A novel arene bonding mode in the mixed-metal cluster Os4Ru( μ-H)3(CO) 12( μ3-η6-C6H5)P(OMe)3

R. A. Al-Mandhary Muna; Jack Lewis; Paul R. Raithby

doi:10.1016/S0022-328X(96)06889-1

A novel arene bonding mode in the mixed-metal cluster Os₄Ru( μ-H)₃(CO) ₁₂( μ₃-η⁶-C₆H₅)P(OMe)₃

R. A. Al-Mandhary Muna, Jack Lewis, Paul R. Raithby^*

^*المؤلف المقابل لهذا العمل

نتاج البحث: المساهمة في مجلة › Article › مراجعة النظراء

17 اقتباسات (Scopus)

ملخص

The ionic coupling of [Os₄H₂(CO)₁₂]_2- with [Ru(η⁶-C₆H₆)(MeCN)₃]^2- affords the neutral mixed metal cluster Os₄Ru( μ-H)₂(CO)₁₂(η⁶-C₆H₆) 1. The reaction of 1 with trimethylphosphite leads to the initial formation of the addition product Os₄Ru( μ-H)₂(CO)₁₂(η⁶-C₆H₆)P(OMe)₃ 2, but this complex rearranges in solution to give Os₄Ru( μ-H)₃(CO)₁₂(μ₃-η⁶-C₆H₅)P(OMe)₃ 3. An X-ray structure of 3 shows that the metal core of the cluster is a ruthenium-spiked Os₄ tetrahedron, with one hydrogen atom from the arene having transferred to the Os₄ core, and one arene carbon bridging an Os-Os edge, while the ring as a whole remains η⁶-bound to the Ru atom.

اللغة الأصلية	English
الصفحات (من إلى)	247-250
عدد الصفحات	4
دورية	Journal of Organometallic Chemistry
مستوى الصوت	530
رقم الإصدار	1-2
المعرِّفات الرقمية للأشياء	https://doi.org/10.1016/S0022-328X(96)06889-1
حالة النشر	Published - مارس 1 1997
منشور خارجيًا	نعم

ASJC Scopus subject areas

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10.1016/S0022-328X(96)06889-1

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@article{0273c2e7256b4b44bbe0eff7911cd306,

title = "A novel arene bonding mode in the mixed-metal cluster Os4Ru( μ-H)3(CO) 12( μ3-η6-C6H5)P(OMe)3",

abstract = "The ionic coupling of [Os4H2(CO)12]2- with [Ru(η6-C6H6)(MeCN)3]2- affords the neutral mixed metal cluster Os4Ru( μ-H)2(CO)12(η6-C6H6) 1. The reaction of 1 with trimethylphosphite leads to the initial formation of the addition product Os4Ru( μ-H)2(CO)12(η6-C6H6)P(OMe)3 2, but this complex rearranges in solution to give Os4Ru( μ-H)3(CO)12(μ3-η6-C6H5)P(OMe)3 3. An X-ray structure of 3 shows that the metal core of the cluster is a ruthenium-spiked Os4 tetrahedron, with one hydrogen atom from the arene having transferred to the Os4 core, and one arene carbon bridging an Os-Os edge, while the ring as a whole remains η6-bound to the Ru atom.",

keywords = "Arene, Crystal structure, Osmium, Phosphite, Ruthenium",

author = "{Al-Mandhary Muna}, {R. A.} and Jack Lewis and Raithby, {Paul R.}",

note = "Funding Information: We are grateful to the Government of the Sultanate of Oman and the Overseas Research Students Awards Scheme for financial support (to M.R.A.A.), and to Johnson Matthey plc for the generous loan of the osmium and ruthenium salts.",

year = "1997",

month = mar,

day = "1",

doi = "10.1016/S0022-328X(96)06889-1",

language = "English",

volume = "530",

pages = "247--250",

journal = "Journal of Organometallic Chemistry",

issn = "0022-328X",

publisher = "Elsevier",

number = "1-2",

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TY - JOUR

T1 - A novel arene bonding mode in the mixed-metal cluster Os4Ru( μ-H)3(CO) 12( μ3-η6-C6H5)P(OMe)3

AU - Al-Mandhary Muna, R. A.

AU - Lewis, Jack

AU - Raithby, Paul R.

N1 - Funding Information: We are grateful to the Government of the Sultanate of Oman and the Overseas Research Students Awards Scheme for financial support (to M.R.A.A.), and to Johnson Matthey plc for the generous loan of the osmium and ruthenium salts.

PY - 1997/3/1

Y1 - 1997/3/1

N2 - The ionic coupling of [Os4H2(CO)12]2- with [Ru(η6-C6H6)(MeCN)3]2- affords the neutral mixed metal cluster Os4Ru( μ-H)2(CO)12(η6-C6H6) 1. The reaction of 1 with trimethylphosphite leads to the initial formation of the addition product Os4Ru( μ-H)2(CO)12(η6-C6H6)P(OMe)3 2, but this complex rearranges in solution to give Os4Ru( μ-H)3(CO)12(μ3-η6-C6H5)P(OMe)3 3. An X-ray structure of 3 shows that the metal core of the cluster is a ruthenium-spiked Os4 tetrahedron, with one hydrogen atom from the arene having transferred to the Os4 core, and one arene carbon bridging an Os-Os edge, while the ring as a whole remains η6-bound to the Ru atom.

AB - The ionic coupling of [Os4H2(CO)12]2- with [Ru(η6-C6H6)(MeCN)3]2- affords the neutral mixed metal cluster Os4Ru( μ-H)2(CO)12(η6-C6H6) 1. The reaction of 1 with trimethylphosphite leads to the initial formation of the addition product Os4Ru( μ-H)2(CO)12(η6-C6H6)P(OMe)3 2, but this complex rearranges in solution to give Os4Ru( μ-H)3(CO)12(μ3-η6-C6H5)P(OMe)3 3. An X-ray structure of 3 shows that the metal core of the cluster is a ruthenium-spiked Os4 tetrahedron, with one hydrogen atom from the arene having transferred to the Os4 core, and one arene carbon bridging an Os-Os edge, while the ring as a whole remains η6-bound to the Ru atom.

KW - Arene

KW - Crystal structure

KW - Osmium

KW - Phosphite

KW - Ruthenium

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U2 - 10.1016/S0022-328X(96)06889-1

DO - 10.1016/S0022-328X(96)06889-1

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EP - 250

JO - Journal of Organometallic Chemistry

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