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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.
Full text not available from this repository, contact author.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 | ||||
| Official Date: | 15 February 2002 | ||||
| Dates: |
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| Volume: | 645 | ||||
| Number: | 1-2 | ||||
| Number of Pages: | 10 | ||||
| Page Range: | pp. 246-255 | ||||
| Publication Status: | Published |
Data sourced from Thomson Reuters' Web of Knowledge
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