Spectroscopic properties of some derivatives of polycyclic aromatic hydrocarbons. 2008

Alfio Catalfo, and Maria Elisabetta Serrentino, and Vito Librando, and Giancarlo Perrini, and Guido de Guidi
Dipartimento di Scienze Chimiche, Università di Catania, Viale Andrea Doria 6, 95125, Catania, Italy.

The aim of this paper is to provide a general picture of the spectral characteristics of some polycyclic aromatic hydrocarbon (PAH) derivatives. A great deal of data concerning PAHs has been reported in the literature, but there is lack of comprehensiveness about important parameters in the same experimental conditions for their nitro (NO(2)) and amino (NH(2)) derivatives such as absorption and emission characteristics. Thus, important parameters such as the molar extinction coefficient, absorption maxima, fluorescence maxima, and fluorescence quantum yield are reported here. The efficiencies of the reduction of NO(2)-PAHs to their corresponding amino compounds were also verified by means of high-performance liquid chromatography (HPLC). This class of derivatives represents one of the most toxic groups of carcinogenic substances and therefore the data reported here should be useful for toxicological research.

UI MeSH Term Description Entries
D009574 Nitro Compounds Compounds having the nitro group, -NO2, attached to carbon. When attached to nitrogen they are nitramines and attached to oxygen they are NITRATES. Nitrated Compounds
D010084 Oxidation-Reduction A chemical reaction in which an electron is transferred from one molecule to another. The electron-donating molecule is the reducing agent or reductant; the electron-accepting molecule is the oxidizing agent or oxidant. Reducing and oxidizing agents function as conjugate reductant-oxidant pairs or redox pairs (Lehninger, Principles of Biochemistry, 1982, p471). Redox,Oxidation Reduction
D011083 Polycyclic Compounds Compounds which contain two or more rings in their structure. Compounds, Polycyclic
D011084 Polycyclic Aromatic Hydrocarbons Aromatic hydrocarbons that contain extended fused-ring structures. Polycyclic Aromatic Hydrocarbon,Polycyclic Hydrocarbons, Aromatic,Polynuclear Aromatic Hydrocarbon,Polynuclear Aromatic Hydrocarbons,Aromatic Hydrocarbon, Polycyclic,Aromatic Hydrocarbon, Polynuclear,Aromatic Hydrocarbons, Polycyclic,Aromatic Hydrocarbons, Polynuclear,Aromatic Polycyclic Hydrocarbons,Hydrocarbon, Polycyclic Aromatic,Hydrocarbon, Polynuclear Aromatic,Hydrocarbons, Aromatic Polycyclic,Hydrocarbons, Polycyclic Aromatic,Hydrocarbons, Polynuclear Aromatic
D002273 Carcinogens Substances that increase the risk of NEOPLASMS in humans or animals. Both genotoxic chemicals, which affect DNA directly, and nongenotoxic chemicals, which induce neoplasms by other mechanism, are included. Carcinogen,Oncogen,Oncogens,Tumor Initiator,Tumor Initiators,Tumor Promoter,Tumor Promoters,Initiator, Tumor,Initiators, Tumor,Promoter, Tumor,Promoters, Tumor
D002851 Chromatography, High Pressure Liquid Liquid chromatographic techniques which feature high inlet pressures, high sensitivity, and high speed. Chromatography, High Performance Liquid,Chromatography, High Speed Liquid,Chromatography, Liquid, High Pressure,HPLC,High Performance Liquid Chromatography,High-Performance Liquid Chromatography,UPLC,Ultra Performance Liquid Chromatography,Chromatography, High-Performance Liquid,High-Performance Liquid Chromatographies,Liquid Chromatography, High-Performance
D004785 Environmental Pollutants Substances or energies, for example heat or light, which when introduced into the air, water, or land threaten life or health of individuals or ECOSYSTEMS. Environmental Pollutant,Pollutant,Pollutants,Pollutants, Environmental,Pollutant, Environmental
D013058 Mass Spectrometry An analytical method used in determining the identity of a chemical based on its mass using mass analyzers/mass spectrometers. Mass Spectroscopy,Spectrometry, Mass,Spectroscopy, Mass,Spectrum Analysis, Mass,Analysis, Mass Spectrum,Mass Spectrum Analysis,Analyses, Mass Spectrum,Mass Spectrum Analyses,Spectrum Analyses, Mass
D015394 Molecular Structure The location of the atoms, groups or ions relative to one another in a molecule, as well as the number, type and location of covalent bonds. Structure, Molecular,Molecular Structures,Structures, Molecular

Related Publications

Alfio Catalfo, and Maria Elisabetta Serrentino, and Vito Librando, and Giancarlo Perrini, and Guido de Guidi
August 1998, Regulatory toxicology and pharmacology : RTP,
Alfio Catalfo, and Maria Elisabetta Serrentino, and Vito Librando, and Giancarlo Perrini, and Guido de Guidi
January 1997, Advances in space research : the official journal of the Committee on Space Research (COSPAR),
Alfio Catalfo, and Maria Elisabetta Serrentino, and Vito Librando, and Giancarlo Perrini, and Guido de Guidi
July 1973, Biochemical pharmacology,
Alfio Catalfo, and Maria Elisabetta Serrentino, and Vito Librando, and Giancarlo Perrini, and Guido de Guidi
December 2015, Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy,
Alfio Catalfo, and Maria Elisabetta Serrentino, and Vito Librando, and Giancarlo Perrini, and Guido de Guidi
August 1975, Analytical biochemistry,
Alfio Catalfo, and Maria Elisabetta Serrentino, and Vito Librando, and Giancarlo Perrini, and Guido de Guidi
August 2013, Environmental monitoring and assessment,
Alfio Catalfo, and Maria Elisabetta Serrentino, and Vito Librando, and Giancarlo Perrini, and Guido de Guidi
May 1980, Bulletin of environmental contamination and toxicology,
Alfio Catalfo, and Maria Elisabetta Serrentino, and Vito Librando, and Giancarlo Perrini, and Guido de Guidi
June 1979, Environmental health perspectives,
Alfio Catalfo, and Maria Elisabetta Serrentino, and Vito Librando, and Giancarlo Perrini, and Guido de Guidi
January 2010, IARC monographs on the evaluation of carcinogenic risks to humans,
Alfio Catalfo, and Maria Elisabetta Serrentino, and Vito Librando, and Giancarlo Perrini, and Guido de Guidi
January 1968, Doklady Akademii nauk SSSR,
Copied contents to your clipboard!