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Reactions of GaCp* with a hemilabile derivative of Rh-6(CO)(16) - Synthesis and structural characterization of two novel heterometallic clusters : Rh-6(CO)(13)(-) (mu,kappa 3-Ph2PC2H3)(mu(3)-GaCp*) and Rh-6(CO)(13)(kappa(1)-Ph2PC2H3)(mu(3)-GaCp*)(2). / Grachova, Elena V.; Linti, Gerald; Stammler, Hans-Georg; Neumann, Beate; Tunik, Sergey P.; Wadepohl, Hubert.

в: European Journal of Inorganic Chemistry, № 1, 01.01.2007, стр. 140-146.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

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@article{5b532705a28040a28ead4a8e94919e30,
title = "Reactions of GaCp* with a hemilabile derivative of Rh-6(CO)(16) - Synthesis and structural characterization of two novel heterometallic clusters: Rh-6(CO)(13)(-) (mu,kappa 3-Ph2PC2H3)(mu(3)-GaCp*) and Rh-6(CO)(13)(kappa(1)-Ph2PC2H3)(mu(3)-GaCp*)(2)",
abstract = "The reaction of Rh-6(CO)(14)(Ph2PCH=CH2) with a twofold excess of GaCp* (Cp* = C5Me5) affords two novel heterometallic clusters Rh-6(CO)(13)(mu. kappa(3)-Ph2PC2H3)(mu(3)-GaCp*) (1) and Rh-6(CO)(13)(kappa(1)-Ph2PC2H3)(mu(3)-GaCp*)(2) (2) in a moderate yield. The hemilabile behavior of coordinated diphenylvinylphosphane in the starting cluster allows the easy insertion of GaCp* into the cluster coordination sphere, which eventually gives the cluster 1 with face-bridging coordination of the gallium fragment and the phosphane ligand recoordinated in an edge-bridging position. The further substitution of the vinyl function in 1 for the second GaCp* ligand affords cluster 2, where recoordination of the double bond is blocked by steric hindrance from adjacent GaCp* fragments. Both clusters were structurally characterized by X-ray crystallography in the solid state and by IR and NMR spectroscopy in solution. Hemildbility of diphenylvinylphosphane in 1 was independently confirmed by the cluster reaction with CO, which gives the Rh-6(CO)(14)(kappa(1)-Ph2PC2H3)(GaCp*) adduct (3) with the phosphane ligand only coordinated through the phosphorus atom. (c) Wiley-VCH Verlag GmbH & Co. KGaA.",
keywords = "cluster compounds, heterometallic complexes, phosphane ligands, DYNAMIC-BEHAVIOR, DISUBSTITUTED-DERIVATIVES, CARBONYL-COMPLEXES, BONDING SITUATION, PHOSPHINE-LIGANDS, ANCILLARY LIGANDS, CHEMISTRY, REACTIVITY, TRIRUTHENIUM, GALLIUM",
author = "Grachova, {Elena V.} and Gerald Linti and Hans-Georg Stammler and Beate Neumann and Tunik, {Sergey P.} and Hubert Wadepohl",
year = "2007",
month = jan,
day = "1",
doi = "10.1002/ejic.200600705",
language = "Английский",
pages = "140--146",
journal = "Berichte der deutschen chemischen Gesellschaft",
issn = "0365-9496",
publisher = "Wiley-Blackwell",
number = "1",

}

RIS

TY - JOUR

T1 - Reactions of GaCp* with a hemilabile derivative of Rh-6(CO)(16) - Synthesis and structural characterization of two novel heterometallic clusters

T2 - Rh-6(CO)(13)(-) (mu,kappa 3-Ph2PC2H3)(mu(3)-GaCp*) and Rh-6(CO)(13)(kappa(1)-Ph2PC2H3)(mu(3)-GaCp*)(2)

AU - Grachova, Elena V.

AU - Linti, Gerald

AU - Stammler, Hans-Georg

AU - Neumann, Beate

AU - Tunik, Sergey P.

AU - Wadepohl, Hubert

PY - 2007/1/1

Y1 - 2007/1/1

N2 - The reaction of Rh-6(CO)(14)(Ph2PCH=CH2) with a twofold excess of GaCp* (Cp* = C5Me5) affords two novel heterometallic clusters Rh-6(CO)(13)(mu. kappa(3)-Ph2PC2H3)(mu(3)-GaCp*) (1) and Rh-6(CO)(13)(kappa(1)-Ph2PC2H3)(mu(3)-GaCp*)(2) (2) in a moderate yield. The hemilabile behavior of coordinated diphenylvinylphosphane in the starting cluster allows the easy insertion of GaCp* into the cluster coordination sphere, which eventually gives the cluster 1 with face-bridging coordination of the gallium fragment and the phosphane ligand recoordinated in an edge-bridging position. The further substitution of the vinyl function in 1 for the second GaCp* ligand affords cluster 2, where recoordination of the double bond is blocked by steric hindrance from adjacent GaCp* fragments. Both clusters were structurally characterized by X-ray crystallography in the solid state and by IR and NMR spectroscopy in solution. Hemildbility of diphenylvinylphosphane in 1 was independently confirmed by the cluster reaction with CO, which gives the Rh-6(CO)(14)(kappa(1)-Ph2PC2H3)(GaCp*) adduct (3) with the phosphane ligand only coordinated through the phosphorus atom. (c) Wiley-VCH Verlag GmbH & Co. KGaA.

AB - The reaction of Rh-6(CO)(14)(Ph2PCH=CH2) with a twofold excess of GaCp* (Cp* = C5Me5) affords two novel heterometallic clusters Rh-6(CO)(13)(mu. kappa(3)-Ph2PC2H3)(mu(3)-GaCp*) (1) and Rh-6(CO)(13)(kappa(1)-Ph2PC2H3)(mu(3)-GaCp*)(2) (2) in a moderate yield. The hemilabile behavior of coordinated diphenylvinylphosphane in the starting cluster allows the easy insertion of GaCp* into the cluster coordination sphere, which eventually gives the cluster 1 with face-bridging coordination of the gallium fragment and the phosphane ligand recoordinated in an edge-bridging position. The further substitution of the vinyl function in 1 for the second GaCp* ligand affords cluster 2, where recoordination of the double bond is blocked by steric hindrance from adjacent GaCp* fragments. Both clusters were structurally characterized by X-ray crystallography in the solid state and by IR and NMR spectroscopy in solution. Hemildbility of diphenylvinylphosphane in 1 was independently confirmed by the cluster reaction with CO, which gives the Rh-6(CO)(14)(kappa(1)-Ph2PC2H3)(GaCp*) adduct (3) with the phosphane ligand only coordinated through the phosphorus atom. (c) Wiley-VCH Verlag GmbH & Co. KGaA.

KW - cluster compounds

KW - heterometallic complexes

KW - phosphane ligands

KW - DYNAMIC-BEHAVIOR

KW - DISUBSTITUTED-DERIVATIVES

KW - CARBONYL-COMPLEXES

KW - BONDING SITUATION

KW - PHOSPHINE-LIGANDS

KW - ANCILLARY LIGANDS

KW - CHEMISTRY

KW - REACTIVITY

KW - TRIRUTHENIUM

KW - GALLIUM

U2 - 10.1002/ejic.200600705

DO - 10.1002/ejic.200600705

M3 - статья

SP - 140

EP - 146

JO - Berichte der deutschen chemischen Gesellschaft

JF - Berichte der deutschen chemischen Gesellschaft

SN - 0365-9496

IS - 1

ER -

ID: 78269724