{"id":20182,"date":"2024-11-12T11:08:04","date_gmt":"2024-11-12T03:08:04","guid":{"rendered":"https:\/\/dac.nycu.edu.tw\/?post_type=portfolio&#038;p=20182"},"modified":"2026-08-05T19:25:51","modified_gmt":"2026-08-05T11:25:51","slug":"%e9%8d%be%e6%96%87%e8%81%96-%e9%80%80%e4%bc%91%e6%95%99%e6%8e%88","status":"publish","type":"portfolio","link":"https:\/\/dac.nycu.edu.tw\/en\/portfolio-item\/%e9%8d%be%e6%96%87%e8%81%96-%e9%80%80%e4%bc%91%e6%95%99%e6%8e%88\/","title":{"rendered":"Retired Professor Wen-Sheng Chung"},"content":{"rendered":"\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-goc19lu-4971c541d612a6c749278de7986ea4ed\">\n.avia-section.av-goc19lu-4971c541d612a6c749278de7986ea4ed{\nmargin-top:-50px;\nmargin-bottom:0px;\n}\n.avia-section.av-goc19lu-4971c541d612a6c749278de7986ea4ed .av-parallax 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class=\"av-section-color-overlay\"><\/div><div class='container av-section-cont-open' style='height:280px'><main  role=\"main\" itemprop=\"mainContentOfPage\"  class='template-page content  av-content-full alpha units'><div class='post-entry post-entry-type-page post-entry-20182'><div class='entry-content-wrapper clearfix'>\n<div  class='flex_column av-gj0k9gi-bc9c927ca250b980a34cc9cd0b7030f9 av_one_full  avia-builder-el-1  avia-builder-el-no-sibling  first flex_column_div  '     ><p>\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-mseqfsxa-31c3086f7adec567afd907acb3de0325\">\n#top .av-special-heading.av-mseqfsxa-31c3086f7adec567afd907acb3de0325{\npadding-bottom:10px;\ncolor:#ffffff;\n}\nbody .av-special-heading.av-mseqfsxa-31c3086f7adec567afd907acb3de0325 .av-special-heading-tag .heading-char{\nfont-size:25px;\n}\n.av-special-heading.av-mseqfsxa-31c3086f7adec567afd907acb3de0325 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\/>\n<\/p><\/div>\n<\/div><\/div><\/main><!-- close content main element --><\/div><\/div><\/div><div id='after_section_1'  class='main_color av_default_container_wrap container_wrap fullsize'  ><div class='container av-section-cont-open' ><div class='template-page content  av-content-full alpha units'><div class='post-entry post-entry-type-page post-entry-20182'><div class='entry-content-wrapper clearfix'>\n\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-fktbug2-723253b1efdaf0bfecff9c954e91a913\">\n#top .hr.hr-invisible.av-fktbug2-723253b1efdaf0bfecff9c954e91a913{\nheight:5px;\n}\n<\/style>\n<div  class='hr av-fktbug2-723253b1efdaf0bfecff9c954e91a913 hr-invisible  avia-builder-el-5  el_after_av_section  el_before_av_hr  avia-builder-el-first  av-small-hide av-mini-hide'><span class='hr-inner '><span class=\"hr-inner-style\"><\/span><\/span><\/div>\n\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" 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av-doxslgi-0ddd0131975c183999ab1929893d2efd av_two_third  avia-builder-el-9  el_after_av_one_third  el_before_av_hr  flex_column_table_cell av-equal-height-column av-align-middle  '     ><p>\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-d6uc3c2-52dc1bdb201eb7635293dd2da676d4de\">\n#top .av-special-heading.av-d6uc3c2-52dc1bdb201eb7635293dd2da676d4de{\nmargin:0 0 0 0;\npadding-bottom:10px;\ncolor:#005daf;\n}\nbody .av-special-heading.av-d6uc3c2-52dc1bdb201eb7635293dd2da676d4de .av-special-heading-tag .heading-char{\nfont-size:25px;\n}\n.av-special-heading.av-d6uc3c2-52dc1bdb201eb7635293dd2da676d4de .special-heading-inner-border{\nborder-color:#005daf;\n}\n.av-special-heading.av-d6uc3c2-52dc1bdb201eb7635293dd2da676d4de .av-subheading{\nfont-size:15px;\n}\n\n@media only screen and (min-width: 480px) and (max-width: 767px){ \n#top .av-special-heading.av-d6uc3c2-52dc1bdb201eb7635293dd2da676d4de{\nmargin:30px 0 0 0;\n}\n}\n\n@media only screen and (max-width: 479px){ \n#top .av-special-heading.av-d6uc3c2-52dc1bdb201eb7635293dd2da676d4de{\nmargin:30px 0 0 0;\n}\n}\n<\/style>\n<div  class='av-special-heading av-d6uc3c2-52dc1bdb201eb7635293dd2da676d4de av-special-heading-h2 custom-color-heading blockquote modern-quote  avia-builder-el-10  el_before_av_heading  avia-builder-el-first '><h2 class='av-special-heading-tag '  itemprop=\"headline\"  >\u937e\u6587\u8056 Wen-Sheng Chung<\/h2><div class=\"special-heading-border\"><div class=\"special-heading-inner-border\"><\/div><\/div><\/div><br \/>\n\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-mseqg1cd-60a2df9c7cd922e04e406b9b9ba1b51c\">\n#top .av-special-heading.av-mseqg1cd-60a2df9c7cd922e04e406b9b9ba1b51c{\nmargin:0 0 0 0;\npadding-bottom:20px;\ncolor:#005daf;\n}\nbody .av-special-heading.av-mseqg1cd-60a2df9c7cd922e04e406b9b9ba1b51c .av-special-heading-tag .heading-char{\nfont-size:25px;\n}\n.av-special-heading.av-mseqg1cd-60a2df9c7cd922e04e406b9b9ba1b51c .special-heading-inner-border{\nborder-color:#005daf;\n}\n.av-special-heading.av-mseqg1cd-60a2df9c7cd922e04e406b9b9ba1b51c .av-subheading{\nfont-size:15px;\n}\n\n@media only screen and (min-width: 480px) and (max-width: 767px){ \n#top .av-special-heading.av-mseqg1cd-60a2df9c7cd922e04e406b9b9ba1b51c{\nmargin:0 0 0 0;\n}\n}\n\n@media only screen and (max-width: 479px){ \n#top .av-special-heading.av-mseqg1cd-60a2df9c7cd922e04e406b9b9ba1b51c{\nmargin:0 0 0 0;\n}\n}\n<\/style>\n<div  class='av-special-heading av-mseqg1cd-60a2df9c7cd922e04e406b9b9ba1b51c av-special-heading-h3 custom-color-heading blockquote modern-quote  avia-builder-el-11  el_after_av_heading  el_before_av_textblock  title-line'><h3 class='av-special-heading-tag '  itemprop=\"headline\"  >Retired Professor\/Adjunct Professor<\/h3><div class=\"special-heading-border\"><div class=\"special-heading-inner-border\"><\/div><\/div><\/div><br \/>\n<section  class='av_textblock_section av-cgvu482-d5dd7cc5f860cd102b0bfa92435de441 '   itemscope=\"itemscope\" itemtype=\"https:\/\/schema.org\/CreativeWork\" ><div class='avia_textblock link_text'  itemprop=\"text\" ><ul>\n<li>TEL | 03-5712121 #31517<\/li>\n<li>OFFICE | SB R307B<\/li>\n<li>Email | wschung@nycu.edu.tw<\/li>\n<li>Lab TEL | 03-5172121 #56553<\/li>\n<\/ul>\n<\/div><\/section><br \/>\n<div  class='avia-buttonrow-wrap av-msg03oti-6e93bf601a7c4d12205a3dbf9dd086c0 avia-buttonrow-left  avia-builder-el-13  el_after_av_textblock  avia-builder-el-last '>\n\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-msg03nt3-aabffa484971667df42f7ba3086e95cb\">\n#top #wrap_all .avia-button.av-msg03nt3-aabffa484971667df42f7ba3086e95cb{\nmargin-bottom:5px;\nmargin-right:5px;\n}\n#top #wrap_all .avia-button.av-msg03nt3-aabffa484971667df42f7ba3086e95cb:hover{\nopacity:1;\ntransition:all 0.4s ease-in-out;\n}\n<\/style>\n<a href='https:\/\/dac.nycu.edu.tw\/en\/portfolio-item\/adjunct-professor-wen-sheng-chung\/'  class='avia-button av-msg03nt3-aabffa484971667df42f7ba3086e95cb avia-icon_select-no avia-size-medium av-icon-on-hover avia-color-theme-color'  target=\"_blank\"  rel=\"noopener noreferrer\"  aria-label=\"Adjunct Professor Wen-Sheng Chung\"><span class='avia_iconbox_title' >Adjunct Professor Wen-Sheng Chung<\/span><\/a>\n<\/div><\/p><\/div><\/div><!--close column table wrapper. Autoclose: 1 -->\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-c4qty76-f3f75816d4fabcacd2a1dc124daa2066\">\n#top .hr.hr-invisible.av-c4qty76-f3f75816d4fabcacd2a1dc124daa2066{\nheight:30px;\n}\n<\/style>\n<div  class='hr av-c4qty76-f3f75816d4fabcacd2a1dc124daa2066 hr-invisible  avia-builder-el-14  el_after_av_two_third  el_before_av_one_full  av-desktop-hide av-medium-hide'><span class='hr-inner '><span class=\"hr-inner-style\"><\/span><\/span><\/div><\/p>\n<div class='flex_column_table av-bnz6jya-3237b9d875645129c1d5af96f0a0c918 sc-av_one_full av-equal-height-column-flextable'>\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-bnz6jya-3237b9d875645129c1d5af96f0a0c918\">\n.flex_column.av-bnz6jya-3237b9d875645129c1d5af96f0a0c918{\nwidth:100%;\nmargin-left:0;\nborder-radius:0 50px 0 0;\npadding:25px 30px 15px 30px;\nbackground-color:#ffeca0;\n}\n#top .flex_column_table.av-equal-height-column-flextable.av-bnz6jya-3237b9d875645129c1d5af96f0a0c918 .av-flex-placeholder{\nwidth:0%;\n}\n<\/style>\n<div  class='flex_column av-bnz6jya-3237b9d875645129c1d5af96f0a0c918 av_one_full  avia-builder-el-15  el_after_av_hr  el_before_av_one_full  double-line-wy titlebox-mob first flex_column_table_cell av-equal-height-column av-align-top  '     ><style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-b2whvs2-55d64ff42833ee7acb7ba25ae75f1d36\">\n#top .av-special-heading.av-b2whvs2-55d64ff42833ee7acb7ba25ae75f1d36{\npadding-bottom:10px;\n}\nbody .av-special-heading.av-b2whvs2-55d64ff42833ee7acb7ba25ae75f1d36 .av-special-heading-tag .heading-char{\nfont-size:25px;\n}\n.av-special-heading.av-b2whvs2-55d64ff42833ee7acb7ba25ae75f1d36 .av-subheading{\nfont-size:15px;\n}\n<\/style>\n<div  class='av-special-heading av-b2whvs2-55d64ff42833ee7acb7ba25ae75f1d36 av-special-heading-h3 blockquote modern-quote  avia-builder-el-16  avia-builder-el-no-sibling '><h3 class='av-special-heading-tag '  itemprop=\"headline\"  >Education<\/h3><div class=\"special-heading-border\"><div class=\"special-heading-inner-border\"><\/div><\/div><\/div><\/div><\/div><!--close column table wrapper. Autoclose: 1 -->\n<div class='flex_column_table av-auda7mq-4a32e0a73d6ab1afcbbc21ecd4972f20 sc-av_one_full av-equal-height-column-flextable'>\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-auda7mq-4a32e0a73d6ab1afcbbc21ecd4972f20\">\n#top .flex_column_table.av-equal-height-column-flextable.av-auda7mq-4a32e0a73d6ab1afcbbc21ecd4972f20{\nmargin-top:0px;\nmargin-bottom:0px;\n}\n.flex_column.av-auda7mq-4a32e0a73d6ab1afcbbc21ecd4972f20{\nwidth:100%;\nmargin-left:0;\nborder-width:2px;\nborder-color:#ffeca0;\nborder-style:solid;\npadding:30px 30px 30px 30px;\n}\n#top .flex_column_table.av-equal-height-column-flextable.av-auda7mq-4a32e0a73d6ab1afcbbc21ecd4972f20 .av-flex-placeholder{\nwidth:0%;\n}\n<\/style>\n<div  class='flex_column av-auda7mq-4a32e0a73d6ab1afcbbc21ecd4972f20 av_one_full  avia-builder-el-17  el_after_av_one_full  el_before_av_one_full  first flex_column_table_cell av-equal-height-column av-align-top  column-top-margin'     ><section  class='av_textblock_section av-11fn3aa-47fd3084a6ff9f0a7b239019c2c5f4ff '   itemscope=\"itemscope\" itemtype=\"https:\/\/schema.org\/CreativeWork\" ><div class='avia_textblock'  itemprop=\"text\" ><p>1978-1982 Undergraduate (B. Sc.), National Tsing Hua University, Hsinchu<br \/>\n1985-1990, Graduate (Ph. D.), Columbia University, New York, USA<\/p>\n<\/div><\/section><\/div><\/div><!--close column table wrapper. Autoclose: 1 -->\n<div class='flex_column_table av-9w3dcea-60685865e07ea4bf3048cff4fa949060 sc-av_one_full av-equal-height-column-flextable'>\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-9w3dcea-60685865e07ea4bf3048cff4fa949060\">\n.flex_column.av-9w3dcea-60685865e07ea4bf3048cff4fa949060{\nwidth:100%;\nmargin-left:0;\nborder-radius:0 50px 0 0;\npadding:25px 30px 15px 30px;\nbackground-color:#3a4586;\n}\n#top .flex_column_table.av-equal-height-column-flextable.av-9w3dcea-60685865e07ea4bf3048cff4fa949060 .av-flex-placeholder{\nwidth:0%;\n}\n<\/style>\n<div  class='flex_column av-9w3dcea-60685865e07ea4bf3048cff4fa949060 av_one_full  avia-builder-el-19  el_after_av_one_full  el_before_av_one_full  double-line-wy titlebox-mob first flex_column_table_cell av-equal-height-column av-align-top  column-top-margin'     ><style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-9mqt04i-f8c1f30c6c4b0c279c65d3d8889000d6\">\n#top .av-special-heading.av-9mqt04i-f8c1f30c6c4b0c279c65d3d8889000d6{\npadding-bottom:10px;\ncolor:#ffffff;\n}\nbody .av-special-heading.av-9mqt04i-f8c1f30c6c4b0c279c65d3d8889000d6 .av-special-heading-tag .heading-char{\nfont-size:25px;\n}\n.av-special-heading.av-9mqt04i-f8c1f30c6c4b0c279c65d3d8889000d6 .special-heading-inner-border{\nborder-color:#ffffff;\n}\n.av-special-heading.av-9mqt04i-f8c1f30c6c4b0c279c65d3d8889000d6 .av-subheading{\nfont-size:15px;\n}\n<\/style>\n<div  class='av-special-heading av-9mqt04i-f8c1f30c6c4b0c279c65d3d8889000d6 av-special-heading-h3 custom-color-heading blockquote modern-quote  avia-builder-el-20  avia-builder-el-no-sibling '><h3 class='av-special-heading-tag '  itemprop=\"headline\"  >Experiences<\/h3><div class=\"special-heading-border\"><div class=\"special-heading-inner-border\"><\/div><\/div><\/div><\/div><\/div><!--close column table wrapper. Autoclose: 1 -->\n<div class='flex_column_table av-93g2abm-0d30ba6b566581db5c53848512f33cbf sc-av_one_full av-equal-height-column-flextable'>\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-93g2abm-0d30ba6b566581db5c53848512f33cbf\">\n#top .flex_column_table.av-equal-height-column-flextable.av-93g2abm-0d30ba6b566581db5c53848512f33cbf{\nmargin-top:0px;\nmargin-bottom:0px;\n}\n.flex_column.av-93g2abm-0d30ba6b566581db5c53848512f33cbf{\nwidth:100%;\nmargin-left:0;\nborder-width:2px;\nborder-color:#3a4586;\nborder-style:solid;\npadding:30px 30px 30px 30px;\n}\n#top .flex_column_table.av-equal-height-column-flextable.av-93g2abm-0d30ba6b566581db5c53848512f33cbf .av-flex-placeholder{\nwidth:0%;\n}\n<\/style>\n<div  class='flex_column av-93g2abm-0d30ba6b566581db5c53848512f33cbf av_one_full  avia-builder-el-21  el_after_av_one_full  el_before_av_one_full  first flex_column_table_cell av-equal-height-column av-align-top  column-top-margin'     ><style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-8ow94aq-1e2da4e3741f94f66ac731267bfbe819\">\n#top .togglecontainer.av-8ow94aq-1e2da4e3741f94f66ac731267bfbe819 p.toggler{\ncolor:#555555;\nbackground-color:#f8f8f8;\nborder-color:#ffffff;\n}\n#top .togglecontainer.av-8ow94aq-1e2da4e3741f94f66ac731267bfbe819 p.toggler:not(.activeTitle):hover{\nbackground-color:#ffeca0;\n}\n#top .togglecontainer.av-8ow94aq-1e2da4e3741f94f66ac731267bfbe819 p.toggler .toggle_icon{\ncolor:#005daf;\nborder-color:#005daf;\n}\n#top .togglecontainer.av-8ow94aq-1e2da4e3741f94f66ac731267bfbe819 p.toggler .toggle_icon > span{\ncolor:#005daf;\nborder-color:#005daf;\n}\n#top .togglecontainer.av-8ow94aq-1e2da4e3741f94f66ac731267bfbe819 .toggle_wrap .toggle_content{\ncolor:#555555;\nbackground-color:#f8f8f8;\nborder-color:#ffffff;\n}\n<\/style>\n<div  class='togglecontainer av-8ow94aq-1e2da4e3741f94f66ac731267bfbe819 av-minimal-toggle  avia-builder-el-22  avia-builder-el-no-sibling ' >\n<section class='av_toggle_section av-86zn3mq-57d253559b9eb66f7d308560997b7871'  itemscope=\"itemscope\" itemtype=\"https:\/\/schema.org\/CreativeWork\" ><div role=\"tablist\" class=\"single_toggle\" data-tags=\"{All} \"  ><p id='toggle-toggle-id-1' data-fake-id='#toggle-id-1' class='toggler  av-title-above av-inherit-border-color'  itemprop=\"headline\"  role='tab' tabindex='0' aria-controls='toggle-id-1' data-slide-speed=\"200\" data-title=\"Academic Positions\" data-title-open=\"\" data-aria_collapsed=\"Click to expand: Academic Positions\" data-aria_expanded=\"Click to collapse: Academic Positions\">Academic Positions<span class=\"toggle_icon\"><span class=\"vert_icon\"><\/span><span class=\"hor_icon\"><\/span><\/span><\/p><div id='toggle-id-1' aria-labelledby='toggle-toggle-id-1' role='region' class='toggle_wrap  av-title-above'  ><div class='toggle_content invers-color av-inherit-border-color'  itemprop=\"text\" ><p>Adjunct Professor, College of Science, National Yang Ming Chiao Tung University (NYCU) (2026-)<br \/>\nDistinguish Professor, College of Science, National Yang Ming Chiao Tung University (NYCU) (2023-2026)<br \/>\nChairman of the Interdisciplinary Program of College of Science, NYCU (2023-2026)<br \/>\nProfessor, Department of Applied Chemistry, NYCU (2021-2022)<br \/>\nDistinguish Professor, College of Science, National Chiao Tung University (NCTU) (2013-2016)<br \/>\nDirector, Advanced Instrumentation Center, NCTU (2013-2015)<br \/>\nDeputy Dean, College of Science, NCTU (2008-2011)<br \/>\nChairman, Department of Applied Chemistry, NCTU (2006-2008)<br \/>\nProfessor, Department of Applied Chemistry, NCTU (1997-2021)<br \/>\nAssociate Professor, Department of Applied Chemistry, NCTU (1991-1997)<br \/>\nPostdoctoral Research Associate, Department of Chemistry, Yale University (1990-1991)<\/p>\n<\/div><\/div><\/div><\/section>\n<section class='av_toggle_section av-7r5kjwi-b7f60c4fa1ca3ed3b220647637d01a5f'  itemscope=\"itemscope\" itemtype=\"https:\/\/schema.org\/CreativeWork\" ><div role=\"tablist\" class=\"single_toggle\" data-tags=\"{All} \"  ><p id='toggle-toggle-id-2' data-fake-id='#toggle-id-2' class='toggler  av-title-above av-inherit-border-color'  itemprop=\"headline\"  role='tab' tabindex='0' aria-controls='toggle-id-2' data-slide-speed=\"200\" data-title=\"Guest Professorship\" data-title-open=\"\" data-aria_collapsed=\"Click to expand: Guest Professorship\" data-aria_expanded=\"Click to collapse: Guest Professorship\">Guest Professorship<span class=\"toggle_icon\"><span class=\"vert_icon\"><\/span><span class=\"hor_icon\"><\/span><\/span><\/p><div id='toggle-id-2' aria-labelledby='toggle-toggle-id-2' role='region' class='toggle_wrap  av-title-above'  ><div class='toggle_content invers-color av-inherit-border-color'  itemprop=\"text\" ><p>National Science Council, Visiting Professor to Mie University, Japan (2005\/March-2005\/July)<\/p>\n<\/div><\/div><\/div><\/section>\n<section class='av_toggle_section av-75qqmzm-6c5492d6c5519c402c4a9d44b3ba9a74'  itemscope=\"itemscope\" itemtype=\"https:\/\/schema.org\/CreativeWork\" ><div role=\"tablist\" class=\"single_toggle\" data-tags=\"{All} \"  ><p id='toggle-toggle-id-3' data-fake-id='#toggle-id-3' class='toggler  av-title-above av-inherit-border-color'  itemprop=\"headline\"  role='tab' tabindex='0' aria-controls='toggle-id-3' data-slide-speed=\"200\" data-title=\"Past Editorial Board Members\" data-title-open=\"\" data-aria_collapsed=\"Click to expand: Past Editorial Board Members\" data-aria_expanded=\"Click to collapse: Past Editorial Board Members\">Past Editorial Board Members<span class=\"toggle_icon\"><span class=\"vert_icon\"><\/span><span class=\"hor_icon\"><\/span><\/span><\/p><div id='toggle-id-3' aria-labelledby='toggle-toggle-id-3' role='region' class='toggle_wrap  av-title-above'  ><div class='toggle_content invers-color av-inherit-border-color'  itemprop=\"text\" ><p>J. Chinese Chemical Society (Editorial board) 2021-2027<br \/>\nAsian Journal of Organic Chemistry, Wiley (Member of International Editorial Board), 2012-present<br \/>\nFrontiers in Chemistry, Supramolecular Chemistry Section (Associate Editor), 2019-present<\/p>\n<\/div><\/div><\/div><\/section>\n<\/div><\/div><\/div><!--close column table wrapper. Autoclose: 1 -->\n<div class='flex_column_table av-6shjpmq-bfbc67bd4fc37d6179e3239613acda51 sc-av_one_full av-equal-height-column-flextable'>\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-6shjpmq-bfbc67bd4fc37d6179e3239613acda51\">\n.flex_column.av-6shjpmq-bfbc67bd4fc37d6179e3239613acda51{\nwidth:100%;\nmargin-left:0;\nborder-radius:0 50px 0 0;\npadding:25px 30px 15px 30px;\nbackground-color:#ffeca0;\n}\n#top .flex_column_table.av-equal-height-column-flextable.av-6shjpmq-bfbc67bd4fc37d6179e3239613acda51 .av-flex-placeholder{\nwidth:0%;\n}\n<\/style>\n<div  class='flex_column av-6shjpmq-bfbc67bd4fc37d6179e3239613acda51 av_one_full  avia-builder-el-23  el_after_av_one_full  el_before_av_one_full  double-line-wy titlebox-mob first flex_column_table_cell av-equal-height-column av-align-top  column-top-margin'     ><style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-mx52si-d4f89a0a37f18447ea0dd9cf5a684807\">\n#top .av-special-heading.av-mx52si-d4f89a0a37f18447ea0dd9cf5a684807{\npadding-bottom:10px;\n}\nbody .av-special-heading.av-mx52si-d4f89a0a37f18447ea0dd9cf5a684807 .av-special-heading-tag .heading-char{\nfont-size:25px;\n}\n.av-special-heading.av-mx52si-d4f89a0a37f18447ea0dd9cf5a684807 .av-subheading{\nfont-size:15px;\n}\n<\/style>\n<div  class='av-special-heading av-mx52si-d4f89a0a37f18447ea0dd9cf5a684807 av-special-heading-h3 blockquote modern-quote  avia-builder-el-24  avia-builder-el-no-sibling '><h3 class='av-special-heading-tag '  itemprop=\"headline\"  >Honors<\/h3><div class=\"special-heading-border\"><div class=\"special-heading-inner-border\"><\/div><\/div><\/div><\/div><\/div><!--close column table wrapper. Autoclose: 1 -->\n<div class='flex_column_table av-5xine82-d180f892ad7daf3c5c8385e71154eea6 sc-av_one_full av-equal-height-column-flextable'>\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-5xine82-d180f892ad7daf3c5c8385e71154eea6\">\n#top .flex_column_table.av-equal-height-column-flextable.av-5xine82-d180f892ad7daf3c5c8385e71154eea6{\nmargin-top:0px;\nmargin-bottom:0px;\n}\n.flex_column.av-5xine82-d180f892ad7daf3c5c8385e71154eea6{\nwidth:100%;\nmargin-left:0;\nborder-width:2px;\nborder-color:#ffeca0;\nborder-style:solid;\npadding:30px 30px 15px 30px;\n}\n#top .flex_column_table.av-equal-height-column-flextable.av-5xine82-d180f892ad7daf3c5c8385e71154eea6 .av-flex-placeholder{\nwidth:0%;\n}\n<\/style>\n<div  class='flex_column av-5xine82-d180f892ad7daf3c5c8385e71154eea6 av_one_full  avia-builder-el-25  el_after_av_one_full  el_before_av_one_full  first flex_column_table_cell av-equal-height-column av-align-top  column-top-margin'     ><section  class='av_textblock_section av-5ajqg4i-4a90982f91d0cde94e5860f15aaddc42 '   itemscope=\"itemscope\" itemtype=\"https:\/\/schema.org\/CreativeWork\" ><div class='avia_textblock'  itemprop=\"text\" ><ul>\n<li>University Excellent Teaching Award in 2000, NCTU, Taiwan<\/li>\n<li>University Outstanding Teaching Award in 2003, NCTU, Taiwan<\/li>\n<li>Guest Editor of J. Chinese Chem. Soc., 2006, memorial issue for Prof. T.-I. Ho<\/li>\n<li>Asian Core Program Lectureship Award to Japan, the 2nd International Conference on Cutting-Edge Organic Chemistry in Asia, September 5th, 2007, Pusan, Korea<\/li>\n<li>Asian Core Program Lectureship Award to Korea, the 4th International Conference on Cutting-Edge Organic Chemistry in Asia, Dec 2nd, 2009 Bangkok, Thailand<\/li>\n<li>Co-organizer of the Organic Symposium No. 47, International Chemical Congress of Pacific Basin Societies (PacifiChem 2010), Hawaii, USA<\/li>\n<li>Asian Core Program Lectureship Award to Singapore, the 6th International Conference on Cutting-Edge Organic Chemistry in Asia, Dec 14th, 2011 Hong-Kong, China<\/li>\n<li>University Outstanding Teaching Award in 2012, NCTU, Taiwan<\/li>\n<li>Organizer of the 7th Taiwan-Japan Bilateral Symposium on the Architecture of Functional Organic Molecules, October 21-24, 2012, Hsinchu, Taiwan<\/li>\n<li>Co-organizer of the Organic Symposium No. 71, \u201cSymposium on Molecular and Supramolecular Photochemistry\u201d, International Chemical Congress of Pacific Basin Societies (PacifiChem 2015), Hawaii, USA<\/li>\n<li>Organizer of the 13th International Symposium on Organic Reactions (ISOR), October 24-26, 2018, Hsinchu, Taiwan<\/li>\n<li>University Outstanding Teaching Award in 2021, NYCU, Taiwan<\/li>\n<li>Elected as an Honorary member of University Teaching Professors, 2021<\/li>\n<\/ul>\n<\/div><\/section><\/div><\/div><!--close column table wrapper. Autoclose: 1 -->\n<div class='flex_column_table av-4qv6h36-054eed8db7b41085062e5b3af42512d5 sc-av_one_full av-equal-height-column-flextable'>\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-4qv6h36-054eed8db7b41085062e5b3af42512d5\">\n.flex_column.av-4qv6h36-054eed8db7b41085062e5b3af42512d5{\nwidth:100%;\nmargin-left:0;\nborder-radius:0 50px 0 0;\npadding:25px 30px 15px 30px;\nbackground-color:#3a4586;\n}\n#top .flex_column_table.av-equal-height-column-flextable.av-4qv6h36-054eed8db7b41085062e5b3af42512d5 .av-flex-placeholder{\nwidth:0%;\n}\n<\/style>\n<div  class='flex_column av-4qv6h36-054eed8db7b41085062e5b3af42512d5 av_one_full  avia-builder-el-27  el_after_av_one_full  el_before_av_one_full  double-line-wy titlebox-mob first flex_column_table_cell av-equal-height-column av-align-top  column-top-margin'     ><style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-4hfxole-eed35ea47d91c46a9b3c19ca5577a7c0\">\n#top .av-special-heading.av-4hfxole-eed35ea47d91c46a9b3c19ca5577a7c0{\npadding-bottom:10px;\ncolor:#ffffff;\n}\nbody .av-special-heading.av-4hfxole-eed35ea47d91c46a9b3c19ca5577a7c0 .av-special-heading-tag .heading-char{\nfont-size:25px;\n}\n.av-special-heading.av-4hfxole-eed35ea47d91c46a9b3c19ca5577a7c0 .special-heading-inner-border{\nborder-color:#ffffff;\n}\n.av-special-heading.av-4hfxole-eed35ea47d91c46a9b3c19ca5577a7c0 .av-subheading{\nfont-size:15px;\n}\n<\/style>\n<div  class='av-special-heading av-4hfxole-eed35ea47d91c46a9b3c19ca5577a7c0 av-special-heading-h3 custom-color-heading blockquote modern-quote  avia-builder-el-28  avia-builder-el-no-sibling '><h3 class='av-special-heading-tag '  itemprop=\"headline\"  >Publication<\/h3><div class=\"special-heading-border\"><div class=\"special-heading-inner-border\"><\/div><\/div><\/div><\/div><\/div><!--close column table wrapper. Autoclose: 1 -->\n<div class='flex_column_table av-3t07l4y-65e1e188b00710cce88eeb763e68ad47 sc-av_one_full av-equal-height-column-flextable'>\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-3t07l4y-65e1e188b00710cce88eeb763e68ad47\">\n#top .flex_column_table.av-equal-height-column-flextable.av-3t07l4y-65e1e188b00710cce88eeb763e68ad47{\nmargin-top:0px;\nmargin-bottom:0px;\n}\n.flex_column.av-3t07l4y-65e1e188b00710cce88eeb763e68ad47{\nwidth:100%;\nmargin-left:0;\nborder-width:2px;\nborder-color:#3a4586;\nborder-style:solid;\npadding:30px 30px 30px 30px;\n}\n#top .flex_column_table.av-equal-height-column-flextable.av-3t07l4y-65e1e188b00710cce88eeb763e68ad47 .av-flex-placeholder{\nwidth:0%;\n}\n<\/style>\n<div  class='flex_column av-3t07l4y-65e1e188b00710cce88eeb763e68ad47 av_one_full  avia-builder-el-29  el_after_av_one_full  el_before_av_one_full  first flex_column_table_cell av-equal-height-column av-align-top  column-top-margin'     ><style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-17exia-113bc4493a6f53e592af90c17fb2781d\">\n#top .togglecontainer.av-17exia-113bc4493a6f53e592af90c17fb2781d p.toggler{\ncolor:#555555;\nbackground-color:#f8f8f8;\nborder-color:#ffffff;\n}\n#top .togglecontainer.av-17exia-113bc4493a6f53e592af90c17fb2781d p.toggler:not(.activeTitle):hover{\nbackground-color:#ffeca0;\n}\n#top .togglecontainer.av-17exia-113bc4493a6f53e592af90c17fb2781d p.toggler .toggle_icon{\ncolor:#005daf;\nborder-color:#005daf;\n}\n#top .togglecontainer.av-17exia-113bc4493a6f53e592af90c17fb2781d p.toggler .toggle_icon > span{\ncolor:#005daf;\nborder-color:#005daf;\n}\n#top .togglecontainer.av-17exia-113bc4493a6f53e592af90c17fb2781d .toggle_wrap .toggle_content{\ncolor:#555555;\nbackground-color:#f8f8f8;\nborder-color:#ffffff;\n}\n<\/style>\n<div  class='togglecontainer av-17exia-113bc4493a6f53e592af90c17fb2781d av-minimal-toggle  avia-builder-el-30  avia-builder-el-no-sibling ' >\n<section class='av_toggle_section av-2x51kqq-c3598708e6d001bc5c80fc56b945ceb4'  itemscope=\"itemscope\" itemtype=\"https:\/\/schema.org\/CreativeWork\" ><div role=\"tablist\" class=\"single_toggle\" data-tags=\"{All} \"  ><p id='toggle-toggle-id-4' data-fake-id='#toggle-id-4' class='toggler  av-title-above av-inherit-border-color'  itemprop=\"headline\"  role='tab' tabindex='0' aria-controls='toggle-id-4' data-slide-speed=\"200\" data-title=\"Publication List: 1-40\" data-title-open=\"\" data-aria_collapsed=\"Click to expand: Publication List: 1-40\" data-aria_expanded=\"Click to collapse: Publication List: 1-40\">Publication List: 1-40<span class=\"toggle_icon\"><span class=\"vert_icon\"><\/span><span class=\"hor_icon\"><\/span><\/span><\/p><div id='toggle-id-4' aria-labelledby='toggle-toggle-id-4' role='region' class='toggle_wrap  av-title-above'  ><div class='toggle_content invers-color av-inherit-border-color'  itemprop=\"text\" ><ol>\n<li>N. J. Turro,* W.-S. Chung, and M. Okamoto <em>J. Photochem. Photobiol. A<\/em>. <strong>1988<\/strong>, <em>45<\/em>, 17. \u201cPressure Effects on the Photocycloaddition of 2-Adamantanone with Fumaronitrile\u201d.<\/li>\n<li>W.-S. Chung, N. J. Turro,* S. Srivastava, H. Li, and W. J. le Noble* <em>J. Am. Chem. Soc<\/em>. <strong>1988<\/strong>, <em>110<\/em>, 7882. \u201cHyperconjucation as a Factor in Face Selectivies.<\/li>\n<li>W.-S. Chung, N. J. Turro,* J. Mertes, and J. Mattay <em>J. Org. Chem<\/em>. <strong>1989<\/strong>, <em>54<\/em>, 4881. \u201cPressure-Induced Diastereoselectivity in Photoinduced Diels-Alder Reactions\u201d.<\/li>\n<li>W.-S. Chung, N. J. Turro,* J. Silver, and W. J. le Noble* <em>J. Am. Chem. Soc.<\/em> <strong>1990<\/strong>, <em>112<\/em>, 1202. \u201cModification of Face Selectivity by Inclusion in Cyclodextrins\u201d.<\/li>\n<li>W.-S. Chung, N. J. Turro,* S. Srivastava, H. Li, and W. J. le Noble* <em>J. Org. Chem<\/em>. <strong>1991<\/strong>, <em>56<\/em>, 5020. \u201cStereochemistry of Photocycloaddition of (E)-1,2-Dicyano- and (Z)-1,2-Diethoxyethylene to 5-Substituted Adamantanones\u201d.<\/li>\n<li>W.-S. Chung, N. J. Turro,* I. R. Gould,* and S. Farid* <em>J. Phys. Chem<\/em>. <strong>1991<\/strong>, <em>95<\/em>, 7752. \u201cEffects of External Pressure on Photoinduced Electron-Transfer Reactions in the Marcus Inverted Region\u201d.<\/li>\n<li>W.-S. Chung, \u201c(I) Pressure as a Tool in the Study of Photoinduced Electron-Transfer, Energy-Transfer and Cycloaddition Reactions, (II) The Influence of Electronic Effects and Inclusion in Cyclodextrins on the Face Selectivities of Photoinduced Oxetane Formation of 5-Substituted Adamantan-2-ones\u201d, Ph. D. Thesis, Columbia University, 1990.<\/li>\n<li>W.-S. Chung,* N.-J. Wang, Y.-D. Liu, Y.-J. Leu and M. Y.-N Chiang, <em>J. Chem. Soc. Perkin Trans. 2<\/em>, <strong>1995<\/strong>, 307.<\/li>\n<li>W.-S. Chung,* Y.-D. Liu and N.-J. Wang, <em>J. Chem. Soc. Perkin Trans. 2<\/em>. <strong>1995<\/strong>, 581. \u201cFace Selectivity in the Paterno-Buchi Reactions of Methacrylonitrile to 5-Substituted Adamantan-2-ones\u201d.<\/li>\n<li>W.-S. Chung,* and J.-Y. Wang, <em>J. Chem. Soc. Chem. Commun<\/em>. <strong>1995<\/strong>, 971, \u201cControl of Regio-selectivity in the Diels-Alder Reactions of Alkyl-substituted 1,4-Benzoquinones by beta-Cyclodextrin and its Derivatives\u201d.<\/li>\n<li>W.-S. Chung,* W.-J. Lin, W.-D. Liu and L.-G. Chen, <em>J. Chem. Soc. Chem. Commun<\/em>. <strong>1995<\/strong>, 2537. \u201cSynthesis of Furan-, Thiophene- and Pyrrole-fused Sultines and their Application in Diels-Alder Reactions\u201d.<\/li>\n<li>S,-H. Tsai, W.-S. Chung* and H.-J. Wu,* <em>J. Chin. Chem. Soc<\/em>. <strong>1996<\/strong>, <em>43<\/em>, 281. \u201cStereochemistry of the Diels-Alder Reaction between (E)-gamma-Oxo-alpha, beta-unsaturated Thioesters with Cyclopentadiene\u201d.<\/li>\n<li>H.-J. Wu,* S,-H. 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Perkin Trans. 2<\/em> <strong>1997<\/strong>, 553. \u201cFace Selectivity in the Photocycloaddition Reactions of Acrylonitrile to 5-Substituted Adamantan-2-ones and Pyrolysis of the Products to Methyleneadamantanes\u201d.<\/li>\n<li>W.-S. Chung* and J.-H. Liu <em>Chem. Commun<\/em>. <strong>1997<\/strong>, 205. \u201cQuinoxalino-fused Sultines and their Application in Diels-Alder Reactions\u201d.<\/li>\n<li>W.-S. Chung* and C.-C. Ho <em>Chem. Commun<\/em>. <strong>1997<\/strong>, 317. \u201cThe Photochemistry of Acetone in the Presence of Exocyclic Olefins: An unexpected Competition between Photo-Conia and Paterno-Buchi Reactions\u201d.<\/li>\n<li>L. C. Bush, R. B. Heath, X.-W. Feng, P. A. Wang, L. Maksimovic, A. I. Song, W.-S. Chung, A. B. Berinstain, J. C. Scaiano, J. A. Berson* <em>J. Am. Chem. Soc<\/em>. <strong>1997<\/strong>, <em>119<\/em>, 1406. \u201cTuning the Singlet-Triplet Energy Gap in a Non-Kekule\u2019 Series by Designed Structural Variation. The Singlet States of N-Substituted-3,4-dimethylenepyrrole Biradicals\u201d.<\/li>\n<li>W.-S. Chung,* T.-L. Tsai, C.-C. Ho, M. Y. N. Chiang and W. J. le Noble,<em> J. Org. Chem<\/em>. <strong>1997<\/strong>, <em>62<\/em>, 4672. \u201cFace Selectivity in the 1,3-Dipolar Cycloaddition Reactions of Benzonitrile Oxide with 5-Substituted Adamantan-2-thiones and 2-Methyleneadamantanes\u201d.<\/li>\n<li>T.-L. Tsai, W.-C. Chen, C.-H. Yu, W. J. le Noble and W.-S. Chung* <em>J. Org. Chem.<\/em> <strong>1999<\/strong>, <em>64<\/em>, 1099. \u201cTemperature and Para-substituent Effects on the Face Selectivity of 1,3-Dipolar Cycloaddition Reactions of Benzonitrile Oxides with 5-Substituted Adamantan-2-thiones, N-benzyladamantyl-2-imines and 2-Methyleneadamantanes\u201d.<\/li>\n<li>C,-M. Shu, W.-S. Chung,* S.-H. Wu, Z.-C. Ho and L.-G. Lin,* <em>J. Org. Chem<\/em>. <strong>1999<\/strong>, <em>64<\/em>, 2673. \u201cSynthesis of Calix[4]arenes with four different \u201cLower Rim Substituents\u201d.<\/li>\n<li>M. Kaselj; W.-S. Chung and W. J. le Noble,* <em>Chem. Rev<\/em>. <strong>1999<\/strong>, <em>99<\/em>, 1387-1414 (May issue) \u201cFace Selectivity in Addition and Elimination in Sterically Unbiased Systems\u201d.<\/li>\n<li>M.-D. Su,* H.-Y. Liao, W.-S. Chung* and S.-Y. Chu,* <em>J. Org. Chem.<\/em> <strong>1999<\/strong>, <em>64<\/em>, 6710. \u201cGas-Phase Cycloadditions of 16-Electron 1,3-Dipoles with Ethylene. A Density Functional and CCSD(T) Study\u201d.<\/li>\n<li>J.-H. Liu, A.-T. Wu, M.-H. Huang, C.-W. Wu and W.-S. Chung,* <em>J. Org. Chem<\/em>. <strong>2000<\/strong>, <em>65<\/em>, 3395, \u201cThe Syntheses of Pyrazino-Containing Sultines and Their Application in Diels-Alder Reactions with Electron-Poor Olefins and [60]Fullerene\u201d.<\/li>\n<li>C.-M. Shu, W.-L. Lin, G.-H. Lee, S.-M. Peng and W.-S. Chung,* <em>J. Chinese Chem. Soc.<\/em> <strong>2000<\/strong>, <em>47<\/em>, 173, \u201cCalix[4]arenes with a Lid in their Upper Rims: 1,3-Dipolar Cycloaddition Reactions of Benzonitrile Oxides with 5-Allyl-, 5,11- and 5,17-Diallylcalix[4]arenes\u201d.<\/li>\n<li>H.-Y. Liao, M.-D. Su,* W.-S. Chung, S.-Y. Chu, <em>Int. J. Quantum Chem<\/em>. <strong>2001<\/strong>, <em>83<\/em>, 318. \u201cDensity Functional Study of the Relative Reactivity in the Concerted 1,3-Dipolar Cycloaddition of Nitrile Ylide to Disubstituted Ethylenes\u201d.<\/li>\n<li>A.-T. Wu, W.-D. Liu, and W.-S. Chung,* <em>J. Chinese Chem. Soc<\/em>. <strong>2002<\/strong>, <em>49<\/em>, 77, \u201cThe Synthesis of Naphthosultine and Benzodisultines and their Pyrolysis with Dienophiles: Studies on o-Naphthoquinodimethane and Bis-o-quinodimethane\u201d.<\/li>\n<li>W.-D. Liu, C.-C. Chi, I.-F. Pai, A.-T. Wu, and W.-S. Chung,*<em> J. Org. Chem<\/em>. <strong>2002<\/strong>, <em>67<\/em>, 9267, \u201cThe Synthesis of 2,5-Disubstituted-thienosultines and their Thermal Reactions with Dienophiles and Nucleophiles\u201d.<\/li>\n<li>W.-S. Li, W.-S. Chung,* and I. Chao,* <em>Chem. Eur. J<\/em>. <strong>2003<\/strong>, <em>9<\/em>, 951, \u201cA Computational Study of Regioselectivity in a Cyclodextrin Mediated Diels-Alder Reaction: Revelation of the Importance of Shallow Binding and Multiple Binding Modes\u201d.<\/li>\n<li>Chu, J.-H.; Li, W.-S.; Ito, C.;* Chung, W.-S.* <em>Tetrahedron<\/em>, <strong>2004<\/strong>, <em>60<\/em>, 9493, \u201cFace Selectivity in the Reactions of 2,4-Disubstituted Adamantanes and Their Modification by Inclusion in Beta-Cyclodextrin Solutions\u201d.<\/li>\n<li>Chi, C.-C.; Pai, I.-F; Chung, W.-S.* <em>Tetrahedron<\/em>, <strong>2004<\/strong>, <em>60<\/em>, 10869, \u201cThermal and Microwave Assisted Diels-Alder Reactions of 2,5-Disubstituted Thienosultines with [60]Fullerene\u201d.<\/li>\n<li>Tang, K.-C.; Lee, S.-J.; Chi, S.-H.; Lu, K.-L; Chen, W.-C.; Yu, C.-h.; Chen, I.-C.;* Wu, S.-L.; Chen, C.-C.; Liu, W.-D.; Chen, L.-J.; Wang, N.-S.* Chung, W.-S.*<em> J. Photochem. Photobiol. A<\/em>, <strong>2005<\/strong>, <em>170<\/em>, 69-81, \u201cPhotochemistry and Photodissociation of Benzosultine and Naphthosultine: Electronic Relaxation of Sultines and Kinetics and Theoretical Studies of Fragment o-Quninodimethanes\u201d.<\/li>\n<li>Kao, T.-L.; Wang, C.-C.; Pan, Y.-T.; Shiao, Y.-J.; Yen, J.-Y.; Shu, C.-M.; Lee, G.-H.; Peng, S.-M.; Chung, W.-S.* <em>J. Org. Chem<\/em>. <strong>2005<\/strong>, 67, 2912, \u201cUpper Rim Allyl and Arylazo Coupled Calix[4]arenes as Highly Sensitive Chromogenic Sensors for Hg+2 Ion\u201d.<\/li>\n<li>Chu, J.-H; Li, W.-S.; Chao, I.;* Lee, G.-H.; Chung, W.-S.* <em>Tetrahedron<\/em>, <strong>2006<\/strong>, <em>62<\/em>, 7380-7389 \u201cRegio Selectivity in the 1,3-Dipolar Cycloaddition of Adamantylidene- fulvene and Its Modification by Inclusion in Cyclodextrins Solutions\u201d.<\/li>\n<li>Senthilvelan, A.; Lee, G.-H.; Chung, W.-S.* <em>Tetrahedron Lett.<\/em> <strong>2006<\/strong>, <em>47<\/em>, 7179-7183. \u201cA Novel Photoinduced Ring Opening and Isomerization of Adamantane-2-spiroisoxazolines Using Mo(CO)6\u201d.<\/li>\n<li>Shiao, Y.-J.; Chiang, P.-J.; Senthilvelan, A.; Tsai, M.-T.; Lee, G.-H.; Chung, W.-S.* <em>Tetrahedron Lett<\/em>. <strong>2006<\/strong>, <em>47<\/em>, 8383-8386. \u201cCapping the upper and lower rims of calix[4]arenes by aryl dinitrile oxide reactions\u201d.<\/li>\n<li>Senthilvelan, A.; Tsai, M.-T.; Chang, K.-C.; Chung, W.-S.* <em>Tetrahedron Lett<\/em>. <strong>2006<\/strong>, <em>47<\/em>, 9077-9081. \u201cMo(CO)6-mediated synthesis of calix[4]arenes carrying beta-hydroxy ketones or alpha,beta-unsaturated-beta-amino ketones\u201d.<\/li>\n<li>Ho, I-T.; Lee, G.-H.; Chung, W.-S.* \u201cSynthesis of upper-rim allyl and p-methoxyphenylazocalix[4]arenes and their efficiencies in chromogenic sensing of Hg+2 Ion\u201d, <em>J. Org. Chem.<\/em> <strong>2007<\/strong>, 72, 2434.<\/li>\n<li>Huang, C.-H.; Chang, Y.-H.; Lin, H.-K.; Pen, C.-W.; Chung, W.-S.; Lee, C.-Y.;* Chiu, H.-T.* \u201cPhase Segregation Assisted Morphology Sculpting: Growth of Graphite and Silicon Crystals via Vapor-Solid Reactions\u201d, <em>J. Phys. Chem. C<\/em> <strong>2007<\/strong>, <em>111<\/em>, 4138.<\/li>\n<\/ol>\n<\/div><\/div><\/div><\/section>\n<section class='av_toggle_section av-2gxghky-ce0f9b49fadc75c2631063fa33bff503'  itemscope=\"itemscope\" itemtype=\"https:\/\/schema.org\/CreativeWork\" ><div role=\"tablist\" class=\"single_toggle\" data-tags=\"{All} \"  ><p id='toggle-toggle-id-5' data-fake-id='#toggle-id-5' class='toggler  av-title-above av-inherit-border-color'  itemprop=\"headline\"  role='tab' tabindex='0' aria-controls='toggle-id-5' data-slide-speed=\"200\" data-title=\"Publication List: 41-80\" data-title-open=\"\" data-aria_collapsed=\"Click to expand: Publication List: 41-80\" data-aria_expanded=\"Click to collapse: Publication List: 41-80\">Publication List: 41-80<span class=\"toggle_icon\"><span class=\"vert_icon\"><\/span><span class=\"hor_icon\"><\/span><\/span><\/p><div id='toggle-id-5' aria-labelledby='toggle-toggle-id-5' role='region' class='toggle_wrap  av-title-above'  ><div class='toggle_content invers-color av-inherit-border-color'  itemprop=\"text\" ><ol>\n<li>Chang, K.-C.; Su, I.-H.; Senthilvelan, A.; Chung, W.-S.* <em>Org. Lett.<\/em> <strong>2007<\/strong>, <em>9<\/em>, 3363-3366. \u201cTriazole-Modified Calix[4]crown as a Novel Fluorescent On-Off Switchable Chemosensor\u201d.<\/li>\n<li>Chang, K.-C.; Su, I.-H.; Lee, G.-H.; Chung, W.-S.* <em>Tetrahedron Lett.<\/em> <strong>2007<\/strong>, <em>48<\/em>, 7274-7278. \u201cTriazole- and Azo-coupled Calix[4]arene as a Highly Sensitive Chromogenic Sensor for Ca2+ and Pb2+ Ions\u201d.<\/li>\n<li>Chang, K.-C.; Luo, L.-Y.; Diau, E. W.-G.; Chung, W.-S.* \u201cHighly Selective Sensing of Cu2+ Ion by an Arylisoxazole Modified Calix[4]arene\u201d, <em>Tetrahedron Lett<\/em>. <strong>2008<\/strong>, <em>49<\/em>, 5013-5016.<\/li>\n<li>Hung, H.-C.; Cheng, C.-W.; Ho, I.-T.; Chung, W.-S.* \u201cDual-mode recognition of transition metal ions by bis-triazoles chained pyrenes\u201d, <em>Tetrahedron Lett<\/em>. <strong>2009<\/strong>, <em>50<\/em>, 302-305.<\/li>\n<li>Senthilvelan, A.; Ho, I.-T.; Chang, K.-C.; Lee, G.-H.; Liu, Y.-H.; Chung, W.-S.* \u201cCooperative Recognition of a Copper Cation and Anion by a Calix[4]arene Substituted at the Lower Rim by a Beta-Amino-alpha,beta-Unsaturated Ketone\u201c, <em>Chem. Eur. J<\/em>. <strong>2009<\/strong>, <em>15<\/em>, 6152-6160.<\/li>\n<li>Chen, Y.-J.; Chung, W.-S.* \u2018Tetrazoles and para-Substituted-phenylazo Coupled Calix[4]arenes as Highly Sensitive Chromogenic sensors for Ca2+\u2019, <em>Eur. J. Org. Chem<\/em>. <strong>2009<\/strong>, 4770-4776.<\/li>\n<li>Hung, H.-C.; Cheng, C.-W.; Wang, Y.-Y.; Cheng, Y.-J.; Chung, W.-S.* \u201cHighly Selective Fluorescence Sensors for Hg2+ and Ag+ Based on Bistriazole Coupled Polyoxyethylenes in MeOH Solution\u201d, <em>Eur. J. Org. Chem<\/em>. <strong>2009<\/strong>, 6360-6366.<\/li>\n<li>Chen, Y.-J.; Hung, H.-C.; Sha, C.-K.*; Chung, W.-S.* \u201cPhotochemistry of Benzene and Quinoxaline Fused Delta2-1,2,3-triazolines and Their Trapping Products\u201c, <em>Tetrahedron<\/em>, <strong>2010<\/strong>, <em>66<\/em>, 176-182.<\/li>\n<li>Luo, J.; Shen, L.-C.; Chung, W.-S.* \u201cInherently Chiral Biscalix[4]arenes: Design and Syntheses\u201d, <em>J. Org. Chem<\/em>. <strong>2010<\/strong>, <em>74<\/em>, 464-467.<\/li>\n<li>Chang, K.-C.; Su, I.-H.; Wang, Y.-Y.; Chung, W.-S.* \u201cA Bifunctional Chromogenic Calix[4]arene Chemosensor for Both Cations and Anions: a Potential Ca2+ and F\uf02d Switched INHIBIT Logic Gate with a YES Logic Function\u201d, <em>Eur. J. Org. Chem<\/em>. <strong>2010<\/strong>, 4700-4704.<\/li>\n<li>Ho, I.-T.; Chu, J.-H.; Chung, W.-S.* \u201cCalix[4]arenes with Lower-rim Beta- Amino-alpha, beta-Unsaturated Ketones Containing bis-Chelating Sites as a Highly Selective Fluorescence Turn-On Chemosensor for Cu(II) Ions\u201d, <em>Eur. J. Org. Chem<\/em>. <strong>2011<\/strong>, 1472-1481.<\/li>\n<li>Chanda, K.; Maiti, B.; Chung, W.-S.*, Sun, C.-M.* \u201cNovel Approach towards 2-Substituted Aminobenzimidazoles on Imidazolium Ion Tag under Focused Microwave Irradiation\u201d, <em>Tetrahedron<\/em> <strong>2011<\/strong>, <em>67<\/em>, 6214-6220.<\/li>\n<li>Wang, N.-J.; Sun, J.-M.*; Chung, W.-S.* \u201cA specific and ratiometric chemosensor for Hg2+ based on triazole coupled ortho-methoxyphenylazocalix[4]arene\u201d, <em>Tetrahedron<\/em> <strong>2011<\/strong>, <em>67<\/em>, 8131-8139.<\/li>\n<li>Ho, I.-T.; Haung, K.-C.; Chung, W.-S.* \u201c1,3-Alternate Calix[4]arene as a Homobinuclear Ditopic Fluorescent Chemosensor for Ag+ Ions\u201d, An invited contribution to the special issue on 10th Anniversary of Click Chemistry. <em>Chem. Asian J.<\/em> <strong>2011<\/strong>, <em>6<\/em>, 2738-2746.<\/li>\n<li>Chiang, S.-Y.;* Lee, P.-Y.; Lai, M.-T.; Shen, L.-C.; Chung, W.-S.; Huang, H.-F.; Wu, K.-y.; Wu, H.-C. \u201cSafrole-2\u2019,3\u2019-oxide Induces Cytotoxic and Genotoxic Effects in HepG2 Cells and in Mice\u201d, <em>Mutat. Res. Gen. Tox. En<\/em>. <strong>2011<\/strong>, <em>726<\/em>, 234-241.<\/li>\n<li>Shen, L.-C.; Chiang, S.-Y.; Ho, I-T.; Wu, K.-Y.*; Chung, W.-S.* \u201cSynthesis and Characterization of Adducts Formed in the Reactions of Safrole-2\u2019,3\u2019-oxide with 2\u2019-Deoxyadenosine, Adenine, and Calf Thymus DNA\u201d, <em>Eur. J. Org. Chem<\/em>. <strong>2012<\/strong>, 792-800.<\/li>\n<li>Tsai, C.-C.; Ho, I-T.; Chu, J.-H.; Shen, L.-C.; Huang, S.-L.; Chung, W.-S.* \u201cSynthesis of 9,10-Bis-ketoenaminoanthryl and 9,10-Bis-isoxazolylanthryl Linked Biscalix[4]arenes: Atropisomers and Molecular Recognitions\u201d, <em>J. Org. Chem<\/em>. <strong>2012<\/strong>, <em>77<\/em>, 2254-2262.<\/li>\n<li>Barve, I. J.; Chen, C.-Y.; Salunke, D. B.; Chung, W.-S.*; Sun, C.-M.* \u201cDesign and Synthesis of New Biprivileged Molecular Scaffolds: Indolo-Fused Benzodiazepinyl\/quinoxalinyl benzimidazoles\u201d, <em>Chem. Asian J<\/em>. <strong>2012<\/strong>, 7, 1684-1690.<\/li>\n<li>Shen, L.-C.; Chiang, S.-Y.; Lin, M.-H.; Chung, W.-S.*; Wu, K.-Y.* \u201cIn vivo Formation of N7-Guanine DNA Adduct by Safrole 2\u2019,3\u2019-oxide in Mice\u201d, <em>Toxicol. Lett<\/em>. <strong>2012<\/strong>, <em>213<\/em>, 309-315.<\/li>\n<li>Wang, N.-J.; Sun, J.-M.*; Chung, W.-S.* \u201cA Highly Selective Fluorescent Chemosensor for Ag+ Based on Calix[4]arene with Lower-rim Proximal Triazolylpyrenes\u201d, <em>Sensors &amp; Actuators B<\/em> <strong>2012<\/strong>, <em>171<\/em>&#8211;<em>172<\/em>, 984-993.<\/li>\n<li>Chung, T.-W. Chen, C.-H.; Lin, C.-C.;* Wu, H.-J.; Sun, C.-M.*; Chung, W.-S.* \u201cExploring a Sulfone Linker Utilizing Trimethyl Aluminum as a Cleavage Reagent: Solid-Phase Synthesis of Sulfonamides and Ureas\u201d, <em>Mol. Divers<\/em> <strong>2012<\/strong>, <em>16<\/em>, 463-476.<\/li>\n<li>Ho, I-T.; Lai, T.-L.; Wu, T.-T.; Tsai, M.-T.; Wu, C.-M.; Lee, G.-H.; Chung, W.-S.*, \u201cDesign and Synthesis of Triazolyl Coumarin as a Selective Fluorescent Chemosensor for Hg2+\u201d, <em>Analyst<\/em> <strong>2012<\/strong>, <em>137<\/em>, 5770-5776.<\/li>\n<li>Su, H.-L. Su; Lee, Y.-P.; Hung, H.-Y.; Lee, C.-Y.; Chung, W.-S.; Hsieh, Y.-Z., \u201cAnalysis of Calix[4]arenes Using Nonaqueous Capillary Electrophoresis\u201d, <em>J. Chin. Chem. Soc<\/em>. <strong>2013<\/strong>, <em>60<\/em>, 113-119.<\/li>\n<li>Tsai, C.-C.; Chang, K.-C. ; Ho, I.-T.; Chu, J.-H.; Cheng, Y.-T.; Shen, L.-C.; Chung, W.-S.*, \u201cEvolution of Nano- to Microsized Spherical Assemblies of Fluorogenic Biscalix[4]arenes into Supramolecular Organogels\u201d, <em>Chem. Commun<\/em>. <strong>2013<\/strong>, <em>49<\/em>, 3037-3039.<\/li>\n<li>Tsai, C.-C.; Cheng, Y.-T.; Shen, L.-C.; Chang, K.-C.; Ho, I.-T.; Chu, J.-H.; Chung, W.-S.*, \u201cBiscalix[4]arene Derivatives As a Very Efficient Phase Selective Gelator for Oil Spill Recovery\u201d, <em>Org. Lett<\/em>. <strong>2013<\/strong>, <em>15<\/em>, 5830-5833.<\/li>\n<li>Chang, Y.-Y.; Ho, I.-T.; Ho, T.-L.*; Chung, W.-S.* \u201cThe Synthesis of Rigid Polycyclic Structures for the Study of Diatropic or Steric Effects of a Phenyl Ring on CF Bond\u201d, <em>J. Org. Chem<\/em>. <strong>2013<\/strong>, <em>78<\/em>, 12790-12794.<\/li>\n<li>Hung, H.-C.; Chang, Y.-Y.; Luo, L.; Hung, C.-H.; Diau, E. W.-G.*; Chung, W.-S.* \u201cDifferent Sensing Modes of Fluoride and Acetate Based on a Calix[4]arene with 25,27-Bistriazolylmethylpyrenylacetamides\u201d, <em>Photochem. Photobiol. Sci<\/em>. <strong>2014<\/strong>, <em>13<\/em>, 370-379.<\/li>\n<li>Chang, Y.-Y.; Ho, T.-L.;* Chung, W.-S.* \u201cDeformative Transition of Menschutkin Reaction and Helical Atropisomers in a Congested Polyheterocyclic System\u201d, <em>J. Org. Chem<\/em>. <strong>2014<\/strong>, <em>79<\/em>, 9970-9978.<\/li>\n<li>Zhang, W.-Z.;Yang, K; Li, S.-Z.; Ma, H.; Luo, J.*; Wang, K.-P.*; Chung, W.-S.*, \u201cInherently Chiral Calix[5]arenes Incorporating an Axially Chiral Binaphthyl Moiety: Synthesis, Structures and Chiral Recognition\u201d, <em>Eur. J. Org. Chem<\/em>. <strong>2015<\/strong>, 765-774.<\/li>\n<li>Huang, C.-C. J.; Wu, C.-F.; Shih, W.-Ch.; Luo, Y.-S.; Chen, M.-F.; Li, C.-M.; Liou, S.-H.; Chung, W.-S.; Chiang, S.-Y.*; Wu, K.-Y.*, \u201cPotential Association of Urinary N7-(2-Carbamoyl-2-hydroxyethyl) Guanine with Dietary Acrylamide Intake of Smokers and Nonsmokers\u201d , <em>Chem. Res. Toxicol<\/em>. <strong>2015<\/strong>, <em>28<\/em>, 43-50.<\/li>\n<li>Chen, Y.-J.; Yang, S.-C.; Tsai, C.-C.; Chang, K.-C.; Chuang, W.-H.; Chu, W.-L.; Kovalev, V.; Chung, W.-S.*, \u201cAnthryl-1,2,4- oxadiazole substituted calix[4]arenes as highly selective fluorescent chemodosimeters for Fe3+\u201d, <em>Chem. Asian. J.<\/em>, <strong>2015<\/strong>, <em>10<\/em>, 1025-1034.<\/li>\n<li>Luo, Y.S.; Tsai, H.-Y.; Chen, H.-C.; Wu, C.; Shen, L.-C.; Chung, W.-S.; Chiang, S.-Y.*; Wu, K.-Y.*, \u201cStudy of urinary 2-[2-(acetylamino)-2-(carboxyethyl)sulfanyl]butanoic acid, a mercapturic acid of rats treated with maleic acid\u201d, <em>Toxicol. Lett<\/em>. <strong>2015<\/strong>, <em>236<\/em>, 131-137.<\/li>\n<li>Fujii, A.; Sekigucchi, Y.; Matsumura, H.*; Inoue, T.; Chung, W.-S.*, Hirota, S.*; Matsuo, T.*, \u201cStatic and kinetic studies on the relationship between pyrene stacking modes and structures of pyrene probes on the protein surface\u201d, <em>Bioconjug. Chem<\/em>. <strong>2015<\/strong>, <em>26<\/em>, 537-548.<\/li>\n<li>Lee, C.-H.; Wu, W.-C.; Dangate, P. S.; Shen, L.-C.; Chung, W.-S.*; Sun, C.-M.*, \u201cSkeletally Diverse Synthesis of Innovative [2,1\u2011c]\u20111,4-Oxazepine and [1,4]-Quinoxaline Systems\u201d, <em>ACS Comb. Sci<\/em>. <strong>2015<\/strong>, <em>17<\/em>, 623-630.<\/li>\n<li>Zhang, W.-Z.; Ma, H.; Xiang, G.-Y.; Luo, J.*; Chung, W.-S.*, \u201cCalix[4]arenes with Combined Axial Chirality and Inherent Chirality: Synthesis, Absolute Configuration and Chiral Recognition\u201d, <em>Chem. Select<\/em> <strong>2016<\/strong>, <em>1<\/em>, 2486-2491.<\/li>\n<li>Chen, L.-H.; Kao, C.-H.; Dhole, S.; Barve, I. J.; Shen, L.-C.; Chung, W.-S.*; Sun, C.-M.*, \u201cRegioselective Synthesis of Imidazo[1,5-a]quinoxalines and methyl N-phenylbenzimidats on and Ionic Liquid Support\u201d, <em>RSC Adv<\/em>. <strong>2016<\/strong>, <em>6<\/em>, 76123-76127.<\/li>\n<li>Yuyama, K.-I.; Marc\u00e9lis, L.; Su, P.-M.; Chung, W.-S.*; Masuhara, H.*, \u201cPhoto-controlled supramolecular assembling of azobenzene based biscalix[4]arenes upon starting and stopping laser trapping\u201d, <em>Langmuir<\/em>, <strong>2017<\/strong>, <em>33<\/em>, 755-763.<\/li>\n<li>Su, P.-M.; Chang, K.-C.*; Yang, C.-J.; Liu, Y.-C.; Chung, W.-S.*, \u201cLight-driven nanofiber and nanoring morphological transformations in organogels based on an azobenzene-bridged biscalix[4]arene\u201d, <em>Chem. Commun<\/em>. <strong>2017<\/strong>, <em>53<\/em>, 13241-13244.<\/li>\n<li>Arumugaperumal, R.; Raghunath, P.; Lin, M-C.; Chung, W.-S.*, \u201cDistinct Nanostructures and Organogel Driven by Reversible Molecular Switching of a Tetraphenylethene-Involved Calix[4]arene-Based Amphiphilic [2]Rotaxane\u201d, <em>Chem. Mater<\/em>., <strong>2018<\/strong>, <em>30<\/em>, 7221\u22127233.<\/li>\n<li>Bolshchikov, B.; Volkov, S.; Sokolova, D.; Gorbunov, A.; Serebryannikova, A.; Gloriozov, I.; Cheshkov, D.; Bezzubov, S.; Chung, W.-S.; Kovalev, V.; Vatsouro, I., \u201cConstructing bridged multifunctional calixarenes by intramolecular indole coupling\u201d, <em>Org. Chem. Front<\/em>. <strong>2019<\/strong>, <em>6<\/em>, 3327-3341.<\/li>\n<\/ol>\n<\/div><\/div><\/div><\/section>\n<section class='av_toggle_section av-256i5fm-438e148a725cfdf2137de3b7c4c08140'  itemscope=\"itemscope\" itemtype=\"https:\/\/schema.org\/CreativeWork\" ><div role=\"tablist\" class=\"single_toggle\" data-tags=\"{All} \"  ><p id='toggle-toggle-id-6' data-fake-id='#toggle-id-6' class='toggler  av-title-above av-inherit-border-color'  itemprop=\"headline\"  role='tab' tabindex='0' aria-controls='toggle-id-6' data-slide-speed=\"200\" data-title=\"Publication List: 41-98\" data-title-open=\"\" data-aria_collapsed=\"Click to expand: Publication List: 41-98\" data-aria_expanded=\"Click to collapse: Publication List: 41-98\">Publication List: 41-98<span class=\"toggle_icon\"><span class=\"vert_icon\"><\/span><span class=\"hor_icon\"><\/span><\/span><\/p><div id='toggle-id-6' aria-labelledby='toggle-toggle-id-6' role='region' class='toggle_wrap  av-title-above'  ><div class='toggle_content invers-color av-inherit-border-color'  itemprop=\"text\" ><ol>\n<li>Chiu, C.-H.; Jheng, T.-C.; Pen, B.-C.; Chung, W.-S.; Mong, K.-K. T., \u201cConvergent Synthesis of Macrocyclic and Linear Desferrioxamines\u201d, <em>Eur. J. Org. Chem. <\/em><strong>2020<\/strong>, 3650\u22123659.<\/li>\n<li>Arumugaperumal, R.; Hua, W.-L.; Raghunath, P.; Lin, M-C.; <strong>Chung, W.-S.<\/strong>*, \u201cControlled Sol-Gel and Diversiform Nanostructure Transitions by Photoresponsive Molecular Switching of Tetraphenylethene- and Azobenzene-Functionalized Organogelators\u201d, <em>ACS Appl. Mater. Interfaces<\/em> <strong>2020<\/strong>, <em>12<\/em>, 29650\u221229660.<\/li>\n<li>Arumugaperumal, R.; Shellaiah, M.; Srinivasadesikan, V.; Awasthi, K. Sun, K.-W.; Lin, M.-C.; Ohta, N. <strong>Chung, W.-S.*<\/strong>. \u201cDiversiform Nanostructures Constructed from Tetraphenylethene and Pyrene-based Acid-Base Controllable Molecular Switching Amphiphilic [2]Rotaxanes with Tunable Aggregation-Induced Static Excimers\u201d, <em>ACS Appl. Mater. Interfaces<\/em>, <strong>2020<\/strong>, 12, 45222-45234.<\/li>\n<li>Chiu, C.-H.; Jheng, T.-C.; Peng, B.-C.; Chung, W.-S.; Mong, K.-K. T.*, \u201cConvergent Synthesis of Macrocyclic and Linear Desferrioxamines\u201d, <em>Eur. J. Org. Chem.<\/em> <strong>2020<\/strong>, 3650-3659.<\/li>\n<li>Chen, Y.-J.; Chen, M.-Y.; Lee, K.-T.; Shen, L.-C.; Hung, H.-C.; Niu, H.-C.; <strong>Chung, W.-S.<\/strong>*, \u201c1,3-Alternate Calix[4]arene Functionalized With Pyrazole and Triazole Ligands as a Highly Selective Fluorescent Sensor for Hg2+ and Ag+ Ions\u201d, <em>Front. Chem.<\/em> <strong>2020<\/strong>, <em>8<\/em>, article 593261.<\/li>\n<li>Hor\u00e1\u010dkov\u00e1, T.; Budka, J.; Eigner, V.; Chung, W.-S.; Cu\u0159\u00ednov\u00e1, P.; Lhot\u00e1k, P.*, \u201cChiral Anion Recognition Using Calix[4]arene-based Ureido Receptors in <em>1,3-Alternate<\/em> Conformation\u201d, <em>Beilstein J. Org. Chem<\/em>. <strong>2020<\/strong>, <em>16<\/em>, 2999-3007.<\/li>\n<li>Alene, D. Y.; Arumugaperumal, R.; Shellaiah, M.; Sun, K. W.; Chung, W.-S.*, \u201cStiff-Stilbene-Bridged Biscalix[4]arene as a Highly Light-Responsive Supramolecular Gelator\u201d, <em>Org. Lett. <\/em><strong>2021<\/strong>, <em>23<\/em>, 2772-2776.<\/li>\n<li>Arumugaperumal, R.; and <strong>Ling, H.-C.<\/strong>*<em> J. Mater. Chem<\/em>. C, 2021 (accepted).<\/li>\n<li>Arumugaperumal, R.; Alene, D. Y.; Shellaiah, M.; Srinivasadesikan, V.; Awasthi, K.; Sun, K. W.; Lin, M.-C.; Ohta<sup>, <\/sup>N.; <strong>Chung, W.-S.<\/strong>*, \u201cConstruction of anisotropic nanostructures by self-assembly of aggregation-induced emission driven from tris-branched [2]rotaxane based molecular zipper\u201d, <em>Mater. Today Chem.<\/em> <strong>2022<\/strong>, <em>24<\/em>, 100997.<\/li>\n<li><strong>Chang, K.-C.<\/strong>;<sup>*<\/sup> Chen, C.-Y.; Hsu, C.-Y.; Lee, L.-W.; <strong>Chung, W.-S.<\/strong>*, \u201cA highly selective chromogenic and fluorogenic chemo-dosimeter for dual detection of Cu<sup>2+<\/sup> based on a redox-active calix[4]arene with isoxazolylchloroanthracene\u201d, <em>Analyst<\/em> <strong>2022<\/strong>, 147, 5105-5112.<\/li>\n<li>Alene, D. Y.; Srinivasadesikan, V.; Lin, M.-C.; <strong>Chung, W.-S.<\/strong>*, \u201cConstruction of Mechanically Interlocked Fluorescence Photoswitchable [2]Rotaxane with Aggregation-Induced Emission and Molecular Shuttling Behaviors\u201d, <em>J. Org. Chem.<\/em> <strong>2023<\/strong>, <em>88<\/em>, 5530-5542.<\/li>\n<li>Yang, F.-M.; Luo, J.; Chen, Y.-C.; <strong>Chung, W.-S.<\/strong>*, \u201cSynthesis and Optical Resolution of Inherently Chiral Fluorescent Calix[4]arenes and Their Application in Chiral Recognition\u201d, <em>Synthesis <\/em><strong>2023<\/strong>, <em>55<\/em>, 2786-2796.<\/li>\n<li>Lian, J.-D.; Hu, H.-Y.; Lin Y.-H.; Raghunath, P.; Lin, M.-C.; <strong>Chung, <\/strong><strong>W.-S.*<\/strong>, \u201cSynthesis of Upper-rim Sulfanylpropyl and <em>p-<\/em>Methoxyphenylazo Substituted Calix[4]arenes as Chromogenic Sensors for Hg<sup>2+<\/sup> and Ag<sup>+<\/sup> Ions\u201d, <em>J. Org. Chem.<\/em> <strong>2023<\/strong>, <em>88<\/em>, 14292-14302.<\/li>\n<li>Wu, K.-Y.; Wei, Y.-T.; Luo, Y.-S.; Shen, L.-C.; Chang, B.-S.; Chen, Y.-Y. Chen; Huang, Y.-C.; Huang, H.-F.; Chung, W.-S.; Chiang, S.-Y., \u201cDose-response formation of <em>N<\/em>7-(3-benzo[1,3]dioxol-5-yl-2-hydroxypropyl) guanine in liver and urine correlates with micronucleated reticulocyte frequencies in mice administered safrole oxide\u201d, <em>Food Chem. Toxicol<\/em>. <strong>2023<\/strong>, <em>181<\/em>, 114056.<\/li>\n<li>Chen, T.-R.; Chang, K.-C.*; Chen, C.-Y.; Wu, T.-W.; Lee, L.-W.; Shen, L.-C.; Chen, H.-N.; <strong>Chung, W.-S.<\/strong><strong>*<\/strong>, \u201cCalix[4]arene-based Supramolecular Gels for Mercury Ions Removal in Water\u201d, <em>Chem. Asian J<\/em>. <strong>2023<\/strong>, 18, e202300739.<\/li>\n<li>Alene, D. Y.; <strong>Chung, W.-S.<\/strong>* \u201cStiff-Stilbene-Linked Bis-Cholesterol: Synthesis and Investigation of its Supramolecular Gelation and Photophysical Behaviors\u201d, ACS Omega, <strong>2025<\/strong>, <em>10<\/em>, 1789-1799.<\/li>\n<li>Yao, C.-Y.; Chang, Y.-Y.; Arumugaperumal, R.; Chao, T.-Y.; Raghunath, P.; Lin, M.-C.; <strong>Chung, W.-S<\/strong>.* \u201cStimuli-Responsive Supramolecular Polymers of Mono- and Bis-triazolylphenylazoaniline-Functionalized Copillar[5]arenes: With Distinctive Binding Modes\u201d, <em>Chem. Asian J<\/em>. <strong>2025<\/strong>, 20, e202500601.<\/li>\n<\/ol>\n<\/div><\/div><\/div><\/section>\n<\/div><\/div><\/div><!--close column table wrapper. Autoclose: 1 -->\n\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-5wogsi-e17ed0c132dc3a217b2b1eea475e7566\">\n.flex_column.av-5wogsi-e17ed0c132dc3a217b2b1eea475e7566{\npadding:30px 30px 15px 30px;\nbackground-color:#e9f3ff;\n}\n<\/style>\n<div  class='flex_column av-5wogsi-e17ed0c132dc3a217b2b1eea475e7566 av_one_full  avia-builder-el-31  el_after_av_one_full  avia-builder-el-last  first flex_column_div  column-top-margin'     ><p>\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-1bmv97m-3063e4ee61f7560feecc97c4d1e26dd2\">\n#top .av-special-heading.av-1bmv97m-3063e4ee61f7560feecc97c4d1e26dd2{\npadding-bottom:10px;\n}\nbody .av-special-heading.av-1bmv97m-3063e4ee61f7560feecc97c4d1e26dd2 .av-special-heading-tag .heading-char{\nfont-size:25px;\n}\n.av-special-heading.av-1bmv97m-3063e4ee61f7560feecc97c4d1e26dd2 .av-subheading{\nfont-size:15px;\n}\n<\/style>\n<div  class='av-special-heading av-1bmv97m-3063e4ee61f7560feecc97c4d1e26dd2 av-special-heading-h3 blockquote modern-quote  avia-builder-el-32  el_before_av_masonry_gallery  avia-builder-el-no-sibling '><h3 class='av-special-heading-tag '  itemprop=\"headline\"  >Research Highlights<\/h3><div class=\"special-heading-border\"><div class=\"special-heading-inner-border\"><\/div><\/div><\/div><br \/>\n<div id='av-masonry-1' class='av-masonry av-q29fqa-d55b26618d9a671b64800ac4fbd784d1 noHover av-fixed-size av-large-gap av-hover-overlay- av-masonry-animation- av-masonry-col-2 av-caption-always av-caption-style- av-masonry-gallery ' data-post_id=\"20182\"><div class=\"av-masonry-container isotope av-js-disabled\"><div class='av-masonry-entry isotope-item av-masonry-item-no-image '><\/div><a href=\"https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u7c21\u58317.jpg\" data-srcset=\"https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u7c21\u58317.jpg 960w, https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u7c21\u58317-300x188.jpg 300w, https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u7c21\u58317-768x480.jpg 768w, https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u7c21\u58317-705x441.jpg 705w\" data-sizes=\"(max-width: 960px) 100vw, 960px\"  aria-label=\"image \u7c21\u58317\"  id='av-masonry-1-item-15246' data-av-masonry-item='15246' class='av-masonry-entry isotope-item post-15246 attachment type-attachment status-inherit hentry  av-masonry-item-with-image' title=\"\" alt=\"\"    itemprop=\"thumbnailUrl\" ><div class='av-inner-masonry-sizer'><\/div><figure class='av-inner-masonry main_color'><div class=\"av-masonry-outerimage-container\"><div class='av-masonry-image-container' style=\"background-image: url(https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u7c21\u58317.jpg);\"  title=\"\u7c21\u58317\" ><\/div><\/div><\/figure><\/a><!--end av-masonry entry--><a href=\"https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u7c21\u58312-1.jpg\" data-srcset=\"https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u7c21\u58312-1.jpg 960w, https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u7c21\u58312-1-267x200.jpg 267w, https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u7c21\u58312-1-768x576.jpg 768w, https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u7c21\u58312-1-705x529.jpg 705w\" data-sizes=\"(max-width: 960px) 100vw, 960px\"  aria-label=\"image \u7c21\u58312\"  id='av-masonry-1-item-14972' data-av-masonry-item='14972' class='av-masonry-entry isotope-item post-14972 attachment type-attachment status-inherit hentry  av-masonry-item-with-image' title=\"\" alt=\"\"    itemprop=\"thumbnailUrl\" ><div class='av-inner-masonry-sizer'><\/div><figure class='av-inner-masonry main_color'><div class=\"av-masonry-outerimage-container\"><div class='av-masonry-image-container' style=\"background-image: url(https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u7c21\u58312-1.jpg);\"  title=\"\u7c21\u58312\" ><\/div><\/div><\/figure><\/a><!--end av-masonry entry--><a href=\"https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u7c21\u58311-1.jpg\" data-srcset=\"https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u7c21\u58311-1.jpg 960w, https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u7c21\u58311-1-267x200.jpg 267w, https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u7c21\u58311-1-768x576.jpg 768w, https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u7c21\u58311-1-705x529.jpg 705w\" data-sizes=\"(max-width: 960px) 100vw, 960px\"  aria-label=\"image \u7c21\u58311\"  id='av-masonry-1-item-14960' data-av-masonry-item='14960' class='av-masonry-entry isotope-item post-14960 attachment type-attachment status-inherit hentry  av-masonry-item-with-image' title=\"\" alt=\"\"    itemprop=\"thumbnailUrl\" ><div class='av-inner-masonry-sizer'><\/div><figure class='av-inner-masonry main_color'><div class=\"av-masonry-outerimage-container\"><div class='av-masonry-image-container' style=\"background-image: url(https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u7c21\u58311-1.jpg);\"  title=\"\u7c21\u58311\" ><\/div><\/div><\/figure><\/a><!--end av-masonry entry--><a href=\"https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u7c21\u58313-1.jpg\" data-srcset=\"https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u7c21\u58313-1.jpg 960w, https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u7c21\u58313-1-267x200.jpg 267w, https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u7c21\u58313-1-768x576.jpg 768w, https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u7c21\u58313-1-705x529.jpg 705w\" data-sizes=\"(max-width: 960px) 100vw, 960px\"  aria-label=\"image \u7c21\u58313\"  id='av-masonry-1-item-14974' data-av-masonry-item='14974' class='av-masonry-entry isotope-item post-14974 attachment type-attachment status-inherit hentry  av-masonry-item-with-image' title=\"\" alt=\"\"    itemprop=\"thumbnailUrl\" ><div class='av-inner-masonry-sizer'><\/div><figure class='av-inner-masonry main_color'><div class=\"av-masonry-outerimage-container\"><div class='av-masonry-image-container' style=\"background-image: url(https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u7c21\u58313-1.jpg);\"  title=\"\u7c21\u58313\" ><\/div><\/div><\/figure><\/a><!--end av-masonry entry--><a href=\"https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u7c21\u58318.jpg\" data-srcset=\"https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u7c21\u58318.jpg 960w, https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u7c21\u58318-300x188.jpg 300w, https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u7c21\u58318-768x480.jpg 768w, https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u7c21\u58318-705x441.jpg 705w\" data-sizes=\"(max-width: 960px) 100vw, 960px\"  aria-label=\"image \u7c21\u58318\"  id='av-masonry-1-item-15251' data-av-masonry-item='15251' class='av-masonry-entry isotope-item post-15251 attachment type-attachment status-inherit hentry  av-masonry-item-with-image' title=\"\" alt=\"\"    itemprop=\"thumbnailUrl\" ><div class='av-inner-masonry-sizer'><\/div><figure class='av-inner-masonry main_color'><div class=\"av-masonry-outerimage-container\"><div class='av-masonry-image-container' style=\"background-image: url(https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u7c21\u58318.jpg);\"  title=\"\u7c21\u58318\" ><\/div><\/div><\/figure><\/a><!--end av-masonry entry--><a href=\"https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u7c21\u58316.jpg\" data-srcset=\"https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u7c21\u58316.jpg 960w, https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u7c21\u58316-267x200.jpg 267w, https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u7c21\u58316-768x576.jpg 768w, https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u7c21\u58316-705x529.jpg 705w\" data-sizes=\"(max-width: 960px) 100vw, 960px\"  aria-label=\"image \u7c21\u58316\"  id='av-masonry-1-item-15138' data-av-masonry-item='15138' class='av-masonry-entry isotope-item post-15138 attachment type-attachment status-inherit hentry  av-masonry-item-with-image' title=\"\" alt=\"\"    itemprop=\"thumbnailUrl\" ><div class='av-inner-masonry-sizer'><\/div><figure class='av-inner-masonry main_color'><div class=\"av-masonry-outerimage-container\"><div class='av-masonry-image-container' style=\"background-image: url(https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u7c21\u58316.jpg);\"  title=\"\u7c21\u58316\" ><\/div><\/div><\/figure><\/a><!--end av-masonry entry--><\/div><a class='av-masonry-pagination av-masonry-load-more' href='#load-more'  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