Nitrothienylporphyrins: Synthesis, crystal structure and, the effect of position and number of nitro groups on the spectral and electrochemical properties

Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy

Volumn 87, Issue , 2012, Pages 258-264

  Prasath, R ^a   Butcher, R J ^b   Bhavana, P ^a  

^a BIRLA INSTITUTE OF TECHNOLOGY AND SCIENCE   (India)

^b HOWARD UNIVERSITY   (United States)

Author keywords

Extended conjugation; Imino hydrogen; Nitration; Nitrothienylporphyrin; Unsymmetrical porphyrins

Indexed keywords

ELECTROPHILIC NITRATION; EXTENDED CONJUGATION; MESO POSITIONS; NITRO GROUP; NITROTHIENYLPORPHYRIN; PROTON NMR; REDOX POTENTIALS; SPECTRAL AND ELECTROCHEMICAL PROPERTIES; THIENYL; THIENYL RING;

ELECTROCHEMICAL PROPERTIES; HYDROGEN; NITRATION; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PORPHYRINS; POSITIVE IONS; REDOX REACTIONS; SYNTHESIS (CHEMICAL);

CRYSTAL ORIENTATION;

NITRO DERIVATIVE; PORPHYRIN;

ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; SYNTHESIS; X RAY CRYSTALLOGRAPHY;

CRYSTALLOGRAPHY, X-RAY; MAGNETIC RESONANCE SPECTROSCOPY; MODELS, MOLECULAR; NITRO COMPOUNDS; PORPHYRINS;

EID: 84855316042     PISSN: 13861425     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.saa.2011.11.049     Document Type: Article

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