Study of intervalence bands due to reversible intramolecular electron transfer phenomena in purely organic mixed-valence high-spin molecules
Up to now, few examples of reversible electron intramolecular transfer phenomena in purely organic mixed-valence molecules have been studied in detail. We present the first example of a purely organic molecule in which, in addition to the observation of an optical electron transfer between open-shel...
Gespeichert in:
Veröffentlicht in: | Synthetic metals 1997-03, Vol.85 (1), p.1651-1654 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1654 |
---|---|
container_issue | 1 |
container_start_page | 1651 |
container_title | Synthetic metals |
container_volume | 85 |
creator | Sedó, J. Ruiz, D. Vidal-Gancedo, J. Rovira, C. Bonvoisin, J. Launay, J.-P. Veciana, J. |
description | Up to now, few examples of reversible electron intramolecular transfer phenomena in purely organic mixed-valence molecules have been studied in detail. We present the first example of a purely organic molecule in which, in addition to the observation of an optical electron transfer between open-shell and anionic sites, two radical centers remain ferromagnetic ally coupled inside the molecule. The intervalence band which arises from the optical ET is clearly observed in the far NIR range and is quantitatively analyzed by means of an
ad hoc model. Since these properties are rather unusual for purely organic compounds, even separately, this and similar molecules offer us a unique chance for studying the reciprocal influence between electron transfer and strong magnetic coupling in organic systems. |
doi_str_mv | 10.1016/S0379-6779(97)80383-9 |
format | Article |
fullrecord | <record><control><sourceid>hal_cross</sourceid><recordid>TN_cdi_hal_primary_oai_HAL_hal_04235979v1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0379677997803839</els_id><sourcerecordid>oai_HAL_hal_04235979v1</sourcerecordid><originalsourceid>FETCH-LOGICAL-c370t-6d350adc296d8013bbaa9a0efe92f38dbd8a977213534a2443339ddafab2e4203</originalsourceid><addsrcrecordid>eNqFkMtKxDAUhoMoOF4eQcjChS6qubRNsxIRbzDgQl2H0-TUiXTaknQGfQcf2tTR2bpKOHz_fzgfISecXXDGy8tnJpXOSqX0mVbnFZOVzPQOmfEqjaXQbJfMtsg-OYjxnTHGtShm5Ot5XLlP2jfUdyOGNbTYWaQ1dC5St0I69jTgGkP0dYsTFGDZt2hXLQSK6TOGvqNp2sUGAx0W2PVL7CChdFgFbFN5eIPOW7r0H-iyvxUL_7bI4pCw3z6MR2SvgTbi8e97SF7vbl9uHrL50_3jzfU8s1KxMSudLBg4K3TpKsZlXQNoYNigFo2sXO0q0EoJLguZg8hzKaV2DhqoBeaCyUNyvuldQGuG4JcQPk0P3jxcz800Y7mQhVZ6zRNbbFgb-hgDNtsAZ2bSb370m8mt0cr86Dc65U43uQGihbZJgqyP27AodVVWE3a1wTDdu_YYTLR-8uN8SG6N6_0_i74Bd7udRQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Study of intervalence bands due to reversible intramolecular electron transfer phenomena in purely organic mixed-valence high-spin molecules</title><source>Elsevier ScienceDirect Journals Complete - AutoHoldings</source><creator>Sedó, J. ; Ruiz, D. ; Vidal-Gancedo, J. ; Rovira, C. ; Bonvoisin, J. ; Launay, J.-P. ; Veciana, J.</creator><creatorcontrib>Sedó, J. ; Ruiz, D. ; Vidal-Gancedo, J. ; Rovira, C. ; Bonvoisin, J. ; Launay, J.-P. ; Veciana, J.</creatorcontrib><description>Up to now, few examples of reversible electron intramolecular transfer phenomena in purely organic mixed-valence molecules have been studied in detail. We present the first example of a purely organic molecule in which, in addition to the observation of an optical electron transfer between open-shell and anionic sites, two radical centers remain ferromagnetic ally coupled inside the molecule. The intervalence band which arises from the optical ET is clearly observed in the far NIR range and is quantitatively analyzed by means of an
ad hoc model. Since these properties are rather unusual for purely organic compounds, even separately, this and similar molecules offer us a unique chance for studying the reciprocal influence between electron transfer and strong magnetic coupling in organic systems.</description><identifier>ISSN: 0379-6779</identifier><identifier>EISSN: 1879-3290</identifier><identifier>DOI: 10.1016/S0379-6779(97)80383-9</identifier><identifier>CODEN: SYMEDZ</identifier><language>eng</language><publisher>Lausanne: Elsevier B.V</publisher><subject>Atomic and molecular physics ; Chemical Sciences ; Electrochemical methods ; Electron-spin resonance ; Electron-transfer ; Exact sciences and technology ; High-spin ; Infrared spectra ; Intervalence band ; Molecular properties and interactions with photons ; Molecular spectra ; Physics ; UV-Vis-NIR absorption</subject><ispartof>Synthetic metals, 1997-03, Vol.85 (1), p.1651-1654</ispartof><rights>1997 Elsevier Science S.A. All rights reserved</rights><rights>1997 INIST-CNRS</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c370t-6d350adc296d8013bbaa9a0efe92f38dbd8a977213534a2443339ddafab2e4203</citedby><cites>FETCH-LOGICAL-c370t-6d350adc296d8013bbaa9a0efe92f38dbd8a977213534a2443339ddafab2e4203</cites><orcidid>0000-0003-3741-9529</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0379-6779(97)80383-9$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,309,310,314,780,784,789,790,885,3548,23928,23929,25138,27922,27923,45993</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2698689$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-04235979$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Sedó, J.</creatorcontrib><creatorcontrib>Ruiz, D.</creatorcontrib><creatorcontrib>Vidal-Gancedo, J.</creatorcontrib><creatorcontrib>Rovira, C.</creatorcontrib><creatorcontrib>Bonvoisin, J.</creatorcontrib><creatorcontrib>Launay, J.-P.</creatorcontrib><creatorcontrib>Veciana, J.</creatorcontrib><title>Study of intervalence bands due to reversible intramolecular electron transfer phenomena in purely organic mixed-valence high-spin molecules</title><title>Synthetic metals</title><description>Up to now, few examples of reversible electron intramolecular transfer phenomena in purely organic mixed-valence molecules have been studied in detail. We present the first example of a purely organic molecule in which, in addition to the observation of an optical electron transfer between open-shell and anionic sites, two radical centers remain ferromagnetic ally coupled inside the molecule. The intervalence band which arises from the optical ET is clearly observed in the far NIR range and is quantitatively analyzed by means of an
ad hoc model. Since these properties are rather unusual for purely organic compounds, even separately, this and similar molecules offer us a unique chance for studying the reciprocal influence between electron transfer and strong magnetic coupling in organic systems.</description><subject>Atomic and molecular physics</subject><subject>Chemical Sciences</subject><subject>Electrochemical methods</subject><subject>Electron-spin resonance</subject><subject>Electron-transfer</subject><subject>Exact sciences and technology</subject><subject>High-spin</subject><subject>Infrared spectra</subject><subject>Intervalence band</subject><subject>Molecular properties and interactions with photons</subject><subject>Molecular spectra</subject><subject>Physics</subject><subject>UV-Vis-NIR absorption</subject><issn>0379-6779</issn><issn>1879-3290</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><recordid>eNqFkMtKxDAUhoMoOF4eQcjChS6qubRNsxIRbzDgQl2H0-TUiXTaknQGfQcf2tTR2bpKOHz_fzgfISecXXDGy8tnJpXOSqX0mVbnFZOVzPQOmfEqjaXQbJfMtsg-OYjxnTHGtShm5Ot5XLlP2jfUdyOGNbTYWaQ1dC5St0I69jTgGkP0dYsTFGDZt2hXLQSK6TOGvqNp2sUGAx0W2PVL7CChdFgFbFN5eIPOW7r0H-iyvxUL_7bI4pCw3z6MR2SvgTbi8e97SF7vbl9uHrL50_3jzfU8s1KxMSudLBg4K3TpKsZlXQNoYNigFo2sXO0q0EoJLguZg8hzKaV2DhqoBeaCyUNyvuldQGuG4JcQPk0P3jxcz800Y7mQhVZ6zRNbbFgb-hgDNtsAZ2bSb370m8mt0cr86Dc65U43uQGihbZJgqyP27AodVVWE3a1wTDdu_YYTLR-8uN8SG6N6_0_i74Bd7udRQ</recordid><startdate>199703</startdate><enddate>199703</enddate><creator>Sedó, J.</creator><creator>Ruiz, D.</creator><creator>Vidal-Gancedo, J.</creator><creator>Rovira, C.</creator><creator>Bonvoisin, J.</creator><creator>Launay, J.-P.</creator><creator>Veciana, J.</creator><general>Elsevier B.V</general><general>Elsevier Science</general><general>Elsevier</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0003-3741-9529</orcidid></search><sort><creationdate>199703</creationdate><title>Study of intervalence bands due to reversible intramolecular electron transfer phenomena in purely organic mixed-valence high-spin molecules</title><author>Sedó, J. ; Ruiz, D. ; Vidal-Gancedo, J. ; Rovira, C. ; Bonvoisin, J. ; Launay, J.-P. ; Veciana, J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c370t-6d350adc296d8013bbaa9a0efe92f38dbd8a977213534a2443339ddafab2e4203</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Atomic and molecular physics</topic><topic>Chemical Sciences</topic><topic>Electrochemical methods</topic><topic>Electron-spin resonance</topic><topic>Electron-transfer</topic><topic>Exact sciences and technology</topic><topic>High-spin</topic><topic>Infrared spectra</topic><topic>Intervalence band</topic><topic>Molecular properties and interactions with photons</topic><topic>Molecular spectra</topic><topic>Physics</topic><topic>UV-Vis-NIR absorption</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sedó, J.</creatorcontrib><creatorcontrib>Ruiz, D.</creatorcontrib><creatorcontrib>Vidal-Gancedo, J.</creatorcontrib><creatorcontrib>Rovira, C.</creatorcontrib><creatorcontrib>Bonvoisin, J.</creatorcontrib><creatorcontrib>Launay, J.-P.</creatorcontrib><creatorcontrib>Veciana, J.</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Synthetic metals</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sedó, J.</au><au>Ruiz, D.</au><au>Vidal-Gancedo, J.</au><au>Rovira, C.</au><au>Bonvoisin, J.</au><au>Launay, J.-P.</au><au>Veciana, J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Study of intervalence bands due to reversible intramolecular electron transfer phenomena in purely organic mixed-valence high-spin molecules</atitle><jtitle>Synthetic metals</jtitle><date>1997-03</date><risdate>1997</risdate><volume>85</volume><issue>1</issue><spage>1651</spage><epage>1654</epage><pages>1651-1654</pages><issn>0379-6779</issn><eissn>1879-3290</eissn><coden>SYMEDZ</coden><abstract>Up to now, few examples of reversible electron intramolecular transfer phenomena in purely organic mixed-valence molecules have been studied in detail. We present the first example of a purely organic molecule in which, in addition to the observation of an optical electron transfer between open-shell and anionic sites, two radical centers remain ferromagnetic ally coupled inside the molecule. The intervalence band which arises from the optical ET is clearly observed in the far NIR range and is quantitatively analyzed by means of an
ad hoc model. Since these properties are rather unusual for purely organic compounds, even separately, this and similar molecules offer us a unique chance for studying the reciprocal influence between electron transfer and strong magnetic coupling in organic systems.</abstract><cop>Lausanne</cop><cop>Amsterdam</cop><cop>New York, NY</cop><pub>Elsevier B.V</pub><doi>10.1016/S0379-6779(97)80383-9</doi><tpages>4</tpages><orcidid>https://orcid.org/0000-0003-3741-9529</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0379-6779 |
ispartof | Synthetic metals, 1997-03, Vol.85 (1), p.1651-1654 |
issn | 0379-6779 1879-3290 |
language | eng |
recordid | cdi_hal_primary_oai_HAL_hal_04235979v1 |
source | Elsevier ScienceDirect Journals Complete - AutoHoldings |
subjects | Atomic and molecular physics Chemical Sciences Electrochemical methods Electron-spin resonance Electron-transfer Exact sciences and technology High-spin Infrared spectra Intervalence band Molecular properties and interactions with photons Molecular spectra Physics UV-Vis-NIR absorption |
title | Study of intervalence bands due to reversible intramolecular electron transfer phenomena in purely organic mixed-valence high-spin molecules |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-09T11%3A57%3A32IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-hal_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Study%20of%20intervalence%20bands%20due%20to%20reversible%20intramolecular%20electron%20transfer%20phenomena%20in%20purely%20organic%20mixed-valence%20high-spin%20molecules&rft.jtitle=Synthetic%20metals&rft.au=Sed%C3%B3,%20J.&rft.date=1997-03&rft.volume=85&rft.issue=1&rft.spage=1651&rft.epage=1654&rft.pages=1651-1654&rft.issn=0379-6779&rft.eissn=1879-3290&rft.coden=SYMEDZ&rft_id=info:doi/10.1016/S0379-6779(97)80383-9&rft_dat=%3Chal_cross%3Eoai_HAL_hal_04235979v1%3C/hal_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rft_els_id=S0379677997803839&rfr_iscdi=true |