Show/Hide Menu
Hide/Show Apps
Logout
Türkçe
Türkçe
Search
Search
Login
Login
OpenMETU
OpenMETU
About
About
Open Science Policy
Open Science Policy
Open Access Guideline
Open Access Guideline
Postgraduate Thesis Guideline
Postgraduate Thesis Guideline
Communities & Collections
Communities & Collections
Help
Help
Frequently Asked Questions
Frequently Asked Questions
Guides
Guides
Thesis submission
Thesis submission
MS without thesis term project submission
MS without thesis term project submission
Publication submission with DOI
Publication submission with DOI
Publication submission
Publication submission
Supporting Information
Supporting Information
General Information
General Information
Copyright, Embargo and License
Copyright, Embargo and License
Contact us
Contact us
Benzotriazole Derivatives as Long Wavelength Photosensitizers for Diaryliodonium Salt Initiators
Date
2011-02-01
Author
Bulut, Umut
Balan, Abidin
Caliskan, Cagin
Metadata
Show full item record
This work is licensed under a
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License
.
Item Usage Stats
138
views
0
downloads
Cite This
Two benzotriazole derivative dyes 4,7-bis(2,3-dihydrothieno[3,4-b][1,4]dioxin-5-yl)-2-dodecyl-2H-benzo[1,2,3]triazole, and 2-dodecyl-4,7-bis(4-hexylthiophen-2-yl)-2H-benzo[d][1,2,3]triazole are shown to work as efficient photosensitizers for a dipheny-liodonium salt initiator in cationic photopolymerization of epoxide and vinyl monomers. Substituted thienyl groups are attached to benzotriazole backbone to extend conjugation and enhance electron density of the molecules. Thereby, it was possible to initiate polymerizations at room temperature using long wavelength UV and visible light. The progress of photopolymerizations was monitored using optical pyrometry. The photopolymerization of an epoxide monomer using solar irradiation was also demonstrated. (C) 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 49: 729-733, 2011
Subject Keywords
Organic Chemistry
,
Materials Chemistry
,
Polymers and Plastics
URI
https://hdl.handle.net/11511/67004
Journal
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY
DOI
https://doi.org/10.1002/pola.24485
Collections
Engineering, Article
Suggestions
OpenMETU
Core
Synthetic Design of Polyester Electrolytes Guided by Hydrophobicity Calculations
Yıldırım, Erol; Peretic, Matthew J.; Pasquinelli, Melissa A.; Mathers, Robert T. (American Chemical Society (ACS), 2016-10-25)
Partition coefficients (LogP) help to quantify hydrophobicity, which can be used to guide the design of polymer electrolytes with properties. Thus, this study combined synthetic experiments and modeling to produce polyester electrolytes that solubilize lithium salts. These polyester electrolytes were derived from natural sources and polymerized with different ratios of polyols (diglycerol, glycerol, and diethylene glycol) and citric acid in the presence of lithium salts (LiTf and LiTFSI). The Fisher esterif...
A Quinoxaline Derivative as a Long Wavelength Photosensitizer for Diaryliodonium Salts
Bulut, Umut; Günbaş, Emrullah Görkem; Toppare, Levent Kamil (Wiley, 2010-01-01)
This article reports the use of a quinoxaline derivative as a photosensitizer for diaryliodonium salt photoinitiators. 2,3-bis(3,4-bis(decyloxy)phenyl)-5,8-bis(2,3-dihydrothieno[3,4-b][1,4]-dioxin-5-yl)quinoxaline (DOPEQ), is a highly conjugated compound with strong absorption bands at wavelengths ranging from 300 to 550 nm and is shown to facilitate photoinitiated cationic polymerization of heterocyclic monomers such as oxiranes and oxetanes. The polymerizations are initiated at room temperature by using l...
Thiophene ended epsilon-caprolactone conducting copolymers and their electrochromic properties
Kerman, I; Toppare, Levent Kamil; Yilmaz, F; Yagci, Y (Informa UK Limited, 2005-04-01)
epsilon-Caprolactone was polymerized by ring-opening polymerization (ROP), using thiophene methanol as the initiator and stannous octoate as the catalyst to yield poly(epsilon-caprolactone) with a thiophene end group. Homopolymerization of thiophene functionalized poly (epsilon-caprolactone) (PCL) was achieved by a constant current electrolysis method. Copolymerizations of PCL with thiophene and pyrrole were achieved in acetonitrile (ACN)-tetrabutylammonium tetrafluoroborate (TBAFB) solvent-electrolyte coup...
Fabrication of a Novel Polymeric Scaffold for Amperometric Laccase Biosensor
Soylemez, Saniye; Bekmezci, Aybüke; Göker, Seza; Toppare, Levent Kamil (Wiley, 2019-11-14)
Present work displays the preparation of an electrochemical biosensor using a conjugated polymer and laccase enzyme for catechol quantification in samples. The biosensing system is based on an enzyme immobilization on polymer modified graphite transducer surface. For that purpose, a random conjugated polymer, thienothiophene-benzoxadiazole-alt-benzodithiophene (BOTT), was coated onto a graphite electrode surface via drop casting method followed by immobilization of a biomolecule (laccase) for sensing experi...
Benzaldehyde lyase-catalyzed enantioselective carboligation of aromatic aldehydes with mono- and dimethoxy acetaldehyde
Demir, Ayhan Sıtkı; Sesenoglu, O; Dunkelmann, P; Muller, M (American Chemical Society (ACS), 2003-06-12)
Benzaldehyde lyase from the Pseudomonas fluorescens catalyzes the reaction of aromatic aldehydes with methoxy and dimethoxy acetaldehyde and furnishes (R)-2-hydroxy-3-methoxy-1-arylpropan-1-one and (R)-2-hydroxy-3,3-dimethoxy-1-arylpropan-1-one in high yields and enantiomeric excess via acyloin linkage. Aromatic aldehydes and benzoins are converted into enamine-carbanion-like intermediates prior to carboligation.
Citation Formats
IEEE
ACM
APA
CHICAGO
MLA
BibTeX
U. Bulut, A. Balan, and C. Caliskan, “Benzotriazole Derivatives as Long Wavelength Photosensitizers for Diaryliodonium Salt Initiators,”
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY
, pp. 729–733, 2011, Accessed: 00, 2020. [Online]. Available: https://hdl.handle.net/11511/67004.