Complexation of Ferrocene Derivatives by the Cucurbit[7]uril Host: A Comparative Study of the Cucurbituril and Cyclodextrin Host Families

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14310%2F05%3A00031282" target="_blank" >RIV/00216224:14310/05:00031282 - isvavai.cz</a>

Výsledek na webu

—

DOI - Digital Object Identifier

—

Jazyk výsledku

angličtina

Název v původním jazyce

Complexation of Ferrocene Derivatives by the Cucurbit[7]uril Host: A Comparative Study of the Cucurbituril and Cyclodextrin Host Families

Popis výsledku v původním jazyce

The formation of inclusion complexes between cucurbit[7]uril (CB[7]) and ferrocene and its derivs. has been investigated. The x-ray crystal structure of the 1:1 inclusion complex between ferrocene and CB[7] revealed that the guest mol. resides in the host cavity with two different orientations. Inclusion of a set of five water-sol. ferrocene derivs. in CB[7] was investigated by 1H NMR spectroscopy and calorimetric and voltammetric techniques. Data indicate that all neutral and cationic guests form highly stable inclusion complexes with CB[7], with binding consts. in the 109-1010 M-1 and 1012-1013 M-1 ranges, resp. However, the anionic ferrocenecarboxylate, the only neg. charged guest among those surveyed, was not bound by CB[7] at all. These results are in sharp contrast to the known binding behavior of the same guests to b-cyclodextrin (b-CD), since all the guests form stable inclusion complexes with b-CD, with binding consts. in the range 103-104 M-1.

Název v anglickém jazyce

Complexation of Ferrocene Derivatives by the Cucurbit[7]uril Host: A Comparative Study of the Cucurbituril and Cyclodextrin Host Families

Popis výsledku anglicky

The formation of inclusion complexes between cucurbit[7]uril (CB[7]) and ferrocene and its derivs. has been investigated. The x-ray crystal structure of the 1:1 inclusion complex between ferrocene and CB[7] revealed that the guest mol. resides in the host cavity with two different orientations. Inclusion of a set of five water-sol. ferrocene derivs. in CB[7] was investigated by 1H NMR spectroscopy and calorimetric and voltammetric techniques. Data indicate that all neutral and cationic guests form highly stable inclusion complexes with CB[7], with binding consts. in the 109-1010 M-1 and 1012-1013 M-1 ranges, resp. However, the anionic ferrocenecarboxylate, the only neg. charged guest among those surveyed, was not bound by CB[7] at all. These results are in sharp contrast to the known binding behavior of the same guests to b-cyclodextrin (b-CD), since all the guests form stable inclusion complexes with b-CD, with binding consts. in the range 103-104 M-1.

Druh

J_x - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)

CEP obor

CD - Makromolekulární chemie

OECD FORD obor

—

Projekt

—

Návaznosti

V - Vyzkumna aktivita podporovana z jinych verejnych zdroju

Rok uplatnění

2005

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Journal of the American Chemical Society

ISSN

0002-7863

e-ISSN

—

Svazek periodika

127

Číslo periodika v rámci svazku

37

Stát vydavatele periodika

CZ - Česká republika

Počet stran výsledku

6

Strana od-do

—

Kód UT WoS článku

000231928800055

EID výsledku v databázi Scopus

—