PENTACOORDINATED NICKEL(II) COMPLEXES WITH THIOLATO LIGATION - SYNTHETIC STRATEGY, STRUCTURES, AND PROPERTIES

被引:76
作者
BAIDYA, N
OLMSTEAD, M
MASCHARAK, PK
机构
[1] UNIV CALIF SANTA CRUZ,DEPT CHEM,JINSHEIMER LABS,SANTA CRUZ,CA 95064
[2] UNIV CALIF DAVIS,DEPT CHEM,DAVIS,CA 95616
关键词
D O I
10.1021/ic00005a011
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Reaction of [Ni(terpy)Cl2] with 2 equiv of thiolates in methanol or acetonitrile affords, depending on the basicity and bulk of the thiolate, the thiolato-bridged dimer [Ni(terpy)(SPh)2]2.6CH3OH (1), solvated monomer [Ni(terpy)(SC6F5)2(CH3CN)]. 3CH3CN (2) and the desired pentacoordinated [Ni(terpy)(S-2,4,6-(i-Pr)3C6H2)2].1.5CH3CN (3). Complex 1 crystallizes in the monoclinic space group P2(1)/c, with a = 9.908 (2) angstrom, b = 20.441 (6) angstrom, c = 14.340 (4) angstrom, beta = 102.20 (2)-degrees, V = 2839 (1) angstrom, and Z = 2. The structure of 1 was refined to R = 5.2% on the basis of 2590 (I > 3-sigma-(I)) data. Complex 2 also crystallizes in the monoclinic space group P2(1)/c, with a = 10.197 (3) angstrom, b = 31.659 (7) angstrom, c = 11.431 (3) angstrom, beta = 105.58 (2)-degrees, V = 3554.6 (6) angstrom 3, and Z = 4. On the basis of 2618 (I > 4-sigma-(I)) data, the structure was refined to R = 7.85%. Complex 3 crystallizes in the triclinic space group P1BAR with a = 16.786 (6) angstrom, b = 17.266 (6) angstrom, c = 18.534 (7) angstrom, alpha = 68.34 (3)-degrees, beta = 64.57 (3)-degrees, gamma = 71.93 (3)-degrees, V = 4286 (3) angstrom 3, and Z = 4. The structure of 3 was refined to 8.06% by using 8587 (I > 4-sigma-(I)) data. In 1 and 2, the coordination geometry around nickel is distorted octahedral while that in 3 is distorted trigonal bipyramidal. In donor solvents, 1 splits into two solvated monomers. The NMR peaks corresponding to the protons of the thiolate ligands in 1-3 have been assigned. In DMF, complexes 2 and 3 are reduced by Na2S2O4 to generate [Ni(terpy)(SR)2]-, R = C6F5, 2,4,6-(i-Pr)3C6H2 (4), which are rather unstable. Binding of CO to 4 affords [Ni(terpy)(SR)2(CO)]-, R = C6F5, 2,4,6-(i-Pr)3C6H2 (5). These CO adducts are quite stable at low temperatures. The EPR spectra of 4 and 5 have been discussed. Evidence for binding of H- to the nickel center in [Ni(terpy)(S-2,4,6-(i-Pr)3C6H2)2] is also presented.
引用
收藏
页码:929 / 937
页数:9
相关论文
共 38 条
[1]  
[Anonymous], 1974, INT TABLES XRAY CRYS, VIV
[2]  
ARRIORTUA MI, 1982, B SOC CHIM BELG, V91, P337
[3]   SYNTHESIS AND STRUCTURAL CHARACTERIZATION OF A TRIMERIC NICKEL(II) COMPLEX OF N-(2-MERCAPTOPROPIONYL)GLYCINE [J].
BAIDYA, N ;
OLMSTEAD, MM ;
MASCHARAK, PK .
INORGANIC CHEMISTRY, 1989, 28 (18) :3426-3432
[4]   MONONUCLEAR NICKEL(II) THIOLATES OF SQUARE-PLANAR GEOMETRY - SYNTHESES, SPECTRAL AND REDOX PROPERTIES OF [NI(SCH2CH2S)2]2- AND [NI(SCH(CH3)CH(CH3)S)2]2- AND THE STRUCTURE OF (PH4P)2[NI(SCH2CH2S)2].4H2O [J].
BAIDYA, N ;
MASCHARAK, PK ;
STEPHAN, DW ;
CAMPAGNA, CF .
INORGANICA CHIMICA ACTA, 1990, 177 (02) :233-238
[5]  
BAIDYA N, UNPUB
[6]   RHENIUM NITROSYL COMPLEXES WITH SIMPLE AND WITH STERICALLY DEMANDING AROMATIC THIOLATE LIGANDS - X-RAY CRYSTAL-STRUCTURES OF [PPH4][RE2(SC6H4-ME-4)7(NO)2].CH2CL2 AND [RE(SC6H3PRI2-2,6)4(NO)] [J].
BLOWER, PJ ;
DILWORTH, JR ;
HUTCHINSON, JP ;
ZUBIETA, JA .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1985, (08) :1533-1541
[7]  
COLPAS GJ, IN PRESS INORG CHEM
[8]   STRUCTURE OF DIAQUACHLORO(2,2'-6',2''-TERPYRIDYL)NICKEL(II) CHLORIDE MONOHYDRATE [J].
CORTES, R ;
ARRIORTUA, MI ;
ROJO, T ;
SOLANS, X ;
MIRAVITLLES, C ;
BELTRAN, D .
ACTA CRYSTALLOGRAPHICA SECTION C-CRYSTAL STRUCTURE COMMUNICATIONS, 1985, 41 :1733-1736
[9]   CRYSTAL-STRUCTURES OF ZN(SR)2 COMPLEXES - STRUCTURAL MODELS FOR THE PROPOSED [ZN(CYS-S)2(HIS)2] CENTER IN TRANSCRIPTION FACTOR-IIIA AND RELATED NUCLEIC-ACID BINDING-PROTEINS [J].
CORWIN, DT ;
KOCH, SA .
INORGANIC CHEMISTRY, 1988, 27 (03) :493-496
[10]   ZINC, COBALT, AND CADMIUM THIOLATE COMPLEXES - MODELS FOR THE ZINC(S-CYS)2(HIS)2 CENTER IN TRANSCRIPTION FACTOR IIIA (CYS = CYSTEINE HIS = HISTIDINE) [J].
CORWIN, DT ;
GRUFF, ES ;
KOCH, SA .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1987, (13) :966-967