Borole Derivatives. 24. Synthesis of Cationic (Arene)(phenylborole)rhodium Complexes. Structures of the Trinuclear Complex (η5-C4H4BPh)Rh(μ3-I)3-Rh(μ,η5:η6-C4H4BPh)Rh(η5-C4H4BMe)·CH2Cl2 and of the Polymeric catena-(μ,η5:η6-1-Phenylborole)rhodium Tetrafluoroborate
The heterocubane [Rh(μ3-I)(C4H4BPh)]4 (1) reacts with Ag+ salts in acetonitrile to give the labile salt [Rh(NCMe)3(C4H4BPh)]BF4 (2). This salt 2 reacts with hexamethylbenzene (hmb) to give the arene complex [Rh(C4H4BPh)(hmb)]BF4 (3), and with mesitylene [Rh(1,3,5-C6H3Me3)(C4H4BPh)]BF4 (4) is obtaine...
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Veröffentlicht in: | Organometallics 1998-02, Vol.17 (4), p.519-523 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The heterocubane [Rh(μ3-I)(C4H4BPh)]4 (1) reacts with Ag+ salts in acetonitrile to give the labile salt [Rh(NCMe)3(C4H4BPh)]BF4 (2). This salt 2 reacts with hexamethylbenzene (hmb) to give the arene complex [Rh(C4H4BPh)(hmb)]BF4 (3), and with mesitylene [Rh(1,3,5-C6H3Me3)(C4H4BPh)]BF4 (4) is obtained. Complex 2 loses acetonitrile under vacuum to produce the polymeric salt catena-[{Rh(μ,η5:η6-C4H4BPh)}BF4] x (5). Insight into the essential structural features of this polymer provided its radial distribution function obtained from a wide-angle X-ray scattering experiment. When treated with acetonitrile, complex 5 regenerates 2 and with pyridine affords [Rh(py)3((C4H4BPh)]BF4 (6). Crystallization from a solution of [Rh(μ3-I)(C4H4BPh)]4 (1) and the corresponding methylborole complex [Rh(μ3-I)(C4H4BMe)]4 (1/1) in CH2Cl2 produces the trinuclear complex (η5-C4H4BPh)Rh(μ3-I)3Rh(μ,η5:η6-C4H4BPh)Rh(η5-C4H4BMe)·CH2Cl2 (7) with a bridging μ,η5:η6-C4H4BPh ligand; complex 7 was characterized by an X-ray structure determination. The resulting molecular structure was used to create a structure model for the monomeric building block of polymer 5. |
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ISSN: | 0276-7333 1520-6041 |
DOI: | 10.1021/om970742+ |