Amphiphilic [5:1]- and [3:3]-hexakisadducts of C 60

Braun M, Hartnagel U, Ravanelli E, Schade B, Boettcher C, Vostrowsky O, Hirsch A (2004)


Publication Type: Journal article, Original article

Publication year: 2004

Journal

Original Authors: Braun M., Hartnagel U., Ravanelli E., Schade B., Böttcher C., Vostrowsky O., Hirsch A.

Publisher: Wiley-VCH Verlag

Pages Range: 1983-2001

Journal Issue: 9

DOI: 10.1002/ejoc.200300663

Abstract

We have synthesized and characterized a variety of new amphiphilic hexakisadducts of C involving mixed octahedral [5:1]- and [3:3]-addition patterns. The [5:1]-adducts 3 and 13 contain five pairs of didodecyl or diethyl malonates as non-polar addends and, as their polar part, an extended bis(malonate) involving C and ethylene glycol chains and two biotin termini. For the first time, amphiphilic [3:3]-hexakisadducts have been prepared using the e,e,e-trisadduct 18, which contains a cyclo-[3]-octyl malonate addend, as the precursor. As polar groups, we used malonates featuring carboxy, amino, or peptide termini. The charge on the termini, which can range from zero up to sixfold positive or sixfold negative, can be built up by protonation or deprotonation. All the amphiphilic [3:3]-hexakisadducts are very soluble in water in their completely charged forms. Initial investigations on the aggregation properties of the amphiphilic [3:3]-hexakisadducts, conducted using transmission electron microscopy (TEM) and pulse-gradient spin echo (PGSE) NMR spectroscopy, reveal the pH-dependent formation of aggregates. © Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004.

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APA:

Braun, M., Hartnagel, U., Ravanelli, E., Schade, B., Boettcher, C., Vostrowsky, O., & Hirsch, A. (2004). Amphiphilic [5:1]- and [3:3]-hexakisadducts of C 60. European Journal of Organic Chemistry, 9, 1983-2001. https://doi.org/10.1002/ejoc.200300663

MLA:

Braun, Martin, et al. "Amphiphilic [5:1]- and [3:3]-hexakisadducts of C 60." European Journal of Organic Chemistry 9 (2004): 1983-2001.

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