Anion Recognition in Supramolecular Chemistry by Brett M. Rambo, Eric S. Silver (auth.), Philip A. Gale, Wim

By Brett M. Rambo, Eric S. Silver (auth.), Philip A. Gale, Wim Dehaen (eds.)

Brett M. Rambo ∙ Eric S. Silver ∙ Christopher W. Bielawski ∙ Jonathan L. Sessler Covalent Polymers Containing Discrete Heterocyclic Anion Receptors Philip A. Gale ∙ Chang-Hee Lee Calix[n]pyrroles as Anion and Ion-Pair Complexants Wim Dehaen Calix[n]phyrins: Synthesis and Anion acceptance Hiromitsu Maeda Acyclic Oligopyrrolic Anion Receptors Jeffery T. Davis Anion Binding and delivery through Prodigiosin and Its Analogs Hemraj Juwarker ∙ Jae-min Suk ∙ Kyu-Sung Jeong Indoles and comparable Heterocycles Pavel Anzenbacher Jr. Pyrrole-Based Anion Sensors, half I: Colorimetric Sensors Pavel Anzenbacher Jr. Pyrrole-Based Anion Sensors, half II: Fluorescence, Luminescence, and Electrochemical Sensors Ermitas Alcalde ∙ Immaculada Dinarès ∙ Neus Mesquida Imidazolium-Based Receptors Nathan L. Kilah ∙ Paul D. Beer Pyridine and Pyridinium-Based Anion Receptors Kevin P. McDonald ∙ Yuran Hua ∙ Amar H. Flood 1,2,3-Triazoles and the increasing software of cost impartial CHlllAnion Interactions

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This observation is most easily rationalized in terms of the hydroxyl groups undergoing deprotonation when exposed to FÀ (an anion recognized for its basicity in organic milieus) a chemical change that was expected to give rise to an intramolecular charge-transfer interaction. Deprotonation also likely accounts for the efficacy of a set of polyhydroxybenzoxazole-based colorimetric and fluorometric chemosensors for fluoride (cf. structure 71) introduced by the Lee group, whose other contributions are featured elsewhere in this chapter [81].

Aldakov D, Anzenbacher P Jr (2004) J Am Chem Soc 126:4752–4753 77. Zhou G, Chen Y, Wang L, Jing X, Wang F (2005) Macromolecules 38:2148–2153 78. Tong H, Zhou G, Wang L, Jing X, Wang F, Zhang J (2003) Tetrahedron Lett 44:131–134 79. Tong H, Wang L, Jing X, Wang F (2003) Macromolecules 36:2584–2586 80. Ma H, Jen AK-Y, Wu J, Wu X, Liu S, Shu C, Dalton LR, Marder SR, Thayumanavan S (1999) Chem Mater 11:2218–2225 81. Lee JK, Na J, Kim TH, Kim Y-S, Park WH, Lee TS (2004) Mater Sci Eng C 24:261–264 82.

45 4 Strapped Systems . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 54 5 Extraction and Transport . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 64 6 Catalysis . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 68 7 Conclusions . . . . . . . . . . . .

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