Conformational inversion of 2,2′-bipyridine 1,1′-dioxide chelate ring in a series of (2,2′,2′′-triaminotriethylamine)(4,4′-disubstituted-2,2′-bipyridine 1,1′-dioxide)cobalt(III) complexes
✍ Scribed by Hideaki Kanno; Mitsutoshi Yamada; Kazuya Nakata; Maiko Nishimura
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- English
- Weight
- 108 KB
- Volume
- 318
- Category
- Article
- ISSN
- 0020-1693
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✦ Synopsis
A new series of cobalt(III) complexes, [Co(2,2%,2%%-triaminotriethylamine)(4,4%-X 2 bpdo)] 3 + (X =Me, MeO, EtO), where 4,4%-X 2 bpdo denotes 4,4%-disubstituted-2,2%-bipyridine 1,1%-dioxide, were prepared. The complexes were resolved into a pair of enantiomers (conformational optical isomers), and gradually racemized in water by conformational inversion of the skewed 4,4%-X 2 bpdo chelate ring, d X l. The rate of racemization is remarkably reduced with an increase in the electron-releasing ability of the 4,4%-X 2 substituents on bpdo.
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A simple method for the preparation of 4,4-disubstituted-3,4-dihydro-1H-2,1,3-benzothiadiazine 2,2dioxides is described. Treatment of N-sulfonyl ketimines 2 and 3 with different carbon nucleophiles afforded the corresponding of 4,4-disubstituted-3,4-dihydro-1H-2,1,3-benzothiadiazine 2,2-dioxides 1 i
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