Time-resolved relaxation studies of spin crossover systems in solution

被引:93
作者
Brady, C
McGarvey, JJ [1 ]
McCusker, JK
Toftlund, H
Hendrickson, DN
机构
[1] Queens Univ Belfast, Sch Chem, Belfast BT9 5AG, Antrim, North Ireland
[2] Michigan State Univ, Dept Chem, E Lansing, MI 48824 USA
[3] Univ So Denmark, Dept Chem, DK-5230 Odense, Denmark
[4] Univ Calif San Diego, Dept Chem & Biochem, La Jolla, CA 92093 USA
来源
SPIN CROSSOVER IN TRANSITION METAL COMPOUNDS III | 2004年 / 235卷
关键词
spin crossover; dynamics; kinetics; ultrafast spectroscopy; photoperturbation; photophysics; activation parameters; time-resolved vibrational spectroscopy;
D O I
10.1007/b95420
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This chapter focuses on the kinetics of spin-state relaxation, primarily in iron(II) complexes in solution. Initial work carried out during the 1970s and early 1980s by chemical relaxation methods is briefly reviewed, followed by a more detailed account of the laser photoperturbation technique and the photophysics which underpin this approach, now widely adopted as the method of choice for spin crossover relaxation studies in solution. The use of time-resolved vibrational spectroscopy as an alternative to conventional spectrophotometric probing of the spin crossover relaxation process is described. The results of variable temperature and pressure studies on a variety of spin crossover complexes are also considered, particularly with reference to strategies for the control of spin state lifetimes through design of ligand structures.
引用
收藏
页码:1 / 22
页数:22
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