Controlling the organization of phosphonium cations relative to p-sulfonatocalix[4]arene anions

Irene Ling; Alexandre Sobolev; Colin Raston

doi:10.1039/c4ce02086c

Controlling the organization of phosphonium cations relative to p-sulfonatocalix[4]arene anions

Irene Ling, Alexandre Sobolev, Colin Raston

Research output: Contribution to journal › Article › peer-review

7 Citations (Scopus)

Abstract

Solution mediated organization of p-sulfonatocalix[4]arene, benzyltriphenylphosphonium cations, and bis(triethylammoniomethyl)-benzene dications in the solid state results in the ammonium dications preferentially binding in the cavities of two opposing calixarenes which take on a -3 charge, with the phosphonium cations arranged in a separate 2D sheet relative to the calixarene bilayer. This journal is

Original language	English
Pages (from-to)	1526-1530
Number of pages	5
Journal	CrystEngComm
Volume	17
Issue number	7
DOIs	https://doi.org/10.1039/c4ce02086c
Publication status	Published - 21 Feb 2015

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abstract = "Solution mediated organization of p-sulfonatocalix[4]arene, benzyltriphenylphosphonium cations, and bis(triethylammoniomethyl)-benzene dications in the solid state results in the ammonium dications preferentially binding in the cavities of two opposing calixarenes which take on a -3 charge, with the phosphonium cations arranged in a separate 2D sheet relative to the calixarene bilayer. This journal is",

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AB - Solution mediated organization of p-sulfonatocalix[4]arene, benzyltriphenylphosphonium cations, and bis(triethylammoniomethyl)-benzene dications in the solid state results in the ammonium dications preferentially binding in the cavities of two opposing calixarenes which take on a -3 charge, with the phosphonium cations arranged in a separate 2D sheet relative to the calixarene bilayer. This journal is

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