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PubMed Publications| Keyword search (4,163 papers available) |  |
"Salzmann I" Authored Publications:
| Title | Authors | PubMed ID | |
|---|---|---|---|
| 1 | Sterically-Hindered Molecular p-Dopants Promote Integer Charge Transfer in Organic Semiconductors | Charoughchi S; Liu JT; Berteau-Rainville M; Hase H; Askari MS; Bhagat S; Forgione P; Salzmann I; | 37220083 CHEMBIOCHEM |
| 2 | Macromolecularly Engineered Thermoreversible Heterogeneous Self-Healable Networks Encapsulating Reactive Multidentate Block Copolymer-Stabilized Carbon Nanotubes | Zhang G; Patel T; Nellepalli P; Bhagat S; Hase H; Jazani AM; Salzmann I; Ye Z; Oh JK; | 33988899 CHEMBIOCHEM |
| 3 | Impact of fluorination on interface energetics and growth of pentacene on Ag(111). | Wang Q, Chen MT, Franco-Cañellas A, Shen B, Geiger T, F Bettinger H, Schreiber F, Salzmann I, Gerlach A, Duhm S | 32974114 CHEMBIOCHEM |
| 4 | An efficient method for indexing grazing-incidence X-ray diffraction data of epitaxially grown thin films | Simbrunner J; Schrode B; Domke J; Fritz T; Salzmann I; Resel R; | 32356785 CERMM |
| 5 | Approaching the Integer-Charge Transfer Regime in Molecularly Doped Oligothiophenes by Efficient Decarboxylative Cross-Coupling | Liu JT; Hase H; Taylor S; Salzmann I; Forgione P; | 31961982 CHEMBIOCHEM |
| 6 | Structural Order in Cellulose Thin Films Prepared from a Trimethylsilyl Precursor. | Jones AOF, Resel R, Schrode B, Machado-Charry E, Röthel C, Kunert B, Salzmann I, Kontturi E, Reishofer D, Spirk S | 31774663 CHEMBIOCHEM |
| 7 | Singlet exciton fission via an intermolecular charge transfer state in coevaporated pentacene-perfluoropentacene thin films | Kim VO; Broch K; Belova V; Chen YS; Gerlach A; Schreiber F; Tamura H; Della Valle RG; D' Avino G; Salzmann I; Beljonne D; Rao A; Friend R; | 31675857 CERMM |
| 8 | Indexing of grazing-incidence X-ray diffraction patterns: the case of fibre-textured thin films. | Simbrunner J, Simbrunner C, Schrode B, Röthel C, Bedoya-Martinez N, Salzmann I, Resel R | 29978847 CHEMBIOCHEM |
| 9 | Indexing grazing-incidence X-ray diffraction patterns of thin films: lattices of higher symmetry | Simbrunner J; Hofer S; Schrode B; Garmshausen Y; Hecht S; Resel R; Salzmann I; | 30996719 CERMM |
| Title: | Approaching the Integer-Charge Transfer Regime in Molecularly Doped Oligothiophenes by Efficient Decarboxylative Cross-Coupling | ||||
| Authors: | Liu JT, Hase H, Taylor S, Salzmann I, Forgione P | ||||
| Link: | https://pubmed.ncbi.nlm.nih.gov/31961982/ | ||||
| DOI: | 10.1002/anie.201914458 | ||||
| Publication: | Angewandte Chemie (International ed. in English) | ||||
| Keywords: | charge transfer; decarboxylative cross-coupling; doping; oligothiophenes; organic semiconductors; | ||||
| PMID: | 31961982 | Category: | Angew Chem Int Ed Engl | Date Added: | 2020-01-22 |
| Dept Affiliation: |
CHEMBIOCHEM
1 Department of Chemistry and Biochemistry, Concordia University, 7141 rue Sherbrooke O., Montréal, QC, H4B 1R6, Canada. 2 Department of Physics, Concordia University, 7141 rue Sherbrooke O., Montréal, QC, H4B 1R6, Canada. 3 Centre for Research in Molecular Modeling (CERMM), Centre for NanoScience Research (CeNSR), Concordia University, 7141 rue Sherbrooke O., Montreal, QC, H4B 1R6, Canada. 4 Center for Green Chemistry and Catalysis, McGill University, 801 rue Sherbrooke O., Montréal, QC, H3A 0B8, Canada. |
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Description: |
A library of symmetrical linear oligothiophene was prepared employing decarboxylative cross-coupling reaction as the key transformation. Thiophene potassium carboxylate salts were used as cross-coupling partners without the need of co-catalyst, base, or additives. This method demonstrates complete chemoselectivity and is a comprehensive greener approach compared to the existing methods. The modularity of this approach is demonstrated with the preparation of discreet oligothiophenes with up to 10 thiophene repeat units. Symmetrical oligothiophenes are prototypical organic semiconductors where their molecular electrical doping as a function of the chain length can be assessed spectroscopically. An oligothiophene critical length for integer charge transfer was observed to be 10 thiophene units, highlighting the potential use of discrete oligothiophenes as doped conduction or injection layers in organic electronics applications. |
