New Electron Donor-Acceptor Compounds, 51. [3](N,N′)-1,8;4,5-Naphthalenetetracarboxdiimido- [3](2,7)Pyrenophane and Its [4,4]Cyclophane Homologue
✍ Scribed by Staab, Heinz A. ;Zhang, De-Quing ;Krieger, Claus
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 736 KB
- Volume
- 1997
- Category
- Article
- ISSN
- 0947-3440
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✦ Synopsis
Abstract
Electron donor‐acceptor cyclophanes 1 and 2, consisting of pyrene as the donor component and 1,8;4,5‐naphthalenete‐tracarboxdiimide as the acceptor component fixed by methylene chains in parallel face‐to‐face orientations, have been synthesized. The structures, based on an X‐ray analysis of 1 and on spectroscopic properties, are discussed with reference to intramolecular charge‐transfer interactions and are compared to those of the related excimer models [3.3]‐ and [4.4]pyrenophanes 3 and 4.
📜 SIMILAR VOLUMES
Two new natural products, N- (2-methyl-3-oxodec-8-enoyl)corresponding acid chloride, in order to acylate Meldrum's acid. Subsequent aminolysis with pyrrolidine, followed by 2-pyrroline (2) and 2-(hept-5-enyl)-3-methyl-4-oxo-6,7,8,8atetrahydro-4H-pyrrolo[2,1-b]-1,3-oxazine (3), have been methylation
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