THE EFFECT OF ACCEPTOR GROUP VARIATION ON THE SOLVATOCHROMISM OF DONOR-ACCEPTOR FLUOROPHORES
✍ Scribed by Gregory M. Anstead; Kathryn E. Carlson; Philip R. Kym; Kwang-Jin Hwang; John A. Katzenellenbogen
- Book ID
- 114896665
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 990 KB
- Volume
- 58
- Category
- Article
- ISSN
- 0031-8655
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
An anomalous solvatochromic behavior of a novel push-pull non-linear optical chromophore containing dithienothiophene (DTF) is described. It indicates that DTI" presents analogies to polyenes as conjugated relay with respect to the sensitivity to solvent polarity.
## Abstract Polymer morphology affects quantum efficiency. The influence of polymer morphology on the emission from charge transfer states within donor–acceptor (D–A) polydioctylfluorene derivatives is investigated. Two D–A copolymers, comprising one‐ and two‐electron‐donating triphenylamines subst
## Abstract In this study, four fluorene‐based conjugated copolymers were synthesized to explore the acceptor effects on the electronic and optoelectronic properties. The studied polymers were poly{[2,7‐(9,9‐dihexylfluorene)]‐__alt__‐[2,2′:5,2″‐terthiophene]} (**PFTT**) and its derivatives of poly{
## Abstract The effect of the substituent groups (alkyl or aryl) on the structure, electronic, optical properties, ionization potentials (IPs), electron affinities (EAs), and reorganization energy of the donor–acceptor monomers 5,8‐di‐2‐thienyl‐quinoxaline (T[Q]T), 4,9‐di‐2‐thienylpyrazine[2,3‐g]qu