GOLD(III)-CYCLAM COMPLEXES - X-RAY CRYSTAL-STRUCTURE AND A USEFUL MACROCYCLIC EFFECT ON THE REDUCTION OF GOLD(III)

被引:29
作者
KIMURA, E [1 ]
KUROGI, Y [1 ]
KOIKE, T [1 ]
SHIONOYA, M [1 ]
IITAKA, Y [1 ]
机构
[1] NISHI TOKYO UNIV,DEPT BIOL SCI,UENOHARA,YAMANASHI 40901,JAPAN
关键词
GOLD(III)-CYCLAM COMPLEXES; X-RAY STRUCTURE; GOLD-PLATING;
D O I
10.1080/00958979308035142
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The X-ray crystal structure of the Au(III)-cyclam complex 1 shows a four-coordinate square-planar N4 geometry with the trans III conformation (or RRSS configuration) of cyclam and an average Au(III)-N bond distance of 2.04 angstrom. A block-diagonal-matrix least-squares refinement yielded a final R value of 0.069 for 2463 independent reflections. Crystals of 1.(NO3)1.5(ClO4)1.5.H2O (C10H26N5.5O11.5AuCl1.5) are triclinic, space group P1 with a = 15.148(8), b = 8.668(5), c = 8.267(5) angstrom, alpha = 109.17(6), beta = 101.08(5), gamma = 82.08(4) angstrom, V = 1003(1) angstrom3, d(calcd) = 2.177 g cm-3, and Z = 2. The reduction potential for Au(III) in 1 to Au0 varies with pH: -0.16 V vs SCE (pH 1.0) to -0.55 V (pH 9.0) at I = 0.50 (NaClO4) and 25-degrees-C, according to the degree of cyclam NH deprotonation. The macrocyclic gold(III) complex 1 has been found to possess very useful electrochemical properties for a novel gold-plating agent. The new properties of gold(III)-cyclam complexes have been characterized by the tetrafluorinated cyclam 7, tetramethylcyclam 8, and aminocyclam 9. Dissociation of two protons from the macrocyclic NH amines in 7 readily occurs with extremely low pK(a) values of 1.6 and 6.5 at 25-degrees-C and I = 0.10 (NaClO4). Cyclic and dc polarograms of 8 in DMF (25-degrees-C, I = 0.10; Et4NClO4) show the Au(III/II) quasi-reversible reduction wave at E1/2 = +0.18 V vs SCE.
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页码:33 / 49
页数:17
相关论文
共 28 条
[1]  
Ali H.O., 1984, GOLD BULL, V17, P118, DOI DOI 10.1007/BF03214674
[2]   ACIDODIETHYLENETRIAMINEGOLD (III) COMPLEXES - PREPARATIONN, SOLUTION CEHMISTRY, AND ELECTRONIC STRUCTURE [J].
BADDLEY, WH ;
NOLTING, C ;
POE, AJ ;
BASOLO, F ;
GRAY, HB .
INORGANIC CHEMISTRY, 1963, 2 (05) :921-&
[3]   MECHANISM OF BASE PROMOTED REDUCTION OF NICKEL(III) COMPLEXES OF MACROCYCLIC AMINES - COORDINATED LIGAND RADICAL INTERMEDIATE [J].
BAREFIELD, EK ;
MOCELLA, MT .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1975, 97 (15) :4238-4246
[4]   COMPLEXES OF SILVER(II) AND SILVER(III) WITH MACROCYCLIC TETRAAZA LIGANDS [J].
BAREFIELD, EK ;
MOCELLA, MT .
INORGANIC CHEMISTRY, 1973, 12 (12) :2829-2832
[5]   TETRAHEDRAL DISTORTION IN PALLADIUM(II) MACROCYCLIC COMPLEXES - THE SINGLE-CRYSTAL X-RAY STRUCTURE OF [PD(TBC)](PF6)2.0.4MENO2 (TBC = 1,4,8,11-TETRABENZYL-1,4,8,11-TETRA-AZACYCLOTETRADECANE) [J].
BLAKE, AJ ;
GOULD, RO ;
HYDE, TI ;
SCHRODER, M .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1987, (22) :1730-1732
[6]   THE REACTION OF GOLD(III) WITH SOME BIDENTATE COORDINATING GROUPS [J].
BLOCK, BP ;
BAILAR, JC .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1951, 73 (10) :4722-4725
[7]   COMPLEXES OF COBALT(3) WITH A CYCLIC TETRADENTATE SECONDARY AMINE [J].
BOSNICH, B ;
POON, CK ;
TOBE, ML .
INORGANIC CHEMISTRY, 1965, 4 (08) :1102-&
[8]  
BOSNICH B, 1965, J CHEM SOC CHEM COMM, P97
[9]   METAL-COMPLEXES WITH MACROCYCLIC LIGANDS .4. SYNTHESIS, PROPERTIES AND KINETICS OF COMPLEXATION WITH 3 N-METHYL SUBSTITUTED 1,4,8,11-TETRAAZACYCLOTETRADECANES [J].
BUXTORF, R ;
KADEN, TA .
HELVETICA CHIMICA ACTA, 1974, 57 (04) :1035-1042
[10]   STABILIZATION OF THE MONO-VALENT NICKEL-COMPLEX WITH 1,4,8,11-TETRAAZACYCLOTETRADECANE IN AQUEOUS-SOLUTIONS BY N-METHYLATION AND C-METHYLATION - AN ELECTROCHEMICAL AND PULSE-RADIOLYSIS STUDY [J].
JUBRAN, N ;
GINZBURG, G ;
COHEN, H ;
KORESH, Y ;
MEYERSTEIN, D .
INORGANIC CHEMISTRY, 1985, 24 (03) :251-258