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
Synthetic Route to Thiophene-Based Double Helical Oligomers
Date
2016-10-01
Author
Swager, Tımothy M.
Dengiz, Çağatay
Metadata
Show full item record
Item Usage Stats
55
views
0
downloads
Cite This
URI
https://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-0036-1589283
https://hdl.handle.net/11511/77683
Journal
Synfacts
Collections
Unverified, Article
Suggestions
OpenMETU
Core
Synthetic methodology toward new propylenedioxythiophene polymers
Reeves, BD; Grenier, CRG; Argun, AA; Çırpan, Ali; Cunningham, GB; McCarley, TD; Reynolds, JR (2004-03-28)
Synthetic applications of biyclic endoperoxides to azasugar : assymetric induction
Bayram, Beyhan; Balcı, Metin; Department of Chemistry (2000)
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...
STRUCTURAL STUDIES OF POLYPYRROLES - OLIGOMERIZATION MECHANISM OF N-METHACRYLOYL PYRROLE
YURTSEVER, E; Toppare, Levent Kamil; HALLENSLEBEN, ML (1993-03-11)
The oligomerization mechanism of N-methacryloyl pyrrole was studied using semiempirical calculations. Starting with the monomer, a large number of dimer, trimer and tetramer structures were optimized. On comparison of alpha-alpha, alpha-beta and beta-beta type pyrrole-pyrrole linkages, it was found that beta-beta type bonding is the most stable form. On average, the introduction of one alpha-type linkage requires about 5 kcal mol-1 of energy.
Selective synthesis of N-substituted pyrrolo[1,2-a]pyrazin-1(2H)-one derivatives via alkyne cyclization
Cetinkaya, Yasin; Balcı, Metin (2014-12-03)
A novel and efficient synthesis of N-substituted pyrrolo-pyrazinone derivatives has been developed. A trichloroacetyl group connected to the pyrrole ring was converted into the desired carboxamide derivatives. Promoted by NaH, the pyrrole carboxamide derivatives underwent a tandem reaction with propargyl bromide to afford pyrrolo-pyrazinones with high efficiency under very mild conditions. The mechanism for the formation of the products is discussed and supported by DFT calculations. (C) 2014 Elsevier Ltd. ...
Citation Formats
IEEE
ACM
APA
CHICAGO
MLA
BibTeX
T. M. Swager and Ç. Dengiz, “Synthetic Route to Thiophene-Based Double Helical Oligomers,”
Synfacts
, pp. 1036–1036, 2016, Accessed: 00, 2021. [Online]. Available: https://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-0036-1589283.