TUNING THE EXCITED STATES IN fac-[Re(X2dppz)(CO)3(L)]: INTRALIGAND, CHARGE TRANSFER OR BOTH?
Excited state lifetime measurements emission, emission lifetime and Resonance Raman have been conducted on the series fac-[Re(X2dppz)(CO)3(L)]0,+ (L = Cl-, 4-ethylpyridine (4-Etpy), 4,4´-bipyridine (4,4´-bpy)), with the X2dppz substituted dipyrido[3,2-a:2',3'-c] phenazine ligands (X = CH3...
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Veröffentlicht in: | Journal of the Chilean Chemical Society 2004-06, Vol.49 (2), p.149-155 |
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container_title | Journal of the Chilean Chemical Society |
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description | Excited state lifetime measurements emission, emission lifetime and Resonance Raman have been conducted on the series fac-[Re(X2dppz)(CO)3(L)]0,+ (L = Cl-, 4-ethylpyridine (4-Etpy), 4,4´-bipyridine (4,4´-bpy)), with the X2dppz substituted dipyrido[3,2-a:2',3'-c] phenazine ligands (X = CH3 and Cl). The results are consistent with closely lying excited states, with pp * lowest, but MLCT contributing significantly to excited state lifetimes for the neutral complexes. fac-[Re(Cl2dppz)(CO)3Cl] appears to undergo a crossover from lowest pp* to lowest MLCT through the glass to fluid transition |
doi_str_mv | 10.4067/S0717-97072004000200009 |
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The results are consistent with closely lying excited states, with pp * lowest, but MLCT contributing significantly to excited state lifetimes for the neutral complexes. fac-[Re(Cl2dppz)(CO)3Cl] appears to undergo a crossover from lowest pp* to lowest MLCT through the glass to fluid transition</description><identifier>ISSN: 0717-9707</identifier><identifier>EISSN: 0717-9707</identifier><identifier>DOI: 10.4067/S0717-97072004000200009</identifier><language>eng</language><publisher>Sociedad Chilena de Química</publisher><subject>CHEMISTRY, MULTIDISCIPLINARY</subject><ispartof>Journal of the Chilean Chemical Society, 2004-06, Vol.49 (2), p.149-155</ispartof><rights>This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c343t-93d43b047f01b0e213e6390ae813b5724729b437e19f8040ef9816317b3a49bf3</citedby></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></links><search><creatorcontrib>LÓPEZ B, ROSA</creatorcontrib><creatorcontrib>LOEB L, BÁRBARA</creatorcontrib><creatorcontrib>STRIPLIN, DURWIN</creatorcontrib><creatorcontrib>DEVENNEY, MARTIN</creatorcontrib><creatorcontrib>OMBERG, KRISTIN</creatorcontrib><creatorcontrib>MEYER, THOMAS J.</creatorcontrib><title>TUNING THE EXCITED STATES IN fac-[Re(X2dppz)(CO)3(L)]: INTRALIGAND, CHARGE TRANSFER OR BOTH?</title><title>Journal of the Chilean Chemical Society</title><addtitle>J. Chil. Chem. Soc</addtitle><description>Excited state lifetime measurements emission, emission lifetime and Resonance Raman have been conducted on the series fac-[Re(X2dppz)(CO)3(L)]0,+ (L = Cl-, 4-ethylpyridine (4-Etpy), 4,4´-bipyridine (4,4´-bpy)), with the X2dppz substituted dipyrido[3,2-a:2',3'-c] phenazine ligands (X = CH3 and Cl). The results are consistent with closely lying excited states, with pp * lowest, but MLCT contributing significantly to excited state lifetimes for the neutral complexes. fac-[Re(Cl2dppz)(CO)3Cl] appears to undergo a crossover from lowest pp* to lowest MLCT through the glass to fluid transition</description><subject>CHEMISTRY, MULTIDISCIPLINARY</subject><issn>0717-9707</issn><issn>0717-9707</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNp1kFFLwzAUhYMoOKe_wTx2YOdNkzWNL1K7rC2UFtoMBiql7RLYmK60-qC_3upEBPHpXO7hu5dzELokMGXg8usCOOG24MAdAAYAgwCIIzT6MY5_zaforO-3ANSZue4IPahlGqchVpHEchXESs5xoXwlCxyn2FSNfZ9ra-Ws2_Z9YgXZhFrJ5PFmMFXuJ3Hop_MrHER-Hko8bNJiIXOc5fguU9HtOTox1a7XF986RsuFVEFkJ1kYB35iN5TRF1vQNaM1MG6A1KAdQrVLBVTaI7SecYdxR9SMck2E8YaI2giPuJTwmlZM1IaO0fRwt282ercvt_vX7nl4WH51U_7pZgD4AWi6fd932pRtt3mqureSQPnZ6r_kB_FoXng</recordid><startdate>20040601</startdate><enddate>20040601</enddate><creator>LÓPEZ B, ROSA</creator><creator>LOEB L, BÁRBARA</creator><creator>STRIPLIN, DURWIN</creator><creator>DEVENNEY, MARTIN</creator><creator>OMBERG, KRISTIN</creator><creator>MEYER, THOMAS J.</creator><general>Sociedad Chilena de Química</general><scope>AAYXX</scope><scope>CITATION</scope><scope>GPN</scope></search><sort><creationdate>20040601</creationdate><title>TUNING THE EXCITED STATES IN fac-[Re(X2dppz)(CO)3(L)]: INTRALIGAND, CHARGE TRANSFER OR BOTH?</title><author>LÓPEZ B, ROSA ; LOEB L, BÁRBARA ; STRIPLIN, DURWIN ; DEVENNEY, MARTIN ; OMBERG, KRISTIN ; MEYER, THOMAS J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c343t-93d43b047f01b0e213e6390ae813b5724729b437e19f8040ef9816317b3a49bf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>CHEMISTRY, MULTIDISCIPLINARY</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>LÓPEZ B, ROSA</creatorcontrib><creatorcontrib>LOEB L, BÁRBARA</creatorcontrib><creatorcontrib>STRIPLIN, DURWIN</creatorcontrib><creatorcontrib>DEVENNEY, MARTIN</creatorcontrib><creatorcontrib>OMBERG, KRISTIN</creatorcontrib><creatorcontrib>MEYER, THOMAS J.</creatorcontrib><collection>CrossRef</collection><collection>SciELO</collection><jtitle>Journal of the Chilean Chemical Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>LÓPEZ B, ROSA</au><au>LOEB L, BÁRBARA</au><au>STRIPLIN, DURWIN</au><au>DEVENNEY, MARTIN</au><au>OMBERG, KRISTIN</au><au>MEYER, THOMAS J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>TUNING THE EXCITED STATES IN fac-[Re(X2dppz)(CO)3(L)]: INTRALIGAND, CHARGE TRANSFER OR BOTH?</atitle><jtitle>Journal of the Chilean Chemical Society</jtitle><addtitle>J. Chil. Chem. Soc</addtitle><date>2004-06-01</date><risdate>2004</risdate><volume>49</volume><issue>2</issue><spage>149</spage><epage>155</epage><pages>149-155</pages><issn>0717-9707</issn><eissn>0717-9707</eissn><abstract>Excited state lifetime measurements emission, emission lifetime and Resonance Raman have been conducted on the series fac-[Re(X2dppz)(CO)3(L)]0,+ (L = Cl-, 4-ethylpyridine (4-Etpy), 4,4´-bipyridine (4,4´-bpy)), with the X2dppz substituted dipyrido[3,2-a:2',3'-c] phenazine ligands (X = CH3 and Cl). The results are consistent with closely lying excited states, with pp * lowest, but MLCT contributing significantly to excited state lifetimes for the neutral complexes. fac-[Re(Cl2dppz)(CO)3Cl] appears to undergo a crossover from lowest pp* to lowest MLCT through the glass to fluid transition</abstract><pub>Sociedad Chilena de Química</pub><doi>10.4067/S0717-97072004000200009</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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title | TUNING THE EXCITED STATES IN fac-[Re(X2dppz)(CO)3(L)]: INTRALIGAND, CHARGE TRANSFER OR BOTH? |
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