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REGIOSELECTIVE FUNCTIONALIZATION OF IMIDAZOAZINES AND DEVELOPMENT OF INDIRECT C-ARYLATION REACTION, TOOLS OF CHOICE TO PREPARE VARIOUS DI- AND TRISUBSTITUTED COMPOUNDS FONCTIONNALISATION REGIOSELECTIVE D’IMIDAZOAZINES, ET DEVELOPPEMENT DE LA REACTION DE C


AHMED EL AKKAOUI 1, 2, JAMAL KOUBACHI 1, 2, SABINE BERTEINA-RABOIN 1 *, ABDERRAHIM MOUADDIB 2, GÉRALD GUILLAUMET 1
(1)INSTITUT DE CHIMIE ORGANIQUE ET ANALYTIQUE, UMR CNRS 6005, UNIVERSITÉ D’ORLÉANS, BP 6759, 45067 ORLÉANS CEDEX 2, FRANCE (2)FACULTÉ DES SCIENCES ET TECHNIQUES DE BÉNI-MELLAL, UNIVERSITÉ SOULTAN MOULAY SLIMAN, BP 523, 23000 BÉNI-MELLAL, MAROC *CORRESPOND

Issue:

SCSCC6, Volume IX, No. 1

Section:

Volume IX, No. 1 (2008)

Abstract:

Electrochemical and in situ AFM studies of cadmium electrodeposition from an aqueous 0.1 M CdSO4 solution have been carried out in the case of (100) n-type silicon single crystal. The mechanisms related to the initial stages of the nucleation and growth mechanism of cadmium have been studied as a function of different potential steps. Within appropriate potential ranges the initial deposition kinetics corresponded to a model including progressive nucleation and diffusion controlled cluster growth. Nucleation rate and the number of atoms in the critical nucleus were determined from the analysis of current transients at different overpotentials. A Ncrit-value of 14 ± 1 atoms was determined in the following potential range: –9 mV = ? = –11 mV. The response of the system at different waiting times at the equilibrium potential was also investigated.

Keywords:

imidazoazines, pallado-catalyzed coupling, regioselective arylation.

Code [ID]:

CSCC6200809V01S01A0002 [0002052]

Full paper:

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