N,N,N′,N′-tetrakis(2-pyridylmethyl)ethylenediamine and its analogues as hypodentate ligands.: Synthesis and characterization of the rhodium(III), ruthenium(II), and palladium(II) complexes

被引:20
作者
Sokolov, M
Umakoshi, K
Sasaki, Y
机构
[1] Novosibirsk Organ Chem Inst, Novosibirsk 630090, Russia
[2] Hokkaido Univ, Grad Sch Sci, Div Chem, Kita Ku, Sapporo, Hokkaido 0600810, Japan
[3] Nagasaki Univ, Fac Engn, Dept Appl Chem, Nagasaki 8528521, Japan
关键词
D O I
10.1021/ic0203264
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
New complexes of Rh(III), Ru(II), and Pd(II) with NNN',N'-tetrakis(2-pyridylmethyl)ethylenediamine (tpen) and its analogues have been prepared. The reaction of RhCl3.nH(2)O with tpen is slow and allows one to isolate the products of three consecutive substitution steps: Rh2Cl6(tpen) (1), cis-[RhCl2(eta(4)-tpen)](+) (2), and [RhCl(eta(5)-tpen)](2+) (3). In acetonitrile the reaction stops at the step of the formation of cis-[RhCl2(eta(4)-tpen)](+), whereas [RhCl(eta(5)-tpen)(2+) is the final product of the further reaction in ethanol. Fully chelated [Rh(tpen)](3+) could not be obtained. Bis(acetylacetonato)palladium(II), Pd(acac)(2), reacts with tpen and its analogues, NNN',N'-tetrakis(2-pyridylmethyl)-1,3-propanediamine (tptn) and N,N,N',N'-tetrakis(2-pyridylmethyl)-(R)-1,2-propylenediamine (R-tppn), to give [Pd(eta(4)-tpen)](2+) (4), [Pd-eta(4)-tppn)](2+) (5), and [Pd(eta(4)-tptn)](2+) (6), respectively. Two pyridyl arms remain uncoordinated in these cases. The formation of unstable Pd(III) complexes from these Pd(II) complexes in solution was suggested on the basis of electrochemical measurements. Ruthenium(III) trichloride, RUCl3.nH(2)O, is reduced to give a Ru(II) complex with fully coordinated tpen, [Ru(tpen)]2+ (7). The same product was obtained in a more straightforward reaction of (RuCl2)-Cl-II(dimethyl sulfoxide)(4) with tpen. Electrochemical studies showed a quasi-reversible [Ru(tpen)](2+/3+) couple for [7](ClO4)(2) (E-1/2 = 1.05 V vs Ag/AgCl). Crystal structures of [2](PF6).2CH(3)CN, [3](PF6)(2).CH3CN, [6](ClO4)(2), and [7](ClO4)(2).0.5H(2)O were determined. Crystal data: [2](PF6).2CH(3)CN, monoclinic, C2, a = 16.974(4) Angstrom, b = 8.064(3) Angstrom, c = 13.247(3) Angstrom, = 106.37(2)degrees, V = 1739.9(8) Angstrom(3), Z = 2; [3](PF6)(2).CH3CN, triclinic, P (1) over bar, a = 11.430(1) Angstrom, b = 19.234(3) Angstrom, c = 8.101 (1) Angstrom, alpha = 99.43(1)degrees, beta = 93.89(1)degrees, gamma = 80.10(1)degrees, V = 1729.3(4) Angstrom(3), Z = 2; [6](ClO4)(2), orthorhombic, Pnna, a = 8.147(1) Angstrom, b 25.57(1) Angstrom, c = 14.770(4) Angstrom, V = 3076(3) Angstrom(3), Z = 4; [7](ClO4)(2).0.5H(2)O, monoclinic, P2(1)/c, a = 10.046(7) Angstrom, b = 19.049(2) Angstrom, c = 15.696(3) Angstrom, beta = 101.46(3)degrees, V 2943(2) Angstrom(3), Z = 4.
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页码:6237 / 6243
页数:7
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