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Volumn 20, Issue 16, 2004, Pages 6580-6585

One-component gels based on peptidic dendrimers: Dendritic effects on materials properties

Author keywords

[No Author keywords available]

Indexed keywords

DIFFERENTIAL SCANNING CALORIMETRY; ENTHALPY; GELATION; GELS; HYDROGEN BONDS; NUCLEAR MAGNETIC RESONANCE; ORGANIC SOLVENTS; SUPRAMOLECULAR CHEMISTRY;

EID: 4043163395     PISSN: 07437463     EISSN: None     Source Type: Journal    
DOI: 10.1021/la049575q     Document Type: Article
Times cited : (72)

References (46)
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    • Our two-component system is held together by carboxylio acid-amine interactions between the focal point of a dendron and a diamine spacer chain: (a) Partridge, K. S.; Smith, D. K.; Dykes, G. M.; McGrail, P. T. Chem. Commun. 2001, 319-320. (b) Hirst, A. R.; Smith, D. K.; Feiters, M. C.; Geurts, H. P. M.; Wright, A. C. J. Am. Chem. Soc. 2003, 125, 9010-9011. We have also illustrated that this design principle can be applied to the formation of gels with the two components held together by interactions between a dendritic crown ether and a protonated aliphatic diamine: (c) Dykes, G. M.; Smith, D. K. Tetrahedron 2003, 59, 3999-4009.
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    • Our two-component system is held together by carboxylio acid-amine interactions between the focal point of a dendron and a diamine spacer chain: (a) Partridge, K. S.; Smith, D. K.; Dykes, G. M.; McGrail, P. T. Chem. Commun. 2001, 319-320. (b) Hirst, A. R.; Smith, D. K.; Feiters, M. C.; Geurts, H. P. M.; Wright, A. C. J. Am. Chem. Soc. 2003, 125, 9010-9011. We have also illustrated that this design principle can be applied to the formation of gels with the two components held together by interactions between a dendritic crown ether and a protonated aliphatic diamine: (c) Dykes, G. M.; Smith, D. K. Tetrahedron 2003, 59, 3999-4009.
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    • 0038634870 scopus 로고    scopus 로고
    • Our two-component system is held together by carboxylio acid-amine interactions between the focal point of a dendron and a diamine spacer chain: (a) Partridge, K. S.; Smith, D. K.; Dykes, G. M.; McGrail, P. T. Chem. Commun. 2001, 319-320. (b) Hirst, A. R.; Smith, D. K.; Feiters, M. C.; Geurts, H. P. M.; Wright, A. C. J. Am. Chem. Soc. 2003, 125, 9010-9011. We have also illustrated that this design principle can be applied to the formation of gels with the two components held together by interactions between a dendritic crown ether and a protonated aliphatic diamine: (c) Dykes, G. M.; Smith, D. K. Tetrahedron 2003, 59, 3999-4009.
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    • For the original report of dendrimers based on L-lysine see: (a) Denkewalter, R. G.; Kolc, J.; Lukasavage, W. J. (Allied Corp) US 4289872, 1981 [Chem. Abstr. 1985, 102, 79324q]. For our synthetic methods see: (b) Dykes, G. M.; Brierley, L. J.; Smith, D. K.; McGrail, P. T.; Seeley, G. J. Chem. Eur. J. 2001, 7, 4730-4739. (c) Driffield, M.; Goodall, D. M.; Smith, D. K. Org. Biomol. Chem. 2003, 1, 2612-2620.
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    • For examples see: (a) Snip, E.; Shinkai, S.; Reinhoudt, D. N. Tetrahedron Lett. 2001, 42, 2153-2156. (b) Ihara, H.; Takafuji, M.; Sakurai, T.; Katsumoto, M.; Ushijima, N.; Shirosaki, T.; Hachisako, H. Org. Biomol. Chem. 2003, 1, 3004-3006. (c) Hanabusa, K.; Maesaka, Y.; Kimura, M.; Shirai, H. Tetrahedron Lett. 1999, 40, 2385-2388. (d) Goto, H.; Zhang, H. Q.; Yashima, E. J. Am. Chem. Soc. 2003, 125, 2516-2523. (e) van Gorp, J. J.; Vekemans, J. A. J. M.; Meijer, E. W. J. Am. Chem. Soc. 2002, 124, 14759-14769.
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