SYNTHESIS AND CHARACTERIZATION OF N-(4-ACETYLPHENYL)-N-(DIPHENYLPHOSPHINO)- P,P-DIPHENYLPHOSPHINOUS AMIDE DERIVATIVES: APPLICATION OF A Pd(ΙΙ) DERIVATIVE AS A PRE-CATALYST IN THE SUZUKI CROSS-COUPLING REACTION

2020 ◽  
Vol 61 (11) ◽  
pp. 1740-1750
Author(s):  
H. T. Al-Masri ◽  
Z. Moussa ◽  
N. M. Al Masaeid
RSC Advances ◽  
2016 ◽  
Vol 6 (103) ◽  
pp. 100690-100695 ◽  
Author(s):  
Tao Wang ◽  
Lantao Liu ◽  
Kai Xu ◽  
Huanping Xie ◽  
Hui Shen ◽  
...  

Five novel trinuclear N-heterocyclic carbene–palladium(ii) complexes 5a–e were conveniently synthesized in one step. The obtained palladium(ii) complexes were the effective catalyst precursors for the Suzuki–Miyaura coupling.


ACS Omega ◽  
2020 ◽  
Vol 5 (16) ◽  
pp. 9598-9604
Author(s):  
Junya Ishida ◽  
Masato Nakatsuji ◽  
Tatsuki Nagata ◽  
Hideya Kawasaki ◽  
Takeyuki Suzuki ◽  
...  

2015 ◽  
Vol 11 ◽  
pp. 951-956 ◽  
Author(s):  
Sandrina Oliveira ◽  
Dulce Belo ◽  
Isabel Cordeiro Santos ◽  
Sandra Rabaça ◽  
Manuel Almeida

A dissymmetric TTF-type electron donor, cyanobenzene-ethylenedithio-tetrathiafulvalene (CNB-EDT-TTF), was obtained in high yield, by a cross-coupling reaction with triethyl phosphite between 2-thioxobenzo[d][1,3]dithiole-5-carbonitrile and 5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-2-one. This new donor was characterized namely by single crystal X-ray diffraction, cyclic voltammetry, NMR, UV-visible and IR spectroscopy.


RSC Advances ◽  
2020 ◽  
Vol 10 (39) ◽  
pp. 23108-23120 ◽  
Author(s):  
Samim Sultana ◽  
Swapna Devi Mech ◽  
Farhaz Liaquat Hussain ◽  
Pallab Pahari ◽  
Geetika Borah ◽  
...  

Here we report the synthesis and characterization of graphene oxide anchored Pd–Cu bimetallic nanoparticles by bio reduction method and its application in Sonogashira cross-coupling reaction.


2020 ◽  
Vol 44 (13) ◽  
pp. 5056-5063
Author(s):  
Amir Hossein Ghasemi ◽  
Hossein Naeimi

The aerogel nanocomposite produces using the sol–gel and supercritical drying method processes. The CO2 supercritical drying (SCD) was taken as the most powerful process, ensuring the best properties of the product.


2021 ◽  
Vol 99 (1) ◽  
pp. 24-30
Author(s):  
M’hamed Chahma ◽  
Somaiah Almubayedh

The synthesis and characterization of a new terthiophene bearing stable radical II is described. Through a cross coupling reaction between 2-tributylstannylthiophene and 6-(2,5-dibromo-thiophene-3-yl)pyridine-2-carboxaldehyde (2), 6-[2,2′:5′,2″]terthiophen-3′-ylpyridine-2-carboxaldehyde (3) was prepared. The condensation of 3 with 2, 4-diisopropylcarbonohydrazide bis-hydrochloride affords the heterocyclic tetrazane (4), which was oxidized with 1,4-benzoquinone to form the stable radical II. II characterized by IR, ESR, and cyclic voltammetry. Oxidative electropolymerization of II and its precursor 4 at oxidation peak potential of the terthiophene using cyclic voltammetric scans produces radical functionalized polyterthiophene on a platinum electrode (poly(II)-Pt).


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