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Doubly cyclopalladated pyridazines: chiral liquid crystals
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UNSPECIFIED. (2002) Doubly cyclopalladated pyridazines: chiral liquid crystals. JOURNAL OF ORGANOMETALLIC CHEMISTRY, 645 (1-2). pp. 246-255. ISSN 0022-328X
Full text not available from this repository.Abstract
The mono and dicyclopalladation of new mesogenic pyridazines and subsequent reaction with beta-diketones yields some novel metallomesogens. The monometallated derivatives have a flat central core. In contrast. the dimetallated derivatives have a sterically induced twist in the molecule that renders them chiral. Smectic A phases are typically exhibited by both the derivatives with transition temperatures in the region of 100-300 degreesC. (C) 2002 Elsevier Science B.V. All rights reserved.
| Item Type: | Journal Article |
|---|---|
| Subjects: | Q Science > QD Chemistry |
| Journal or Publication Title: | JOURNAL OF ORGANOMETALLIC CHEMISTRY |
| Publisher: | ELSEVIER SCIENCE SA |
| ISSN: | 0022-328X |
| Date: | 15 February 2002 |
| Volume: | 645 |
| Number: | 1-2 |
| Number of Pages: | 10 |
| Page Range: | pp. 246-255 |
| Publication Status: | Published |
| URI: | http://wrap.warwick.ac.uk/id/eprint/11133 |
Data sourced from Thomson Reuters' Web of Knowledge
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