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Volumn 16, Issue 11, 2010, Pages 3467-3475

Self-assembly of calix[6]arene-diazapyrenium pseudorotaxanes: Interplay of molecular recognition and ion-pairing effects

Author keywords

Calixarenes; Ion pairs; Molecular devices; Pseudorotaxanes; Supramolecular chemistry

Indexed keywords

CALIX[6]ARENES; CALIXARENES; COMPLEX STRUCTURE; CONCENTRATED SOLUTION; CONCENTRATION OF; COORDINATING ANIONS; COUNTERIONS; DIAZAPYRENIUM; DILUTE SOLUTION; ELECTRON-ACCEPTOR; HETERODITOPIC RECEPTORS; ION PAIRS; ION-PAIRING; MACROCYCLICS; MOLECULAR DEVICE; PSEUDOROTAXANES; SELF-ASSEMBLED; SUPRAMOLECULAR COMPLEXES; SUPRAMOLECULAR SPECIES; THREE COMPONENT;

EID: 77949304942     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200903049     Document Type: Article
Times cited : (31)

References (57)
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    • The reduction of the magnitude of the diffusion coefficient measured upon binding (≈ 1.7%) is comparable to that found in similar studies in which an α-cyclodextrin was used as a wheel for the formation of pseudorotaxane compounds
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    • - salt causes the exchange of the counterions, see: ref. [15]
    • - salt causes the exchange of the counterions, see: ref. [15];
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    • In this case we could not perform, the experiment on 1·2TsO because of precipitation
    • b) In this case we could not perform, the experiment on 1·2TsO because of precipitation.
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    • Any attempt to obtain crystals of the 2:1 adduct suitable for X-ray analysis failed
    • Any attempt to obtain crystals of the 2:1 adduct suitable for X-ray analysis failed.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.