101446-65-5Relevant academic research and scientific papers
Phase controlled synthesis of bifunctional TiO2 nanocrystallites: Via d-mannitol for dye-sensitized solar cells and heterogeneous catalysis
Al-Enizi, Abdullah M.,Mane, Rajaram S.,Rana, Abu Ul Hassan Sarwar,Shaikh, Shoyebmohamad F.,Siddiqui, T. A. J.,Ubaidullah, Mohd,Yousef, Ayman
, p. 14826 - 14836 (2020)
The crystal architecture of TiO2 was successfully tailored via a low-temperature (≤200 °C) hydrothermal process in the presence of d-mannitol for feasible applications in dye-sensitized solar cells (DSSCs) and heterogeneous catalysis. In the development of anatase-TiO2 (A-TiO2), d-mannitol does not merely acts as a complexing agent to manage the zigzag chains of octahedral TiO62- with dominant edge sharing but also performs as a capping agent by influencing the hydrolysis process during nucleation, as confirmed by Fourier-transform infrared spectroscopy and dynamic light scattering studies. After physical measurements, the as-synthesized nanocrystallites (NCs) of A-TiO2 were used in DSSCs, where a fascinating power conversion efficiency (PCE) of 6.0% was obtained, which showed excellent performance compared with commercial anatase-TiO2 (CA-TiO2: 5.7%) and rutile-TiO2 (R-TiO2) obtained without d-mannitol (3.7%). Moreover, a smart approach was developed via the A-TiO2 catalyst to synthesize pharmaceutically important C-3 alkylated 4-hydroxycoumarins through different activated secondary alcohols under solvent-free, and heat/visible light conditions. In addition, the catalytic activity of the so-produced A-TiO2 catalyst under solvent-free conditions exhibited remarkable recyclability with up to five consecutive runs with negligible reduction, which is superior to existing reports, and clearly reveals the novelty, and green, sustainable nature of the as-synthesized A-TiO2 catalyst. A plausible reaction mechanism of both coupling partners was activated through the interaction with the A-TiO2 catalyst to produce valuable C-3 alkylated 4-hydroxycoumarins with 95% yield and high selectivity.
An expedient solvent-free C-benzylation of 4-hydroxycoumarin with styrenes
Chatterjee, Rana,Mukherjee, Anindita,Santra, Sougata,Zyryanov, Grigory V.,Chupakhin, Oleg N.,Majee, Adinath
, p. 123 - 124 (2021/02/16)
An efficient straightforward solvent-free C(3)-benzylation of 4-hydroxycoumarin with styrenes is performed by heating the reactants in the presence of p-toluenesulfonic acid. By this procedure, benzylated 4-hydroxycoumarin derivatives which exhibit variou
An efficient greener copper triflate-catalyzed C-3 benzylation of 4-hydroxycoumarin and some active methylene compounds
Ganguly, Nemai C.,Chandra, Sumanta
, p. 547 - 555 (2012/10/29)
4-Hydroxycoumarin has been directly benzylated at C-3 position with a good number of secondary benzylic alcohols using copper triflate catalyst (2 mol%) in toluene under reflux. The protocol provides an efficient, expedient and atom-economic access to warfarin and coumatetralyl analogues with potential anticoagulant activity. The protocol has been extended to benzylation of 4-hydroxy-1-methylquinolin-2(1H)-1-one, N-methylbarbiturate and some other active methylene compounds with remarkable success.
Benzylation of β-dicarbonyl compounds and 4-hydroxycoumarin using TMSOTf catalyst: A simple, mild, and efficient method
Theerthagiri, Palani,Lalitha, Appaswami
supporting information; experimental part, p. 5454 - 5458 (2010/11/02)
The direct benzylation of 1,3-dicarbonyl compounds and 4-hydroxycoumarin with a wide variety of benzylic alcohols was achieved using trimethylsilyl trifluoromethanesulfonate as an efficient catalyst. The reaction proceeded under very mild conditions at ro
