SYNTHESIS OF MOLYBDENUM AND TUNGSTEN COMPLEXES THAT CONTAIN TRIAMIDOAMINE LIGANDS OF THE TYPE (C6F5NCH2CH2)(3)N AND ACTIVATION OF DINITROGEN MOLYBDENUM

Citation
M. Kol et al., SYNTHESIS OF MOLYBDENUM AND TUNGSTEN COMPLEXES THAT CONTAIN TRIAMIDOAMINE LIGANDS OF THE TYPE (C6F5NCH2CH2)(3)N AND ACTIVATION OF DINITROGEN MOLYBDENUM, Journal of the American Chemical Society, 116(10), 1994, pp. 4382-4390
Citations number
50
Categorie Soggetti
Chemistry
ISSN journal
00027863
Volume
116
Issue
10
Year of publication
1994
Pages
4382 - 4390
Database
ISI
SICI code
0002-7863(1994)116:10<4382:SOMATC>2.0.ZU;2-1
Abstract
Three new ligands of the type (ArNHCH2CH2)(3)N (Ar = 3,5-bis(trifluoro methyl)phenyl, 2-(trifluoromethyl)phenyl, and pentafluorophenyl) have been prepared. Only Mo and W complexes containing the [(C6F5NCH2CH2)(3 )N](3-) ([N3N](3-)) ligand were found to be stable. Stable complexes t hat have been prepared include Mo[N3N](NMe(2)), M[N3N]Cl(M = Mo or W), Mo[N3N](OTf) (M = Mo or W), [N3N]M=N (M = Mo or W), and {[N3N]Mo=NMe} (OTf). An X-ray study of Mo[N3N]Cl showed it to be a monomeric distort ed trigonal bipyramidal species having a pseudo-C-3 symmetry (space gr oup P (1) over bar, a = 11.265(2) Angstrom, b = 11.371(2) Angstrom, c = 21.805(4) Angstrom, alpha = 82.40(1)degrees, beta = 79.07(1)degrees, gamma = 74.89(1)degrees, V = 2637.4 Angstrom(3), Z = 4, fw = 772.75, rho(calcd) = 1.946 g/cm(3), R = 0.032, R(W) = 0.034). Reduction of Mo[ N3N](OTf) with 1 equiv of sodium amalgam yields a dinuclear bridging d initrogen species, [N3N]Mo(mu N-2)Mo[N3N]. In the presence of 2 equiv of sodium amalgam in ether Mo[N3N](OTf) is reduced to [N3N]Mo(N-2)[Na( ether)(x)] (1 < x < 2). A more stable 15-crown-5 derivative can be pre pared and more fully characterized. [N3N]Mo(mu-N-2)Mo[N3N] can be redu ced to [N3N]Mo(N-2)[NaL(x)] by sodium amalgam under dinitrogen and the latter can be oxidized to the former by ferrocenium triflate or air. [N3N]Mo(N-2)[NaL(x)] reacts with Mo[N3N](OTf) to give [N3N]Mo(mu-N-2)M o[N3N], with triisopropylsilyl chloride to give [N3N]MoN=NSi(i-Pr)(3), and with tributyltin chloride to give [N3N]MoN=NSn(Bu)(3). An X-ray s tudy of [N3N]MoN=NSi(i-Pr)(3) (space group P2(1)/n, a 13.524(3) Angstr om, b = 18.016(4) Angstrom, c = 16.248(3) Angstrom, beta = 98.74(2)deg rees, V = 3913(1) Angstrom(3), Z = 4, fw = 922.67, rho(calcd) = 1.566 g/cm(3), R = 0.069, R(W) = 0.072) showed it to be a trigonal bipyramid al complex containing a slightly bent diazenido ligand (Mo-N-alpha = 1 .788(9) Angstrom, Mo-N-alpha-N-beta = 171.1(8)degrees, N-alpha-N-beta- Si = 154(1)degrees).