[Synthesis and spectroscopic properties of tetra-(dimethylaminophenyl) porphyrin and its metal complexes].

Porphyrin and metalloporphyrin distribute widely in nature and they play an important role in the life. Synthesis of porphyrin compounds with special function has been the focus of attention. In the present paper, porphyrin and metalloporphyrin compound were synthesized by the following method: by one-step synthesis, tetra-(dimethylaminophenyl) porphyrin (T(DMAP) P) was synthesized with propionic acid, acetic acid and nitrobenzene as solvent and 4-dimethylaminobenzaldehyde and pyrrole as raw material.

[Study on spectral behavior of meso-tetra-(3, 5-dibromo-4-hydroxyphenyl) porphyrin with calf thymus DNA].

The binding characteristics of meso-tetra-(3, 5-dibromo-4-hydroxphenyl) porphyrin [T(DBHP)P] with calf thymus DNA (ct DNA) in pH 4.92 HAc-NaAc buffer solution were studied by the techniques of spectrophotometry. At the maxium absorption wavelength for T(DBHP)P, the decrease in the absorbance was linear with the amount of ct DNA.

[Microemulsion sensitized fluorophotometric determination of protein with probe of phenylfluorone-molybdenum (VI) complex].

The fluorescence spectral behavior of interaction of phenylfluorone(PF)-Mo(VI) and protein was investigated in Triton X-100 microemulsion medium at pH 2.0. A novel method for the determination of protein using phenylfluorone (PF)-Mo(VI) as a fluorescence spectrum probe was developed.

Rapid and highly sensitive determination of trace proteins using dibromomethyl carboxyazo-Pb(II) complex as a spectroscopic reagent.

Background: The concentration of protein in body fluids is an important measure in disease diagnosis and in analytical biochemistry. Searching for a sensitive and rapid method for proteins is an ongoing subject of investigation. We describe the reaction of dibromomethyl carboxyazo-Pb(II) with proteins found in urine.