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178 related items for PubMed ID: 25757046
1. Stille Catalyst-Transfer Polycondensation Using Pd-PEPPSI-IPr for High-Molecular-Weight Regioregular Poly(3-hexylthiophene). Qiu Y, Mohin J, Tsai CH, Tristram-Nagle S, Gil RR, Kowalewski T, Noonan KJ. Macromol Rapid Commun; 2015 May; 36(9):840-4. PubMed ID: 25757046 [Abstract] [Full Text] [Related]
2. Palladium-catalyzed dehydrohalogenative polycondensation of 2-bromo-3-hexylthiophene: an efficient approach to head-to-tail poly(3-hexylthiophene). Wang Q, Takita R, Kikuzaki Y, Ozawa F. J Am Chem Soc; 2010 Aug 25; 132(33):11420-1. PubMed ID: 20684550 [Abstract] [Full Text] [Related]
3. Influence of the boron moiety and water on suzuki-miyaura catalyst-transfer condensation polymerization. Kosaka K, Ohta Y, Yokozawa T. Macromol Rapid Commun; 2015 Feb 25; 36(4):373-7. PubMed ID: 25504582 [Abstract] [Full Text] [Related]
4. Chain-growth polymerization of aryl Grignards initiated by a stabilized NHC-Pd precatalyst. Bryan ZJ, Smith ML, McNeil AJ. Macromol Rapid Commun; 2012 May 14; 33(9):842-7. PubMed ID: 22488735 [Abstract] [Full Text] [Related]
5. Precision synthesis of poly(3-hexylthiophene) from catalyst-transfer Suzuki-Miyaura coupling polymerization. Yokozawa T, Suzuki R, Nojima M, Ohta Y, Yokoyama A. Macromol Rapid Commun; 2011 Jun 01; 32(11):801-6. PubMed ID: 21509845 [Abstract] [Full Text] [Related]
6. Synthesis of end-capped regioregular poly(3-hexylthiophene)s via direct arylation. Wang Q, Wakioka M, Ozawa F. Macromol Rapid Commun; 2012 Jul 26; 33(14):1203-7. PubMed ID: 22539499 [Abstract] [Full Text] [Related]
7. An efficient low-temperature Stille-Migita cross-coupling reaction for heteroaromatic compounds by Pd-PEPPSI-IPent. Dowlut M, Mallik D, Organ MG. Chemistry; 2010 Apr 12; 16(14):4279-83. PubMed ID: 20209529 [Abstract] [Full Text] [Related]
8. Preparation of an Aurylated Alkylthiophene Monomer via C-H Activation for Use in Pd-PEPPSI-iPr Catalyzed-Controlled Chain Growth Polymerization. Suraru SL, Lee JA, Luscombe CK. ACS Macro Lett; 2016 Apr 19; 5(4):533-536. PubMed ID: 35607224 [Abstract] [Full Text] [Related]
9. Catalyst-transfer polycondensation. mechanism of Ni-catalyzed chain-growth polymerization leading to well-defined poly(3-hexylthiophene). Miyakoshi R, Yokoyama A, Yokozawa T. J Am Chem Soc; 2005 Dec 14; 127(49):17542-7. PubMed ID: 16332106 [Abstract] [Full Text] [Related]
10. Direct Synthesis of Chain-end-functionalized Poly(3-hexylthiophene) without Protecting Groups Using a Zincate Complex. Inagaki S, Yamamoto T, Higashihara T. Macromol Rapid Commun; 2020 Jun 14; 41(11):e2000148. PubMed ID: 32364289 [Abstract] [Full Text] [Related]
11. Two flavors of PEPPSI-IPr: activation and diffusion control in a single NHC-ligated Pd catalyst? Larrosa I, Somoza C, Banquy A, Goldup SM. Org Lett; 2011 Jan 07; 13(1):146-9. PubMed ID: 21133362 [Abstract] [Full Text] [Related]
16. "Hairy" poly(3-hexylthiophene) particles prepared via surface-initiated Kumada catalyst-transfer polycondensation. Senkovskyy V, Tkachov R, Beryozkina T, Komber H, Oertel U, Horecha M, Bocharova V, Stamm M, Gevorgyan SA, Krebs FC, Kiriy A. J Am Chem Soc; 2009 Nov 18; 131(45):16445-53. PubMed ID: 19860410 [Abstract] [Full Text] [Related]
17. Rational exploration of N-heterocyclic carbene (NHC) palladacycle diversity: a highly active and versatile precatalyst for Suzuki-Miyaura coupling reactions of deactivated aryl and alkyl substrates. Peh GR, Kantchev EA, Er JC, Ying JY. Chemistry; 2010 Apr 06; 16(13):4010-7. PubMed ID: 20175159 [Abstract] [Full Text] [Related]
18. Random catalyst walking along polymerized poly(3-hexylthiophene) chains in Kumada catalyst-transfer polycondensation. Tkachov R, Senkovskyy V, Komber H, Sommer JU, Kiriy A. J Am Chem Soc; 2010 Jun 09; 132(22):7803-10. PubMed ID: 20465260 [Abstract] [Full Text] [Related]
19. The Selective Cross-Coupling of Secondary Alkyl Zinc Reagents to Five-Membered-Ring Heterocycles Using Pd-PEPPSI-IHept(Cl). Atwater B, Chandrasoma N, Mitchell D, Rodriguez MJ, Pompeo M, Froese RD, Organ MG. Angew Chem Int Ed Engl; 2015 Aug 10; 54(33):9502-6. PubMed ID: 26110577 [Abstract] [Full Text] [Related]