Detail of "6319-40-0"

Reference

Monomers, oligomers and polymers of 2-functionalized and 2,7-difunctionalized carbazoles

Monomers, oligomers and polymers of 2-functionalized and 2,7-difunctionalized carbazoles. Leclerc, Mario; Morin, Jean-Francois (Universite Laval, Can.). PCT Int. Appl. WO 2005016882 A1 24 Feb 2005, 72 pp.There are some reagents like 6319-40-0 is used in this study. DESIGNATED STATES: W: AE, AG, AL, AM, AT, AU, AZ, BA, BB, BG, BR, BW, BY, BZ, CA, CH, CN, CO, CR, CU, CZ, DE, DK, DM, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, HR, HU, ID, IL, IN, IS, JP, KE, KG, KP, KR, KZ, LC, LK, LR, LS, LT, LU, LV, MA, MD, MG, MK, MN, MW, MX, MZ, NA, NI, NO, NZ, OM, PG, PH, PL, PT, RO, RU, SC, SD, SE, SG, SK, SL, SY, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, YU, ZA, ZM, ZW; RW: AT, BE, BF, BJ, CF, CG, CH, CI, CM, CY, DE, DK, ES, FI, FR, GA, GB, GR, IE, IT, LU, MC, ML, MR, NE, NL, PT, SE, SN, TD, TG, TR. (English). (World Intellectual Property Organization). CODEN: PIXXD2. CLASS: ICM: C07D209-86. ICS: C08F026-12.Except for chemicals metioned above, 6319-40-0 is also used. APPLICATION: WO 2004-CA1509 16 Aug 2004. PRIORITY: US 2003-2003/PV495113 15 Aug 2003. DOCUMENT TYPE: Patent CA Section: 35 (Chemistry of Synthetic High Polymers) Section cross-reference(s): 76 The present invention relates to 2-functionalized and 2,7-difunctionalized carbazoles and 2,7 -carbazolenevinylene oligomers and polymers. More specifically, the present invention relates to a compd. of formula (I): wherein R1 is selected from the group consisting of H, alkyl, and aryl; and wherein R2 and R3 are independently selected from the group consisting of H, alkyl, formyl, hydroxymethyl, trityloxymethyl, acetonitrile, chloromethyl, methylphosphonate, methyltriphenylphosphonium and vinyl. The oligomers and polymers are used in field-effect transistors, light-emitting devices such as light-emitting diodes, and solar cells. ..

Monomers, oligomers and polymers of 2-functionalized and 2,7-difunctionalized carbazoles

Monomers, oligomers and polymers of 2-functionalized and 2,7-difunctionalized carbazoles. Leclerc, Mario; Morin, Jean-Francois (Universite Laval, Can.). PCT Int. Appl. WO 2005016882 A1 24 Feb 2005, 72 pp.There are some reagents like 6319-40-0 is used in this study. DESIGNATED STATES: W: AE, AG, AL, AM, AT, AU, AZ, BA, BB, BG, BR, BW, BY, BZ, CA, CH, CN, CO, CR, CU, CZ, DE, DK, DM, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, HR, HU, ID, IL, IN, IS, JP, KE, KG, KP, KR, KZ, LC, LK, LR, LS, LT, LU, LV, MA, MD, MG, MK, MN, MW, MX, MZ, NA, NI, NO, NZ, OM, PG, PH, PL, PT, RO, RU, SC, SD, SE, SG, SK, SL, SY, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, YU, ZA, ZM, ZW; RW: AT, BE, BF, BJ, CF, CG, CH, CI, CM, CY, DE, DK, ES, FI, FR, GA, GB, GR, IE, IT, LU, MC, ML, MR, NE, NL, PT, SE, SN, TD, TG, TR. (English). (World Intellectual Property Organization). CODEN: PIXXD2. CLASS: ICM: C07D209-86. ICS: C08F026-12.Except for chemicals metioned above, 6319-40-0 is also used. APPLICATION: WO 2004-CA1509 16 Aug 2004. PRIORITY: US 2003-2003/PV495113 15 Aug 2003. DOCUMENT TYPE: Patent CA Section: 35 (Chemistry of Synthetic High Polymers) Section cross-reference(s): 76 The present invention relates to 2-functionalized and 2,7-difunctionalized carbazoles and 2,7 -carbazolenevinylene oligomers and polymers. More specifically, the present invention relates to a compd. of formula (I): wherein R1 is selected from the group consisting of H, alkyl, and aryl; and wherein R2 and R3 are independently selected from the group consisting of H, alkyl, formyl, hydroxymethyl, trityloxymethyl, acetonitrile, chloromethyl, methylphosphonate, methyltriphenylphosphonium and vinyl. The oligomers and polymers are used in field-effect transistors, light-emitting devices such as light-emitting diodes, and solar cells. ..