Cotton F. Albert, Schmid Günter
Department of Chemistry, Texas A&M University, College Station, Texas 77843-3255.
Inorg Chem. 1997 May 21;36(11):2267-2278. doi: 10.1021/ic961071v.
A series of molybdenum(IV) complexes of the type trans-Mo(Q)(Q')(P&arcraise;P)(2) has been prepared where Q and Q' are chalcogen ligands (O, S, Se, Te) and P&arcraise;P is either cis-1,2-bis(diphenylphosphino)ethylene (dppee) or 1,2-bis(diphenylphosphino)ethane (dppe). X-ray crystallographic studies were carried out to investigate how the Mo-Q distance is influenced by the mutually competitive d(pi)-p(pi) interactions between the p(x)() and p(y)() orbitals of the chalcogen ligands and the d(xz)() and d(yz)() orbitals of the molybdenum center. trans-Mo(O)(2)(dppee)(2) (1) has been prepared by the hydrolysis and deprotonation reaction of [Mo(O)(Cl)(dppee)(2)]Cl with NaOH in methanol. The compounds where Q represents the heavier chalcogens (S, Se, Te) have been prepared by the reaction between trans-Mo(N(2))(2)(P&arcraise;P)(2) and a chalcogen source: trans-Mo(S)(2)(dppee)(2) (2), BzS(3)Bz (dibenzyl trisulfide); trans-Mo(Se)(2)(dppee)(2) (3), elemental Se; trans-Mo(Te)(2)(dppee)(2) (4), TePEt(3) (Et = ethyl); trans-Mo(S)(2)(dppe)(2) (5), BzS(3)Bz; trans-Mo(Se)(2)(dppe)(2) (6), Se. trans-Mo(O)(S)(dppee)(2) (7) was obtained from the reaction of MoCl(3)(THF)(3) (THF = tetrahydrofuran), dppee, and NaHS in a mixture of THF and methanol. The attempted preparation of 7 by the reaction of SO(2) and trans-Mo(N(2))(2)(dppee)(2) yielded Mo(SO(2))(2)(dppee)(2) (8). 1 crystallizes in the monoclinic space group P2(1)/c (No. 14, Z = 2) with a = 11.1340(15) Å, b = 18.435(2) Å, c = 12.515(2) Å, and beta = 110.999(9) degrees; 2 crystallizes in the triclinic space group P&onemacr; (No. 2, Z = 1) with a = 10.102(4) Å, b = 10.722(4) Å, c = 12.195(3) Å, alpha = 100.95(3) degrees, beta = 95.04(4) degrees, and gamma = 117.81(2) degrees; 3 crystallizes in the monoclinic space group P2(1)/c (No. 14, Z = 2) with a = 11.186(5) Å, b = 18.005(8) Å, c = 12.761(9) Å, and beta = 110.35(4) degrees; 4 crystallizes in the triclinic space group P&onemacr; (No. 2, Z = 2) with a = 12.681(4) Å, b = 19.280(5) Å, c = 10.454(3) Å, alpha = 104.60(2) degrees, beta = 111.61(2) degrees, and gamma = 75.12(2) degrees; 5 crystallizes in the monoclinic space group C2/c (No. 15, Z = 8) with a = 49.515(7) Å, b = 10.9286(12) Å, c = 18.203(3) Å, and beta = 98.306(12) degrees; 6 crystallizes in the monoclinic space group C2/c (No. 15, Z = 8) with a = 49.566(9) Å, b = 10.9765(15) Å, c = 18.282(3) Å, and beta = 98.541(13) degrees; 7 crystallizes in the triclinic space group P&onemacr; (No. 2, Z = 1) with a = 10.040(1) Å, b = 10.563(1) Å, c = 12.162(2) Å, alpha = 75.30(1) degrees, beta = 85.93(1) degrees, and gamma = 63.21(1) degrees; 8 crystallizes in the monoclinic space group C2/c (No. 15, Z = 4) with a = 21.534(6) Å, b = 12.4271(13) Å, c = 19.550(5) Å, and beta = 118.480(14) degrees. The UV/vis and the (31)P{(1)H} NMR data for compounds 1-7 are also reported and discussed.
已制备出一系列通式为trans-Mo(Q)(Q')(P∧P)(2)的钼(IV)配合物,其中Q和Q'为硫属元素配体(O、S、Se、Te),P∧P为顺式-1,2-双(二苯基膦基)乙烯(dppee)或1,2-双(二苯基膦基)乙烷(dppe)。进行了X射线晶体学研究,以探究硫属元素配体的p(x)和p(y)轨道与钼中心的d(xz)和d(yz)轨道之间相互竞争的d(π)-p(π)相互作用如何影响Mo-Q键长。trans-Mo(O)(2)(dppee)(2)(1)通过[Mo(O)(Cl)(dppee)(2)]Cl与NaOH在甲醇中的水解和去质子化反应制备。Q代表较重硫属元素(S、Se、Te)的化合物通过trans-Mo(N(2))(2)(P∧P)(2)与硫属元素源反应制备:trans-Mo(S)(2)(dppee)(2)(2),二苄基三硫化物BzS(3)Bz;trans-Mo(Se)(2)(dppee)(2)(3),元素硒;trans-Mo(Te)(2)(dppee)(2)(4),三乙基碲TePEt(3)(Et = 乙基);trans-Mo(S)(2)(dppe)(2)(5),BzS(3)Bz;trans-Mo(Se)(2)(dppe)(2)(6),硒。trans-Mo(O)(S)(dppee)(2)(7)由MoCl(3)(THF)(3)(THF = 四氢呋喃)、dppee和NaHS在四氢呋喃与甲醇的混合物中反应得到。尝试通过SO(2)与trans-Mo(N(2))(2)(dppee)(2)反应制备7,得到了Mo(SO(2))(2)(dppee)(2)(8)。1在单斜空间群P2(1)/c(编号14,Z = 2)中结晶,a = 11.1340(15) Å,b = 18.435(2) Å,c = 12.515(2) Å,β = 110.999(9)°;2在三斜空间群P1(编号2,Z = 1)中结晶,a = 10.102(4) Å,b = 10.722(4) Å,c = 12.195(3) Å,α = 100.95(3)°,β = 95.04(4)°,γ = 117.81(2)°;