Academic Journal
Synthesis and characterization of new ruthenium N-heterocyclic carbene Hoveyda II-type complexes. Study of reactivity in ring closing metathesis reactions
| العنوان: | Synthesis and characterization of new ruthenium N-heterocyclic carbene Hoveyda II-type complexes. Study of reactivity in ring closing metathesis reactions |
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| المؤلفون: | Merino Marcos, Estibaliz, Poli, Evelyne, Díaz Morales, Urbano Manuel, Brunel, Daniel |
| المساهمون: | Universitat Politècnica de València. Instituto Universitario Mixto de Tecnología Química - Institut Universitari Mixt de Tecnologia Química, Ministerio de Ciencia e Innovación |
| المصدر: | Repositorio Institucional de la Universitat Politècnica de València |
| بيانات النشر: | Royal Society of Chemistry |
| سنة النشر: | 2012 |
| مصطلحات موضوعية: | musiq, hisphilso |
| الوصف: | Senia ; [EN] This manuscript describes the synthesis and structural study of new second generation Hoveyda¿Grubbs catalysts: 1,3-dimesitylacenaphthylenyl- 4,5-imidazolin-2-ylidene (BIAN-NHC) ruthenium isopropoxybenzylidene dichloride 3 and 1,3-bis- (2,6-dimethylphenyl)-2,3-dihydro-1H-imidazole Cl2Ru(vCHo- O-i-PrC6H4) 4. The electrochemical and catalytic behavior of these new complexes was compared with the conventional NHC carbene Hoveyda II IMes-type complexes 1 and 2 for ring closing metathesis reactions. We thank Dr Berta Gomez-Lor for allowing us to use the cyclic voltammetry instrumentation, Dr J. A. Vidal-Moya for his support in the kinetic experiments and Dr Marcelo Domine for the HRMS measurements. We thank Avelino Corma, Felix Sanchez and Marta Iglesias for helpful discussions. E. M. also thanks Ministerio de Ciencia e Innovacion for a contract of the "Juan de la Cierva" program. Financial support by Consolider-Ingenio 2010 (MULTICAT project) and MAT2011-29020-C02-01 is additionally acknowledged. Merino Marcos, E.; Poli, E.; Díaz Morales, UM.; Brunel, D. (2012). Synthesis and characterization of new ruthenium N-heterocyclic carbene Hoveyda II-type complexes. Study of reactivity in ring closing metathesis reactions. DALTON TRANSACTIONS. 41(36):10913-10918. doi:10.1039/c2dt31540h ; 10913 10918 41 36 |
| نوع الوثيقة: | article in journal/newspaper |
| اللغة: | English |
| تدمد: | 1477-9226 1477-9234 |
| Relation: | http://hdl.handle.net/10251/31696; http://dx.doi.org/10.1039/c2dt31540h |
| DOI: | 10.1039/c2dt31540h |
| الاتاحة: | https://doi.org/10.1039/c2dt31540h http://hdl.handle.net/10251/31696 |
| رقم الانضمام: | edsbas.D9EDCF37 |
| قاعدة البيانات: | BASE |
| تدمد: | 14779226 14779234 |
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| DOI: | 10.1039/c2dt31540h |