Steric bulkness of diamondoidyl substituents

dc.contributor.authorBarabash, Anastasia
dc.contributor.authorBiletskiy, Bogdan
dc.contributor.authorMaksimyuk, Yuriy
dc.contributor.authorButova, Ekaterina
dc.contributor.authorFokin, Andrey
dc.date.accessioned2013-06-14T13:38:49Z
dc.date.available2013-06-14T13:38:49Z
dc.date.issued2011
dc.description.abstractThe influence of the diamondoidyl substituent on the reaction center was investigated experimentally and computationally. Calculations were provided at DFT and DFT-D,using B3LYP, B97D and M062X functionals. Experimental investigation was made by studying the Corey-Chaykovsky reaction. The latter was explored with dimethylsulfoxonium methylide and diamondoidyl ketones, which has different distance between the carbonyl group and the cage. Diamondoidyl substituent was shown to have negligible effect on the reactive center within 2 CH2 groups. While in ketones, bearing one CH2 group between cage and carbonyl, it hampers tetrahedization of the reactive center. In case of methyl diamondoidyl ketones the cage hinders the access of the reagent.uk_UA
dc.identifier.citationSteric bulkness of diamondoidyl substituents / Anastasia Barabash, Bogdan Biletskiy, Yuri Maksimyuk, Ekaterina Butova, Andrey Fokin // Хімія та хімічні технології : матеріали ІI Міжнародної конференції молодих вчених CCT-2011, 24–26 листопада 2011 року, Україна, Львів / Національний університет "Львівська політехніка". – Львів : Видавництво Львівської політехніки, 2011. – С. 98–99. – (3-й Міжнародний молодіжний фестиваль науки "Litteris et Artibus"). – Bibliography: 1 titel.uk_UA
dc.identifier.urihttps://ena.lpnu.ua/handle/ntb/19782
dc.language.isoenuk_UA
dc.publisherВидавництво Львівської політехнікиuk_UA
dc.subjectdiamondoidsuk_UA
dc.subjectDFT calculationsuk_UA
dc.subjectkineticsuk_UA
dc.subjectreaction centeruk_UA
dc.titleSteric bulkness of diamondoidyl substituentsuk_UA
dc.typeArticleuk_UA

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