Loading…
1,3,5‐Benzene Tricarboxylic Acid Based Cocrystals With Selective Semiconductivity via H‐coupled Charge Transfer
Two organic cocrystals, one (1) based on benzene 1,3,5 tricarboxylic acid (TMA) plus 4‐amino pyridine and another (2) based on benzene 1,3,5 tricarboxylic acid (TMA) plus urea is reported. Cocrystals 1 and 2 are fully characterized by single crystal X ray diffraction, NMR and IR spectroscopy. The si...
Saved in:
Published in: | ChemistrySelect (Weinheim) 2024-02, Vol.9 (8), p.n/a |
---|---|
Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | cdi_FETCH-LOGICAL-c2446-c1770b5fc1855998a858e13f204fffda65b39aab621b3157f2d67871fa4f5a813 |
container_end_page | n/a |
container_issue | 8 |
container_start_page | |
container_title | ChemistrySelect (Weinheim) |
container_volume | 9 |
creator | Sarkar, Sudip Shil, Suranjan De, Gobinda Chandra Ghosh, Sushobhan |
description | Two organic cocrystals, one (1) based on benzene 1,3,5 tricarboxylic acid (TMA) plus 4‐amino pyridine and another (2) based on benzene 1,3,5 tricarboxylic acid (TMA) plus urea is reported. Cocrystals 1 and 2 are fully characterized by single crystal X ray diffraction, NMR and IR spectroscopy. The single crystal X ray diffraction shows the intermolecular H‐bonding interaction between components of the pairs TMA‐TMA as well as TMA‐4 amino pyridine and TMA‐Urea molecules. The conductivity studies for the cocrystal 1 shows semiconducting behavior whereas cocrystal 2remain as insulator under the same experimental condition. Computational studies with theoretically optimized structures as well as experimental X‐ray structures of both the cocrystals reveal the origin of conductivity as the H‐atom coupled charge transfer through the intermolecular H‐bonding between TMA and 4‐amino pyridine in cocrystal 1.
Selective Semiconductivity via H‐coupled Charge Transfer of Benzene 1,3,5 Tricarboxylic acid based cocrystals 1 and 2. Cocrystal 1 is supposed to give semiconductive state by H atom transfer over charge assisted H‐bond formation between trimesic acid and 4‐amino pyridine which is absent in Cocrystal 2 as it gives normal H‐bonding between urea and trimesic acid. |
doi_str_mv | 10.1002/slct.202304666 |
format | article |
fullrecord | <record><control><sourceid>wiley_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1002_slct_202304666</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>SLCT202304666</sourcerecordid><originalsourceid>FETCH-LOGICAL-c2446-c1770b5fc1855998a858e13f204fffda65b39aab621b3157f2d67871fa4f5a813</originalsourceid><addsrcrecordid>eNqFkL1OwzAUhS0EElXpyuwHaIJ_YscZ2wgoUiSGBjFGjmNTozSp7LQQJh6BZ-RJSFQEbEz3XOl833AAuMQoxAiRK1-rLiSIUBRxzk_AhFDOAs6i5PRPPgcz758RQpgLTlg8AR7P6Zx9vn8sdfOmGw1zZ5V0Zfva11bBhbIVXEqvK5i2yvW-k7WHj7bbwLWutersQQ9pa1XbVPvxtV0PD1bC1eBU7X5Xj-hGuqdRLRtvtLsAZ2bQ6Nn3nYKHm-s8XQXZ_e1dusgCRaKIBwrHMSqZUVgwliRCCiY0poagyBhTSc5KmkhZcoJLillsSMVjEWMjI8OkwHQKwqNXudZ7p02xc3YrXV9gVIyrFeNqxc9qA5AcgRdb6_6fdrHO0vyX_QK-0XQU</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>1,3,5‐Benzene Tricarboxylic Acid Based Cocrystals With Selective Semiconductivity via H‐coupled Charge Transfer</title><source>Wiley-Blackwell Read & Publish Collection</source><creator>Sarkar, Sudip ; Shil, Suranjan ; De, Gobinda Chandra ; Ghosh, Sushobhan</creator><creatorcontrib>Sarkar, Sudip ; Shil, Suranjan ; De, Gobinda Chandra ; Ghosh, Sushobhan</creatorcontrib><description>Two organic cocrystals, one (1) based on benzene 1,3,5 tricarboxylic acid (TMA) plus 4‐amino pyridine and another (2) based on benzene 1,3,5 tricarboxylic acid (TMA) plus urea is reported. Cocrystals 1 and 2 are fully characterized by single crystal X ray diffraction, NMR and IR spectroscopy. The single crystal X ray diffraction shows the intermolecular H‐bonding interaction between components of the pairs TMA‐TMA as well as TMA‐4 amino pyridine and TMA‐Urea molecules. The conductivity studies for the cocrystal 1 shows semiconducting behavior whereas cocrystal 2remain as insulator under the same experimental condition. Computational studies with theoretically optimized structures as well as experimental X‐ray structures of both the cocrystals reveal the origin of conductivity as the H‐atom coupled charge transfer through the intermolecular H‐bonding between TMA and 4‐amino pyridine in cocrystal 1.
Selective Semiconductivity via H‐coupled Charge Transfer of Benzene 1,3,5 Tricarboxylic acid based cocrystals 1 and 2. Cocrystal 1 is supposed to give semiconductive state by H atom transfer over charge assisted H‐bond formation between trimesic acid and 4‐amino pyridine which is absent in Cocrystal 2 as it gives normal H‐bonding between urea and trimesic acid.</description><identifier>ISSN: 2365-6549</identifier><identifier>EISSN: 2365-6549</identifier><identifier>DOI: 10.1002/slct.202304666</identifier><language>eng</language><subject>Cocrystal ; H Stacking ; Semiconductor</subject><ispartof>ChemistrySelect (Weinheim), 2024-02, Vol.9 (8), p.n/a</ispartof><rights>2024 Wiley‐VCH GmbH</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c2446-c1770b5fc1855998a858e13f204fffda65b39aab621b3157f2d67871fa4f5a813</cites><orcidid>0000-0002-8440-7494</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Sarkar, Sudip</creatorcontrib><creatorcontrib>Shil, Suranjan</creatorcontrib><creatorcontrib>De, Gobinda Chandra</creatorcontrib><creatorcontrib>Ghosh, Sushobhan</creatorcontrib><title>1,3,5‐Benzene Tricarboxylic Acid Based Cocrystals With Selective Semiconductivity via H‐coupled Charge Transfer</title><title>ChemistrySelect (Weinheim)</title><description>Two organic cocrystals, one (1) based on benzene 1,3,5 tricarboxylic acid (TMA) plus 4‐amino pyridine and another (2) based on benzene 1,3,5 tricarboxylic acid (TMA) plus urea is reported. Cocrystals 1 and 2 are fully characterized by single crystal X ray diffraction, NMR and IR spectroscopy. The single crystal X ray diffraction shows the intermolecular H‐bonding interaction between components of the pairs TMA‐TMA as well as TMA‐4 amino pyridine and TMA‐Urea molecules. The conductivity studies for the cocrystal 1 shows semiconducting behavior whereas cocrystal 2remain as insulator under the same experimental condition. Computational studies with theoretically optimized structures as well as experimental X‐ray structures of both the cocrystals reveal the origin of conductivity as the H‐atom coupled charge transfer through the intermolecular H‐bonding between TMA and 4‐amino pyridine in cocrystal 1.
Selective Semiconductivity via H‐coupled Charge Transfer of Benzene 1,3,5 Tricarboxylic acid based cocrystals 1 and 2. Cocrystal 1 is supposed to give semiconductive state by H atom transfer over charge assisted H‐bond formation between trimesic acid and 4‐amino pyridine which is absent in Cocrystal 2 as it gives normal H‐bonding between urea and trimesic acid.</description><subject>Cocrystal</subject><subject>H Stacking</subject><subject>Semiconductor</subject><issn>2365-6549</issn><issn>2365-6549</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqFkL1OwzAUhS0EElXpyuwHaIJ_YscZ2wgoUiSGBjFGjmNTozSp7LQQJh6BZ-RJSFQEbEz3XOl833AAuMQoxAiRK1-rLiSIUBRxzk_AhFDOAs6i5PRPPgcz758RQpgLTlg8AR7P6Zx9vn8sdfOmGw1zZ5V0Zfva11bBhbIVXEqvK5i2yvW-k7WHj7bbwLWutersQQ9pa1XbVPvxtV0PD1bC1eBU7X5Xj-hGuqdRLRtvtLsAZ2bQ6Nn3nYKHm-s8XQXZ_e1dusgCRaKIBwrHMSqZUVgwliRCCiY0poagyBhTSc5KmkhZcoJLillsSMVjEWMjI8OkwHQKwqNXudZ7p02xc3YrXV9gVIyrFeNqxc9qA5AcgRdb6_6fdrHO0vyX_QK-0XQU</recordid><startdate>20240226</startdate><enddate>20240226</enddate><creator>Sarkar, Sudip</creator><creator>Shil, Suranjan</creator><creator>De, Gobinda Chandra</creator><creator>Ghosh, Sushobhan</creator><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0002-8440-7494</orcidid></search><sort><creationdate>20240226</creationdate><title>1,3,5‐Benzene Tricarboxylic Acid Based Cocrystals With Selective Semiconductivity via H‐coupled Charge Transfer</title><author>Sarkar, Sudip ; Shil, Suranjan ; De, Gobinda Chandra ; Ghosh, Sushobhan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2446-c1770b5fc1855998a858e13f204fffda65b39aab621b3157f2d67871fa4f5a813</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Cocrystal</topic><topic>H Stacking</topic><topic>Semiconductor</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sarkar, Sudip</creatorcontrib><creatorcontrib>Shil, Suranjan</creatorcontrib><creatorcontrib>De, Gobinda Chandra</creatorcontrib><creatorcontrib>Ghosh, Sushobhan</creatorcontrib><collection>CrossRef</collection><jtitle>ChemistrySelect (Weinheim)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sarkar, Sudip</au><au>Shil, Suranjan</au><au>De, Gobinda Chandra</au><au>Ghosh, Sushobhan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>1,3,5‐Benzene Tricarboxylic Acid Based Cocrystals With Selective Semiconductivity via H‐coupled Charge Transfer</atitle><jtitle>ChemistrySelect (Weinheim)</jtitle><date>2024-02-26</date><risdate>2024</risdate><volume>9</volume><issue>8</issue><epage>n/a</epage><issn>2365-6549</issn><eissn>2365-6549</eissn><abstract>Two organic cocrystals, one (1) based on benzene 1,3,5 tricarboxylic acid (TMA) plus 4‐amino pyridine and another (2) based on benzene 1,3,5 tricarboxylic acid (TMA) plus urea is reported. Cocrystals 1 and 2 are fully characterized by single crystal X ray diffraction, NMR and IR spectroscopy. The single crystal X ray diffraction shows the intermolecular H‐bonding interaction between components of the pairs TMA‐TMA as well as TMA‐4 amino pyridine and TMA‐Urea molecules. The conductivity studies for the cocrystal 1 shows semiconducting behavior whereas cocrystal 2remain as insulator under the same experimental condition. Computational studies with theoretically optimized structures as well as experimental X‐ray structures of both the cocrystals reveal the origin of conductivity as the H‐atom coupled charge transfer through the intermolecular H‐bonding between TMA and 4‐amino pyridine in cocrystal 1.
Selective Semiconductivity via H‐coupled Charge Transfer of Benzene 1,3,5 Tricarboxylic acid based cocrystals 1 and 2. Cocrystal 1 is supposed to give semiconductive state by H atom transfer over charge assisted H‐bond formation between trimesic acid and 4‐amino pyridine which is absent in Cocrystal 2 as it gives normal H‐bonding between urea and trimesic acid.</abstract><doi>10.1002/slct.202304666</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0002-8440-7494</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2365-6549 |
ispartof | ChemistrySelect (Weinheim), 2024-02, Vol.9 (8), p.n/a |
issn | 2365-6549 2365-6549 |
language | eng |
recordid | cdi_crossref_primary_10_1002_slct_202304666 |
source | Wiley-Blackwell Read & Publish Collection |
subjects | Cocrystal H Stacking Semiconductor |
title | 1,3,5‐Benzene Tricarboxylic Acid Based Cocrystals With Selective Semiconductivity via H‐coupled Charge Transfer |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T01%3A02%3A05IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-wiley_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=1,3,5%E2%80%90Benzene%20Tricarboxylic%20Acid%20Based%20Cocrystals%20With%20Selective%20Semiconductivity%20via%20H%E2%80%90coupled%20Charge%20Transfer&rft.jtitle=ChemistrySelect%20(Weinheim)&rft.au=Sarkar,%20Sudip&rft.date=2024-02-26&rft.volume=9&rft.issue=8&rft.epage=n/a&rft.issn=2365-6549&rft.eissn=2365-6549&rft_id=info:doi/10.1002/slct.202304666&rft_dat=%3Cwiley_cross%3ESLCT202304666%3C/wiley_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c2446-c1770b5fc1855998a858e13f204fffda65b39aab621b3157f2d67871fa4f5a813%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |