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Volumn 20, Issue 3, 2008, Pages 782-820

Inorganic and hybrid nanofibrous materials templated with organogelators

Author keywords

[No Author keywords available]

Indexed keywords

GELATION; MOLECULAR WEIGHT; NANOSTRUCTURES; SELF ASSEMBLED MONOLAYERS; SUPRAMOLECULAR CHEMISTRY; TRANSCRIPTION;

EID: 39849093496     PISSN: 08974756     EISSN: None     Source Type: Journal    
DOI: 10.1021/cm702141e     Document Type: Article
Times cited : (240)

References (200)
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    • An interesting an recent example of a blue-emitting hydro-gel, with a pH-responsive, gelation-induced fluorescence emission: Kim, T. H, Seo, J, Lee, S. J, Kim, J, Jung, J. H. Chem. Mater. 2007 [Online Nov. 17, 2007] DOI: 10.1021/cm071391k
    • (b) An interesting an recent example of a blue-emitting hydro-gel, with a pH-responsive, gelation-induced fluorescence emission: Kim, T. H.; Seo, J.; Lee, S. J.; Kim, J.; Jung, J. H. Chem. Mater. 2007 [Online Nov. 17, 2007] DOI: 10.1021/cm071391k.
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    • See also ref 10
    • (d) See also ref 10.
  • 37
    • 7244253291 scopus 로고    scopus 로고
    • LMOGs may also be used as templating agents of organics, i.e., for the polymerization of organic monomers. For instance, Shinkai et al. have recently directed the polymerization of organic monomers (like aniline, pyrrole, ethylendioxythiophene, etc.) through electrostatic interactions with cationic (protonated cyclohexane diamines) or anionic (sulphonated synthetic lipids) assemblies of LMOGs as templates; see, e.g., (a) Hatano, T.; Bae, A.-H.; Takeuchi, M.; Fujita, N.; Kaneko, K.; Ihara, H.; Takafuji, M.; Shinkai, S. Chem.-Eur. J. 2004, 10, 5067.
    • LMOGs may also be used as templating agents of organics, i.e., for the polymerization of organic monomers. For instance, Shinkai et al. have recently directed the polymerization of organic monomers (like aniline, pyrrole, ethylendioxythiophene, etc.) through electrostatic interactions with cationic (protonated cyclohexane diamines) or anionic (sulphonated synthetic lipids) assemblies of LMOGs as templates; see, e.g., (a) Hatano, T.; Bae, A.-H.; Takeuchi, M.; Fujita, N.; Kaneko, K.; Ihara, H.; Takafuji, M.; Shinkai, S. Chem.-Eur. J. 2004, 10, 5067.
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    • A review on the gelation of liquids by cholesterol derivatives may be found in ref d. More detailed and comprehensive overviews-monographic chapters-of the gelating and structural properties of cholesterol-based gelators can be found in ref 7.
    • A review on the gelation of liquids by cholesterol derivatives may be found in ref d. More detailed and comprehensive overviews-monographic chapters-of the gelating and structural properties of cholesterol-based gelators can be found in ref 7.
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    • Murata, K. Ph-D. Thesis, Graduate School of Engineering, Kyushu University, Fukuoka, Japan, 1997.
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    • in a rather different but related approach, hexagonal patterns of au nanorods have been recently grown onto coassembled poly(n-isopropylacrylamide) microgel particles: kumar, v. r. r.; samal, a. k.; sreeprasad, t. s.; pradeep, t. langmuir 2007, 23, 8667. in this case, thus, the strategy consisted of the assembly of polymer microgel particles previously coated with gold nanoparticles (surface-modified with ctab surfactant).
    • in a rather different but related approach, hexagonal patterns of au nanorods have been recently grown onto coassembled poly(n-isopropylacrylamide) microgel particles: kumar, v. r. r.; samal, a. k.; sreeprasad, t. s.; pradeep, t. langmuir 2007, 23, 8667. in this case, thus, the strategy consisted of the assembly of polymer microgel particles previously coated with gold nanoparticles (surface-modified with ctab surfactant).
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    • Similarly, some organometallic compounds (bearing direct transition-metal-to-carbon bonds) can also lead to fibrous hybrid organogels (i.e., the pentacarbonyl chromate hybrid gelator synthesized by Bühler et al.), but they are not reported herein. Bühler; et al. Angew. Chem., Int. Ed. 2003, 42, 2494.
    • Similarly, some organometallic compounds (bearing direct transition-metal-to-carbon bonds) can also lead to fibrous hybrid organogels (i.e., the pentacarbonyl chromate hybrid gelator synthesized by Bühler et al.), but they are not reported herein. Bühler; et al. Angew. Chem., Int. Ed. 2003, 42, 2494.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.