Login

Samar Bahzad Eid

Associate professor
Chemistry - Biochemistry department - Section II - Fanar
Speciality: Chemistry
Specific Speciality: Chimie

Positions
2007 - 2015 : Enseignante

(Université Libanaise - Faculté des Sciences II
Fanar

2011 - 2012 : Enseignante

Université Notre Dame
Louaize

2007 - 2007 : Enseignante

Université de Rennes 1
France

2007 - 2009 : Enseignante

Université Saint Esprit de Kaslik
Kaslik

1999 - 2003 : Enseignante

Institut Byblos
Dora

Teaching 9 Taught Courses
(2014-2015) Chim 402 - Organic Chemistry (organic synthesis)

M1 Molecular Chemistry

(2014-2015) Chim 462 - Organic Chemistry Lab (organic synthesis)

M1 Molecular Chemistry

(2014-2015) TPCC 510 - Advanced organic synthesis and medicinal chemistry

M2 Technology of Perfumes, Cosmetics and Dyes

(2014-2015) Chim 426 - Laboratory training

M1 Molecular Chemistry

(2014-2015) TPCC 580 - Training

M2 Technology of Perfumes, Cosmetics and Dyes

(2014-2015) Chim 242 - Organic Chemistry II Lab

BS Chemistry

(2014-2015) Bioc 241 - Chemistry Lab for Biochemistry (organic and inorganic)

BS Biochemistry

(2014-2015) Chim 331 - Methods of structural analysis

BS Biochemistry

(2014-2015) Chim 335 - Organic Chemistry III

BS Chemistry

Education
2004 - 2007: Doctorat

Université de Rennes 1-France
Chimie Organique

2003 - 2004: DEA

Université de Rennes 1-France
Chimie Moléculaire

1995 - 1999: Maîtrise

Université Libanaise-Faculté des Sciences (Section II)
Chimie

1992 - 1995: Baccalauréat

Lycée Officiel de Jdeidé (Liban)
Diplôme en Sciences Expérimentales

Publications 5 publications
Debbab, M.; Renault, S.; Eid, S.; Lozach, O.; Meijer, L.; Carreaux, F., Bazureau, J.P An efficient method for the preparation of new analogs of Leucettamine B under solvent-free microwave irradiation. The Japan Institute of Heterocyclic Chemistry(Heterocycles) 2009

A simple and efficient microwave-assisted protocol has been developed for the synthesis of new 2-amino-3,4-dihydro-4H-imidazol-4-one derivatives of leucettamine B. This solvent-free protocol involves sulphur/nitrogen displacement of 2-ethylthio-5-arylidene-imidazolone 5 with a variety of functionalized polar primary amines 6 and this general method afforded a small library of the desired pure products 7a-n in yields ranging from 33 to 92% in moderate reaction times (30-100 minutes).

Eid, S.; Roisnel, T.; Lorcy, D. Titanocene complexes of the N-methyl and N-phenyl-1,3-thiazoline-2-thione-4,5-dithiolates and 4,5-diselenolate ligands Elsevier (Journal of Organometallic Chemistry) 2008

Cp2Ti(dithiolene) and Cp2Ti(diselenolene) complexes containing the N-methyl-1,3-thiazoline-2-thione- 4,5-dithiolate ligand (Me-thiazdt), the N-phenyl-1,3-thiazoline-2-thione-4,5-dithiolate ligand (Ph-thiazdt) and the N-methyl-1,3-thiazoline-2-thione-4,5-diselenolate ligand (Me-thiazds) have been synthesized. Three approaches have been developed in order to generate the dithiolene or the diselenolene ligands which were reacted with Cp2TiCl2 to form the corresponding heteroleptic complexes. Their Xray crystal structures, UV–Vis absorption spectra as well as their redox properties, determined by cyclic voltammetry have been investigated and discussed. Variable-temperature 1H NMR experiments have been performed in order to determine the activation energies of the chelate ring inversion.

Eid, S.; Fourmigué, M.; Roisnel, T.; Lorcy, D. Influence of the Thiazole Backbone on the Structural, Redox, and Optical Properties of Dithiolene and Diselenolene Complexes ACS publications (Inorganic chemistry) 2007

Metalation of N-methyl-1,3-thiazoline-2-thione followed by reaction with elemental S or Se affords a simple and efficient approach to N-methyl-1,3-thiazoline-2-thione-4,5-dithiolate (Me-thiazdt) and the diselenolate (Me-thiazds) analogue. In the presence of metal II centers such as Zn, Ni, and Pd these ligands afford the corresponding dianionic dithiolene and diselenolene complexes. The Ni and Pd dianionic complexes are easily oxidized into the monoanionic species. Complexes were isolated and characterized by single-crystal X-ray crystallography. Most often a substitutional S/N-Me disorder is observed, attributable to the square-planar trans complexes disordered on two positions or coexistence of both cis and trans isomers on inversion centers. Monoanionic complexes exhibit a strong NIR absorption band with  values up to 33 750 M-1 cm-1.

Eid, S.; Guerro, M.; Roisnel, T.; Lorcy, D. Trithiaazafulvalene : A Promising Building Block between Tetrathiafulvalene and Dithiadiazafulvalene ACS publications (Organic letters) 2006

New electroactive building blocks, the trithiaazafulvalenes (TTAFs), were synthesized. These redox-active molecules, intermediate between tetrathiafulvalene (TTF) and dithiadiazafulvalene (DTDAF), show promising features for the elaboration of molecular materials.

Eid, S.; Guerro, M.; Lorcy, D. 1,3-Thiazoline-2-thione-4,5-dithiolato, an efficient building block towards functionalized dithiadiazafulvalenes Elsevier (Tetrahedron Letters) 2006

The first synthesis and X-ray structural determination of the bis(tetraethylammonium) Zn dithiolene complex involving N-methyl-1,3-thiazoline-2-thione-4,5-dithiolate, [NEt4]2[Zn(Me-thiazdt)2], are reported. The reactivity of this dithiolene complex as a nucleophilic dithiolate synthon and as a precursor of the air sensitive electron rich olefine, the bis ethylenedithiodithiadiazafulvalene (BEDT–DTDAF), is also described.

Languages
English

Professional working proficiency

French

Full professional proficiency