1,8-Dipyrenylnaphthalenes: Syntheses, Molecular Structure, and Spectroscopic Properties
β Scribed by Wahl, Peter ;Krieger, Claus ;Schweitzer, Dieter ;Staab, H. A.
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1984
- Tongue
- English
- Weight
- 778 KB
- Volume
- 117
- Category
- Article
- ISSN
- 0009-2940
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π SIMILAR VOLUMES
tively unsaturated equilibrium partner 5 react preferentially and thus open the way for the formation of 7 from 3 and tert-butyl Isonitrile. These examples show that organometallic betaine compounds with a combination of transition metal and main group metal are easily accessible and that they make
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The syntheses of 1,8-diazacyclotetradeca-3,5,10,12-tetrayne (2a), its N,NΠ-dimethyl (2b), N,NΠ-diethyl (2c), N,NΠ-diisopropyl (2d), N,NΠ-diallyl (2e), and N,NΠ-dibenzyl (2f) derivatives were achieved in a one-pot procedure from primary amines and 1,6-dibromo-2,4-hexadiyne (4). Diffraction studies on