Complexing ability of p-tert-butylthiacalix[6]arene toward metal ions. Predominant effect of coordination by the bridging sulfur rather than that of the ring-size

Naoya Morohashi; Nobuhiko Iki; Mitsuru Aono; Sotaro Miyano

doi:10.1246/cl.2002.494

Complexing ability of p-tert-butylthiacalix[6]arene toward metal ions. Predominant effect of coordination by the bridging sulfur rather than that of the ring-size

Naoya Morohashi, Nobuhiko Iki, Mitsuru Aono, Sotaro Miyano

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

8 Citations (Scopus)

Abstract

p-tert-Butylthiacalix[6]arene extracted soft to intermediate metal ions to the same extent as the [4] counterpart did, indicating that the O^-,S,O^- -tridentate binding manner rather than the effect of ring extension is critical to determine the complexing ability.

Original language	English
Pages (from-to)	494-495
Number of pages	2
Journal	Chemistry Letters
Issue number	5
DOIs	https://doi.org/10.1246/cl.2002.494
Publication status	Published - 2002 May 5

ASJC Scopus subject areas

Chemistry(all)

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10.1246/cl.2002.494

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title = "Complexing ability of p-tert-butylthiacalix[6]arene toward metal ions. Predominant effect of coordination by the bridging sulfur rather than that of the ring-size",

abstract = "p-tert-Butylthiacalix[6]arene extracted soft to intermediate metal ions to the same extent as the [4] counterpart did, indicating that the O-,S,O- -tridentate binding manner rather than the effect of ring extension is critical to determine the complexing ability.",

author = "Naoya Morohashi and Nobuhiko Iki and Mitsuru Aono and Sotaro Miyano",

year = "2002",

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AU - Morohashi, Naoya

AU - Iki, Nobuhiko

AU - Aono, Mitsuru

AU - Miyano, Sotaro

PY - 2002/5/5

Y1 - 2002/5/5

N2 - p-tert-Butylthiacalix[6]arene extracted soft to intermediate metal ions to the same extent as the [4] counterpart did, indicating that the O-,S,O- -tridentate binding manner rather than the effect of ring extension is critical to determine the complexing ability.

AB - p-tert-Butylthiacalix[6]arene extracted soft to intermediate metal ions to the same extent as the [4] counterpart did, indicating that the O-,S,O- -tridentate binding manner rather than the effect of ring extension is critical to determine the complexing ability.

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ER -

Complexing ability of p-tert-butylthiacalix[6]arene toward metal ions. Predominant effect of coordination by the bridging sulfur rather than that of the ring-size

Abstract

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