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A kinetic study of guest displacement reactions on a host-guest complex with a photoswitchable calixarene
Authors:Letzel Matthias C  Schäfer Christian  Novara Francesca R  Speranza Maurizio  Rozhenko Alexander B  Schoeller Wolfgang W  Mattay Jochen
Affiliation:1. Fakult?t für Chemie, Universit?t Bielefeld, Postfach 100131, 33501 Bielefeld, Germany;2. Institut für Chemie der Technischen Universit?t Berlin, Strasse des 17. Juni 135, 10623 Berlin, Germany;3. Dipartimento di Studi di Chimica e Tecnologia delle Sostanze Biologicamente Attive, Università ‘La Sapienza’, P.le Aldo Moro 5, 00185 Roma, Italy;4. Institute of Organic Chemistry, National Academy of Sciences of Ukraine, 5 Murmanskaya street, 02660, Kiev, Ukraine;5. Department of Chemistry, University of California, Riverside, CA 92521‐0403, USA
Abstract:The displacement processes of several guests, incorporated in a calixarene host system, were investigated in the gas phase by electrospray ionization-Fourier transform-ion cyclotron resonance (ESI-FT-ICR) mass spectrometry. The complexes resulting from a resorcin[4]arene host with ammonia and sec-butylamine guests were isolated in an ICR-cell, separately using both states of the photoswitch as well as two reference systems for the open and closed forms of the photoswitchable host. The isolated complexes were forced to exchange the guest by using methylamine, ethylamine and sec-butylamine, resulting in different reaction rates for all the measured systems. Especially, the reaction rates of both states of the photoswitch are dependent on the provided guest. Potential side effects like proton exchanges were examined by an H/D-exchange experiment. The results were investigated and supported by quantum chemical calculations (DFT).
Keywords:host–guest chemistry  gas‐phase ion chemistry  photochemistry  resorcin[4]arene  electrospray mass spectrometry  computational modeling  DFT
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