{"id":16742,"date":"2024-12-01T07:58:20","date_gmt":"2024-11-30T23:58:20","guid":{"rendered":"https:\/\/dac.nycu.edu.tw\/?post_type=portfolio&#038;p=16742"},"modified":"2026-07-31T19:08:48","modified_gmt":"2026-07-31T11:08:48","slug":"professor-shih-ching-chuang","status":"publish","type":"portfolio","link":"https:\/\/dac.nycu.edu.tw\/en\/portfolio-item\/professor-shih-ching-chuang\/","title":{"rendered":"Professor Shih-Ching Chuang"},"content":{"rendered":"\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-20a21c2-b47a1133bbec8357adf63a46bb2789b9\">\n.avia-section.av-20a21c2-b47a1133bbec8357adf63a46bb2789b9{\nmargin-top:-50px;\nmargin-bottom:0px;\n}\n.avia-section.av-20a21c2-b47a1133bbec8357adf63a46bb2789b9 .av-parallax .av-parallax-inner{\nbackground-repeat:no-repeat;\nbackground-image:url(https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/03\/trnava.jpg);\nbackground-position:50% 50%;\nbackground-attachment:scroll;\n}\n.avia-section.av-20a21c2-b47a1133bbec8357adf63a46bb2789b9 .av-section-color-overlay{\nopacity:0.5;\nbackground-color:#2a2a59;\n}\n<\/style>\n<div id='av_section_1'  class='avia-section av-20a21c2-b47a1133bbec8357adf63a46bb2789b9 main_color avia-section-default avia-no-border-styling  avia-builder-el-0  el_before_av_hr  avia-builder-el-first  avia-full-stretch av-parallax-section avia-bg-style-parallax av-section-color-overlay-active av-minimum-height av-minimum-height-custom av-height-custom  container_wrap fullsize'  data-section-bg-repeat='stretch' data-av_minimum_height_px='280'><div class='av-parallax' data-avia-parallax-ratio='0.3' ><div class='av-parallax-inner main_color avia-full-stretch'><\/div><\/div><div class=\"av-section-color-overlay-wrap\"><div 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-16742'><div class='entry-content-wrapper clearfix'>\n<div  class='flex_column av-1y4o44i-5554cda8ce8a4fe27f821626e33b3fec 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-1whscea-228a4148139776565bfbb6b71bfa1712\">\n#top .av-special-heading.av-1whscea-228a4148139776565bfbb6b71bfa1712{\npadding-bottom:10px;\ncolor:#ffffff;\n}\nbody .av-special-heading.av-1whscea-228a4148139776565bfbb6b71bfa1712 .av-special-heading-tag .heading-char{\nfont-size:25px;\n}\n.av-special-heading.av-1whscea-228a4148139776565bfbb6b71bfa1712 .special-heading-inner-border{\nborder-color:#ffffff;\n}\n.av-special-heading.av-1whscea-228a4148139776565bfbb6b71bfa1712 .av-subheading{\nfont-size:15px;\n}\n<\/style>\n<div  class='av-special-heading av-1whscea-228a4148139776565bfbb6b71bfa1712 av-special-heading-h3 custom-color-heading  avia-builder-el-2  el_before_av_heading  avia-builder-el-first '><h3 class='av-special-heading-tag '  itemprop=\"headline\"  >Professor<\/h3><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-1uuhkjm-b3c1dcc79ce658e449b430a9859e27de\">\n#top .av-special-heading.av-1uuhkjm-b3c1dcc79ce658e449b430a9859e27de{\npadding-bottom:10px;\ncolor:#ffffff;\n}\nbody .av-special-heading.av-1uuhkjm-b3c1dcc79ce658e449b430a9859e27de .av-special-heading-tag .heading-char{\nfont-size:25px;\n}\n.av-special-heading.av-1uuhkjm-b3c1dcc79ce658e449b430a9859e27de .special-heading-inner-border{\nborder-color:#ffffff;\n}\n.av-special-heading.av-1uuhkjm-b3c1dcc79ce658e449b430a9859e27de .av-subheading{\nfont-size:15px;\n}\n\n@media only screen and (min-width: 990px){ \n#top #wrap_all .av-special-heading.av-1uuhkjm-b3c1dcc79ce658e449b430a9859e27de .av-special-heading-tag{\nfont-size:40px;\n}\n}\n\n@media only screen and (min-width: 768px) and (max-width: 989px){ \n#top #wrap_all .av-special-heading.av-1uuhkjm-b3c1dcc79ce658e449b430a9859e27de .av-special-heading-tag{\nfont-size:40px;\n}\n}\n<\/style>\n<div  class='av-special-heading av-1uuhkjm-b3c1dcc79ce658e449b430a9859e27de av-special-heading-h1 custom-color-heading blockquote modern-quote modern-right  avia-builder-el-3  el_after_av_heading  el_before_av_codeblock '><h1 class='av-special-heading-tag '  itemprop=\"headline\"  >Professor Shih-Ching Chuang<\/h1><div class=\"special-heading-border\"><div class=\"special-heading-inner-border\"><\/div><\/div><\/div><br \/>\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-16742'><div class='entry-content-wrapper clearfix'>\n\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-1ras3aa-8bfc677e3bf297e64c006744a58957b2\">\n#top .hr.hr-invisible.av-1ras3aa-8bfc677e3bf297e64c006744a58957b2{\nheight:5px;\n}\n<\/style>\n<div  class='hr av-1ras3aa-8bfc677e3bf297e64c006744a58957b2 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\" id=\"style-css-av-1qtvdpe-a466d8bd76f4ae92940c881782addaf9\">\n#top .hr.hr-invisible.av-1qtvdpe-a466d8bd76f4ae92940c881782addaf9{\nheight:30px;\n}\n<\/style>\n<div  class='hr av-1qtvdpe-a466d8bd76f4ae92940c881782addaf9 hr-invisible  avia-builder-el-6  el_after_av_hr  el_before_av_one_third  av-desktop-hide av-medium-hide'><span class='hr-inner 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id=\"style-css-av-1ni2r2q-61d620addeeb74597592c8db8492d311\">\n.avia-image-container.av-1ni2r2q-61d620addeeb74597592c8db8492d311 img.avia_image{\nbox-shadow:none;\n}\n.avia-image-container.av-1ni2r2q-61d620addeeb74597592c8db8492d311 .av-image-caption-overlay-center{\ncolor:#ffffff;\n}\n<\/style>\n<div  class='avia-image-container av-1ni2r2q-61d620addeeb74597592c8db8492d311 av-styling-no-styling avia-align-center  avia-builder-el-8  avia-builder-el-no-sibling '   itemprop=\"image\" itemscope=\"itemscope\" itemtype=\"https:\/\/schema.org\/ImageObject\" ><div class=\"avia-image-container-inner\"><div class=\"avia-image-overlay-wrap\"><img decoding=\"async\" fetchpriority=\"high\" class='wp-image-11871 avia-img-lazy-loading-not-11871 avia_image ' src=\"https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2025\/05\/\u838a\u58eb\u537fShih-Ching-Chuang.png\" alt='\u838a\u58eb\u537fShih-Ching Chuang' title='\u838a\u58eb\u537fShih-Ching Chuang'  height=\"510\" width=\"600\"  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data-created_by=\"avia_inline_auto\" id=\"style-css-av-1k7hmsy-ef90c87e210bce7550ae2d0e4f6f644b\">\n#top .av-special-heading.av-1k7hmsy-ef90c87e210bce7550ae2d0e4f6f644b{\nmargin:0 0 0 0;\npadding-bottom:10px;\ncolor:#005daf;\n}\nbody .av-special-heading.av-1k7hmsy-ef90c87e210bce7550ae2d0e4f6f644b .av-special-heading-tag .heading-char{\nfont-size:25px;\n}\n.av-special-heading.av-1k7hmsy-ef90c87e210bce7550ae2d0e4f6f644b .special-heading-inner-border{\nborder-color:#005daf;\n}\n.av-special-heading.av-1k7hmsy-ef90c87e210bce7550ae2d0e4f6f644b .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-1k7hmsy-ef90c87e210bce7550ae2d0e4f6f644b{\nmargin:30px 0 0 0;\n}\n}\n\n@media only screen and (max-width: 479px){ \n#top .av-special-heading.av-1k7hmsy-ef90c87e210bce7550ae2d0e4f6f644b{\nmargin:30px 0 0 0;\n}\n}\n<\/style>\n<div  class='av-special-heading av-1k7hmsy-ef90c87e210bce7550ae2d0e4f6f644b 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\"  >\u838a\u58eb\u537f Shih-Ching Chuang<\/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-1igdwea-11efabe87fe9fdfe19b0bef282a5dbce\">\n#top .av-special-heading.av-1igdwea-11efabe87fe9fdfe19b0bef282a5dbce{\nmargin:0 0 0 0;\npadding-bottom:20px;\ncolor:#005daf;\n}\nbody .av-special-heading.av-1igdwea-11efabe87fe9fdfe19b0bef282a5dbce .av-special-heading-tag .heading-char{\nfont-size:25px;\n}\n.av-special-heading.av-1igdwea-11efabe87fe9fdfe19b0bef282a5dbce .special-heading-inner-border{\nborder-color:#005daf;\n}\n.av-special-heading.av-1igdwea-11efabe87fe9fdfe19b0bef282a5dbce .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-1igdwea-11efabe87fe9fdfe19b0bef282a5dbce{\nmargin:0 0 0 0;\n}\n}\n\n@media only screen and (max-width: 479px){ \n#top .av-special-heading.av-1igdwea-11efabe87fe9fdfe19b0bef282a5dbce{\nmargin:0 0 0 0;\n}\n}\n<\/style>\n<div  class='av-special-heading av-1igdwea-11efabe87fe9fdfe19b0bef282a5dbce 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\"  >Professor<\/h3><div class=\"special-heading-border\"><div class=\"special-heading-inner-border\"><\/div><\/div><\/div><br \/>\n<section  class='av_textblock_section av-1gh6gg2-3b86527e20b8f2cb9d42c8a80184cef8 '   itemscope=\"itemscope\" itemtype=\"https:\/\/schema.org\/CreativeWork\" ><div class='avia_textblock link_text'  itemprop=\"text\" ><p>Tel\u00a0+886-35712121 ext 31858<\/p>\n<p>OfficeScience Building 2, R531<\/p>\n<p>Email\u00a0jscchuang@nycu.edu.tw<\/p>\n<p>Lab\u00a0\u00a0Science Building 2, R539<\/p>\n<p>Lab Tel\u00a0+886-35712121 ext 56513<\/p>\n<\/div><\/section><br \/>\n\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-1eax0z6-b101e1cacf6a4814b6d9f02a82da4f65\">\n#top .hr.hr-invisible.av-1eax0z6-b101e1cacf6a4814b6d9f02a82da4f65{\nheight:15px;\n}\n<\/style>\n<div  class='hr av-1eax0z6-b101e1cacf6a4814b6d9f02a82da4f65 hr-invisible  avia-builder-el-13  el_after_av_textblock  el_before_av_buttonrow '><span class='hr-inner '><span class=\"hr-inner-style\"><\/span><\/span><\/div><br \/>\n<div  class='avia-buttonrow-wrap av-1cbxxya-80ea16f335b9853e9713c52869dee603 avia-buttonrow-left  avia-builder-el-14  el_after_av_hr  avia-builder-el-last '>\n\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-1ammxsi-762a459b32404f9a85d57a88ec99849d\">\n#top #wrap_all .avia-button.av-1ammxsi-762a459b32404f9a85d57a88ec99849d{\nmargin-bottom:5px;\nmargin-right:5px;\n}\n#top #wrap_all .avia-button.av-1ammxsi-762a459b32404f9a85d57a88ec99849d:hover{\nopacity:1;\ntransition:all 0.4s ease-in-out;\n}\n<\/style>\n<a href='https:\/\/sites.google.com\/site\/thechuanggroup\/home'  class='avia-button av-1ammxsi-762a459b32404f9a85d57a88ec99849d avia-icon_select-yes-right-icon avia-size-medium av-icon-on-hover avia-color-theme-color'  target=\"_blank\"  rel=\"noopener noreferrer\"  aria-label=\"The Chuang Research Group\/\u838a\u58eb\u537f\u8001\u5e2b\u5be6\u9a57\u5ba4\u7db2\u7ad9\"><span class='avia_iconbox_title' >The Chuang Research Group\/\u838a\u58eb\u537f\u8001\u5e2b\u5be6\u9a57\u5ba4\u7db2\u7ad9<\/span><span class='avia_button_icon avia_button_icon_right avia-iconfont avia-font-entypo-fontello' data-av_icon='\ue881' data-av_iconfont='entypo-fontello' ><\/span><\/a>\n<\/div><\/p><\/div><\/div><!--close column table wrapper. Autoclose: 1 -->\n\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-19ibof6-29a1d6bf8e4eff9ede078760c6bcaf6d\">\n#top .hr.hr-invisible.av-19ibof6-29a1d6bf8e4eff9ede078760c6bcaf6d{\nheight:30px;\n}\n<\/style>\n<div  class='hr av-19ibof6-29a1d6bf8e4eff9ede078760c6bcaf6d hr-invisible  avia-builder-el-15  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>\n<div class='flex_column_table av-17ajlcy-3f9d067815737765c12c3884b3640669 sc-av_one_full av-equal-height-column-flextable'>\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-17ajlcy-3f9d067815737765c12c3884b3640669\">\n.flex_column.av-17ajlcy-3f9d067815737765c12c3884b3640669{\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-17ajlcy-3f9d067815737765c12c3884b3640669 .av-flex-placeholder{\nwidth:0%;\n}\n<\/style>\n<div  class='flex_column av-17ajlcy-3f9d067815737765c12c3884b3640669 av_one_full  avia-builder-el-16  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-15uv61u-9e3baa965e0ccba1dae931920466fe54\">\n#top .av-special-heading.av-15uv61u-9e3baa965e0ccba1dae931920466fe54{\npadding-bottom:10px;\n}\nbody .av-special-heading.av-15uv61u-9e3baa965e0ccba1dae931920466fe54 .av-special-heading-tag .heading-char{\nfont-size:25px;\n}\n.av-special-heading.av-15uv61u-9e3baa965e0ccba1dae931920466fe54 .av-subheading{\nfont-size:15px;\n}\n<\/style>\n<div  class='av-special-heading av-15uv61u-9e3baa965e0ccba1dae931920466fe54 av-special-heading-h3 blockquote modern-quote  avia-builder-el-17  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-152asg2-2541a896423f2fe4cdc28b1eb8fcb6a0 sc-av_one_full av-equal-height-column-flextable'>\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-152asg2-2541a896423f2fe4cdc28b1eb8fcb6a0\">\n#top .flex_column_table.av-equal-height-column-flextable.av-152asg2-2541a896423f2fe4cdc28b1eb8fcb6a0{\nmargin-top:0px;\nmargin-bottom:0px;\n}\n.flex_column.av-152asg2-2541a896423f2fe4cdc28b1eb8fcb6a0{\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-152asg2-2541a896423f2fe4cdc28b1eb8fcb6a0 .av-flex-placeholder{\nwidth:0%;\n}\n<\/style>\n<div  class='flex_column av-152asg2-2541a896423f2fe4cdc28b1eb8fcb6a0 av_one_full  avia-builder-el-18  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-12pu8ki-1ab0d7d603b2edf75923bd4862e4aac7 '   itemscope=\"itemscope\" itemtype=\"https:\/\/schema.org\/CreativeWork\" ><div class='avia_textblock'  itemprop=\"text\" ><p><strong>2005<\/strong>\u00a0Ph.D. Department of Chemistry and Biochemistry, UCLA, USA<\/p>\n<p><strong>1997<\/strong>\u00a0M.S. Department of Chemistry, National Tsing Hua University, Taiwan<\/p>\n<p><strong>1995<\/strong>\u00a0B.S. Department of Chemistry, Tunghai University, Taiwan<\/p>\n<\/div><\/section><\/div><\/div><!--close column table wrapper. Autoclose: 1 -->\n<div class='flex_column_table av-115rf3m-05be6f33068422b33e6706e2ac67f6da sc-av_one_full av-equal-height-column-flextable'>\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-115rf3m-05be6f33068422b33e6706e2ac67f6da\">\n.flex_column.av-115rf3m-05be6f33068422b33e6706e2ac67f6da{\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-115rf3m-05be6f33068422b33e6706e2ac67f6da .av-flex-placeholder{\nwidth:0%;\n}\n<\/style>\n<div  class='flex_column av-115rf3m-05be6f33068422b33e6706e2ac67f6da av_one_full  avia-builder-el-20  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-yxtrf6-a7ecf70387891c83d4469f81edd6b6df\">\n#top .av-special-heading.av-yxtrf6-a7ecf70387891c83d4469f81edd6b6df{\npadding-bottom:10px;\ncolor:#ffffff;\n}\nbody .av-special-heading.av-yxtrf6-a7ecf70387891c83d4469f81edd6b6df .av-special-heading-tag .heading-char{\nfont-size:25px;\n}\n.av-special-heading.av-yxtrf6-a7ecf70387891c83d4469f81edd6b6df .special-heading-inner-border{\nborder-color:#ffffff;\n}\n.av-special-heading.av-yxtrf6-a7ecf70387891c83d4469f81edd6b6df .av-subheading{\nfont-size:15px;\n}\n<\/style>\n<div  class='av-special-heading av-yxtrf6-a7ecf70387891c83d4469f81edd6b6df av-special-heading-h3 custom-color-heading blockquote modern-quote  avia-builder-el-21  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-sac606-25243140b49d21c00f8f575d093e5f50 sc-av_one_full av-equal-height-column-flextable'>\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-sac606-25243140b49d21c00f8f575d093e5f50\">\n#top .flex_column_table.av-equal-height-column-flextable.av-sac606-25243140b49d21c00f8f575d093e5f50{\nmargin-top:0px;\nmargin-bottom:0px;\n}\n.flex_column.av-sac606-25243140b49d21c00f8f575d093e5f50{\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-sac606-25243140b49d21c00f8f575d093e5f50 .av-flex-placeholder{\nwidth:0%;\n}\n<\/style>\n<div  class='flex_column av-sac606-25243140b49d21c00f8f575d093e5f50 av_one_full  avia-builder-el-22  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-mh4cco6u-dea7dd2d2f4b0507d4e8a87fed5d8393 '   itemscope=\"itemscope\" itemtype=\"https:\/\/schema.org\/CreativeWork\" ><div class='avia_textblock'  itemprop=\"text\" ><ul>\n<li>2nd Lieutenant, Army, Taiwan (1997.7-1999.6)<\/li>\n<li>Research Assistant., Department of Chemistry, National Tsing Hua University, Hsinchu, Taiwan (1999.11-2000.6)<\/li>\n<li>Ph.D., Department of Chemistry and Biochemistry, University of California, Los Angeles, USA (2005.8)<\/li>\n<li>PhD Thesis: \u201cNanosurgery of C60\u201d (Advisor: Prof. Yves Rubin, UCLA)<\/li>\n<li>Postdoctoral Fellow, Institute for Chemical Research, Kyoto University, Japan (2005.9-2007.7)<\/li>\n<li>Advisor: Prof. Koichi Komatsu; Prof. Yasujiro Murata<\/li>\n<li>Assistant Professor, Department of Applied Chemistry, National Chiao Tung University, Hsinchu, Taiwan (2007.08\u20132012.07)<\/li>\n<li>Associate Professor, Department of Applied Chemistry, National Chiao Tung University, Hsinchu, Taiwan (2012.08\u20132016.07)<\/li>\n<li>Professor, Department of Applied Chemistry, National Chiao Tung University, Hsinchu, Taiwan (2016.08\u20132021.01)<\/li>\n<li>Professor, Department of Applied Chemistry, National Yang Ming Chiao Tung University, Hsinchu, Taiwan (2021.02\u2013now)<\/li>\n<\/ul>\n<\/div><\/section><\/div><\/div><!--close column table wrapper. Autoclose: 1 -->\n<div class='flex_column_table av-perd82-19d21d09f6e165a350e8f5c03ce17936 sc-av_one_full av-equal-height-column-flextable'>\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-perd82-19d21d09f6e165a350e8f5c03ce17936\">\n.flex_column.av-perd82-19d21d09f6e165a350e8f5c03ce17936{\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-perd82-19d21d09f6e165a350e8f5c03ce17936 .av-flex-placeholder{\nwidth:0%;\n}\n<\/style>\n<div  class='flex_column av-perd82-19d21d09f6e165a350e8f5c03ce17936 av_one_full  avia-builder-el-24  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-ojvtsi-2d66ca25564d736307bbc83af79fb6d3\">\n#top .av-special-heading.av-ojvtsi-2d66ca25564d736307bbc83af79fb6d3{\npadding-bottom:10px;\n}\nbody .av-special-heading.av-ojvtsi-2d66ca25564d736307bbc83af79fb6d3 .av-special-heading-tag .heading-char{\nfont-size:25px;\n}\n.av-special-heading.av-ojvtsi-2d66ca25564d736307bbc83af79fb6d3 .av-subheading{\nfont-size:15px;\n}\n<\/style>\n<div  class='av-special-heading av-ojvtsi-2d66ca25564d736307bbc83af79fb6d3 av-special-heading-h3 blockquote modern-quote  avia-builder-el-25  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-lsxsrm-95e0e75ee4964150ab24dbe3be576ae8 sc-av_one_full av-equal-height-column-flextable'>\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-lsxsrm-95e0e75ee4964150ab24dbe3be576ae8\">\n#top .flex_column_table.av-equal-height-column-flextable.av-lsxsrm-95e0e75ee4964150ab24dbe3be576ae8{\nmargin-top:0px;\nmargin-bottom:0px;\n}\n.flex_column.av-lsxsrm-95e0e75ee4964150ab24dbe3be576ae8{\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-lsxsrm-95e0e75ee4964150ab24dbe3be576ae8 .av-flex-placeholder{\nwidth:0%;\n}\n<\/style>\n<div  class='flex_column av-lsxsrm-95e0e75ee4964150ab24dbe3be576ae8 av_one_full  avia-builder-el-26  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-k5mdrm-4aeca5a53b2042c369d68bd81c7e3e76 '   itemscope=\"itemscope\" itemtype=\"https:\/\/schema.org\/CreativeWork\" ><div class='avia_textblock'  itemprop=\"text\" ><ul>\n<li>2018 Asian Core Program Lectureship (Korea)<\/li>\n<li>2017 Young Scholar Research Award, Shui-Mu Foundation of Chemistry<\/li>\n<li>Asian Core Program Lectureship (Japan)<\/li>\n<li>Dr. Ta-You Wu Award Ministry of Science and Technology, Taiwan<\/li>\n<li>Teaching Award National Chiao Tung University<\/li>\n<li>2000 Academician, Academia Sinica, Taiwan<\/li>\n<li>Young Investigator Research Award College of Science, National Chiao Tung University<\/li>\n<li>UCLA Chancellor&#8217;s Dissertation Year Fellowship, UCLA<\/li>\n<li>2001-2004 Teaching Fellowship, UCLA<\/li>\n<\/ul>\n<\/div><\/section><\/div><\/div><!--close column table wrapper. Autoclose: 1 --><div class='flex_column_table av-jb4cg2-55ff245b22b6b0835121705282f1b7be sc-av_one_full av-equal-height-column-flextable'>\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-jb4cg2-55ff245b22b6b0835121705282f1b7be\">\n.flex_column.av-jb4cg2-55ff245b22b6b0835121705282f1b7be{\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-jb4cg2-55ff245b22b6b0835121705282f1b7be .av-flex-placeholder{\nwidth:0%;\n}\n<\/style>\n<div  class='flex_column av-jb4cg2-55ff245b22b6b0835121705282f1b7be av_one_full  avia-builder-el-28  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-h8b8aa-3854dcdbf00fade1ab7b8353a8285bc8\">\n#top .av-special-heading.av-h8b8aa-3854dcdbf00fade1ab7b8353a8285bc8{\npadding-bottom:10px;\ncolor:#ffffff;\n}\nbody .av-special-heading.av-h8b8aa-3854dcdbf00fade1ab7b8353a8285bc8 .av-special-heading-tag .heading-char{\nfont-size:25px;\n}\n.av-special-heading.av-h8b8aa-3854dcdbf00fade1ab7b8353a8285bc8 .special-heading-inner-border{\nborder-color:#ffffff;\n}\n.av-special-heading.av-h8b8aa-3854dcdbf00fade1ab7b8353a8285bc8 .av-subheading{\nfont-size:15px;\n}\n<\/style>\n<div  class='av-special-heading av-h8b8aa-3854dcdbf00fade1ab7b8353a8285bc8 av-special-heading-h3 custom-color-heading blockquote modern-quote  avia-builder-el-29  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 --><\/p>\n<div class='flex_column_table av-gfra42-191a84875922be5618c28c4ce866952c sc-av_one_full av-equal-height-column-flextable'>\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-gfra42-191a84875922be5618c28c4ce866952c\">\n#top .flex_column_table.av-equal-height-column-flextable.av-gfra42-191a84875922be5618c28c4ce866952c{\nmargin-top:0px;\nmargin-bottom:0px;\n}\n.flex_column.av-gfra42-191a84875922be5618c28c4ce866952c{\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-gfra42-191a84875922be5618c28c4ce866952c .av-flex-placeholder{\nwidth:0%;\n}\n<\/style>\n<div  class='flex_column av-gfra42-191a84875922be5618c28c4ce866952c av_one_full  avia-builder-el-30  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-e6a3z6-7454201097b73b3afbd2e494e28458db\">\n#top .togglecontainer.av-e6a3z6-7454201097b73b3afbd2e494e28458db p.toggler{\ncolor:#555555;\nbackground-color:#f8f8f8;\nborder-color:#ffffff;\n}\n#top .togglecontainer.av-e6a3z6-7454201097b73b3afbd2e494e28458db p.toggler:not(.activeTitle):hover{\nbackground-color:#ffeca0;\n}\n#top .togglecontainer.av-e6a3z6-7454201097b73b3afbd2e494e28458db p.toggler .toggle_icon{\ncolor:#005daf;\nborder-color:#005daf;\n}\n#top .togglecontainer.av-e6a3z6-7454201097b73b3afbd2e494e28458db p.toggler .toggle_icon > span{\ncolor:#005daf;\nborder-color:#005daf;\n}\n#top .togglecontainer.av-e6a3z6-7454201097b73b3afbd2e494e28458db .toggle_wrap .toggle_content{\ncolor:#555555;\nbackground-color:#f8f8f8;\nborder-color:#ffffff;\n}\n<\/style>\n<div  class='togglecontainer av-e6a3z6-7454201097b73b3afbd2e494e28458db av-minimal-toggle  avia-builder-el-31  avia-builder-el-no-sibling ' >\n<section class='av_toggle_section av-cbe25u-177bac5d10810828fd751cb87e256014'  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=\"Publikations\" data-title-open=\"\" data-aria_collapsed=\"Click to expand: Publikations\" data-aria_expanded=\"Click to collapse: Publikations\">Publikations<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\" ><ol>\n<li style=\"list-style-type: none;\">\n<ol>\n<li style=\"list-style-type: none;\">\n<ol>\n<li style=\"list-style-type: none;\">\n<ol>\n<li style=\"list-style-type: none;\">\n<ol>\n<li style=\"list-style-type: none;\">\n<ol>\n<li>Chen, S.-H.; Chen, Y.-L.; Chen, C.-Y.; Wu, C.-S.; Su, M.-D.*; Chuang, S.-C.* &#8220;Spirocyclopropanes and Substituted Furans by Controlling Reactivity of 1,3-Enynoates: \u03b3- and \u03b4-Addition of Phosphines to Conjugate Acceptors&#8221; Chem. Eur. J. 2024, 30, e202402688 . https:\/\/doi.org\/10.1002\/chem.202402688<\/li>\n<li>Wang, W.-Q.; Nallapati, S.; Chen, C.-Y.; Yaoita, T.; Yamaoka, S.; Murata, M.*; Chuang, S.-C.* \u201cPhosphine-promoted synthesis of naphthoquinones fused with cyclopentadienyl moiety via ring expansion: synthesis, reactivity, and ring contraction via [1,5] sigmatropic rearrangement\u201c Org. Lett. 2024, 26, 8730-8735.<\/li>\n<li>Hsiao, H.-C.; Li, M.-C.; Vedarethinam, G.; Chen, P.-L.; Chuang, S.-C.* &#8220;Synthesis of Benzo[c]cinnolinium Salts from 2-Azobiaryls by Copper(\u2161) or Electrochemical Oxidation&#8221; Org. Lett. 2024, 26,1694-1698. Open Access Link: https:\/\/pubs.acs.org\/doi\/full\/10.1021\/acs.orglett.4c00213<\/li>\n<li>Hsiao, H.-C.; Chen, P.-L.; Chuang, S.-C.* \u201cSynthesis and Photophysical Properties of Fluorescent Benzo[def]carbazoles\u201d J. Chin. Chem. Soc. 2023, 70, 1591-1598.<\/li>\n<li>Jayabal, K.*; Elumalai, D.; Leelakrishnan, S.; Bhattacharya, S.; Rengarajan, V.; Kannan, T.; Chuang, S.-C.* &#8220;Green and Regioselective Approach for the Synthesis of 3-Substituted Indole Based 1,2-Dihydropyridine and Azaxanthone Derivatives as a Potential Lead for SARS-CoV-2 and Delta Plus Mutant Virus: DFT and Docking Studies&#8221; ACS Omega 2022, 7, 43856-43876.<\/li>\n<li>Ueda, K.; Fukuzaki, R.; Ito, T.; Toyama, N.; Muraoka, M.; Terao, T.; Manabe, K.; Hirai, T.; Wu, C.-J.; Chuang, S.-C.; Kawano, S.; Murata, M.* \u201cA Highly Conductive n-Type Coordination Complex with Thieno[3,2-b]thiophene Units: Facile Synthesis, Orientation, and Thermoelectric Properties\u201d J. Am. Chem. Soc. 2022, 144, 18744-18749.<\/li>\n<li>Hsieh, C.-M.; Hsiao, H.-C.; Yamada, Y.; Wu, W.-R.; Jeng, U.-S.; Su, C.-J.;* Lin, Y.-S.; Murata, M.;* Chang, Y. J.;* Chuang, S.-C.* &#8220;Promoting the Efficiency and Stability of Nonfullerene Organic Photovoltaics by Incorporating Open-Cage [60]Fullerenes in the Nonfullerene Nanocrystallites&#8221; ACS Appl. Mater. Interfaces, 2022, 14, 39109.<\/li>\n<li>Nallapati, S.; Tseng, M.-F.; Chen, P.-L.; Chuang, S.-C.* \u201cPhosphine-Mediated [4 + 3] Annulation of Diynoates and 2-Arylidene Indane-1,3-diones: Access of Indeno[1,2-b]oxepin-4-ylidenes and Beyond\u201d Org. Lett. 2022, 24, 2993\u20132997.<\/li>\n<li>Hsiao, H.-C.; Chen, P.-L.; Chuang, S.-C.* \u201cCrystal structure and fluorescence of 1-[8-phenyl-9-(phenylethynyl)-4H-benzo[def]carbazol-4-yl]-ethan-1-one\u201d Acta Cryst. 2022. E78, 590-593.<\/li>\n<li>Hsieh, C.-M.; Chuang, M.-R.; Yamada, Y.; Su, C.-J.; Chang, Y. J.*; Murata, M.*; Jeng, U.-S.*; Chuang, S.-C.* &#8220;p-Tetrafluorophenylene divinylene-Bridged Nonfullerene Acceptors as Binary Components and Additives for High-efficiency Organic Solar Cells&#8221; ACS Appl. Mater. Interfaces, 2021, 13, 61473-61486.<\/li>\n<li>Sun, S.-Y.; Raju, S.; Vedarethinam, G.; Chen, P.-L.; Chuang, S.-C.* \u201cTfOH-Promoted Classical Nazarov-type Cyclization of Benzofulvenes: Synthesis of Polycyclic 5H,10&#8217;H-spiro[benzo[k]phenanthridine-5,6&#8242;-dibenzopentalenes]\u201d Org. Lett. 2021, 23, 6212\u20136216.<\/li>\n<li>Seo, J; Chen, C.-W.; Lee, W.; Jeon, J. E.; Chen, P.-L.; Chuang, S.-C.*; Joo, J. M.* Pd-Catalyzed C\u2013H \u201cBenzannulation of Functionalized Furans and Pyrroles with Alkynes\u201d Synthesis 2021, 53, 3001-3010.<\/li>\n<\/ol>\n<\/li>\n<\/ol>\n<p>Song, J. Y.; Jang, J. H.; Chuang, S.-C.*; Joo, J. M.* \u201cPalladium-catalyzed Aerobic Benzannulation of Pyrazoles with Alkynes\u201d Bull. Kor. Chem. Soc. 2021, 42, 489-491.<\/p>\n<p>Hsiao, H.-C.; Annamalai, P.; Jayakumar, J.; Sun, S.-Y.; Chuang, S.-C.* \u201cSynthesis of Fluorescent 4-Azapyrenes by Palladium(II)-Catalyzed Dual C\u2212H Bond Activation and Annulation\u201d Adv. Synth. Catal. 2021, 363, 1695-1701.<\/p>\n<p>Jillella, R.; Raju, S.; Hsiao, H.-C.; Hsu, D.-S.; Chuang, S.-C.* &#8220;Pd-Catalyzed Redox-Neutral C\u2013N Coupling Reaction of Iminoquinones with Electron-Deficient Alkenes without External Oxidants: Access of Tertiary (E)-Enamines and Application to the Synthesis of Indoles and Quinolin-4-ones&#8221; Org. Lett. 2020, 22, 6252-6256.<\/p>\n<p>Jayakumar, J.; Vedarethinam, G.; Hsiao, H.-C.; Sun, S.-Y.; Chuang, S.-C.* \u201cCascade One-Pot Synthesis of Orange-Red Fluorescent Polycyclic Cinnolino[2,3-f]phenanthridin-9-ium Salts by Palladium(II)-Catalyzed C-H Bond Activation of 2-Azobiaryls and Alkenes\u201d Angew. Chem. Int. Ed. 2020, 59, 689-694.<\/p>\n<p>Tseng, P.-Y.; Hsiao, H.-C.; Hsieh, C.-M.;Wu, A.-J.; Chuang, S.-C.* &#8220;Organic bulk heterojunction photovoltaics incorporating cyclopenteno[60]fullerene monoadducts as n-type materials display superior power conversion efficiency than with PC61BM&#8221; J. Chin. Chem. Soc. 2020, 67, 430 (Invited).<\/p>\n<p>Annamalai, P.; Hsiao, H.-C.; Raju, S.; Fu, Y.-H.; Chen, P.-L.; Horng, J.-C.; Liu, Y.-H.; Chuang, S.-C.* \u201cSynthesis, Isolation, and Characterization of Mono- and Bis-Norbornene Annulated Biarylamines Through Pseudo-Catellani Intermediates\u201d Org. Lett. 2019, 21, 1182-1186.<\/p>\n<p>Raju, S.; Hsiao, H.-C.; Thirupathi, S.; Chen, P.-L.; Chuang, S.-C.* &#8220;Palladium-Catalyzed Benzofulvenation of o-Arylanilines through C\u2013H Bond Activation by Using Two Diarylacetylenes as an Implicit Benzofulvene&#8221; Adv. Synth. Catal. 2019, 361, 683-689.<\/p>\n<p>Nallapati, S. B.; Chuang, S.-C.* &#8220;Phosphine-catalyzed Reactions with Unsaturated Carbonyl Compounds&#8221; Asian J. Org. Chem. 2018, 7, 1743-1757 (Invited review).<\/p>\n<p>Chiou, M.-F.; Jayakumar, J.; Cheng, C.-H.; Chuang, S.-C.* \u201cImpact of the Valence Charge of Transition Metals on the Cobalt- and Rhodium-Catalyzed Synthesis of Indenamines, Indenols, and Isoquinolinium Salts: A Catalytic Cycle Involving MIII\/MV [M = Co, Rh] for [4+2] Annulation\u201d J. Org. Chem. 2018, 83, 7814-7824.<\/p>\n<p>Hsieh, C.-M.; Liao, Y.-S.; Lin, Y.-R.; Chen, C.-P.; Tsai, C.-M.; Diau, E. W.-G.; Chuang, S.-C.* \u201cLow-Temperature, Simple and Efficient Preparation of Perovskite Solar Cells Using Lewis Bases Urea and Thiourea as Additives: Stimulating Large Grain Growth and Providing a PCE up to 18.8%\u201d RSC Adv. 2018, 8, 19610-19615. (selected for the RSC Advances 10th Anniversary collection: Solar energy)<\/p>\n<p>Annamalai, P.; Hsu, K.-C.; Raju, S.; Hsiao, H.-C.; Chou, C.-W.; Lin, G.-Y.; Hsieh, C.-M.; Chen, P.-L.; Liu, Y.-H.; Chuang, S.-C.* \u201cPalladium (II)-catalyzed mono- and bis-alkenylation of N-acetyl-2-aminobiaryls through regioselective C\u2013H bond activation\u201d J. Org. Chem. 2018, 83, 3840-3856.<\/p>\n<p>Upadhyay, N. S.; Thorat, V. H.; Sato, R.; Annamalai, P.; Chuang, S.-C.*; Cheng, C.-H.* &#8220;Synthesis of Isoquinolone via Rh-catalyzed C-H Activation of Substituted Benzamides as Air as the Sole Oxidant in Water&#8221; Green Chemistry, 2017, 19, 3219-3224.<\/p>\n<p>Raju, S.; Annamalai, P.; Chen, P.-L.; Liu, Y.-H.; Chuang, S.-C.* &#8220;Palladium-Catalyzed C\u2013H Bond Activation by Using Iminoquinone as a Directing Group and an Internal Oxidant or a Co-oxidant: Production of Dihydrophenanthridines, Phenanthridines, and Carbazoles&#8221; Org. Lett. 2017, 19, 4134-4137.<\/p>\n<p>Raju, S.; Annamalai, P.; Chen, P.-L.; Liu, Y.-H.; Chuang, S.-C.* &#8220;Iptycenes with an acridinone motif developed through [4+2]cycloaddition of tethered naphthalene and iminoquinone via a radical reaction&#8221; Chem. Commun., 2017, 53, 6247-6250.<\/p>\n<p>Raju, S.; Annamalai, P.; Chan, F.-W. Tseng, P.-Y.; Chen, P.-Y.; Kuo, T.-S.; Chuang, S.-C. &#8220;Palladium-Catalyzed Regio- and Stereoselective Hydrosulfonation of Propiolate Esters&#8221; Synthesis 2017, 49, 5007-5016.<\/p>\n<p>Annamalai, P.; Chen, W.-Y.; Raju, S.; Hsu, K.-C.; Upadhyay, N. S.; Cheng, C.-H.*; Chuang, S.-C.* &#8221; Palladium-Catalyzed Selective Aryl Ring C\u2013H Activation of N-Acyl 2-Aminobiaryls: Efficient Access of Multiaryl Substituted Naphthalenes&#8221; Adv. Synth. Catal. 2016, 358, 3642\u20133648.<\/p>\n<p>Chuang, S.-C.*; Sung, S.-P.; Deng, J.-C.; Chiou, M.-F.; Hsu, D.-S. &#8220;Multicomponent reactions of phosphines, enynedioates and benzylidene malononitriles generated highly substituted cyclopentenes through an unexpected phosphine alpha-addition-delta-evolvement of an anion pathway&#8221; Org. Biomol. Chem. 2016, 14, 2306\u20132317.<\/p>\n<p>Wu, A.-J.; Tseng, P,-Y.; Hsu, W.-H.; Chuang, S.-C.* &#8220;Tricyclohexylphosphine-catalyzed Cycloaddition of Enynoates with [60]Fullerene and the Application of Cyclopentenofullerenes as n-Type Materials in Organic Photovoltaics&#8221; Org. Lett. 2016,18, 224\u2013227.<\/p>\n<p>Tai, H.-C.; Chavan, A. S.; Chuang, S.-C.* &#8220;Nucleophilic Conjugate 1,5-Addition of (E)-Hex-2-en-4-ynedioates towards Gilman Reagents: An Access toward b(g&#8217;)-Substituted Muconates&#8221; Synthesis 2015, 47, 2223\u20132232.<\/p>\n<p>Deng, J.-C.; Chen, W.-Y.; Zhu, C.; Chuang, S.-C.* &#8221; Multicomponent Reactions of Phosphines, Enynedioates and Cinnamaldimines Give \u03b3-Lactams with a 1,3,5-Hexatriene Moiety for Facile 6p Electrocyclization: Access to Oxindoles, Isatins and Isoxazolinones&#8221; Adv. Synth. &amp; Catal. 2015, 357, 1453\u20131462.<\/p>\n<p>Chen, C.-P.*; Huang, C.-Y.; Chuang, S.-C.* &#8220;Highly Thermal Stable and Efficient Organic Photovoltaic Cells with Crosslinked Networks Appending Open-Cage Fullerenes as Additives&#8221; Adv. Funct. Mater., 2015, 15, 207\u2013213 (Selected as a Frontispiece).<\/p>\n<p>Deng, J.-C.; Chuang, S.-C.* \u201cMulticomponent Reactions of Phosphines, Diynedioates and Aryl Aldehydes Generated Furans Appending Reactive Phosphorus Ylides through Cumulated Trienoates as Key Intermediates: A Phosphine a-Addition-d-Evolvement of an Anion Pathway\u201d Org. Lett. 2014, 16, 5792\u20135795.<\/p>\n<p>Jayakumar, J.; Parthasarathy, K.; Chen, Y.-H.; Lee, T.-H.; Chuang, S.-C.;* Cheng, C.-H.* \u201cOne-Pot Synthesis of Highly Substituted Polyheteroaromatic Compounds by Rhodium(III)-Catalyzed Multiple C-H Activation and Annulation\u201d Angew. Chem. Int. Ed. 2014, 53, 9889\u20139892.<\/p>\n<p>Deng, J.-C.; Kuo, C.-W.; Chuang, S.-C.* \u201cNucleophilic Conjugate 1,3-Addition of Phosphines to Oligoynoates\u201d Chem. Commun., 2014, 50, 10580\u201310583 (Selected as an Inside Back Cover).<\/p>\n<p>Lin, Y.-W., Deng, J.-C., Hsieh, Y.-Z.; Chuang, S.-C.* \u201cOne-Pot Formation of Fluorescent g-Lactams Having an a-Phosphorus Ylide Moiety through Three-Component a(d&#8217;)-Michael Reaction of Phosphines with an Enyne and N-Tosyl Aldimines\u201d Org. Biomol. Chem. 2014, 12, 162\u2013170.<\/p>\n<p>Lee, T.-H.; Jayakumar, J.; Cheng, C.-H.;* Chuang, S.-C.* \u201cOne Pot Synthesis of Bioactive Benzopyranones through Palladium-Catalyzed C\u2212H Activation and CO Insertion to 2-Arylphenols\u201d Chem. Commun., 2013, 49, 11797\u201311799.<\/p>\n<p>Murata, Y.; Chuang, S.-C.; Tanabe, F.; Murata, M.; Komatsu, K. \u201cRecognition of hydrogen isotopomers by an open-cage fullerene\u201d Philosophical Transactions of the Royal Society, A: Mathematical, Physical &amp; Engineering Sciences 2013, 371(1998), 20110629\/1-20110629\/6.<\/p>\n<p>Tseng, B.-Y.; Chuang, S.-C.* \u201cChemo-, Regio- and Stereoselective Tricyclohexylphosphine-Catalyzed [3+2]Cycloaddition of Enynes with [60]Fullerene Initiated by 1,4-Michael Addition: Synthesis of Cyclopenteno[60]fullerenes and Their Electrochemical Properties\u201d Adv. Synth. &amp; Catal. 2013, 355, 2165\u20132171.<\/p>\n<p>Rajeshkumar, V.; Lee, T.-H.; Chuang, S.-C.* \u201cPalladium-Catalyzed Oxidative Insertion of Carbon Monoxide to N-Sulfonyl-2-aminobiaryls through C\u2013H Bond Activation: Access to Bioactive Phenanthridinone Derivatives in One Pot\u201d Org. Lett. 2013, 15, 1468\u20131471.<\/p>\n<p>Chavan, A. S.; Deng, J.-C.; Chuang, S.-C.* \u201c\u03b1(\u03b4&#8217;)-Michael Addition of Alkyl amines to Dimethyl (E)-Hex-2-en-4-ynedioate: Synthesis of a,b-Dehydroamino Acid Derivatives\u201d Molecules, 2013, 18, 2611\u20132622.<\/p>\n<p>Rajeshkumar, V.; Chan, F.-W.; Chuang, S.-C.* \u201cPalladium-Catalyzed and Hybrid Acids-Assisted Synthesis of [60]Fulleroazepines in One Pot Under Mild Conditions: Annulation of N-sulfonyl-2-aminobiaryls with [60]Fullerene through Sequential C\u2013H Bond Activation, C\u2013C and C\u2013N Bond Formation\u201d Adv. Synth. &amp; Catal. 2012, 354, 2473\u20132483.<\/p>\n<p>Deng, J.-C.; Chan, F.-W.; Kuo, C.-W.; Cheng, C.-A.; Huang, C.-Y. Chuang, S.-C.* \u201cAssembly of Dimethyl Acetylenedicarboxylate and Phosphanes with Aldehydes Leading to g-Lactones Having a-Phosphorus Ylides as Wittig Reagents\u201d Eur. J. Org. Chem. 2012, 5738\u20135747.<\/p>\n<p>Rajeshkumar, V.; Chuang, S.-C.* \u201cEvolution of Late Transition-Metal-Catalyzed Intermolecular Reductive Coupling Reaction of [60]Fullerene and N-sulfonylaldimines: Competing Formation of Hydrobenzylated [60]Fullerenes and 1,2-Dihydrofullerene\u201d Eur. J. Org. Chem. 2012, 3795\u20133805.<\/p>\n<p>Chuang, S.-C.;* Deng, J.-C.; Chan, F.-W.; Chen, S.-Y.; Huang, W.-J.; Lai, L.-H.; Rajeshkumar, V. \u201c[3+2] Cycloaddition of Dialkyl (E)-Hex-2-en-4-ynedioates to [60]Fullerene by Phosphane-Promoted Tandem \u03b1(\u03b4&#8217;)-Michael Additions\u201d Eur. J. Org. Chem. 2012, 2606\u20132613.<\/p>\n<p>Chen, C.-P.;* Lin, Y.-W.; Horng; J.-C.; Chuang, S.-C.* \u201cOpen-cage Fullerenes as n-Type Materials in Organic Photovoltaics: Relevance of Frontier Energy Levels, Carrier Mobility and Morphology of Different Sizable Open-cage Fullerenes with Power Conversion Efficiency in Devices\u201d Adv. Energy Mat. 2011, 1, 776\u2013780.<\/p>\n<p>Chen, C.-P.;* Chen, Y.-D.; Chuang, S.-C.* \u201cHigh-Performance and Highly-Durable Inverted Organic Photovoltaics Embedding Solution-Processable Vanadium Oxides as an Interfacial Hole-Transporting Layer\u201d Adv. Mat. 2011, 11, 3859\u20133863.<\/p>\n<p>Chuang, S.-C.;* Chiu, C.-W.; Chien, S.-C.; Chu, C.-W.; Chen, F.-C.* \u201c1-(3-Methoxycarbonyl)propyl-2-selenyl-[6,6]-methanofullerene as a n-Type Material for Organic Solar Cells\u201d Syn. Met. 2011, 161, 1624\u20131629.<\/p>\n<p>Deng, J.-C.; Chuang, S.-C.* \u201cThree-Component and Nonclassical Reaction of Phosphines with Enynes and Aldehydes: Formation of g-Lactones Featuring a-Phosphorus Ylides\u201d Org. Lett. 2011, 13, 2248\u20132251.<\/p>\n<p>Chuang, S.-C.*; RajeshKumar, V.; Cheng, C.-A.; Deng, J.-C.; Wang, G.-W.* \u201cAnnulation of Benzamides with [60]Fullerenes Through Palladium(II)-Catalyzed C-H Bond Activation\u201d J. Org. Chem. 2011, 76, 1599\u20131604.<\/p>\n<p>Chen, C.-P.; Luo, C.; Ting, C.; Chuang, S.-C.* \u201cOrganic Photovoltaics Incorporating Fulleroisoquinolinone as n-type Materials\u201d Chem. Commun. 2011, 47, 1845\u20131847.<\/p>\n<p>Su, H.-L.; Kao, W.-C.; Lee, C.-Y.; Chuang, S.-C.; Hsieh, Y.-Z.* \u201cSeparation of open-cage fullerenes using nonaqueous capillary electrophoresis\u201d J. Chromatography A 2010, 1217, 4471\u20134475.<\/p>\n<p>Chen, S.-Y.; Cheng, R.-L.; Tseng, C.-K.; Lin, Y.-S.; Lai,L.-H.; Venkatachalam, R. K.; Chen, Y.-C.; Cheng, C.-H.; Chuang, S.-C.* \u201cFullerene Derivatives Incorporating Phosphoramidous Ylide and Phosphoramidate: Synthesis and Property\u201d J. Org. Chem. 2009, 74, 4866\u20134869.<\/p>\n<p>Turro, N. J.; Marti, A. A.; Chen, J. Y.-C.; Jockusch, S.; Lawler, R. G.; Ruzzi, M.; Sartori, E.; Chuang, S.-C.; Komatsu, K.; Murata, Y. \u201cDemonstration of a Chemical Transformation Inside a Fullerene. The Reversible Conversion of the Allotropes of H2@C60\u201d J. Am. Chem. Soc. 2008, 130, 10506\u201310507.<\/p>\n<p>Chin, K. K.; Chuang, S.-C.; Hernandez, B.; Selke, M.; Foote, C. S.; Garcia-Garibay, M. A. \u201cPhotophysical Properties of non-Homoconjugated 1,2-disubstituted, 1,2,3,4-tetrasubstituted, and 1,2,3,4,5,6-Hexasubstituted Fullerene Derivatives\u201d, Photochemistry and Photobiological Science, 2008, 7, 49\u201355.<\/p>\n<p>Chuang, S.-C.; Murata, Y.; Murata, M.; Komatsu, K. \u201cAn Orifice-Size Index for Open-Cage Fullerenes\u201d J. Org. Chem. 2007, 72, 6447\u20136453.<\/p>\n<p>Chuang, S.-C.; Murata, Y.; Murata, M.; Komatsu, K. \u201cThe Outside Knows the Difference Inside: Trapping Helium by Immediate Reduction of Orifice Size of an Open-Cage Fullerene and the Effect of Encapsulated Helium and Hydrogen upon NMR of the Proton Directly Attached to the Outside\u201d Chem. Commun. 2007, 1751\u20131753.<\/p>\n<p>Sander, M.; Jarrosson, T.; Chuang, S.-C.; Khan, S. I.; Rubin, Y. \u201cApproaches to Open Fullerenes: Synthesis and Thermal Stability of cis-1 Bis(isobenzofuran) Diels-Alder Adducts of C60\u201d J. Org. Chem. 2007, 72, 2724\u20132731.<\/p>\n<p>Chuang, S.-C.; Jarrosson, T.; Sander, M.; James, S.; Rozumov, E.; Khan, S. I.; Rubin, Y. \u201cApproaches to Open Fullerenes: Synthesis and Kinetic Stability of Diels-Alder Adducts of Substituted Isobenzofurans and C60\u201d J. Org. Chem. 2007, 72, 2716\u20132723.<\/p>\n<p>Chuang, S.-C.; Murata, Y.; Murata, M.; Mori, S.; Maeda, S.; Tanabe, F.; Komatsu, K. \u201cFine Tuning of the Orifice Size of an Open-Cage Fullerene by Placing Selenium in the Rim: Insertion\/Release of Molecular Hydrogen\u201d, Chem. Commun. 2007, 1278\u20131280.<\/p>\n<p>Chin, K. K.; Chuang, S.-C.; Hernandez, B.; Selke, M.; Foote, C. S.; Garcia-Garibay, M. A. \u201cPhotophysical Properties of a 1,2,3,4,5,6-Hexasubstituted Fullerene Derivative\u201d, J. Phy. Chem. A, 2006, 110, 13662\u201313666.<\/p>\n<p>Chuang, S.-C.; Clemente, F.; Khan, S. I.; Houk, K. N.; Rubin, Y. \u201cApproaches to Open Fullerenes: A 1,2,3,4,5,6-Hexaadduct of C60\u201d, Org. Lett. 2006, 8, 4525\u20134528.<\/p>\n<p>Chuang, S.-C.; Khan, Saeed I.; Rubin, Y. \u201cSwitch of Electronic Reactivity in Fullerene C60: Activation of Three trans-4 Positions via Temporary Saturation of the cis-1 Positions\u201d, Org. Lett. 2006, 8, 6075\u20136078.<\/p>\n<p>Chuang, S.-C. \u201cNano Sugery of C60\u201d PhD dissertation, University of California, Los Angeles, 2005.<\/p>\n<p>Qian, W.; Chuang, S.-C.; Amador, R. B.; Jarrosson, T.; Sander, M.; Pieniazek, S.; Khan, S. I.; Rubin, Y. \u201cSynthesis of Stable Derivatives of C62: The First Nonclassical Fullerene Incorporating a Four-Membered Ring\u201d J. Am. Chem. Soc., 2003, 125, 2066\u20132067.<\/p>\n<p>Chuang, S.-C.; Islam, A.; Huang, C.-W.; Shih, H.-T.; Cheng, C.-H. \u201cNovel Acid-Catalyzed Rearrangement of Methanofullerenes Bearing an -Ylidic Ester to Cyclopentanofullerenes: A Vinyl Cyclopropane-Type Ring Expansion\u201d J. Org. Chem. 2003, 68, 3811\u20133816.<\/p>\n<p>Chuang, S.-C.; Shih, H.-T.; Cheng, C.-H. \u201cInteraction of Magnesium and Lithium Ions with [60]Fullerene Derivatives Bearing a Phosphorus Ylide Group\u201d Fullerene Science and Technology 2001, 233\u2013239.<\/p>\n<p>Chuang, S.-C.; Lee, D.-D.; Santhosh, K. C.; Cheng, C.-H. \u201cFullerene Derivatives Bearing a Phosphite Ylide, Phosphonate, Phosphine Oxide, and Phosphonic Acid: Synthesis and Reactivities\u201d J. Org. Chem. 1999, 64, 8868\u20138872.<\/p>\n<p>Chuang, S.-C.; Santhosh, K. C.; Lin, C.-H.; Wang, S.-L.; Cheng, C.-H. \u201cSynthesis and Chemistry of Fullerene Derivatives Bearing Phosphorus Substituents. Unusual Reaction of Phosphines with Electron-Deficient Acetylenes and C60\u201d J. Org. Chem. 1999, 64, 6664\u20136669.<\/li>\n<\/ol>\n<\/li>\n<\/ol>\n<\/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-j6hxe-5fb49e4c0ad7cd690d1f1e1f6b8c601e\">\n.flex_column.av-j6hxe-5fb49e4c0ad7cd690d1f1e1f6b8c601e{\npadding:30px 30px 15px 30px;\nbackground-color:#e9f3ff;\n}\n<\/style>\n<div  class='flex_column av-j6hxe-5fb49e4c0ad7cd690d1f1e1f6b8c601e av_one_full  avia-builder-el-32  el_after_av_one_full  el_before_av_textblock  first flex_column_div  column-top-margin'     ><p>\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-436ozm-a296f8b40374534ea3d140d196ec7c42\">\n#top .av-special-heading.av-436ozm-a296f8b40374534ea3d140d196ec7c42{\npadding-bottom:10px;\n}\nbody .av-special-heading.av-436ozm-a296f8b40374534ea3d140d196ec7c42 .av-special-heading-tag .heading-char{\nfont-size:25px;\n}\n.av-special-heading.av-436ozm-a296f8b40374534ea3d140d196ec7c42 .av-subheading{\nfont-size:15px;\n}\n<\/style>\n<div  class='av-special-heading av-436ozm-a296f8b40374534ea3d140d196ec7c42 av-special-heading-h3 blockquote modern-quote  avia-builder-el-33  el_before_av_masonry_gallery  avia-builder-el-no-sibling '><h3 class='av-special-heading-tag '  itemprop=\"headline\"  >Teaching Achievements<\/h3><div class=\"special-heading-border\"><div class=\"special-heading-inner-border\"><\/div><\/div><\/div><br \/>\n<\/p><\/div>\n<section  class='av_textblock_section av-2gax9e-08307241190a12da63bf7df25d3d5c4d '   itemscope=\"itemscope\" itemtype=\"https:\/\/schema.org\/CreativeWork\" ><div class='avia_textblock'  itemprop=\"text\" ><p>Click here to add your own text<\/p>\n<\/div><\/section>\n<div  class='flex_column av-av_one_full-7714eba142aeda1f8b5272a3c372b279 av_one_full  avia-builder-el-36  el_after_av_textblock  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-ms8u3uwk-e6d61706cb0097715289bf95ef714951\">\n#top .av-special-heading.av-ms8u3uwk-e6d61706cb0097715289bf95ef714951{\npadding-bottom:0;\n}\nbody .av-special-heading.av-ms8u3uwk-e6d61706cb0097715289bf95ef714951 .av-special-heading-tag .heading-char{\nfont-size:25px;\n}\n.av-special-heading.av-ms8u3uwk-e6d61706cb0097715289bf95ef714951 .av-subheading{\nfont-size:15px;\n}\n<\/style>\n<div  class='av-special-heading av-ms8u3uwk-e6d61706cb0097715289bf95ef714951 av-special-heading-h3 blockquote modern-quote  avia-builder-el-37  el_before_av_image  avia-builder-el-first '><h3 class='av-special-heading-tag '  itemprop=\"headline\"  ><\/p>\n<div class=\"title-style-1\">Research Highlights<\/div>\n<p><\/h3><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-ms8u4a6k-ab406317aa0605198154fad9bbe74316\">\n.avia-image-container.av-ms8u4a6k-ab406317aa0605198154fad9bbe74316 img.avia_image{\nbox-shadow:none;\n}\n.avia-image-container.av-ms8u4a6k-ab406317aa0605198154fad9bbe74316 .av-image-caption-overlay-center{\ncolor:#ffffff;\n}\n<\/style>\n<div  class='avia-image-container av-ms8u4a6k-ab406317aa0605198154fad9bbe74316 av-styling-no-styling avia-align-center  avia-builder-el-38  el_after_av_heading  avia-builder-el-last '   itemprop=\"image\" itemscope=\"itemscope\" itemtype=\"https:\/\/schema.org\/ImageObject\" ><div class=\"avia-image-container-inner\"><div class=\"avia-image-overlay-wrap\"><img decoding=\"async\" fetchpriority=\"high\" class='wp-image-19898 avia-img-lazy-loading-not-19898 avia_image ' src=\"https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u6295\u5f71\u72474-1030x713.png\" alt='Shih-Ching Chuang' title='\u6295\u5f71\u72474'  height=\"713\" width=\"1030\"  itemprop=\"thumbnailUrl\" srcset=\"https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u6295\u5f71\u72474-1030x713.png 1030w, https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u6295\u5f71\u72474-289x200.png 289w, https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u6295\u5f71\u72474-768x532.png 768w, https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u6295\u5f71\u72474-705x488.png 705w, https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u6295\u5f71\u72474.png 1040w\" sizes=\"(max-width: 1030px) 100vw, 1030px\" \/><\/div><\/div><\/div><\/p><\/div><\/li>\n<\/ol>\n","protected":false},"excerpt":{"rendered":"<p>Shih-Ching Chuang \u838a\u58eb\u537f<br \/>\nTransition-Metal-Catalyzed C-H Bond Activation, Synthetic Methodology, Organic Photovoltaics<br \/>\nTel | 03-5712121 #31858<br \/>\nEmail | jscchuang@nycu.edu.tw<br \/>\nOffice | Science Building II R531<\/p>\n","protected":false},"author":20,"featured_media":16744,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"footnotes":""},"tags":[],"portfolio_entries":[198,196],"class_list":["post-16742","portfolio","type-portfolio","status-publish","has-post-thumbnail","hentry","portfolio_entries-01-en","portfolio_entries--en"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.2 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Professor Shih-Ching Chuang - \u570b\u7acb\u967d\u660e\u4ea4\u901a\u5927\u5b78\u61c9\u7528\u5316\u5b78\u7cfb<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/dac.nycu.edu.tw\/en\/portfolio-item\/professor-shih-ching-chuang\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" 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