Effect of peracetylation on the conformation of γ-cyclodextrin

Mino R. Caira; Giampiero Bettinetti; Milena Sorrenti; Laura Catenacci; Dyanne Cruickshank; Kate Davies

doi:10.1039/b616681d

Effect of peracetylation on the conformation of γ-cyclodextrin

Mino R. Caira, Giampiero Bettinetti, Milena Sorrenti, Laura Catenacci, Dyanne Cruickshank, Kate Davies

IRCCS Fondazione Policlinico San Matteo

Research output: Contribution to journal › Article › peer-review

Abstract

The well-known, fourfold symmetry of the γ-CD molecule in its solid inclusion complexes is lost on peracetylation, which yields a highly distorted host molecule in which self-inclusion of acetyl residues divides the macrocyclic cavity into two distinct sub-cavities that accommodate solvent molecules.

Original language	English
Pages (from-to)	1221-1223
Number of pages	3
Journal	Chemical Communications
Issue number	12
DOIs	https://doi.org/10.1039/b616681d
Publication status	Published - 2007

ASJC Scopus subject areas

Chemistry(all)

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10.1039/b616681d

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title = "Effect of peracetylation on the conformation of γ-cyclodextrin",

abstract = "The well-known, fourfold symmetry of the γ-CD molecule in its solid inclusion complexes is lost on peracetylation, which yields a highly distorted host molecule in which self-inclusion of acetyl residues divides the macrocyclic cavity into two distinct sub-cavities that accommodate solvent molecules.",

author = "Caira, {Mino R.} and Giampiero Bettinetti and Milena Sorrenti and Laura Catenacci and Dyanne Cruickshank and Kate Davies",

year = "2007",

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journal = "Chemical Communications",

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publisher = "Royal Society of Chemistry",

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AU - Caira, Mino R.

AU - Bettinetti, Giampiero

AU - Sorrenti, Milena

AU - Catenacci, Laura

AU - Cruickshank, Dyanne

AU - Davies, Kate

PY - 2007

Y1 - 2007

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AB - The well-known, fourfold symmetry of the γ-CD molecule in its solid inclusion complexes is lost on peracetylation, which yields a highly distorted host molecule in which self-inclusion of acetyl residues divides the macrocyclic cavity into two distinct sub-cavities that accommodate solvent molecules.

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Effect of peracetylation on the conformation of γ-cyclodextrin

Abstract

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