The different natures of the weakly coordinating anions –triflate or perchlorate–in the Cu2+-mediatedself-assembly of cytidine monophosphate nucleotide play a fundamental role in the homochiralresolution 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 circulardichroism experiments both in solution and in the solid state.

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

Marino N;ARMENTANO, Donatella
;
NEVE, Francesco;DI DONNA, Leonardo;DE MUNNO, Giovanni
2015-01-01

Abstract

The different natures of the weakly coordinating anions –triflate or perchlorate–in the Cu2+-mediatedself-assembly of cytidine monophosphate nucleotide play a fundamental role in the homochiralresolution 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 circulardichroism experiments both in solution and in the solid state.
2015
self-assembly; copper; biocoordination polymers
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11770/145014
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