Metal-free polymerization: synthesis and properties of fused benzo[1,2-b:4,5-b′]bis[b]benzothiophene (BBBT) polymers
Literature Information
Hailiang Liao, Mahesh Kumar Ravva, Yanjun Guo, Jiayao Duan, Yazhou Wang, Yaping Yu, Zhengke Li, Wan Yue
We report the “green” synthesis and characterization of a series of fused benzo[1,2-b:4,5-b′]bis[b]benzothiophene (BBBT) polymers containing a phenyl ring and naphthalene as comonomers, as well as BBBT homopolymers. These novel fused polymers have been obtained from simple acid and hexaethyltriaminophosphine catalyzed polymerization without involving any metal catalyst. The effect of the different aromatic units on the optical and electronic properties of the resulting polymers has been studied. It was found that these polymers possess high electron affinities due to the presence of electron-deficient lactams on each repeat unit. BBBT-P and BBBT-N exhibit NIR absorption spectra with the tail extending to 1000 nm, while the BBBT homopolymer exhibits a large blue-shifted absorption.
Related Literature
Activity-based protein profiling reveals deubiquitinase and aldehyde dehydrogenase targets of a cyanopyrrolidine probe
Nattawadee Panyain, Aurélien Godinat, Aditya Raymond Thawani, Sofía Lachiondo-Ortega, Katie Mason, Sarah Elkhalifa, Lisa M. Smith, Jeanine A. Harrigan
DOI: 10.1039/D1MD00218J
Second-generation tricyclic pyrimido-pyrrolo-oxazine mTOR inhibitor with predicted blood–brain barrier permeability
Chiara Borsari, Erhan Keles, Andrea Treyer, Martina De Pascale, Matthias Hamburger, Matthias P. Wymann
DOI: 10.1039/D0MD00408A
Comprehensive overview of biased pharmacology at the opioid receptors: biased ligands and bias factors‡
Jolien De Neve, Thomas M. A. Barlow, Dirk Tourwé, Frédéric Bihel, Frédéric Simonin, Steven Ballet
DOI: 10.1039/D1MD00041A
Monobodies as tool biologics for accelerating target validation and druggable site discovery
Padma Akkapeddi, Kai Wen Teng
DOI: 10.1039/D1MD00188D
Novel fluorinated ring-fused chlorins as promising PDT agents against melanoma and esophagus cancer
Nelson A. M. Pereira, Bruno F. O. Nascimento, João Pina, Gonçalo Brites, J. Sérgio Seixas de Melo, Marta Pineiro, Teresa M. V. D. Pinho e Melo
DOI: 10.1039/D0MD00433B
Porphyromonas gingivalis: where do we stand in our battle against this oral pathogen?
Kaitlind C. Howard, Octavio A. Gonzalez, Sylvie Garneau-Tsodikova
DOI: 10.1039/D0MD00424C
N-Aryl mercaptoacetamides as potential multi-target inhibitors of metallo-β-lactamases (MBLs) and the virulence factor LasB from Pseudomonas aeruginosa
Samir Yahiaoui, Katrin Voos, Jörg Haupenthal, Thomas A. Wichelhaus, Denia Frank, Lilia Weizel, Marco Rotter, Steffen Brunst, Jan S. Kramer, Ewgenij Proschak, Christian Ducho
DOI: 10.1039/D1MD00187F
Structural evolution of toll-like receptor 7/8 agonists from imidazoquinolines to imidazoles
Deepender Kaushik, Arshpreet Kaur
DOI: 10.1039/D1MD00031D
A review of the latest research on Mpro targeting SARS-COV inhibitors
Huihui Yang
DOI: 10.1039/D1MD00066G
Target 2035 – update on the quest for a probe for every protein
Susanne Müller, Suzanne Ackloo, Arij Al Chawaf, Hartmut Beck, Shaunna Beedie, Ulrich A. K. Betz, Gustavo Arruda Bezerra, Paul E. Brennan, David Brown, Peter J. Brown, Alex N. Bullock, Adrian J. Carter, Apirat Chaikuad, Mathilde Chaineau, Alessio Ciulli, Ian Collins, Jan Dreher, Kristina Edfeldt, Aled M. Edwards, Ursula Egner, Stephen M. Fuchs, Matthew D. Hall, Ingo V. Hartung, Alexander Hillisch, Stephen H. Hitchcock, Evert Homan, Natarajan Kannan, James R. Kiefer, Stefan Knapp, Milka Kostic, Stefan Kubicek, Andrew R. Leach, Sven Lindemann, Hisanori Matsui, Jordan L. Meier, Maurice Michel, Maxwell R. Morgan, Anke Mueller-Fahrnow, Dafydd R. Owen, Benjamin G. Perry, Saul H. Rosenberg, Kumar Singh Saikatendu, Cora Scholten, Sujata Sharma, Anton Simeonov, Michael Sundström, Matthew H. Todd, Claudia Tredup, Timothy M. Willson, Georg E. Winter
DOI: 10.1039/D1MD00228G
You might also like
How should waste containing 6-Chloro-5-(2'-hydroxy-3'-methoxy-4-biphenylyl)-3-(3-methoxyphenyl)-1H-pyrrolo[3,2-d]pyrimidine-2,4(3H,5H)-dione (CAS: 1346607-05-3) be handled?
Waste containing 6-Chloro-5-(2'-hydroxy-3'-methoxy-4-biphenylyl)-3-(3-methoxyphe...
What are the main uses of (3alpha,5alpha)-3-Hydroxypregnane-11,20-dione (CAS: 23930-19-0)?
(3alpha,5alpha)-3-Hydroxypregnane-11,20-dione is primarily used in the pharmaceu...
What is the market or research trend for 4-Amino-6-chloro-2-pyridinecarboxylic acid (CAS: 546141-56-4)?
The market for 4-Amino-6-chloro-2-pyridinecarboxylic acid (CAS: 546141-56-4) is ...
Are there alternatives to (2-Benzoylethyl)trimethylammonium chloride (CAS: 24472-88-6) in synthesis?
Alternatives to (2-Benzoylethyl)trimethylammonium chloride (CAS: 24472-88-6) in ...
Is N-[4-Nitro-3-(trifluoromethyl)phenyl]acetamide (CAS: 393-12-4) safe?
N-[4-Nitro-3-(trifluoromethyl)phenyl]acetamide (CAS: 393-12-4) is generally safe...
Are there alternatives to [(4R,5R,6S)-5-hydroxy-10-imino-3,7-dioxa-1,9-diazatricyclo[6.4.0.02,6]dodeca-8,11-dien-4-yl]methyl dihydrogen phosphate (CAS: 39679-56-6) in synthesis?
Alternative reagents such as other phosphates or similar functional groups can b...
Are there alternatives to N,N'-Bis(3-aminopropyl)-1,3-propanediamine (CAS: 4605-14-5) in synthesis?
There are alternatives to N,N'-Bis(3-aminopropyl)-1,3-propanediamine (CAS: 4605-...
What precautions should be taken when handling Aluminium trihexadecanoate (CAS: 555-35-1)?
When handling Aluminium trihexadecanoate, it is important to use appropriate per...
What is (1,1-Dioxido-3-oxo-1,2-benzothiazol-2(3H)-yl)acetic acid (CAS: 52188-11-1)?
(1,1-Dioxido-3-oxo-1,2-benzothiazol-2(3H)-yl)acetic acid is a chemical compound ...
Are there alternatives to 5,5-dimethyloxolan-2-one (CAS: 3123-97-5) in synthesis?
Several alternatives to 5,5-dimethyloxolan-2-one (CAS: 3123-97-5) can be used in...
Source Journal
Polymer Chemistry

Polymer Chemistry welcomes submissions in all areas of polymer science that have a strong focus on macromolecular chemistry. Manuscripts may cover a broad range of fields, yet no direct application focus is required.










![Benzo[b]naphtho[2,1-d]thiophene structure Benzo[b]naphtho[2,1-d]thiophene structure](https://static.chemtradehub.com/structs/239/239-35-0-ff90.webp)



