Six [Tp*WS_3Cu_2]-based clusters derived from [Et_4N][Tp*WS_3], Cu(I) salts and phosphine ligands: syntheses, structures and enhanced third-order NLO properties

摘要

Treatment of [Et_4N][Tp*WS_3] (Tp* = hydridotris(3,5-dimethylpyrazol-1-yl)borate) (1) with CuX (X = Br, SCN) and PPh3 or 1,1-bis(diphenylphosphino)methane (dppm) produced two neutral trinuclear clusters [Tp*W(μ_3-S)(μ-S)_2Cu_2Br(PPh3)] (2) and [Tp*W(μ_3-S)(μ-S)_2Cu_2(SCN)(dppm)]_2·MeCN·Et_2O (3·MeCN·Et_2O). Reactions of 1 with [Cu(MeCN)_4]PF_6, NH_4PF_6 and 1,3-bis(diphenylphosphino)propane (dppp), N,N-bi- (diphenylphosphanylmethyl)-2-aminopyridine (bdppmapy), N,N,N',N'-tetra(diphenylphosphanylmethyl)- ethylenediamine (dppeda), or 1,4-N,N,N',N'-tetra(diphenylphosphanylmethyl)benzenediamine (dpppda) afforded four clusters containing butterfly-shaped [Tp*WS_3Cu_2] cores, [Tp*W(μ_3-S)(μ-S)_2Cu_2(dpppds)]- (PF6)·1.25MeCN (dpppds = 1,3-bis(diphenylphosphino)propane disulfide) (4·1.25MeCN), [Tp*W(μ_3-S)- (μ-S)_2Cu_2(bdppmapy)](PF6)·3MeCN (5·3MeCN) and {[Tp*W(μ_3-S)(μ-S)_2Cu_2]_2(L)]}(PF_6)_2·Sol (6·Et_2O: L = dppeda, Sol = Et_2O; 7·1.25MeCN: L = dpppda, Sol = 1.25MeCN). Compounds 2-7 were characterized by elemental analysis, IR, UV-Vis, ~1H and ~(31)P{~1H} NMR spectra, electrospray ion mass spectra (ESI-MS) and single-crystal X-ray diffraction. Compound 2 or 3 has a butterfly-shaped [Tp*WS_3Cu_2] core in which one [Tp*WS_3] unit binds two Cu(I) centers via one μ_3-S and two μ-S atoms. In the cationic structure of 4 or 5, one in situ-formed dpppds or bdppmapy combines with the [Tp*WS_3Cu_2] core via each of its two S atoms or two P atoms coordinated at each Cu(I) center. In the bicationic structure of 6 or 7, two [Tp*WS_3Cu_2] cores are linked by one dppeda or dpppda bridge to form a bicyclic structure. The isolation of 2-7 with unstable [Tp*WS_3Cu_2] cores may be ascribed to the coordination of P- or S-donor ligands at Cu(I) centers of these cores. The third-order nonlinear optical (NLO) properties of 2-7 in DMF were also investigated by using the femtosecond degenerate four-wave mixing (DFWM) technique at 800 nm.