Preparation of highly pure quaterthiophene and role of impurities on its photoluminescence properties

被引:41
作者
Trabattoni, S
Laera, S
Mena, R
Papagni, A
Sassella, A
机构
[1] Univ Milano Bicocca, INFM, I-20125 Milan, Italy
[2] Univ Milano Bicocca, Dipartimento Sci Mat, I-20125 Milan, Italy
[3] Nikem Res SRL, I-20021 Baranzate Di Bollate, Mi, Italy
关键词
D O I
10.1039/b309150c
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Highly pure quaterthiophene (4T) has been prepared from monobromobithiophene by a Ni-0-mediated coupling reaction. The analysis of impurities produced by the synthetic procedure, performed by mass spectrometry and gas chromatography with a mass spectrometer detector, has allowed the identification of at least four contaminants, among them, alpha-bromoquaterthiophene (Br-4T). Studies of photoluminescence carried out at low temperatures ( from 70 to 4 K) on 4T thin films grown by organic molecular beam deposition are demonstrated to be a powerful tool in detecting impurities that can act as traps for 4T emission. Indeed, it was possible to assign the anomalous emission observed in some 4T thin films to Br-4T. A protocol for removal of 4T contaminants is also proposed.
引用
收藏
页码:171 / 178
页数:8
相关论文
共 18 条
[1]   ARYL MIGRATION REACTIONS IN THE ALKALINE-HYDROLYSIS OF VINYLPHOSPHONIUM IONS - ROLE OF THE ELECTRON SINK AND THE EFFECTS OF SUBSTITUTION AT THE MIGRATION TERMINUS [J].
ALLEN, DW ;
HUTLEY, BG .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1979, (06) :1499-1502
[2]  
Bansal R.C., 1988, ACTIVE CARBON
[3]   SELECTIVE SYNTHESIS OF ALPHA-SUBSTITUTED OLIGOTHIOPHENES [J].
BAUERLE, P ;
WURTHNER, F ;
GOTZ, G ;
EFFENBERGER, F .
SYNTHESIS-STUTTGART, 1993, (11) :1099-1103
[4]   Conformational analysis and optical characterization of oligothiophene inclusion compounds [J].
Bongiovanni, G ;
Botta, C ;
Bredas, JL ;
Cornil, J ;
Ferro, DR ;
Mura, A ;
Piaggi, A ;
Tubino, R .
CHEMICAL PHYSICS LETTERS, 1997, 278 (1-3) :146-153
[5]   SOME PHENYL MIGRATIONS IN ORGANOPHOSPHORUS COMPOUNDS [J].
BROPHY, JJ ;
FREEMAN, KL ;
GALLAGHE.MJ .
JOURNAL OF THE CHEMICAL SOCIETY C-ORGANIC, 1968, (22) :2760-&
[6]  
Fichou D., 1999, HDB OLIGO POLYTHIOPH
[7]   Aryl-aryl bond formation one century after the discovery of the Ullmann reaction [J].
Hassan, J ;
Sévignon, M ;
Gozzi, C ;
Schulz, E ;
Lemaire, M .
CHEMICAL REVIEWS, 2002, 102 (05) :1359-1469
[8]   A polystyrene-oligothiophene-polystyrene triblock copolymer [J].
Hempenius, MA ;
Langeveld-Voss, BMW ;
van Haare, JAEH ;
Janssen, RAJ ;
Sheiko, SS ;
Spatz, JP ;
Möller, M ;
Meijer, EW .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1998, 120 (12) :2798-2804
[9]   Synthetic chemistry for ultrapure, processable, and high-mobility organic transistor semiconductors [J].
Katz, HE ;
Bao, ZN ;
Gilat, SL .
ACCOUNTS OF CHEMICAL RESEARCH, 2001, 34 (05) :359-369
[10]   Characterization of activated carbon using X-ray photoelectron spectroscopy and inelastic neutron scattering spectroscopy [J].
Lennon, D ;
Lundie, DT ;
Jackson, SD ;
Kelly, GJ ;
Parker, SF .
LANGMUIR, 2002, 18 (12) :4667-4673