Loading…
A Donor–Acceptor–Donor Structured Organic Conductor with S···S Chalcogen Bonding
A novel thiophene derivative 7,9-di(thiophen-2-yl)-8H-cyclopenta[a]acenaphthylen-8-one (DTCPA) is shown to exhibit high electrical conductivity (1.97 × 10–2 ± 0.0018 S/cm at RT) in the crystalline state. The material shows two orders of increase in conductivity from normal solid to single crystalli...
Saved in:
Published in: | Crystal growth & design 2014-02, Vol.14 (2), p.459-466 |
---|---|
Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-a289t-a3d59d5bd2b4f41be6c5159d0fbe58d759133631d4c84e0fde4d9da913990d033 |
---|---|
cites | cdi_FETCH-LOGICAL-a289t-a3d59d5bd2b4f41be6c5159d0fbe58d759133631d4c84e0fde4d9da913990d033 |
container_end_page | 466 |
container_issue | 2 |
container_start_page | 459 |
container_title | Crystal growth & design |
container_volume | 14 |
creator | Bai, Monalisa Thomas, Sajesh P Kottokkaran, Ranjith Nayak, Susanta K Ramamurthy, Praveen C Guru Row, T. N |
description | A novel thiophene derivative 7,9-di(thiophen-2-yl)-8H-cyclopenta[a]acenaphthylen-8-one (DTCPA) is shown to exhibit high electrical conductivity (1.97 × 10–2 ± 0.0018 S/cm at RT) in the crystalline state. The material shows two orders of increase in conductivity from normal solid to single crystalline state. The crystal structure has S···S chalcogen bonding, C–H···O hydrogen bonding, and π···π stacking as the major intermolecular interactions. The nature and strength of the S···S interactions in this structure have been evaluated by theoretical charge density analysis, and its contribution to the crystal packing quantified by Hirshfeld surface analysis. Further, thermal and morphological characterizations have been carried out, and the second harmonic generation (SHG) efficiency has been measured using the Kurtz–Perry method. |
doi_str_mv | 10.1021/cg401069y |
format | article |
fullrecord | <record><control><sourceid>acs_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1021_cg401069y</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>a853225041</sourcerecordid><originalsourceid>FETCH-LOGICAL-a289t-a3d59d5bd2b4f41be6c5159d0fbe58d759133631d4c84e0fde4d9da913990d033</originalsourceid><addsrcrecordid>eNptkL9OwzAQxi0EEqUw8AZeGBgC59hOnLGEv1KlDgUxRo7tpKmCU9mpUDfegYdh51F4EtwWyoJuuE_f_e6T7hA6JXBBICaXqmZAIMlWe2hAeCyilAPf_9VM0EN05P0cANKE0gF6HuHrznbu6-19pJRZ9Bu5sfC0d0vVL53ReOJqaRuF887q4IXha9PP8PTzY11TnM9kq7raWHwViMbWx-igkq03Jz99iJ5ubx7z-2g8uXvIR-NIxiLrI0k1zzQvdVyyipHSJIqT4EBVGi50yjNCaUKJZkowA5U2TGdaBjfLQAOlQ3S-zVWu896Zqli45kW6VUGgWH-k2H0ksGdbdiG9km3lpFWN3y3EIgagqfjjpPLFvFs6Gy74J-8bnllw2w</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>A Donor–Acceptor–Donor Structured Organic Conductor with S···S Chalcogen Bonding</title><source>American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list)</source><creator>Bai, Monalisa ; Thomas, Sajesh P ; Kottokkaran, Ranjith ; Nayak, Susanta K ; Ramamurthy, Praveen C ; Guru Row, T. N</creator><creatorcontrib>Bai, Monalisa ; Thomas, Sajesh P ; Kottokkaran, Ranjith ; Nayak, Susanta K ; Ramamurthy, Praveen C ; Guru Row, T. N</creatorcontrib><description>A novel thiophene derivative 7,9-di(thiophen-2-yl)-8H-cyclopenta[a]acenaphthylen-8-one (DTCPA) is shown to exhibit high electrical conductivity (1.97 × 10–2 ± 0.0018 S/cm at RT) in the crystalline state. The material shows two orders of increase in conductivity from normal solid to single crystalline state. The crystal structure has S···S chalcogen bonding, C–H···O hydrogen bonding, and π···π stacking as the major intermolecular interactions. The nature and strength of the S···S interactions in this structure have been evaluated by theoretical charge density analysis, and its contribution to the crystal packing quantified by Hirshfeld surface analysis. Further, thermal and morphological characterizations have been carried out, and the second harmonic generation (SHG) efficiency has been measured using the Kurtz–Perry method.</description><identifier>ISSN: 1528-7483</identifier><identifier>EISSN: 1528-7505</identifier><identifier>DOI: 10.1021/cg401069y</identifier><language>eng</language><publisher>Washington,DC: American Chemical Society</publisher><subject>Condensed matter: electronic structure, electrical, magnetic, and optical properties ; Condensed matter: structure, mechanical and thermal properties ; Exact sciences and technology ; Optical properties and condensed-matter spectroscopy and other interactions of matter with particles and radiation ; Optical properties of bulk materials and thin films ; Physics ; Structure of solids and liquids; crystallography ; Structure of specific crystalline solids</subject><ispartof>Crystal growth & design, 2014-02, Vol.14 (2), p.459-466</ispartof><rights>Copyright © 2013 American Chemical Society</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a289t-a3d59d5bd2b4f41be6c5159d0fbe58d759133631d4c84e0fde4d9da913990d033</citedby><cites>FETCH-LOGICAL-a289t-a3d59d5bd2b4f41be6c5159d0fbe58d759133631d4c84e0fde4d9da913990d033</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=28200378$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Bai, Monalisa</creatorcontrib><creatorcontrib>Thomas, Sajesh P</creatorcontrib><creatorcontrib>Kottokkaran, Ranjith</creatorcontrib><creatorcontrib>Nayak, Susanta K</creatorcontrib><creatorcontrib>Ramamurthy, Praveen C</creatorcontrib><creatorcontrib>Guru Row, T. N</creatorcontrib><title>A Donor–Acceptor–Donor Structured Organic Conductor with S···S Chalcogen Bonding</title><title>Crystal growth & design</title><addtitle>Cryst. Growth Des</addtitle><description>A novel thiophene derivative 7,9-di(thiophen-2-yl)-8H-cyclopenta[a]acenaphthylen-8-one (DTCPA) is shown to exhibit high electrical conductivity (1.97 × 10–2 ± 0.0018 S/cm at RT) in the crystalline state. The material shows two orders of increase in conductivity from normal solid to single crystalline state. The crystal structure has S···S chalcogen bonding, C–H···O hydrogen bonding, and π···π stacking as the major intermolecular interactions. The nature and strength of the S···S interactions in this structure have been evaluated by theoretical charge density analysis, and its contribution to the crystal packing quantified by Hirshfeld surface analysis. Further, thermal and morphological characterizations have been carried out, and the second harmonic generation (SHG) efficiency has been measured using the Kurtz–Perry method.</description><subject>Condensed matter: electronic structure, electrical, magnetic, and optical properties</subject><subject>Condensed matter: structure, mechanical and thermal properties</subject><subject>Exact sciences and technology</subject><subject>Optical properties and condensed-matter spectroscopy and other interactions of matter with particles and radiation</subject><subject>Optical properties of bulk materials and thin films</subject><subject>Physics</subject><subject>Structure of solids and liquids; crystallography</subject><subject>Structure of specific crystalline solids</subject><issn>1528-7483</issn><issn>1528-7505</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNptkL9OwzAQxi0EEqUw8AZeGBgC59hOnLGEv1KlDgUxRo7tpKmCU9mpUDfegYdh51F4EtwWyoJuuE_f_e6T7hA6JXBBICaXqmZAIMlWe2hAeCyilAPf_9VM0EN05P0cANKE0gF6HuHrznbu6-19pJRZ9Bu5sfC0d0vVL53ReOJqaRuF887q4IXha9PP8PTzY11TnM9kq7raWHwViMbWx-igkq03Jz99iJ5ubx7z-2g8uXvIR-NIxiLrI0k1zzQvdVyyipHSJIqT4EBVGi50yjNCaUKJZkowA5U2TGdaBjfLQAOlQ3S-zVWu896Zqli45kW6VUGgWH-k2H0ksGdbdiG9km3lpFWN3y3EIgagqfjjpPLFvFs6Gy74J-8bnllw2w</recordid><startdate>20140205</startdate><enddate>20140205</enddate><creator>Bai, Monalisa</creator><creator>Thomas, Sajesh P</creator><creator>Kottokkaran, Ranjith</creator><creator>Nayak, Susanta K</creator><creator>Ramamurthy, Praveen C</creator><creator>Guru Row, T. N</creator><general>American Chemical Society</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20140205</creationdate><title>A Donor–Acceptor–Donor Structured Organic Conductor with S···S Chalcogen Bonding</title><author>Bai, Monalisa ; Thomas, Sajesh P ; Kottokkaran, Ranjith ; Nayak, Susanta K ; Ramamurthy, Praveen C ; Guru Row, T. N</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a289t-a3d59d5bd2b4f41be6c5159d0fbe58d759133631d4c84e0fde4d9da913990d033</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Condensed matter: electronic structure, electrical, magnetic, and optical properties</topic><topic>Condensed matter: structure, mechanical and thermal properties</topic><topic>Exact sciences and technology</topic><topic>Optical properties and condensed-matter spectroscopy and other interactions of matter with particles and radiation</topic><topic>Optical properties of bulk materials and thin films</topic><topic>Physics</topic><topic>Structure of solids and liquids; crystallography</topic><topic>Structure of specific crystalline solids</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bai, Monalisa</creatorcontrib><creatorcontrib>Thomas, Sajesh P</creatorcontrib><creatorcontrib>Kottokkaran, Ranjith</creatorcontrib><creatorcontrib>Nayak, Susanta K</creatorcontrib><creatorcontrib>Ramamurthy, Praveen C</creatorcontrib><creatorcontrib>Guru Row, T. N</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Crystal growth & design</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bai, Monalisa</au><au>Thomas, Sajesh P</au><au>Kottokkaran, Ranjith</au><au>Nayak, Susanta K</au><au>Ramamurthy, Praveen C</au><au>Guru Row, T. N</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Donor–Acceptor–Donor Structured Organic Conductor with S···S Chalcogen Bonding</atitle><jtitle>Crystal growth & design</jtitle><addtitle>Cryst. Growth Des</addtitle><date>2014-02-05</date><risdate>2014</risdate><volume>14</volume><issue>2</issue><spage>459</spage><epage>466</epage><pages>459-466</pages><issn>1528-7483</issn><eissn>1528-7505</eissn><abstract>A novel thiophene derivative 7,9-di(thiophen-2-yl)-8H-cyclopenta[a]acenaphthylen-8-one (DTCPA) is shown to exhibit high electrical conductivity (1.97 × 10–2 ± 0.0018 S/cm at RT) in the crystalline state. The material shows two orders of increase in conductivity from normal solid to single crystalline state. The crystal structure has S···S chalcogen bonding, C–H···O hydrogen bonding, and π···π stacking as the major intermolecular interactions. The nature and strength of the S···S interactions in this structure have been evaluated by theoretical charge density analysis, and its contribution to the crystal packing quantified by Hirshfeld surface analysis. Further, thermal and morphological characterizations have been carried out, and the second harmonic generation (SHG) efficiency has been measured using the Kurtz–Perry method.</abstract><cop>Washington,DC</cop><pub>American Chemical Society</pub><doi>10.1021/cg401069y</doi><tpages>8</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1528-7483 |
ispartof | Crystal growth & design, 2014-02, Vol.14 (2), p.459-466 |
issn | 1528-7483 1528-7505 |
language | eng |
recordid | cdi_crossref_primary_10_1021_cg401069y |
source | American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list) |
subjects | Condensed matter: electronic structure, electrical, magnetic, and optical properties Condensed matter: structure, mechanical and thermal properties Exact sciences and technology Optical properties and condensed-matter spectroscopy and other interactions of matter with particles and radiation Optical properties of bulk materials and thin films Physics Structure of solids and liquids crystallography Structure of specific crystalline solids |
title | A Donor–Acceptor–Donor Structured Organic Conductor with S···S Chalcogen Bonding |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-24T01%3A58%3A45IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-acs_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20Donor%E2%80%93Acceptor%E2%80%93Donor%20Structured%20Organic%20Conductor%20with%20S%C2%B7%C2%B7%C2%B7S%20Chalcogen%20Bonding&rft.jtitle=Crystal%20growth%20&%20design&rft.au=Bai,%20Monalisa&rft.date=2014-02-05&rft.volume=14&rft.issue=2&rft.spage=459&rft.epage=466&rft.pages=459-466&rft.issn=1528-7483&rft.eissn=1528-7505&rft_id=info:doi/10.1021/cg401069y&rft_dat=%3Cacs_cross%3Ea853225041%3C/acs_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-a289t-a3d59d5bd2b4f41be6c5159d0fbe58d759133631d4c84e0fde4d9da913990d033%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 |