ARYLDIAZENE, ARYLDIAZENIDO, AND HYDRAZINE COMPLEXES OF MANGANESE - PREPARATION, CHARACTERIZATION, AND X-RAY CRYSTAL-STRUCTURES OF [MN(CO)(3)(4-CH3C6H4N=NH)(PPH(OET)(2))(2)]BF4 AND [MN(CO)(3)(NH2NH2)(PPH(OET)(2))(2)]BPH4 DERIVATIVES

Citation
G. Albertin et al., ARYLDIAZENE, ARYLDIAZENIDO, AND HYDRAZINE COMPLEXES OF MANGANESE - PREPARATION, CHARACTERIZATION, AND X-RAY CRYSTAL-STRUCTURES OF [MN(CO)(3)(4-CH3C6H4N=NH)(PPH(OET)(2))(2)]BF4 AND [MN(CO)(3)(NH2NH2)(PPH(OET)(2))(2)]BPH4 DERIVATIVES, Inorganic chemistry, 36(7), 1997, pp. 1296-1305
Citations number
65
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
00201669
Volume
36
Issue
7
Year of publication
1997
Pages
1296 - 1305
Database
ISI
SICI code
0020-1669(1997)36:7<1296:AAAHCO>2.0.ZU;2-R
Abstract
Aryldiazene complexes [Mn(CO)(3)(ArN=NH)P-2]BF4 (1, 2) and [{Mn(CO)(3) P-2}(2)(mu-HN=NArArN=NH)](BF4)(2) (3, 4) [P = PPh(OEt)(2), PPh(2)OEt; Ar = C6H5, 2-CH3C6H4, 4-CH3C6H4, 4-CH3OC6H4; ArAr = 4,4'-C6H4C6H4, 4,4 '-(2-CH3)C6H3C6H3(2-CH3), 4,4'-C6H6CH2C6H4] were prepared by reacting hydride species MnH(CO)(3)P-2 with the appropriate aryldiazonium catio ns in CH2Cl2 or acetone solutions at -80 degrees C. The compounds were characterized by IR, H-1 and P-31 NMR spectra (with N-15 isotopic sub stitution), and a single-crystal X-ray structure determination. The co mplex [Mn(CO)(3)(4-CH3C6H4N=NH) {PPh(OEt)(2)}(2)]BF4 (1c) crystallizes in the space group C2/c with a 31.857(5) Angstrom, b = 11.119(2) Angs trom, c = 22.414(3) Angstrom, beta = 97.82(1)degrees, and Z = 8. Treat ment of aryldiazene compounds 1-4 with NEt(3) gave the pentacoordinate aryldiazenido [Mn(CO)(2)(ArN2)P-2] (5, 6) and [{Mn(CO)(2)P-2}(2)(mu-N -2-ArArN2)] (7, 8) [P = PPh(OEt)(2), PPh(2)OEt; Ar = C6H5, 4-CH3C6H4; ArAr = 4,4'-C6H4C6H4, 4,4'-(2-CH3)C6H3C6H3(2-CH3)] derivatives. Proton ation reactions of these aryldiazenido complexes 5-8 with HCl afforded the aryldiazene [MnCl(CO)(2)(ArN=NH)P-2] (9) and [{MnCl(CO)(2)P-2}(2) (mu-HN=NArArN=NH)] (10) derivatives. Hydrazine complexes [Mn(CO)(3)(RN HNH(2))P-2]BPh(4) (11, 12) [P = PPh(OEt)(2), PPh(2)OEt; R = H, CH3, C6 H5, 4-NO2C6H4] were prepared by allowing hydride species MnH(CO)(3)P-2 to react first with triflic acid and then with the appropriate hydraz ine. Their characterization by IR, H-1 and P-31 NMR spectra, and an X- ray crystal structure determination is reported. The compound [Mn(CO)( 3)(NH2NH2){PPh(OEt)(2)}(2)]BPh(4) (11a) crystallizes in the space grou p P (1) over bar with a = 13.772(3) Angstrom, b = 14.951(4) Angstrom, c = 13.319(3) Angstrom, alpha = 104.47(1)degrees, beta = 100.32(1)degr ees, gamma = 111.08(1)degrees, and Z = 2. Oxidation reactions of hydra zine compounds 11 and 12 with Pb(OAc)(4) at -40 degrees C gave stable aryldiazene [Mn(CO)(3)(RN=NH)P-2]BPh(4) and thermally unstable (upon r eaching -40 degrees C) diazene [Mn(CO)(3)(HN=NH)P-2]BPh(4) derivatives .