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Synthesis of Tin(II) Phosphate Open Frameworks Using Isomers of 1,2‐Diaminocyclohexane as Template
Author(s) -
Yuan Xuejun,
Li YiZhi,
Xu Yan,
You Xiaozeng,
Linhardt Robert J.
Publication year - 2007
Publication title -
european journal of inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 1434-1948
DOI - 10.1002/ejic.200600912
Subject(s) - chemistry , triclinic crystal system , tin , monoclinic crystal system , hydrothermal synthesis , oxalate , phosphate , phosphoric acid , protonation , crystallography , medicinal chemistry , stereochemistry , crystal structure , inorganic chemistry , hydrothermal circulation , organic chemistry , ion , seismology , geology
Abstract A novel layered framework of tin(II) phosphate, [Sn 4 (PO 4 ) 3 (OH)] 2– · [ trans ‐1,2‐C 6 H 10 (NH 3 ) 2 ] 2+ , has been synthesized under hydrothermal conditions with tin(II) oxalate, phosphoric acid and a mixture of trans ‐ and cis ‐1,2‐diaminocyclohexane (1,2‐DACH). The compound crystallizes in the monoclinic space group P 2 1 / n (No. 14). The channels of the trans ‐1,2‐DACH are occluded by hydrogen bonding in the doubly protonated form, which is leached out from the framework. Reaction using only tran ‐DACH gives the same compound. For comparison, when cis ‐DACH is used as template under the same conditions instead of the mixture of trans and cis isomers, the neutral inorganic phosphate framework (Sn 3 O) 2 (Sn 2 O) 2 (PO 4 ) 4 is formed. It crystallizes in the triclinic space group P $\bar {1}$ (No. 2). These results suggest that trans ‐1,2‐DACH is selectively occluded in the framework [Sn 4 (PO 4 ) 3 (OH)] 2– · [ trans ‐1,2‐C 6 H 10 (NH 3 ) 2 ] 2+ . (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007)