Перейти к основному содержанию
AkademIndex

Продукты

Для разработчиков

AkademBaseскороОткрытый API экосистемы
Латиница
Русский
Статья

Formation and polymorphic phase transitions of crystalline inclusion compounds between 2,2′‐bis(9‐hydroxy‐9‐fluorenyl)biphenyl host and acetone guest

Б. Т. ИбрагимовInstitute of Bioorganic Chemistry, Uzbekistan Academy of Sciences, H. Abdullaev Str. 83, Tashkent 700143, UzbekistanК. М. БекетовInstitute of Bioorganic Chemistry, Uzbekistan Academy of Sciences, H. Abdullaev Str. 83, Tashkent 700143, UzbekistanEdwin WeberInstitut für Organische Chemie der Technischen Universität Bergakademie Freiberg, Leipziger Str. 29, D-09596 Freiberg/Sachsen, GermanyJürgen SeidelInstitut für Physikalische Chemie der Technischen Universität Bergakademie Freiberg, Leipziger Str. 29, D-09596, Freiberg/Sachsen, GermanyO. SumarnaInstitut für Physikalische Chemie der Technischen Universität Bergakademie Freiberg, Leipziger Str. 29, D-09596, Freiberg/Sachsen, GermanyK.K. MakhkamovInstitut für Organische Chemie der Technischen Universität Bergakademie Freiberg, Leipziger Str. 29, D-09596 Freiberg/Sachsen, GermanyK. KöhnkeInstitut für Physikalische Chemie der Technischen Universität Bergakademie Freiberg, Leipziger Str. 29, D-09596, Freiberg/Sachsen, Germany
ABI

Аннотация

Abstract The 2,2′‐bis(9‐hydroxy‐9‐fluorenyl)biphenyl host compound ( 1 ) was found to form various crystalline inclusion compounds with acetone depending on the crystallization conditions or on the method of preparation (inclusion of acetone vapour, co‐crystallization from solution). In order to understand and control the formation of these pseudopolymorphic phases regarding potential uses, single crystals of the existing phases (two 1:2 and one 1:1 compound) were prepared, their structures were solved by single‐crystal x‐ray diffraction (XRD) analysis and the desolvation and phase transformations were studied using simultaneous thermogravimetry–differential scanning calorimetry (TG–DSC) and variable‐temperature powder XRD. The results explain the inclusion and desolvation behaviour and also clarify the observed, apparently accidental formation of a 1:1 or 1:2 inclusion compound at ambient temperature. Copyright © 2001 John Wiley & Sons, Ltd.

Темы

Идентификаторы

Цитирования и источники

Показатели — AkademScholar · Скоро