25417-58-7Relevant articles and documents
Polyelectrolyte templated polymerization in langmuir films: Nanoscopic control of polymer chain organization
Chandra, M. Sharath,Radhakrishnan
, p. 2982 - 2986 (2006)
Polyelectrolytes introduced in the aqueous subphase are shown to have a profound impact on the kinetics of polymerization of N-octadecylaniline at the air/water interface. This can be attributed to changes effected in molecular organization and reorientation behavior in the Langmuir film. The polyelectrolyte templates lead to considerable modification of the morphology of the monomer and polymer Langmuir films. Polyelectrolyte complexation is found to be an elegant and efficient methodology to achieve enhanced alignment of the polyaniline chains in the transferred Langmuir-Blodgett (Langmuir-Schafer) film.
In water alkylation of amines with alcohols through a borrowing hydrogen process catalysed by ruthenium nanoparticles
Risi, Caterina,Calamante, Massimo,Cini, Elena,Faltoni, Valentina,Petricci, Elena,Rosati, Filippo,Taddei, Maurizio
supporting information, p. 327 - 331 (2020/02/13)
A simple and environmentally benign procedure for the synthesis of secondary amines in water has been developed. Combining Ru3(CO)12, tetraphenylcyclopentadienone and a small quantity of TGPS-750-M surfactant, primary and secondary alcohols were alkylated at N employing equimolar amounts of aromatic amines in water. The reaction occurs under microwave (MW) dielectric heating with high conversion and high yield. When required, the use of biomass-derived 2-MeTHF or GVL as a co-solvent is possible. Under the influence of MWs, a Ru nanoparticle-nanomicelle combination was formed acting as an effective and recyclable catalyst. This protocol was also employed for "in water" cyclisation to synthesise biologically relevant pyrrolobenzodiazepines (PBDs).
Efficient nickel-catalysed: N -alkylation of amines with alcohols
Afanasenko, Anastasiia,Elangovan, Saravanakumar,Stuart, Marc C. A.,Bonura, Giuseppe,Frusteri, Francesco,Barta, Katalin
, p. 5498 - 5505 (2018/11/20)
The selective N-alkylation of amines with alcohols via the borrowing hydrogen strategy represents a prominent sustainable catalytic method, which produces water as the only by-product and is ideally suited for the catalytic transformation of widely available alcohol reaction partners that can be derived from renewable resources. Intensive research has been devoted to the development of novel catalysts that are mainly based on expensive noble metals. However, the availability of homogeneous or heterogeneous non-precious metal catalysts for this transformation is very limited. Herein we present a highly active and remarkably easy-to-prepare Ni based catalyst system for the selective N-alkylation of amines with alcohols, that is in situ generated from Ni(COD)2 and KOH under ligand-free conditions. This novel method is very efficient for the functionalization of aniline and derivatives with a wide range of aromatic and aliphatic alcohols as well as diols and exhibits excellent functional group tolerance including halides, benzodioxane and heteroaromatic groups. Several TEM measurements combined with elemental analysis were conducted in order to gain insight into the nature of the active catalyst and factors influencing reactivity.
Copper-TBAF catalyzed arylation of amines and amides with aryl trimethoxysilane
Lin, Baoda,Liu, Miaochang,Ye, Zhishi,Ding, Jinchang,Wu, Huayue,Cheng, Jiang
supporting information; experimental part, p. 869 - 873 (2009/05/30)
A copper-catalyzed C-N bond forming reaction among aryl siloxane and primary, secondary amines as well as amides has been described. The reaction was conducted in the presence of P(C6F5)3 and 4 A molecular sieves in CHsub
