Understanding the reactivity of transition metal complexes involving multiple spin states

被引:313
作者
Harvey, JN
Poli, R
Smith, KM
机构
[1] Univ Bourgogne 1, Lab Synthese & Electrosynthese Organomet, Fac Sci Gabriel, F-21000 Dijon, France
[2] Univ Bristol, Sch Chem, Bristol BS8 1TS, Avon, England
[3] Univ Prince Edward Isl, Dept Chem, Charlottetown, PE C1A 4P3, Canada
关键词
coordination chemistry; organometallic chemistry; spin crossover; minimum energy crossing point; spin acceleration; two-state reactivity;
D O I
10.1016/S0010-8545(02)00283-7
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
In coordination chemistry. many reactions involve several electronic states, in particular states of different spin. This phenomenon of 'Multiple-State Reactivity' has been recognized for some time, both for gas-phase reactions of 'bare' metal ions, and for transition metal complexes in solution. Until recently, however, much of the discussion of these systems has remained qualitative, because standard computational methods do not allow the location of the critical points for these processes, the Minimum Energy Crossing Points (MECPs) between states of different spin. Increased computational resources and new algorithms now enable MECPs to be located for large. realistic transition metal containing systems, yielding important new insight into the mechanisms of important reactions such as oxidative addition of C-H bonds to metal centers and ligand association/dissociation processes. Several examples will be presented for inorganic, organometallic and bioinorganic reactions. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:347 / 361
页数:15
相关论文
共 88 条
[1]   (Salen)Mn(III)-catalyzed epoxidation reaction as a multichannel process with different spin states. Electronic tuning of asymmetric catalysis: A theoretical study [J].
Abashkin, YG ;
Collins, JR ;
Burt, SK .
INORGANIC CHEMISTRY, 2001, 40 (16) :4040-4048
[2]   INSTABILITY OF 15-ELECTRON CP(STAR)MOCL(2)L (L=2-ELECTRON DONOR) DERIVATIVES - X-RAY STRUCTURE OF CP(STAR)MOCL(2)(PME(2)PH)(2) AND [CP(STAR)MOCL(2)(PME(2)PH)(2)]ALCL4 [J].
ABUGIDEIRI, F ;
KEOGH, DW ;
KRAATZ, HB ;
PEARSON, W ;
POLI, R .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1995, 488 (1-2) :29-38
[3]   A DIRECT METHOD FOR THE LOCATION OF THE LOWEST ENERGY POINT ON A POTENTIAL SURFACE CROSSING [J].
BEARPARK, MJ ;
ROBB, MA ;
SCHLEGEL, HB .
CHEMICAL PHYSICS LETTERS, 1994, 223 (03) :269-274
[4]   EVIDENCE FOR THE FORMATION OF FREE 16-ELECTRON SPECIES RATHER THAN SOLVATE COMPLEXES IN THE ULTRAVIOLET-IRRADIATION OF CPCO(CO)(2) IN LIQUEFIED NOBLE-GAS SOLVENTS [J].
BENGALI, AA ;
BERGMAN, RG ;
MOORE, CB .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (13) :3879-3880
[5]   A PHYSICAL ORGANIC ROAD TO ORGANOMETALLIC C-H OXIDATIVE ADDITION-REACTIONS [J].
BERGMAN, RG .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1990, 400 (1-2) :273-282
[6]   MECHANISMS FOR THE REACTIONS BETWEEN METHANE AND THE NEUTRAL TRANSITION-METAL ATOMS FROM YTTRIUM TO PALLADIUM [J].
BLOMBERG, MRA ;
SIEGBAHN, PEM ;
SVENSSON, M .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (15) :6095-6102
[7]   New developments in matrix isolation spectroscopy [J].
Bondybey, VE ;
Smith, AM ;
Agreiter, J .
CHEMICAL REVIEWS, 1996, 96 (06) :2113-2134
[8]   Time-resolved optical and infrared spectral studies of intermediates generated by photolysis of trans-RhCl(CO)PR3)2.: Roles played in the photocatalytic activation of hydrocarbons [J].
Bridgewater, JS ;
Netzel, TL ;
Schoonover, JR ;
Massick, SM ;
Ford, PC .
INORGANIC CHEMISTRY, 2001, 40 (07) :1466-1476
[9]   Theoretical study of the 15- and 17-electron structures of cyclopentadienylchromium(III) and cyclopentadienylmolybdenum(III) complexes. Dichloride and dimethyl compounds [J].
Cacelli, I ;
Keogh, DW ;
Poli, R ;
Rizzo, A .
JOURNAL OF PHYSICAL CHEMISTRY A, 1997, 101 (50) :9801-9812
[10]   New ansa-2,2-bis(eta-cyclopentadienyl)propane molybdenum and tungsten compounds and intramolecular hydrogen-deuterium exchange in methyl-hydride and ethyl-hydride derivatives [J].
Chernega, A ;
Cook, J ;
Green, MLH ;
Labella, L ;
Simpson, SJ ;
Souter, J ;
Stephens, AHH .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1997, (18) :3225-3243