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Volumn 49, Issue 48, 2010, Pages 9170-9173

Acid/base- and anion-controllable organogels formed from a urea-based molecular switch

Author keywords

host guest chemistry; molecular recognition; molecular switches; organogels; rotaxanes

Indexed keywords

1-PENTANOL; ANION EXCHANGE; GEL STATE; GEL-SOL TRANSITIONS; GELATORS; HOSTGUEST CHEMISTRY; MACROCYCLES; MOLECULAR SWITCHES; ORGANOGELS; ROTAXANES; SOLVENT EXPOSURE;

EID: 78649627683     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201004090     Document Type: Article
Times cited : (97)

References (35)
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    • 6] contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • 6] contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via.
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    • 6] in 1-pentanol was 1.2 wt%
    • 6] in 1-pentanol was 1.2 wt%.
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    • For examples of organogels that aggregate through the recognition of urea units, see
    • For examples of organogels that aggregate through the recognition of urea units, see
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    • For other anion-controllable rotaxane-based molecular switches, see
    • For other anion-controllable rotaxane-based molecular switches, see
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    • 6], associated through the proposed amide-urea hydrogen bonding interactions, to be 3 nm by using CS Chem. 3D computer simulation. This value is reasonably close to the thickness of the fibers observed using AFM (Figure 4d)
    • 6], associated through the proposed amide-urea hydrogen bonding interactions, to be 3 nm by using CS Chem. 3D computer simulation. This value is reasonably close to the thickness of the fibers observed using AFM (Figure 4d).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.