Protonated sapphyrins. Highly effective phosphate receptors

Vladimír Král, Hiroyuki Furuta, Kevin Shreder, Vincent Lynch, Jonathan L. Sessler

研究成果: ジャーナルへの寄稿学術誌査読

159 被引用数 (Scopus)

抄録

The phosphate anion chelation properties of several sapphyrin derivatives, namely 3,12,13,22-tetraethyl-8,17-bis[bis(hydroxyethyl)amino)carbonylethyl]-2 ,7,18,23-tetramethylsapphyrin (1), 3,12,13,22-tetraethyl-2,7,18,23-tetramethyl-8,17-bis(hydroxypropyl)sap phyrin (2), and 3,8,12,13,17,22-hexaethyl-2,7,18,23-tetramethylsapphyrin (3) are reported. X-ray diffraction studies of the dihydroxylated and decaalkyl derivatives 2 and 3 reveal that the diprotonated forms of sapphyrin are capable of stabilizing 1:2 inner-sphere complexes with phosphate-derived monoanions, such as diphenyl phosphate and monobasic phenyl phosphate. Similar analyses reveal that the diprotonated form of dihydroxysapphyrin 2 is capable of forming a 1:1 chelate complex in the solid state with either mono- or dibasic phosphoric acid. Solution-phase studies, involving 1H and 31P NMR spectroscopy, confirm that these same sapphyrins are capable of binding phosphate anions in organic solution, a conclusion that is supported by qualitative fast atom bombardment mass spectrometric (FAB MS) and extractive partition studies. In the case of phenylphosphonic acid and sapphyrin 2, extraction studies were consistent with 2:1 and 1:1 phosphate-to-sapphyrin binding stochiometries at pH 1.68 and 5.6, respectively. Similar studies using NMR and visible spectroscopy carried out with the water-soluble tetrahydroxy sapphyrin derivative, 1, and 2 indicate that these species bind phosphate anion in both methanolic and aqueous solution. Calculated association constants are on the order of 104 M-1 in methanol and 102 M-1 in 10 mM aqueous bis-Tris, pH 6.1.

本文言語英語
ページ(範囲)1595-1607
ページ数13
ジャーナルJournal of the American Chemical Society
118
7
DOI
出版ステータス出版済み - 2月 21 1996
外部発表はい

!!!All Science Journal Classification (ASJC) codes

  • 触媒
  • 化学一般
  • 生化学
  • コロイド化学および表面化学

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