MOLECULAR ROUTES FOR THE SYNTHESIS OF METAL CARBIDES, NITRIDES, AND OXIDES .1. STUDIES OF THE THERMAL-DECOMPOSITION OF M(2)(OR)(6) AND M(2)(CH(2)PH)(2)(OR)(4) COMPOUNDS WHERE M=MO AND W

被引:15
|
作者
BAXTER, DV
CHISHOLM, MH
DISTASI, VF
HAUBRICH, ST
机构
[1] INDIANA UNIV,DEPT CHEM,BLOOMINGTON,IN 47405
[2] INDIANA UNIV,DEPT PHYS,BLOOMINGTON,IN 47405
关键词
D O I
10.1021/cm00049a014
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Thermolysis of the homoleptic alkoxides M(2)(OR)(6) and the mixed benzyl alkoxides M(2)(CH(2)Ph)(2)(O-i-Pr)(4), where M = Mo and W, have been studied under a purified helium flow by a coupled thermogravimetric analyzer/mass spectrometer (TGA-MS) system installed in a VAC atmosphere Dri-Lab. Under rigorously purified He, Mo-2(OR)(6), where R = t-Bu and i-Pr, sublimed without decomposition at ca. 100-200 degrees C, 1 atm. In the presence of a trace of O-2/H2O, Mo-2(O-t-Bu)(6) gave MoO2 The related W-2(OR)(6) compounds were transformed to WO2 when R = t-Bu at ca. 200 degrees C and when R = i-Pr to a mixture of WO2 and W(m) after heating to 750 degrees C. In contrast, the cyclohexoxides M(2)(O-c-C6H11)(6) gave upon heating Mo2C and W(m), respectively, by way of a metastable amorphous phase of approximate composition M(2)C(4)O(4). The introduction of two benzyl ligands in the compound M(2)(CH(2)Ph)(2)(O-i-Pr)(4) significantly alters the molecular decomposition. For instance, for M = Mo the addition of the benzyl Ligands causes the compound to decompose prior to sublimation and gives Mo2C with traces of Mo(m). For M = W the decomposition pathway is altered considerably, with the initial decomposition temperature range lower than that of the homoleptic alkoxide W-2(O-i-Pr)(6) by ca. 100-250 degrees C. This decomposition gives the product W2C (>65%) with traces of W(m) and WC as the only detectable products by X-ray diffraction (XRD) powder patterns. The formation of the residues after thermal decomposition is based on XRD and the percentage weight retained in the TGA experiments. A variety of isotopically labeled compounds were prepared and the gases evolved during thermolysis were analyzed by MS, CC-MS, and H-1 and C-13 NMR spectroscopy. On the basis of these studies, some insights into the initial mechanisms of the thermolyses are proposed.
引用
收藏
页码:84 / 92
页数:9
相关论文
共 50 条
  • [21] AMINOCARBYNE COUPLING REACTIONS AT M(PH(2)PCH(2)CH(2)PPH(2))(2) (M=MO OR W) SITES - DETAILED MECHANISTIC STUDIES ON THE PROTONATION OF COORDINATED ISOCYANIDES AND COUPLING OF LIGANDS IN TRANS-[M(CNR)(2)(PH(2)PCH(2)CH(2)-PPH(2))(2)] (R=BU(T) OR ME)
    HENDERSON, RA
    POMBEIRO, AJL
    RICHARDS, RL
    DASILVA, JJRF
    WANG, Y
    JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1995, (07): : 1193 - 1199
  • [22] PREPARATION AND CHARACTERIZATION OF M2(SEAR)6 AND MIXED-LIGAND M2(OR)2(SEAR')4 SPECIES (M = MO, W)
    CHISHOLM, MH
    HUFFMAN, JC
    PARKIN, IP
    STREIB, WE
    POLYHEDRON, 1990, 9 (24) : 2941 - 2952
  • [23] THE MOLYBDENUM MOLYBDENUM TRIPLE BOND .15. COMPOUNDS WITH CHAINS OF METAL ATOMS HAVING M-M SINGLE AND TRIPLE BONDS - M2(M'(M'ME3)3)2(NME2)4(M=M) WHERE M = MO AND W AND M' = SI AND SN
    CHISHOLM, MH
    CHIU, HT
    FOLTING, K
    HUFFMAN, JC
    INORGANIC CHEMISTRY, 1984, 23 (24) : 4097 - 4102
  • [24] SYNTHESIS AND STRUCTURE OF [M(CO)(4)((PPH(2))(2)CHAU(PPH(3)))] (M=CR,MO,W)
    FERNANDEZ, EJ
    GIMENO, MC
    JONES, PG
    LAGUNA, A
    LAGUNA, M
    OLMOS, E
    INORGANICA CHIMICA ACTA, 1995, 238 (1-2) : 173 - 177
  • [25] Convenient synthesis of [Et4N]2[M2(CO)8(μ-H)2] (M = Mo, W)
    Lin, JT
    Huang, PH
    ORGANOMETALLICS, 1998, 17 (16) : 3619 - 3620
  • [26] CHEMICAL OXIDATION AND ELECTRONIC-SPECTRA OF THE COMPLEXES TRANS-[M(CNR)2(PH2PCH2CH2PPH2)2] (M=MO OR W)
    POMBEIRO, AJL
    RICHARDS, RL
    JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1979, 179 (04) : 459 - 477
  • [28] Synthesis, Structure, Bonding, and Reactivity of Metal Complexes Comprising Diborane(4) and Diborene(2): [{Cp*Mo(CO)2}2{μ-η2:η2-B2H4}] and [{Cp*M(CO)2}2B2H2M(CO)4], M=Mo,W
    Mondal, Bijan
    Bag, Ranjit
    Ghorai, Sagar
    Bakthavachalam, K.
    Jemmis, Eluvathingal D.
    Ghosh, Sundargopal
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2018, 57 (27) : 8079 - 8083
  • [29] Facile synthesis of M(=NtBu)2(CH2SiMe3)2 (M = Mo or W) as potential precursors for thin film deposition
    Tang, Younian
    Wu, Fan
    Chen, Huiying
    Chai, Jia-Lu
    Chen, Xu-Dong
    Xi, Bin
    INORGANIC CHEMISTRY COMMUNICATIONS, 2023, 151
  • [30] FORMATION AND FAC-MER ISOMERIZATION OF CATIONIC PHOSPHENIUM TRANSITION-METAL COMPLEXES FORMULATED AS [M(BPY)(CO)(3)(PN(ME)CH(2)CH(2)NME)](+) (M=CR, MO, W) AND [M(DPPE)(CO)(3)(PN(ME)CH(2)CH(2)NME)](+) (M=MO, W)
    NAKAZAWA, H
    YAMAGUCHI, Y
    MIYOSHI, K
    JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1994, 465 (1-2) : 193 - 198