Yi Ren, Ph.D. - Publications

Affiliations: 
Chemistry University of Calgary, Calgary, Alberta, Canada 

25 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Li X, Liu Z, Li C, Gao R, Qi Y, Ren Y. Synthesis and Photophysical Properties of Carbazole-Functionalized Diazaphosphepines via Sequent P-N Chemistry. The Journal of Organic Chemistry. PMID 37691267 DOI: 10.1021/acs.joc.3c01351  0.312
2022 Yang Z, Li X, Yang K, Zhang Z, Wang Y, Yu N, Baumgartner T, Ren Y. Tailored Solvatochromic NIR Phosphorus-Chromophores via Selective P-N and P-C Chemistry in P-Heteropines. Organic Letters. 24: 2045-2049. PMID 35244405 DOI: 10.1021/acs.orglett.2c00570  0.443
2018 Adachi Y, Ooyama Y, Ren Y, Yin X, Jäkle F, Ohshita J. Hybrid conjugated polymers with alternating dithienosilole or dithienogermole and tricoordinate boron units Polymer Chemistry. 9: 291-299. DOI: 10.1039/C7Py01790A  0.309
2018 Ren Y, Li Z, Allcock HR. Molecular Engineering of Polyphosphazenes and SWNT Hybrids with Potential Applications as Electronic Materials Macromolecules. 51: 5011-5018. DOI: 10.1021/Acs.Macromol.8B00779  0.304
2017 Yin X, Liu K, Ren Y, Lalancette RA, Loo YL, Jäkle F. Pyridalthiadiazole acceptor-functionalized triarylboranes with multi-responsive optoelectronic characteristics. Chemical Science. 8: 5497-5505. PMID 30155227 DOI: 10.1039/C6Sc03097A  0.327
2016 Ren Y, Sezen M, Guo F, Jäkle F, Loo YL. []-Carbon-carbon double bond engineering in diazaphosphepines: a pathway to modulate the chemical and electronic structures of heteropines. Chemical Science. 7: 4211-4219. PMID 30155067 DOI: 10.1039/C6Sc00519E  0.348
2016 Ren Y, Jäkle F. Merging thiophene with boron: new building blocks for conjugated materials. Dalton Transactions (Cambridge, England : 2003). PMID 27491626 DOI: 10.1039/C6Dt02756C  0.35
2016 Ren Y, Baumgartner T. A structure-property study toward π-extended phosphole chromophores with ambipolar redox properties Canadian Journal of Chemistry. 94: 297-304. DOI: 10.1139/Cjc-2015-0347  0.565
2016 Ren Y, Gao J, Hailey AK, Baumgartner T, Loo Y. Cooperative Assembly of Phosphole Lipids and Single-Walled Carbon Nanotubes Chemistry of Materials. 28: 8407-8414. DOI: 10.1021/Acs.Chemmater.6B03987  0.514
2015 Ren Y, Hiszpanski AM, Loo YL. Self-Assembly of Axially Functionalized Subphthalocyanines in Thin Films Chemistry of Materials. 27: 4008-4014. DOI: 10.1021/Acs.Chemmater.5B00941  0.317
2014 Ren Y, Hailey AK, Hiszpanski AM, Loo YL. Isoindigo-Containing Molecular Semiconductors: Effect of Backbone Extension on Molecular Organization and Organic Solar Cell Performance. Chemistry of Materials : a Publication of the American Chemical Society. 26: 6570-6577. PMID 25678745 DOI: 10.1021/Cm503312C  0.316
2014 Ren Y, Hiszpanski AM, Whittaker-Brooks L, Loo YL. Structure-property relationship study of substitution effects on isoindigo-based model compounds as electron donors in organic solar cells. Acs Applied Materials & Interfaces. 6: 14533-42. PMID 25089728 DOI: 10.1021/Am503812F  0.35
2014 Chua CJ, Ren Y, Stolar M, Xing S, Linder T, Baumgartner T. P-terthienyl-functionalized dithieno[3,2-b:2′,3′-d]phospholes European Journal of Inorganic Chemistry. 1767-1774. DOI: 10.1002/Ejic.201301065  0.567
2013 Ren Y, Orthaber A, Pietschnig R, Baumgartner T. Perfluorophenylene-bridged bisphospholes: synthesis and unexpected photophysical properties. Dalton Transactions (Cambridge, England : 2003). 42: 5314-21. PMID 23403450 DOI: 10.1039/C3Dt33058C  0.561
2013 Ren Y, Biegger F, Baumgartner T. Molecular engineering of the physical properties of highly luminescent π-conjugated phospholes Journal of Physical Chemistry C. 117: 4748-4758. DOI: 10.1021/Jp3115012  0.578
2012 Ren Y, Baumgartner T. Combining form with function--the dawn of phosphole-based functional materials. Dalton Transactions (Cambridge, England : 2003). 41: 7792-800. PMID 22414898 DOI: 10.1039/C2Dt00024E  0.545
2012 Ren Y, Kan WH, Thangadurai V, Baumgartner T. Bio-inspired phosphole-lipids: from highly fluorescent organogels to mechanically responsive FRET. Angewandte Chemie (International Ed. in English). 51: 3964-8. PMID 22389225 DOI: 10.1002/Anie.201109205  0.536
2012 Chua CJ, Ren Y, Baumgartner T. Charge-transfer properties of lateral triphenylamine-dithienophosphole diads. Organic Letters. 14: 1588-91. PMID 22385325 DOI: 10.1021/Ol300331F  0.514
2012 Ren Y, Baumgartner T. Structure-property studies toward the stimuli-responsive behavior of benzyl-phospholium acenes. Inorganic Chemistry. 51: 2669-78. PMID 22283643 DOI: 10.1021/Ic2026335  0.554
2012 Chua CJ, Ren Y, Baumgartner T. Structure-property studies of bichromophoric, PAH-functionalized dithieno[3,2-b:2′,3′-d]phospholes Organometallics. 31: 2425-2436. DOI: 10.1021/Om3000407  0.569
2012 Ren Y, Kan WH, Thangadurai V, Baumgartner T. Bioinspirierte Phosphol-Lipide: von stark fluoreszierenden Organogelen zu mechanisch induziertem FRET Angewandte Chemie. 124: 4031-4035. DOI: 10.1002/Ange.201109205  0.454
2011 Ren Y, Kan WH, Henderson MA, Bomben PG, Berlinguette CP, Thangadurai V, Baumgartner T. External-stimuli responsive photophysics and liquid crystal properties of self-assembled "phosphole-lipids". Journal of the American Chemical Society. 133: 17014-26. PMID 21958374 DOI: 10.1021/ja206784f  0.533
2011 Ren Y, Baumgartner T. Dually switchable heterotetracenes: addressing the photophysical properties and self-organization of the P-S system. Journal of the American Chemical Society. 133: 1328-40. PMID 21210689 DOI: 10.1021/Ja108081B  0.576
2010 Ren Y, Baumgartner T. Ladder-type pi-conjugated 4-hetero-1,4-dihydrophosphinines: a structure-property study. Chemistry, An Asian Journal. 5: 1918-29. PMID 20544789 DOI: 10.1002/Asia.201000196  0.554
2009 Ren Y, Dienes Y, Hettel S, Parvez M, Hoge B, Baumgartner T. Highly fluorinated dithieno[3,2-b:2′,3′-d]phospholes with stabilized LUMO levels Organometallics. 28: 734-740. DOI: 10.1021/Om800874D  0.56
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