Indicator characteristics of bromothymol blue derivatives

Some Bromothymol Blue derivatives with a nitro, amino, isothiocyanato or sulfonamide group substituted on the sulfonated ring of the dibromothymolsulfonephthalein have been studied spectrometrically. All the dyes have two characteristic absorption peaks which can be used to measure pH in the physiological range. The molar absorptivities, wavelengths of maximum absorption and pK(a) values have been determined from the absorbances, and are similar for all four dyes.     

The direct determination of cadmium in biological samples by selective volatilization and graphite tube reservoir atomic absorption spectrometry

The utilization of modifications of the rate of metal-catalyzed reactions (mainly redox reactions involving organic dyes of relatively high molar absorptivities) by other organic species (ligands) is outlined. This extension of catalytic reaction-rate methods in solution is of recent development and suggests the possibility of further analytical procedures. Three main types of modifications, (a) inhibition, (b) true metal complex catalysis, and (c) promotion, are distinguished, and their applications to analytical determinations are discussed.     

Syntheses of azo dyes containing 4,5-diphenylimidazole and their evaluation as analytical reagents

Eight azo dyes containing the 4,5-diphenylimidazole group have been synthesized, and their potential for determinations of metals has been studied spectrophotometrically. Of these reagents, the pyridylazo and quinolylazo derivatives are suitable as chromogenic reagents, the best being 2-(quinolylazo)-4,5-diphenylimidazole (QAI), which reacts with several metal ions. The copper and mercury complexes of QAI show molar absorptivities of the order of 80 000 l mol^?1 cm^?1.     

Simultaneous quantitation of 1,8,9-anthracenetriol, 1,8-dihydroxy-9,10-anthraquinone, and 1,8,1',8'-tetrahydroxy-10,10'-dianthrone by reversed-phase high-performance liquid chromatography

A sensitive and specific reversed-phase high-performance liquid chromatographic method was developed for the simultaneous analysis of anthralin (1,8,9-anthracenetriol) and its known degradation products: quinone (1,8-dihydroxy-9,10-anthraquinone) and dimer (1,8,1',8'-tetrahydroxy-10,10'-dianthrone). The method provides for rapid and simple quantitation of nanogram amounts of the three compounds. The molar absorptivities for anthralin in different solvents and solvent systems, including the mobile phase, are presented.     

Spectroscopic study of chloranil charge-transfer complexes of amino acids and related compounds

The absorption maxima, molar absorptivities, infrared spectra, compositions, formation constants, and pH dependence of amino acid—chloranil complexes have been determined with purified chloranil The n-π charge-transfer interaction depends on the presence of an unprotonated amino group; pH 9 is optimal for complex formation, but once formed, the complex is stable in a highly acidic medium and may be quantitatively extracted by hexanol. The molar absorptivities of the chloranil complexes of glycine, iminodiacetic acid, NTA, EDTA, DTPA and TTHA were measured. There is a linear relationship between the logarithm of the molar absorptivities of their chloranil complexes and the number of carboxylic groups in the molecule. There is an inverse linear relationship between the molar absorptivities of chloranil—metal—EDTA complexes and the logarithm of the stability constants of the EDTA chelates. This leads to a new method of determining the stability constants of complexes involving a nitrogen-donating group.     

分光光度法测定络合物稳定常数及摩尔吸光系数的通用算法

提出了一个用单纯形法与线性最小二乘法结合的方法计算络合物稳定的常数及摩尔吸光系 的新算法,并处理了Ｃｊ＾２＋－ＰＡＮ－Ｓ络合体系的数据,求得了该络合物的第一,二级稳定常数。     

Densitometric quantification of individual phospholipids. Improvement and evaluation of a method using molybdenum blue reagent for detection

A densitometric method for simultaneous quantification of individual phospholipids based on visualization with molybdenum blue reagent is presented. Previously reported problems concerning colour instability have been solved. The method is specific for phosphorus-containing compounds and independent of the degree of fatty acid unsaturation. The molar absorptivities of most analysed phospholipids do not differ more than 10% from that for phosphatidylcholine from egg yolk. For cases of greater deviation (sphingomyelin, lysophosphatidylcholine and phosphatidylserine), analysis is accomplished by use of appropriate standard mixtures. The between-series coefficient of variation is ca. 9%. The method is compared to a preparative thin-layer chromatographic assay and another commonly used densitometric method.     

Application of sulphanilamides disazo dyes with Tropaeolin O for simple, rapid and sensitive spectrophotometric assay of medicines

A rapid, simple and sensitive spectrophotometric method for the determination of some sulphanilamides is described. The method is based on the formation of blue coloured disazo dyes by the diazotization of sulphonamides viz. sulphanilamide (SA), sulphamerazine (SMR), sulphamethazine (SMZ), sulphadimethoxine (SDM), sulphamethoxazole (SMX), sulphadiazine (SDA), sulfathiazole (STZ), sulphaguanidine (SGN), sulphamonomethoxine (SMM), sulphamethoxypyridazine (SMP) in 0.5M hydrochloric acid media at ice bath followed by the azocoupling reaction with acid monoazo dye Tropaeolin O (TrO) at pH=10.5. Formed products are stable for 10h at room temperature. Effective molar absorptivities at absorbance maxima 595nm for disazo dyes were ～10(4)M(-1)cm(-1). Stoichiometric ratios of the components of disazo dyes were determined by means of mole ratio and continuous variations methods. Linear ranges for sulphanilamides determination were 0.4-14.0μgml(-1). The methods were successfully approved at suphanilamides determination in model solutions and commercial pharmaceutical preparations.     

Colorimetric determination of amino acids using genipin from Gardenia jasminoides

Genipin, a hydrolysate of geniposide from gardenia fruits, produces blue pigments on reaction with amino acids. The colorimetric detection of amino acids using this genipin reaction was evaluated and compared with the well-known ninhydrin reaction. The molar absorptivities of the blue pigments, the reaction products of genipin with various amino acids, were greater than those of the respective ninhydrin reaction products. When asparagine was reacted with genipin, the molar absorptivity was about 14 times higher than with ninhydrin. The absorbance of the genipin–amino acids increased linearly with increase of amino acid concentration, indicating that genipin could be a useful reagent for quantitation of amino acids. Thin layer chromatographic analysis showed that the genipin reaction produces clear and stable colored spots. The blue ninhydrin reaction spots were usually bleached in 24 h at room temperature, while the genipin reaction spots remained unchanged for several months. The addition of 0.1 mM Cu²⁺ and Fe³⁺ decreased the absorbance of Gly–ninhydrin pigment by 50% and 98%, respectively, but those metal ions did not affect the absorbance of the Gly–genipin pigment.     

Cd(II) determination in the presence of aqueous micellar solutions

The equilibrium constants and molar absorptivities for the fast formation of a 1:3 complex between cadmium(II) (Cd(II)) and dithizonate anion, in the presence of cationic and non-ionic surfactants, allowed a simple and fast spectrophotometric determination of total cadmium. Indeed, the molar absorptivities of the Cd(II)-dithizone (Dz) complex formed in the presence of the neutral Triton X-100 and cationic cetyltrimethylammonium bromide (CTAB) surfactants are almost twice the value observed in the standard method and the maxima of absorption are shifted by about 40 nm when compared with the standard method. Clearly, the use of neutral and cationic surfactants promotes a higher value of the molar absorptivities of the complex, resulting in an increase in the sensitivity of the method. Application of the method to the desorption of Cd(II) ions from clays is illustrated.     

Some azo-dye reagents for the spectrophotometric determination of cadmium

2-[2-(5-Bromopyridyl)azol-4,5-dimethylphenol (BrPDMP) and 2-[2-benzothiazolylazo)-5-dimethylaminophenol (BTADAP) have been synthesised and compared, as reagents for cadmium, with the related dyes BrPADAP and BTDMP. The new dyes both form stable highly coloured 2:1 complexes with cadmium, with molar absorptivities (in o-xylene solution) of 3.8 x 10(4) 1.mole(-1).cm(-1) at 590 nm (BrPDMP) and 4.5 x 10(4) 1.mole(-1).cm(-1) at 600 nm (BTADAP). Cadmium can be determined by extraction under alkaline conditions with a solution of BTADAP in xylene. Beer's law is obeyed up to at least 16 mug of cadmium. A limit of detection of 0.15 mug has been estimated and a coefficient of variation of 3.3% at the 5 mug level was found. The only species which interfere seriously are Co(2+), Ni(2+), and Ca(2+). A 200-fold excess of zinc may be tolerated. The method has been applied to the determination of cadmium in water samples, plant materials and hair. Interferences were overcome by preliminary extraction into Aliquat/carbon tetrachloride. The acid dissociation constant of BTADAP (pK = 9.5) and formation constant of the cadmium-BTADAP complex (log beta = 15.1) have been determined.     

Synthesis and fluorescence characteristics of novel asymmetric cyanine dyes for DNA detection

Sixteen new asymmetric monomethine cyanine dyes have been synthesized and their spectral characteristics and interaction with double stranded DNA have been investigated. The dyes absorb in the region 453–519 nm and have molar absorptivities in the range 37.900–93.100 l M^?1 cm^?1. The dyes do not have intrinsic fluorescence, but in the presence of dsDNA they exhibited a significant enhancement in fluorescence. The most pronounced increase was found for D9, D10, D12 and D16 allowing the recommendation of these dyes as the most sensitive DNA markers. Thermodynamic analysis of cyanine–DNA complexation was carried out using the McGhee & von Hippel non-cooperative excluded site model, and binding parameters have been derived. A hypothesis describing the DNA–dye binding mode has been proposed.     

HPLC separation of heterocyclic beta-diketonates of actinide, lanthanide and transition metals

Liquid-chromatography conditions for the separation of neutral chelates of 1-phenyl-3-methyl-4-benzoyl-5-pyrazolone with transition metals, lanthanides and actinides have been established. The use of reverse-phase liquid chromatography, instead of ion-exchange, is a novel approach for actinide separation. The high molar absorptivities of the beta-diketonates in the ultraviolet region allow for their detection at the nanogram level. The potential exists, therefore, for the rapid solvent extraction, concentration and determination of traces of actinides and other metals.     

Characterization of synthetic dyes for environmental and forensic assessments: A chromatography and mass spectrometry approach

Dyes have become common substances since they are employed in mostly all objects surrounding our daily activities such as clothing and upholstery. Based on the usage and disposal of these objects, the transfer of the dyes to other media such as soil and water increases their prevalence in our environment. However, this prevalence could help to solve crimes and pollution problems if detection techniques are proper. For that reason, the detection and characterization of dyes in complex matrices is important to determine the possible events leading to their deposition (natural degradation, attempts of removal, possible match with evidence, among others). Currently, there are several chromatographic and mass spectrometric approaches used for the identification of these organic molecules and their derivatives with high specificity and accuracy. This review presents current chromatographic and mass spectrometric methods that are used for the detection and characterization of disperse, acid, basic, and reactive dyes, and their derivatives.     

拓扑指数法研究显色剂结构与反应性能关系

本文讨论了２９个不对称色酸双偶氮膦酸型显色剂的分子联接性指数，并将其与结构选择性因子相结合，用于偶氮类剂结构与铈显色反应灵敏度的相关性研究，讨论了显色剂结构对显色反应灵敏度的影响。     

Quantitation of phenacyl esters of retinal fatty acids by high-performance liquid chromatography.

A high-performance liquid chromatographic (HPLC) method for the separation and quantitation of retinal fatty acids containing long-chain polyunsaturated fatty acids is described. Fatty acids from frog retinal lipids were converted to the corresponding phenacyl derivatives which were separated on a C18 reversed-phase column and detected at 242 nm. Molar absorptivities (peak area units/nmol) of up to seventeen fatty acid phenacyl derivatives were determined and used for quantitation of fatty acids separated by HPLC. Compared with gas chromatography, the HPLC method gave a similar molar percent distribution of the fatty acids and was twenty to fifty times more sensitive. This HPLC method provides a useful means for the study of chemistry and metabolism of long-chain polyunsaturated fatty acids in retina and other tissues where amounts of material may be limited or recovery of individual components desirable.     

High-performance liquid chromatography analysis of ten dyes for control of safety of commercial articles

Two high-performance liquid chromatographic methods, with ultraviolet-visible spectrophotometry detection (HPLC-UV/Vis) and with tandem mass spectrometry triple quadrupole interfaced with positive ion mode electrospray ionization detection (HPLC-ESI+-QqQ-MS/MS), for determination and quantification of ten commercial dyes are proposed for control in commercial products. Multiple peaks observed for some of the studied dyes in HPLC-UV/Vis chromatograms forced to obtain structural information by HPLC-ESI-MS/MS method with scan mode. The quality parameters of the two proposed chromatographic methods were evaluated for different requirements of normative, showing detection (LODs) and quantification (LOQs) limits around 60-890 and 200-2990 microg L(-1) for HPLC-UV/Vis, and 4.54-14.3 and 15.0-47.6 microg L(-1) for HPLC-ESI+-QqQ-MS/MS.     

Spectrophotometric Determination of Microamounts of Ruthenium Using 2-(3,5-Dichloro-2-Pyridylazo)-5-Dimethylaminophenol and its Application

Binary component colour systems of spectrophotometric determination of Ru using heterocyclic-azo reagents have been reported, but their apparent molar absorptivities are low.     

Spectrophotometric study of the complexation and extraction of chromium(VI) with cyanine dyes

Solvent extraction of chromium(VI) ion associates with symmetric cyanine dyes including the heterocyclic radicals of 1,3,3-trimethyl-3N-indoline, benzooxazol, benzothiazol and quinoline has been studied by means of spectrophotometric method. In the acidic medium in the presence of chloride ions, extractable by aromatic hydrocarbons and esters of acetic acids, chromium(VI) ion associates are formed. The molar absorptivities of ion associates are 2.5-3.6x10(5) l mol(-1) cm(-1) in dependence on extractant and dye. The absorbance of the coloured extracts obeys the Beer's law in the range 0.01-2.1 mg l(-1). The extraction of chromium is the highest during extraction from the sulphuric acid medium in the range 0.05-03 M H(2)SO(4). It was found that the Cr(VI):Cl:R molar ratio is 1:1:1. A novel procedure of chromium(VI) extraction and spectrophotometric determination in various types of soils and sewage doped with chromium(VI) was examined.     

Trace determination of some aromatic molecules by laser two-photon ionization

A simplified yet sensitiive system is described for the detection of the two-photon ionization signal in solution. The photo-ionization cell consists of a quartz cuvette and a pair of stainless steel electrodes. Several aromatic compounds, including quinones, can be detected in the ng l^?1–mg l^?1 range both in hexane and in methanol; detection limits of pyrene in hexane and in methanol are 0.02 μg l^?1 and 4 μg l^?1, respectively. The detectability in hexane is much better than that in methanol. The detection limits and the molar absorptivities at the excitation wavelength are shown to be correlated.