Open shell organometallics: a general analysis of their electronic structure and reactivity

被引:73
作者
Poli, R [1 ]
机构
[1] Chim Coordinat Lab, F-31077 Toulouse, France
基金
美国国家科学基金会;
关键词
open-shell; organometallic chemistry; pairing energy; molecular orbital theory; spin crossover reactivity; minimum energy crossing point;
D O I
10.1016/j.jorganchem.2004.05.040
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Transition metal organometallic compounds that contain fewer than 18-electrons and two or more unpaired electrons are generally excluded from treatises of either Werner-type coordination compounds or organometallic chemistry. However, they can be seen as the bridge filling the gap between these two traditional areas of coordination chemistry. Their magnetic and optical properties are reminiscent of the Werner-type complexes, whereas their chemical reactivity parallels that of the lower-valent organometallies. Spin state change phenomena are of paramount importance in this area. This paper provides a broad perspective of this area, with particular attention to: (i) how the ground state properties can be related to the metal and ligands nature; (ii) under which circumstances the often inappropriately invoked concept of "spin block" is meaningful; (iii) the spin acceleration concept; (iv) how the coordination sphere affects the topology of the reaction coordinate in the vicinity of spin crossing points; and (v) the effect of spin state changes on reaction selectivities. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:4291 / 4304
页数:14
相关论文
共 68 条
[1]   Four-legged piano stool Molybdenum(II) compounds without carbonyl ligands .4. Cyclopentadienylmolybdenum(II) complexes with 16-electron and 18-electron configurations [J].
Abugideiri, F ;
Fettinger, JC ;
Keogh, DW ;
Poli, R .
ORGANOMETALLICS, 1996, 15 (21) :4407-4416
[2]   NEOPENTYL, NEOPHYL, AND TRIMETHYLSILYLMETHYL COMPOUNDS OF MANGANESE - MANGANESE(II) DIALKYLS - MANGANESE(II) DIALKYL AMINE ADDUCTS - TETRA-ALKYLMANGANATE(II) IONS AND LITHIUM-SALTS - MANGANESE(IV) TETRA-ALKYLS [J].
ANDERSEN, RA ;
CARMONAGUZMAN, E ;
GIBSON, JF ;
WILKINSON, G .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1976, (21) :2204-2211
[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]   A TRANSIENT INFRARED-SPECTROSCOPY STUDY OF COORDINATIVELY UNSATURATED OSMIUM CARBONYL-COMPOUNDS [J].
BOGDAN, PL ;
WEITZ, E .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1990, 112 (02) :639-644
[5]   A TRANSIENT INFRARED-SPECTROSCOPY STUDY OF COORDINATIVELY UNSATURATED RUTHENIUM CARBONYLS [J].
BOGDAN, PL ;
WEITZ, E .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1989, 111 (09) :3163-3167
[6]   TRANSITION-METAL BICYCLO[2.2.1]HEPT-1-YLS [J].
BOWER, BK ;
TENNENT, HG .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1972, 94 (07) :2512-&
[7]   PREPARATION AND CRYSTAL-STRUCTURE OF A 2-CO-ORDINATE MANGANESE COMPOUND, BIS[TRIS(TRIMETHYL)SILYLMETHYL]MANGANESE [J].
BUTTRUS, NH ;
EABORN, C ;
HITCHCOCK, PB ;
SMITH, JD ;
SULLIVAN, AC .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1985, (20) :1380-1381
[8]   Synthesis and characterization of the monomeric molybdenum trithiolate Mo(η7-dmpt)(η1-dmpt)2 (dmpt = 2,6-dimesitylphenylthiolate) [J].
Buyuktas, BS ;
Olmstead, MM ;
Power, PP .
CHEMICAL COMMUNICATIONS, 1998, (16) :1689-1690
[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]   A density functional study of open-shell cyclopentadienyl-molybdenum(II) complexes.: A comparison of stabilizing factors:: Spin-pairing, Mo-X π bonding, and release of steric pressure [J].
Cacelli, I ;
Poli, R ;
Quadrelli, EA ;
Rizzo, A ;
Smith, KM .
INORGANIC CHEMISTRY, 2000, 39 (03) :517-524