121680-23-7Relevant articles and documents
Gold Catalysis Meets Materials Science – A New Approach to π-Extended Indolocarbazoles
Hendrich, Christoph M.,Bongartz, Lukas M.,Hoffmann, Marvin T.,Zschieschang, Ute,Borchert, James W.,Sauter, Désirée,Kr?mer, Petra,Rominger, Frank,Mulks, Florian F.,Rudolph, Matthias,Dreuw, Andreas,Klauk, Hagen,Hashmi, A. Stephen K.
supporting information, p. 549 - 557 (2020/12/07)
Herein we describe a modular, convergent synthesis of substituted benzo[a]benzo[6,7]-indolo[2,3-h]carbazoles (BBICZs) using a bidirectional gold-catalyzed cyclization reaction as a key step. A building block strategy enabled the easy variation of substituents at different positions of the core structure and a general analysis of substitution effects on the materials properties of the target compounds. All BBICZs were fully characterized and their optical and electronic properties were studied experimentally as well as by computational methods. Organic thin-film transistors based on eight selected derivatives were fabricated by vacuum deposition and charge-carrier mobilities up to 1 cm2/Vs were measured. (Figure presented.).
Preparation, characterization and application of 1,4-disulfopiperazine-1,4-diium chloride ([Piper-(SO3H)2]·2Cl) as an efficient dicationic ionic catalyst for the N-Boc protection of amines
Koodehi, Tahereh Ghauri,Shirini, Farhad,Goli-Jolodar, Omid
, p. 443 - 456 (2017/01/10)
In this work, 1,4-disulfopiperazine-1,4-diium chloride ([Piper-(SO3H)2]·2Cl), as a novel Br?nsted acidic ionic catalyst is synthesized and characterized using a series of techniques including FT-IR, TGA, DTA, SEM, pH analysis and Hammett acidity function. This substance can significantly catalyze the N-Boc protection of amines without solvent interference at room temperature. The advantages of this manner are chemoselectivity, short reaction times, suitable yields, excellent yields of the products, without solvent interference and ease of preparation as well as reusability of the catalyst.
Fulleropyrrolidine end-capped molecular wires for molecular electronics-synthesis, spectroscopic, electrochemical, and theoretical characterization
Sorensen, Jakob Kryger,Fock, Jeppe,Pedersen, Anders Holmen,Petersen, Asger B.,Jennum, Karsten,Bechgaard, Klaus,Kilsa, Kristine,Geskin, Victor,Cornil, Jerome,Bjornholm, Thomas,Nielsen, Mogens Brondsted
experimental part, p. 245 - 263 (2011/03/20)
In continuation of previous studies showing promising metal-molecule contact properties a variety of C60 end-capped "molecular wires" for molecular electronics were prepared by variants of the Prato 1,3-dipolar cycloaddition reaction. Either benzene or fluorene was chosen as the central wire, and synthetic protocols for derivatives terminated with one or two fullero[c]pyrrolidine "electrode anchoring" groups were developed. An aryl-substituted aziridine could in some cases be employed directly as the azomethine ylide precursor for the Prato reaction without the need of having an electron-withdrawing ester group present. The effect of extending the π-system of the central wire from 1,4-phenylenediamine to 2,7-fluorenediamine was investigated by absorption, fluorescence, and electrochemical methods. The central wire and the C60 end-groups were found not to electronically communicate in the ground state. However, the fluorescence of C60 was quenched by charge transfer from the wire to C60. Quantum chemical calculations predict and explain the collapse of coherent electronic transmission through one of the fulleropyrrolidine-terminated molecular wires.
