𝔖 Bobbio Scriptorium
✦   LIBER   ✦

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


Solvatochromism of non-linear optical ch
✍ Oh-Kil Kim; Jean-Marie Lehn 📂 Article 📅 1996 🏛 Elsevier Science 🌐 English ⚖ 264 KB

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.

Solvatochromic Effects on the Photoinduc
✍ Dr. Caryl E. Richards; Prof. Richard T. Phillips 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 260 KB 👁 2 views

## 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

Effects of Acceptors on the Electronic a
✍ Wen-Ya Lee; Kai-Fang Cheng; Then-Fu Wang; Chu-Chen Chueh; Wen-Chang Chen; Chih-S 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 240 KB

## 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{

Density functional study on the effect o
✍ Lei Sun; Fu-Quan Bai; Zeng-Xia Zhao; Bao-Zhu Yang; Hong-Xing Zhang 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 326 KB

## 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