Self-assembled monolayers of a water-insoluble porphyrin, tetraphenyl porphyrin (TPP), in the presence of an aqueous electrolyte were characterized in situ with electrochemical scanning tunneling microscopy (EC-STM) at working electrode potentials of between 0.5 and -0.2 V. Isolated domains of TPP monolayers with differing orientation were observed on Au(111) in 0.1 M HClO(4) over this entire p...

A general chiroptical protocol for determination of absolute configuration of secondary amines including acyclic and cyclic aliphatic amines, aromatic amines, amino acids, and amino alcohols is described. The chiral substrate is linked to the achiral carrier moiety (3-N-Boc-amino-propyl-N-Boc-amino)acetic acid 1 (BocHNCH(2)CH(2)CH(2)BocNCH(2)COOH), which after deprotection, yields a bidentate c...

Recently cationic porphyrin-peptide conjugates were synthesized to enhance the cellular uptake of porphyrins or deliver the peptide moiety to the close vicinity of nucleic acids. DNA binding of such compounds was not systematically studied yet. We synthesized two new porphyrin-tetrapeptide conjugates which can be considered as a typical monomer unit corresponding to the branches of porphyrin-po...

The absolute configuration of gymnocin-B has been determined to be (S)-10 and (S)-37. Three challenges toward the configurational assignment of this largest of the polyether marine toxin include (i) introduction of p-(meso-triphenylporphyrin)-cinnamate group (TPPcinnamate) on sterically hindered 10-, 37-hydroxyls under mild conditions, (ii) conformational analysis in the presence of TPPcinnamat...

We employed Circular Dichroism (CD) and UV/Vis-spectrophotometric methods to study the interaction of two Fe-containg cationic porphyrins: meso-tetra (4N-butylpyridyl) porphyrin [FeTButPyP4] and meso-tetra (4N-oxyethylpyridyl) porphyrin [FeTOEtPyP4] with DNA at various ionic strengths. The temperature-dependent absorption titration data were used to determine the binding constants and stoichiom...

Porphyrins molecules are gaining importance in the present era. Porphyrins are important part of biological molecules like hemoglobin and chlorophyll .Photo system 1 and photo system 2 is important sunlight trap in chloroplast. Electron transport chain is a series of chemical reaction in which energy is formed in the form of ATP (Adenosine triphosphate).The members of electron transport chains ...

We have studied the UV-vis absorption and chiroptical properties, binding affinity and photostability of a conjugated positively charged butadiyne-linked Zn(ii) porphyrin dimer bound to DNA sequence poly(dG-dC)2. Right-handed B-DNA, spermine-induced Z-DNA and Co(iii)-induced Z-DNA have been explored. Resonance light scattering (RLS) spectra showed formation of porphyrin aggregates in the presen...

New types of steroid-porphyrin conjugates derived from 20-hydroxyecdysone (20E) and 24-epibrassinolide (EBl) were synthesized. An exceptional regioselectivity in the reaction of both steroids with porphyrin boronic acids was found to give side-chain-conjugated boronic esters as sole products. UV-Vis-, fluorescence and NMR spectroscopy yielded similar data for all the studied compounds confirmin...

Environmental pollution with chiral organic compounds is an emerging problem requiring innovative sensing methods. Amino-functionalized thioureas, such as 2-(dimethylamino)cyclohexyl-(3,5-bis(trifluoromethyl)phenyl)thiourea (Takemoto’s catalyst), are widely used organocatalysts virtually unknown environmental safety data. Ecotoxicity studies based on the Vibrio fischeri luminescence inhibition ...

The interactions of 5,10,15,20-tetrakis(4-sulfonatophenyl)-porphyrin (TSPP, a singlet oxygen photosensitiser molecule) with a hexa-2,4-diynediyl bridged β-cyclodextrin dimer (CD-CD) in aqueous solutions of pH 7 were studied using steady-state UV-visible absorption/emission and femto- to millisecond time-resolved spectroscopy. TSPP forms 1 : 1 complexes with CD-CD (K(e) = 1.9 × 10(8) M(-1) at 29...