1988
DOI: 10.1039/c39880001192
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Co-ordination complexes of polyoxomolybdates with a hexanuclear core: synthesis and structural characterization of (NBun 4)2[Mo6O18(NNMePh)]

Abstract: Reaction of [MoCI4(NNMePh)] with ( B u ~~N ) ~[ M o ~O ~] yields a co-ordination complex with the hexanuclear oxomolybdate core, ( B u ~~N ) ~[ M o & ~( NNMePh)]; the reaction is general with appropriate precursors in providing a ready entry into the class of co-ordination compounds of the types [Mo5018(ML)]* and [W5018(ML)]*, with M = Mo or W and L = NNR2, NR, or N.

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Cited by 66 publications
(41 citation statements)
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“…[43][44][45] For example, imidoylization of POMs was first discovered by Zubieta and Kang, [20] and then largely investigated and developed by Maatta et al, [21,[24][25][26] Proust et al, [22] and Errington et al [23] by introducing three basic approaches including reactions with phosphinimines, isocyanates, and aromatic amines. [43][44][45] For example, imidoylization of POMs was first discovered by Zubieta and Kang, [20] and then largely investigated and developed by Maatta et al, [21,[24][25][26] Proust et al, [22] and Errington et al [23] by introducing three basic approaches including reactions with phosphinimines, isocyanates, and aromatic amines.…”
Section: Introductionmentioning
confidence: 99%
“…[43][44][45] For example, imidoylization of POMs was first discovered by Zubieta and Kang, [20] and then largely investigated and developed by Maatta et al, [21,[24][25][26] Proust et al, [22] and Errington et al [23] by introducing three basic approaches including reactions with phosphinimines, isocyanates, and aromatic amines. [43][44][45] For example, imidoylization of POMs was first discovered by Zubieta and Kang, [20] and then largely investigated and developed by Maatta et al, [21,[24][25][26] Proust et al, [22] and Errington et al [23] by introducing three basic approaches including reactions with phosphinimines, isocyanates, and aromatic amines.…”
Section: Introductionmentioning
confidence: 99%
“…The discovery of these new compounds occurred serendipitously during our investigation of the hydroamination of alkynes by anilines with the imido catalyst [Bn 3 Ta=NtBu] (1). [7] Reaction mixtures often developed a red color during the course of the reaction, and catalyst deactivation was always observed within 24 hours regardless of the amount of 1 added (Scheme 1).…”
mentioning
confidence: 99%
“…[1] The terminal oxo ligands in hexamolybdate and hexatungstate have been replaced to varying degrees by imido [2] or hydrazido [3] groups, and cyclopentadienyl-functionalized hetero-hexanuclear clusters have been prepared. [4] Still, incorporation of organic groups into the bridging sites has been more challenging.…”
mentioning
confidence: 99%
“…L] nÀ in which L is a nitrogenous ligand. Following the pioneering investigations by Zubieta and co-workers, [46] this family of polyanions has been extended by Errington, Maatta, Proust, Peng and Wei groups [32] and now includes nitrosyl, [47][48][49] hydrazido, [50] diazenido [46,[51][52] nitrido [50] and imido [53][54][55][56][57][58] derivatives. One diazoalkane derivative has been also reported by Maatta and coworkers.…”
Section: X-ray Diffraction Studiesmentioning
confidence: 97%