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Merck

Enantioselective nanofiber-spinning of chiral calixarene receptor with guest.

Chemical communications (Cambridge, England) (2007-11-21)
Yan-Song Zheng, Ao Ji, Xian-Jie Chen, Jin-Lan Zhou
RESUMEN

Chiral para-tert-butylcalix[4]arene bearing (S)-alpha-methylbenzylamine groups at lower rim only self-assembles with one of two enantiomers of 2,3-dibenzoyltartaric acid into coiled nanofibers and the coiled nanofibers only stack with the nanofibers having the same handedness to construct bigger ribbon-like fibers bearing porosity.

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Sigma-Aldrich
(S)-(−)-α-Methylbenzylamine, 98%
Sigma-Aldrich
(R)-(+)-α-Methylbenzylamine, 98%
Sigma-Aldrich
α-Methylbenzylamine, 99%
Sigma-Aldrich
Dibenzoyl-L-tartaric acid, 98%
Sigma-Aldrich
(+)-2,3-Dibenzoyl-D-tartaric acid, ≥98%, made from synthetic tartaric acid
Sigma-Aldrich
(R)-(+)-α-Methylbenzylamine, ChiPros®, produced by BASF, ≥99.0%
Sigma-Aldrich
(+)-2,3-Dibenzoyl-D-tartaric acid, ≥99.0% (T)
Sigma-Aldrich
(R)-(+)-α-Methylbenzylamine, purum, ≥98.0% (sum of enantiomers, GC)
Supelco
(R)-(+)-α-Methylbenzylamine, for chiral derivatization, LiChropur, ≥99.0%