Mechanism of metal-to-ligand charge transfer sensitization of olefin trans-to-cis isomerization in the fac-[ReI(phen)(CO)3(1,2-bpe)]+ cation

被引:54
作者
Dattelbaum, DM
Itokazu, MK
Iha, NYM
Meyer, TJ
机构
[1] Univ Sao Paulo, Inst Quim, BR-05508900 Sao Paulo, Brazil
[2] Univ N Carolina, Dept Chem, Chapel Hill, NC 27599 USA
[3] Los Alamos Natl Lab, Los Alamos, NM 87545 USA
关键词
D O I
10.1021/jp021660o
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Near-UV, largely Re-I --> phen, bpe metal-to-ligand charge transfer (MLCT) excitation of fac-[Re-I(phen)(CO)3(trans-bpe)](+) [where phen is 1,10-phenanthroline and bpe is 1,2-bis(4-pyridyl)ethylene] in CH3CN results in isomerization at the bpe ligand and formation of fac-[Re-I(phen)(CO)(3)(cis-bpe)](+). Time-resolved absorption and infrared (TRIR) measurements reveal the existence of an intermediate with a lifetime of similar to28 ns (k = 3.6 x 10(7) s(-1)). According to the results of the transient IR measurements, the intermediate is ligand-based, presumably the olefin-localized twisted triplet (3)p. TRIR measurements in the nu(C=C) region point to a significant twisting around the C=C bond in (3)p.
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页码:4092 / 4095
页数:4
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