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Rational Design and X‐ray Molecular Structure of the First Irido‐Cryptand and Encapsulation of a Tetrafluoroborate Anion
Author(s) -
Amouri Hani,
Rager Marie Noelle,
Cagnol Florence,
Vaissermann Jacqueline
Publication year - 2001
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/1521-3773(20011001)40:19<3636::aid-anie3636>3.0.co;2-i
Subject(s) - tetrafluoroborate , cryptand , denticity , iridium , chemistry , stereochemistry , ion , rhodium , crystallography , crystal structure , organic chemistry , ionic liquid , catalysis
Iridium and rhodium coordination chemistry has been used to self‐assemble metallocryptands: Treatment of two equivalents of [Cp*M(solv) 3 ][BF 4 ] 2 (Cp*=C 5 (CH 3 ) 5 ; M=Rh, Ir; solv=acetone) with three equivalents of the bidentate ligand 1,3‐bis(aminomethyl)‐2,5‐dimethoxy‐4,6‐dimethylbenzene (L) afforded the first irido‐ and rhodio‐cryptands [(Cp*M) 2 L 3 ][BF 4 ] 4 in high yields (70–85 %). The use of less congested ligands increased the accessibility of the cavity of the metallocryptands and enabled the encapsulation of tetrafluoroborate ions (see scheme).

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