A facile one-pot synthesis of deep blue luminescent lead bromide perovskite microdisks

2015 ◽  
Vol 51 (91) ◽  
pp. 16385-16388 ◽  
Author(s):  
Zhao Yuan ◽  
Yu Shu ◽  
Yu Tian ◽  
Yan Xin ◽  
Biwu Ma
Keyword(s):  
Thin Films ◽  
Room Temperature ◽  
Quantum Yields ◽  
Synthetic Method ◽  
Lateral Size ◽  
One Pot ◽  
One Pot Synthesis ◽  
Deep Blue ◽  
Lead Bromide

We report a facile one-pot synthetic method to prepare highly luminescent layered lead(ii) bromide perovskite microdisks with the lateral size of a few micrometers and thickness of 100–150 nm, featuring narrow deep blue emissions with quantum yields of up to 53% in toluene solutions and thin films at room temperature.

A facile room temperature chemical transformation approach for binder-free thin film formation of Ag2Te and lithiation/delithiation chemistry of the film

2016 ◽  
Vol 45 (43) ◽  
pp. 17312-17318 ◽  
Author(s):  
Eun-Kyung Kim ◽  
Dasom Park ◽  
Nabeen K. Shrestha ◽  
Jinho Chang ◽  
Cheol-Woo Yi ◽  
...  
Keyword(s):  
Thin Film ◽  
Thin Films ◽  
Aqueous Solution ◽  
Ion Exchange ◽  
Chemical Transformation ◽  
Room Temperature ◽  
Film Formation ◽  
Synthetic Method ◽  
Binder Free ◽  
Thin Film Formation

An aqueous solution based synthetic method for binder-free Ag2Te thin films using ion exchange induced chemical transformation of Ag/AgxO thin films.

scholarly journals A rare γ-pyranopyrazole skeleton: design, one-pot synthesis and computational study

2016 ◽  
Vol 14 (31) ◽  
pp. 7490-7494 ◽  
Author(s):  
Muhammed Üçüncü ◽  
Ceren Cantürk ◽  
Erman Karakuş ◽  
Hüseyin Zeybek ◽  
Uğur Bozkaya ◽  
...  
Keyword(s):  
Computational Study ◽  
Synthetic Method ◽  
One Pot ◽  
One Pot Synthesis

A base mediated one-pot, two-step synthetic method for constructing γ-pyranopyrazoles.

scholarly journals A Facile Synthesis of Polysubstituted Pyrroles by One-Pot Three-Component Reaction

2012 ◽  
Vol 9 (4) ◽  
pp. 2239-2244 ◽  
Author(s):  
Hossein Anaraki-Ardakani ◽  
Maziar Noei ◽  
Mina Karbalaei-Harofteh ◽  
Shahab Zomorodbakhsh
Keyword(s):  
Room Temperature ◽  
Facile Synthesis ◽  
One Pot ◽  
Pyrrole Derivatives ◽  
Dialkyl Acetylenedicarboxylates ◽  
One Pot Synthesis ◽  
Three Component Reaction ◽  
High Yields ◽  
Neutral Conditions

A new and efficient one-pot synthesis of polysubstituted pyrrole derivatives by three-component reaction between dialkyl acetylenedicarboxylates, triphenylphosphine, 2-aminopyridin derivatives in the presence of arylglyoxals is described. The reactions were performed in dichloromethane at room temperature and neutral conditions and afforded high yields of products.

One-pot synthesis of chitosan–dehydropregnenolone acetate ketimine nanoparticles and their antifungal bioevaluation

RSC Advances ◽  
2015 ◽  
Vol 5 (13) ◽  
pp. 10065-10071 ◽  
Author(s):  
Archana M. Das ◽  
Raju Khan ◽  
Manash P. Hazarika ◽  
Debjani Baruah ◽  
Purnajyoti D. Bhuyan
Keyword(s):  
Room Temperature ◽  
Polymeric Nanoparticles ◽  
Communicable Diseases ◽  
New Method ◽  
One Pot ◽  
One Pot Synthesis ◽  
Dehydropregnenolone Acetate

This paper presents a new method for fabricating biodegradable bio-polymeric nanoparticles via a convenient one-pot strategy at room temperature under stirring conditions for application to communicable diseases.

A Quick Micelle-Catalyzed One-Pot Synthesis of Spiro[indoline-3, 4′-pyrano[2, 3-c]pyrazoles] in Water at Room Temperature

2018 ◽  
Vol 3 (5) ◽  
pp. 1512-1516 ◽  
Author(s):  
Jutika Devi ◽  
Subarna Jyoti Kalita ◽  
Dibakar Chandra Deka
Keyword(s):  
Room Temperature ◽  
One Pot ◽  
One Pot Synthesis

Palladium-Catalyzed One-Pot Stereospecific Synthesis of 2-Deoxy Aryl C-Glycosides from Glycals and Anilines in the Presence of tert-Butyl Nitrite

Synthesis ◽  
2019 ◽  
Vol 51 (22) ◽  
pp. 4215-4230 ◽  
Author(s):  
Adesh Kumar Singh ◽  
Rapelly Venkatesh ◽  
Jeyakumar Kandasamy
Keyword(s):  
Room Temperature ◽  
Stereospecific Synthesis ◽  
One Pot ◽  
Tert Butyl ◽  
Mild Conditions ◽  
One Pot Synthesis ◽  
Palladium Catalyzed ◽  
Aryl Glycosides

The palladium-catalyzed one-pot synthesis of 2,3-deoxy-3-keto aryl C-glycosides is achieved from glycals and anilines in the presence of tert-butyl nitrite and aqueous HBF4 under mild conditions. This one-pot method stereospecifically provides α- and β-aryl glycosides (≥19:1 by NMR) in good yields at room temperature. The configuration at the C-3 position in the glycal determines the anomeric selectivity (i.e., α or β) of the desired products.

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