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Novel carbonyl complexes of ruthenium with alpha-substituted oxime derivatives of terpenes Full article

Journal Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya
ISSN: 1070-3284
Output data Year: 2008, Volume: 34, Number: 4, Pages: 286-294 Pages count : 9 DOI: 10.1134/S1070328408040088
Authors Shabalina I.Yu. 1 , Kirin V.P. 2 , Maksakov V.A. 2 , Virovets A.V. 2 , Golovin A.V. 1 , Agafontsev A.M. 3 , Tkachev A.V. 3
Affiliations
1 (Данные Web of science) Novosibirsk State Univ, Novosibirsk 630090, Russia
2 (Данные Web of science) Russian Acad Sci, Siberian Div, Nikolaev Inst Inorgan Chem, Novosibirsk 630090, Russia
3 (Данные Web of science) Russian Acad Sci, Siberian Div, Vorozhstov Inst Organ Chem, Novosibirsk, Russia

Abstract: The reactions of Ru-3(CO)(12) with 1R, 4S, 6S-4-dimethylamino-4,7,7-trimethylbicyclo[4.1.0] heptane-3- one oxime (dimethylaminocaraneoxime) (I), 1R, 4S, 6S-4-methylamino-4,7,7-trimethylbicyclo[4.1.0] heptane-3- one oxime (methylaminocarane oxime) (II), and 1R, 2R, 5R-2-benzylthio-2,6,6-trimethylbicyclo[3.1.1] heptane-3- one oxime (benzylthiopinaneoxime) (III) were studied. The binuclear complex Ru-2(CO)(4){mu-eta(3)(O, N, X)-L}(2) was formed as the main product in every reaction, when Ru-3(CO)(12) was heated with terpenoid to 80 degrees C. In the above complex, two terpene ligands are coordinated in the form of 'head-to tail' bridge by the oxime groups at a binuclear metal fragment Ru-Ru. The heteroatom of the second functional group of every bridging ligand ( nitrogen of amino group in I and II, sulfur of the thio group in III) is additionally coordinated to the ruthenium atom to give the chelate five-membered ring. Also the reactions of terpenoids I, II, III with Ru-3(CO)(12) were performed at room temperature using Me3NO. In this case, as in the thermal reactions, the main product was the binuclear complex. However, in the reactions of Ru-3(CO)(12) with I and II, the trinuclear clusters were isolated that readily transformed to binuclear complexes in a solution. The complexes synthesized can exist as two diastereomers due to their chiral metal core. However, in all the cases, only one diastereomer was isolated, which indicates stereospecific nature of the above reactions. The compounds obtained were characterized by IR, H-1-, C-13{H-1}-, COSY, and HXCOBI-NMR spectroscopy, the specific optical rotation angles were measured. For the binuclear complexes with ligands I, III and for trinuclear cluster with ligand II, single crystals were obtained and studied by X-ray diffraction.
Cite: Shabalina I.Y. , Kirin V.P. , Maksakov V.A. , Virovets A.V. , Golovin A.V. , Agafontsev A.M. , Tkachev A.V.
Novel carbonyl complexes of ruthenium with alpha-substituted oxime derivatives of terpenes
Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya. 2008. V.34. N4. P.286-294. DOI: 10.1134/S1070328408040088 WOS Scopus РИНЦ OpenAlex
Original: Шабалина И.Ю. , Кирин В.П. , Максаков В.А. , Вировец А.В. , Головин А.В. , Агафонцев А.М. , Ткачев А.В.
Новые карбонильные комплексы рутения с -замещенными оксимными производными терпенов
Координационная химия (RUSS J COORD CHEM+). 2008. Т.34. №4. С.293-301. РИНЦ
Dates:
Published print: Apr 1, 2008
Published online: May 4, 2008
Identifiers:
Web of science: WOS:000255586800008
Scopus: 2-s2.0-43249117505
Elibrary: 13577161
OpenAlex: W2079559951
Citing:
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Web of science 4
Scopus 4
Elibrary 4
OpenAlex 5
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