Pollution of a Tropical Lagoon by the Determination of Organochlorine Coumpounds

The lagoon system of Ivory Coast with 1,200 km2 of area is one among the important in West Africa. In the context of national quality water assessment, study of chemicals has been carried out in the central basin and its surroundings. The samples taken in different stations have been extracted with hexane and purified on column of florisil deactivated at 5% at chemical treatment. The analysis by CPG/ECD has permitted to identify the organochlorine compound wastes such as the Lindan, Heptachlor, Dieldrin, Endrin, the metabolites of DDT (PP'DDD and PP'DDE) and PCBs. The PCA method showed the highest stations of contamination located to Abidjan, the main industrial and urban zones (PCB: 15-227 ng/g and DDT + DDD + DDE: 1.7-130 ng/g)

Benzophénanthridines isolées de Zanthoxylum psammophilum

Dix-huit composés dont deux nouvelles benzophénanthridines la 8-méthoxy-7,8-dihydrofagaridine 1 et la 8-acétonyl-7,8-dihydrofagaridine 2 ont été isolés des racines de Zanthoxylum psammophilum (Rutaceae). La structure de ces composés (1-18) a été déterminée principalement par l’utilisation de la spectroscopie de RMN 1D (1H et 13C) et 2D (COSY, NOESY, HSQC, HMBC). Le composé 1 a montré une activité antimicrobienne sur S. Aureus.Mots clés: Rutaceae, alcaloïdes, 8-méthoxy-7,8-dihydrofagaridine, 8- acétonyl-7,8-dihydrofagaridin

Combined Analysis of the Root Bark Oil of Cleistopholis glauca by Chromatographic and Spectroscopic Techniques

International audienceThe composition of root bark oil from Cleistopholis glauca Pierre ex Engler & Diels growing wild in Ivory Coast was investigated by GC (in combination with retention indices) and 13C NMR spectroscopy after partition of hydrocarbons and oxygenated compounds on silica gel. Thirty-one compounds have been identified. C. glauca produces a sesquiterpene-rich oil, patchoulenone (33.5%), cyperene (9.5%) and germacrene D (6.6%) being the main components. Special attention was paid to the identification and quantification of germacrene C (a heat-sensitive compound) and d-elemene, which were achieved by a combination of GC(FID) and 13C NMR spectroscopy. The composition of C. glauca root bark and leaf oils differed drastically

The key role of 13C NMR analysis in the identification of individual components of Polyalthia longifolia leaf oil

International audiencePolyalthia longifolia produces sesquiterpene-rich essential oils (EOs) whose compositions varied substantially from sample to sample depending on the origin of the plant (Nigeria and Vietnam). Nothing is known about the phytochemistry of Ivoirian P. longifolia. The aim of the present study was to characterize Ivoirian P. longifolia through the chemical composition of the leaf oil and to develop a strategy that allows the identification of minor oxygenated sesquiterpenes whose MS data are not compiled in commercial or laboratory-constructed MS libraries. The EO was submitted to gas chromatography (GC) retention index (RI), GC-mass spectrometry (MS) and 13C nuclear magnetic resonance (NMR) analysis. Then hydrocarbons and oxygenated components were separated and the oxygenated fraction was chromatographed on silica gel. The fractions were analysed by GC(RI) and 13C NMR. Seventy compounds accounting for 91.8% of the EO were identified. Sesquiterpene hydrocarbons, (E)-β-caryophyllene (27.8%), α-zingiberene (20.0%) and allo-aromadendrene (15.0%), were the major components. Various oxygenated sesquiterpenes whose MS data were not compiled in commercial and laboratory-made MS libraries were identified by comparison of their chemical shift values in the spectrum of the fraction of CC with those reported in the literature and compiled in a laboratory-constructed 13C NMR data library. The composition of the investigated Ivoirian P. longifolia oil sample presented similarities and differences with Nigerian and Vietnamese oils. Combined analysis of Ivoirian P. longifolia EO by chromatographic and spectroscopic techniques including 13C NMR without isolation of the components, appeared particularly efficient to identify minor components of EOs, whose MS spectra are insufficiently differentiated or MS data are not compiled in commercial and lab-constructed MS libraries