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Homochiral self-assembly of biocoordination polymers: anion-triggered helicity and absolute configuration inversion†
Donatella Armentano,Emilio Pardo,Julia Vallejo,Francesco Neve,Leonardo Di Donna,Giovanni De Munno
Chemical Science Pub Date : 04/30/2015 00:00:00 , DOI:10.1039/C5SC01089F
Abstract

The different natures of the weakly coordinating anions – triflate or perchlorate – in the Cu2+-mediated self-assembly of cytidine monophosphate nucleotide play a fundamental role in the homochiral resolution process, yielding one-dimensional copper(II) coordination polymers of opposite helicity that can be easily inverted, in a reversible way, by changing the nature of the anion as revealed by circular dichroism experiments both in solution and in the solid state.

Graphical abstract: Homochiral self-assembly of biocoordination polymers: anion-triggered helicity and absolute configuration inversion
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