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Selective inclusion of cesium ion in a cryptand-type Ti(IV) complex derived from a tripodal tris-2,3-dihydroxynaphthalene ligand

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Abstract

A novel tripodand-type ligand (L1) having three 2,3-dihydroxynaphthalene end groups and a C3 symmetric 1,3,5-tryimethylbenzene based backbone was prepared by the reaction of 1,3,5-tris(bromomethyl)-2,4,6-trimethylbenzene with 3-(2-(hydroxymethyl)allyloxy)naphthalene-2-ol followed by triple Claisen rearrangement. A 1:1 titanium complex which acts as a metallo-cryptand is obtained by the reaction of ligand (L1) with Ti(IV)(=O)(acac)2 in the presence of base. The formation of the metallo-cryptand strongly depends on templating effects by counter cations and it shows a high selectively for the encapsulation of cesium cations in its cavity.

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Acknowledgement

Financial support by the DAAD for an exchange scholarship for S. B. and support by the Deutsche Forschungsgemeinschaft (Schwerpunktprogramm 1118) is gratefully acknowledged. We would also like to thank Dr. Masatoshi Kanesato at National Institute of Advanced Industrial Science and Technology, Tsukuba, Japan for helpful discussion on the ESI mass spectrometry. One of the authors (K.H.) thanks the Ministry of Education, Culture, Sports, Science and Technology (MEST) for partial support through a Grant-in-Aid for Scientific Research (No. 19550132).

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Correspondence to Kazuhisa Hiratani.

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Burk, S., Albrecht, M. & Hiratani, K. Selective inclusion of cesium ion in a cryptand-type Ti(IV) complex derived from a tripodal tris-2,3-dihydroxynaphthalene ligand. J Incl Phenom Macrocycl Chem 61, 353–359 (2008). https://doi.org/10.1007/s10847-008-9429-1

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