STRUCTURE AND BONDING IN LOW-SPIN OCTAHEDRAL MANGANESE(II) CARBONYLS - LIGAND-SET CONTROL OF SPIN DELOCALIZATION

被引:25
作者
CARRIEDO, GA
CONNELLY, NG
PEREZCARRENO, E
ORPEN, AG
RIEGER, AL
RIEGER, PH
RIERA, V
ROSAIR, GM
机构
[1] BROWN UNIV,DEPT CHEM,PROVIDENCE,RI 02912
[2] UNIV BRISTOL,SCH CHEM,BRISTOL BS8 1TS,AVON,ENGLAND
来源
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS | 1993年 / 20期
关键词
D O I
10.1039/dt9930003103
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
X-Ray structural studies on the redox pair trans-[Mn(CN)(CO)(dppm)2] (dppm = Ph2PCH2PPh2) and trans-[Mn(CN)(CO)(dppm)2][PF6].CH2Cl2 showed that one-electron oxidation results in changes consistent with depopulation of an orbital involved in Mn-P pi-back bonding. The ESR spectra of trans-[Mn(CN)(CO)(dppm)2]+, [Mn(CO)(CNCH2CH=CH2)(dppm)2]2+, trans-[Mn(CN)(CO)2(PEt3)(dppe)]+ (dppe = PhCH2CH2PPh2) and trans-[MnBr(CO)2(PEt3)(dppe)]+ in frozen dichloromethane-dichloroethane (1:1) solutions at 90 K, and extended-Huckel molecular-orbital calculations on the model compounds [Mn(CN)(CO)(H2PCH2PH2)2]+, [Mn(CO)(CNMe)(H2PCH2PH2)2]2+, cis- and trans-[Mn(CN)(CO)2(PH3)3]+ and trans-[MnBr(CO)2(PH3)3]+, showed that the semi-occupied molecular orbital of these low-spin octahedral cyanomanganese(II) carbonyls is always primarily manganese d(pi) in character and in the plane of the phosphorus ligands, either aligned along the Mn(CN) axis as in trans-[Mn(CO)2(PEt3)(dppe)]+ or perpendicular to this axis as in trans-[Mn(CN)(CO)(dppm)2]. The relative arrangement of the cyanide and carbonyl ligands is shown to control the extent of spin delocalisation onto the cyanide ligand.
引用
收藏
页码:3103 / 3110
页数:8
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