Charge transfer in mixed and segregated stacks of tetrathiafulvalene, tetrathianaphthalene and naphthalene diimide: a structural, spectroscopic and computational study
Tetrathiafulvalene (TTF) is a highly tunable electron donor that has been widely studied in charge transfer (CT) complexes, including Bechgaard salts which are superconductors at low temperatures. Its close relative, tetrathianaphthalene (TTN) has received considerably less attention than its TTF co...
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Veröffentlicht in: | New journal of chemistry 2022-05, Vol.46 (21), p.126-136 |
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creator | Leong, Chanel F Chan, Bun Liu, Tianfu Moore, Harrison S Hod, Idan Solomon, Marcello B Usov, Pavel M Hupp, Joseph T Farha, Omar D'Alessandro, Deanna M |
description | Tetrathiafulvalene (TTF) is a highly tunable electron donor that has been widely studied in charge transfer (CT) complexes, including Bechgaard salts which are superconductors at low temperatures. Its close relative, tetrathianaphthalene (TTN) has received considerably less attention than its TTF counterpart but is potentially a versatile electron donor. Three novel CT complexes containing mixed and segregated stack donor-acceptor (D-A) complexes of tetrathiafulvalene (TTF), tetrathianaphthalene (TTN) and naphthalene diimide (NDI) are reported. We demonstrate a facile mechanochemical synthesis of two salts, TTF-DPNI and TTN-DPNI (DPNI =
N
,
N
′-di-(4-pyridyl)-1,4,5,8-naphthalenetetracarboxydiimide), which is uncommon for these materials. Despite the detection of a very low partial charge transfer in the three salts using UV-Vis-NIR, Raman and EPR spectroscopies, we elucidated the properties of the TTN core with support from DFT calculations for the first time. We highlight the performance of TTN in a CT complex and demonstrate the importance of a combined approach to the characterisation of CT in organic D-A complexes.
We report the synthesis of novel charge transfer complexes consisting of TTF or TTN, and DPNI. A spectroscopic and computational approach is taken to elucidate charge transfer in these complexes. |
doi_str_mv | 10.1039/d2nj00643j |
format | Article |
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N
,
N
′-di-(4-pyridyl)-1,4,5,8-naphthalenetetracarboxydiimide), which is uncommon for these materials. Despite the detection of a very low partial charge transfer in the three salts using UV-Vis-NIR, Raman and EPR spectroscopies, we elucidated the properties of the TTN core with support from DFT calculations for the first time. We highlight the performance of TTN in a CT complex and demonstrate the importance of a combined approach to the characterisation of CT in organic D-A complexes.
We report the synthesis of novel charge transfer complexes consisting of TTF or TTN, and DPNI. A spectroscopic and computational approach is taken to elucidate charge transfer in these complexes.</description><identifier>ISSN: 1144-0546</identifier><identifier>EISSN: 1369-9261</identifier><identifier>DOI: 10.1039/d2nj00643j</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Charge transfer ; Diimide ; Low temperature ; Naphthalene ; Superconductors</subject><ispartof>New journal of chemistry, 2022-05, Vol.46 (21), p.126-136</ispartof><rights>Copyright Royal Society of Chemistry 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c344t-a5e404dbaa11906c338cd71dbd725b56695bae3a7758a349dda9f268531ce0f53</citedby><cites>FETCH-LOGICAL-c344t-a5e404dbaa11906c338cd71dbd725b56695bae3a7758a349dda9f268531ce0f53</cites><orcidid>0000-0002-1497-2543 ; 0000-0002-9904-9845 ; 0000-0001-9096-6981 ; 0000-0003-3982-9812 ; 0000-0003-4837-8793 ; 0000-0002-0082-5497 ; 0000-0003-0732-676X ; 0000000214972543 ; 0000000348378793 ; 000000030732676X ; 0000000339829812 ; 0000000299049845 ; 0000000200825497 ; 0000000190966981</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.osti.gov/biblio/1866873$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Leong, Chanel F</creatorcontrib><creatorcontrib>Chan, Bun</creatorcontrib><creatorcontrib>Liu, Tianfu</creatorcontrib><creatorcontrib>Moore, Harrison S</creatorcontrib><creatorcontrib>Hod, Idan</creatorcontrib><creatorcontrib>Solomon, Marcello B</creatorcontrib><creatorcontrib>Usov, Pavel M</creatorcontrib><creatorcontrib>Hupp, Joseph T</creatorcontrib><creatorcontrib>Farha, Omar</creatorcontrib><creatorcontrib>D'Alessandro, Deanna M</creatorcontrib><title>Charge transfer in mixed and segregated stacks of tetrathiafulvalene, tetrathianaphthalene and naphthalene diimide: a structural, spectroscopic and computational study</title><title>New journal of chemistry</title><description>Tetrathiafulvalene (TTF) is a highly tunable electron donor that has been widely studied in charge transfer (CT) complexes, including Bechgaard salts which are superconductors at low temperatures. Its close relative, tetrathianaphthalene (TTN) has received considerably less attention than its TTF counterpart but is potentially a versatile electron donor. Three novel CT complexes containing mixed and segregated stack donor-acceptor (D-A) complexes of tetrathiafulvalene (TTF), tetrathianaphthalene (TTN) and naphthalene diimide (NDI) are reported. We demonstrate a facile mechanochemical synthesis of two salts, TTF-DPNI and TTN-DPNI (DPNI =
N
,
N
′-di-(4-pyridyl)-1,4,5,8-naphthalenetetracarboxydiimide), which is uncommon for these materials. Despite the detection of a very low partial charge transfer in the three salts using UV-Vis-NIR, Raman and EPR spectroscopies, we elucidated the properties of the TTN core with support from DFT calculations for the first time. We highlight the performance of TTN in a CT complex and demonstrate the importance of a combined approach to the characterisation of CT in organic D-A complexes.
We report the synthesis of novel charge transfer complexes consisting of TTF or TTN, and DPNI. A spectroscopic and computational approach is taken to elucidate charge transfer in these complexes.</description><subject>Charge transfer</subject><subject>Diimide</subject><subject>Low temperature</subject><subject>Naphthalene</subject><subject>Superconductors</subject><issn>1144-0546</issn><issn>1369-9261</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNpN0U1P3DAQBuCoKlIpcOFeyWpvFaF2_JGkt2r5aBEqFzhHs_Zk423WTm0HwS_ib2J2q8LJntHj0VhvURwzesoob7-Zyq0pVYKv3xX7jKu2bCvF3uc7E6KkUqgPxccYs2GsVmy_eFoMEFZIUgAXewzEOrKxD2gIOEMirgKuIOUyJtB_IvE9SZhxGiz083gPIzo8ee05mIY0bLvbCW9rY-3GGvxOIE8Ls05zgPGExAl1Cj5qP1m9faT9ZpoTJOsdjNnO5vGw2OthjHj07zwo7i7Obxc_y-uby1-LH9el5kKkEiQKKswSgLGWKs15o03NzNLUlVxKpVq5BORQ17IBLlpjoO0r1UjONNJe8oPi826uj8l2UduEetDeubxjxxqlmppn9GWHpuD_zhhTt_ZzyLvGrlI1a6VoWJ3V153S-XMxYN9NwW4gPHaMdi9pdWfV76ttWlcZf9rhEPV_95omfwYVaJXD</recordid><startdate>20220530</startdate><enddate>20220530</enddate><creator>Leong, Chanel F</creator><creator>Chan, Bun</creator><creator>Liu, Tianfu</creator><creator>Moore, Harrison S</creator><creator>Hod, Idan</creator><creator>Solomon, Marcello B</creator><creator>Usov, Pavel M</creator><creator>Hupp, Joseph T</creator><creator>Farha, Omar</creator><creator>D'Alessandro, Deanna M</creator><general>Royal Society of Chemistry</general><general>Royal Society of Chemistry (RSC)</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>H9R</scope><scope>JG9</scope><scope>KA0</scope><scope>OTOTI</scope><orcidid>https://orcid.org/0000-0002-1497-2543</orcidid><orcidid>https://orcid.org/0000-0002-9904-9845</orcidid><orcidid>https://orcid.org/0000-0001-9096-6981</orcidid><orcidid>https://orcid.org/0000-0003-3982-9812</orcidid><orcidid>https://orcid.org/0000-0003-4837-8793</orcidid><orcidid>https://orcid.org/0000-0002-0082-5497</orcidid><orcidid>https://orcid.org/0000-0003-0732-676X</orcidid><orcidid>https://orcid.org/0000000214972543</orcidid><orcidid>https://orcid.org/0000000348378793</orcidid><orcidid>https://orcid.org/000000030732676X</orcidid><orcidid>https://orcid.org/0000000339829812</orcidid><orcidid>https://orcid.org/0000000299049845</orcidid><orcidid>https://orcid.org/0000000200825497</orcidid><orcidid>https://orcid.org/0000000190966981</orcidid></search><sort><creationdate>20220530</creationdate><title>Charge transfer in mixed and segregated stacks of tetrathiafulvalene, tetrathianaphthalene and naphthalene diimide: a structural, spectroscopic and computational study</title><author>Leong, Chanel F ; Chan, Bun ; Liu, Tianfu ; Moore, Harrison S ; Hod, Idan ; Solomon, Marcello B ; Usov, Pavel M ; Hupp, Joseph T ; Farha, Omar ; D'Alessandro, Deanna M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c344t-a5e404dbaa11906c338cd71dbd725b56695bae3a7758a349dda9f268531ce0f53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Charge transfer</topic><topic>Diimide</topic><topic>Low temperature</topic><topic>Naphthalene</topic><topic>Superconductors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Leong, Chanel F</creatorcontrib><creatorcontrib>Chan, Bun</creatorcontrib><creatorcontrib>Liu, Tianfu</creatorcontrib><creatorcontrib>Moore, Harrison S</creatorcontrib><creatorcontrib>Hod, Idan</creatorcontrib><creatorcontrib>Solomon, Marcello B</creatorcontrib><creatorcontrib>Usov, Pavel M</creatorcontrib><creatorcontrib>Hupp, Joseph T</creatorcontrib><creatorcontrib>Farha, Omar</creatorcontrib><creatorcontrib>D'Alessandro, Deanna M</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Illustrata: Natural Sciences</collection><collection>Materials Research Database</collection><collection>ProQuest Illustrata: Technology Collection</collection><collection>OSTI.GOV</collection><jtitle>New journal of chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Leong, Chanel F</au><au>Chan, Bun</au><au>Liu, Tianfu</au><au>Moore, Harrison S</au><au>Hod, Idan</au><au>Solomon, Marcello B</au><au>Usov, Pavel M</au><au>Hupp, Joseph T</au><au>Farha, Omar</au><au>D'Alessandro, Deanna M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Charge transfer in mixed and segregated stacks of tetrathiafulvalene, tetrathianaphthalene and naphthalene diimide: a structural, spectroscopic and computational study</atitle><jtitle>New journal of chemistry</jtitle><date>2022-05-30</date><risdate>2022</risdate><volume>46</volume><issue>21</issue><spage>126</spage><epage>136</epage><pages>126-136</pages><issn>1144-0546</issn><eissn>1369-9261</eissn><abstract>Tetrathiafulvalene (TTF) is a highly tunable electron donor that has been widely studied in charge transfer (CT) complexes, including Bechgaard salts which are superconductors at low temperatures. Its close relative, tetrathianaphthalene (TTN) has received considerably less attention than its TTF counterpart but is potentially a versatile electron donor. Three novel CT complexes containing mixed and segregated stack donor-acceptor (D-A) complexes of tetrathiafulvalene (TTF), tetrathianaphthalene (TTN) and naphthalene diimide (NDI) are reported. We demonstrate a facile mechanochemical synthesis of two salts, TTF-DPNI and TTN-DPNI (DPNI =
N
,
N
′-di-(4-pyridyl)-1,4,5,8-naphthalenetetracarboxydiimide), which is uncommon for these materials. Despite the detection of a very low partial charge transfer in the three salts using UV-Vis-NIR, Raman and EPR spectroscopies, we elucidated the properties of the TTN core with support from DFT calculations for the first time. We highlight the performance of TTN in a CT complex and demonstrate the importance of a combined approach to the characterisation of CT in organic D-A complexes.
We report the synthesis of novel charge transfer complexes consisting of TTF or TTN, and DPNI. A spectroscopic and computational approach is taken to elucidate charge transfer in these complexes.</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/d2nj00643j</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-1497-2543</orcidid><orcidid>https://orcid.org/0000-0002-9904-9845</orcidid><orcidid>https://orcid.org/0000-0001-9096-6981</orcidid><orcidid>https://orcid.org/0000-0003-3982-9812</orcidid><orcidid>https://orcid.org/0000-0003-4837-8793</orcidid><orcidid>https://orcid.org/0000-0002-0082-5497</orcidid><orcidid>https://orcid.org/0000-0003-0732-676X</orcidid><orcidid>https://orcid.org/0000000214972543</orcidid><orcidid>https://orcid.org/0000000348378793</orcidid><orcidid>https://orcid.org/000000030732676X</orcidid><orcidid>https://orcid.org/0000000339829812</orcidid><orcidid>https://orcid.org/0000000299049845</orcidid><orcidid>https://orcid.org/0000000200825497</orcidid><orcidid>https://orcid.org/0000000190966981</orcidid><oa>free_for_read</oa></addata></record> |
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source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
subjects | Charge transfer Diimide Low temperature Naphthalene Superconductors |
title | Charge transfer in mixed and segregated stacks of tetrathiafulvalene, tetrathianaphthalene and naphthalene diimide: a structural, spectroscopic and computational study |
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