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Crystal structures of polymorphs of 2-(2'-hydroxyphenyl)benzimidazole (HPBI), Forms α and β, are analyzed by X-ray crystallography. The fluorescence excitation (FE) and fluorescence spectra of the polymorphs are separately observed at temperatures 77-298 K. It has been found that the electronic spectra of the two crystal forms are significantly different from each other. Photo-excitation of the enol forms in Forms α and β induces the excited-state intramolecular proton transfer (ESIPT) to produce the S(1) state of the keto forms. In the FE spectra of Forms α and β, the S(1) ← S(0) (ππ*) transition of the keto form is observed in the 360-420 nm region in addition to that of the enol form in the 250-420 nm region. In the FE spectrum of Form β a new band peaking at 305 nm is observed, which is assigned to the S(1) ← S(0) transition of a non-planar enol form based on the observation of dual fluorescence in the UV and visible regions and quantum chemical calculation on the transition energy against the twisted angle between the benzimidazole and hydroxyphenyl rings. The fluorescence quantum yield (φ(T)) for the keto form is remarkably dependent on polymorphs at room temperature; φ(T) = 0.53 for Form α is much larger than φ(T) ≤ 0.23 for Form β. At 77 K the φ(T) values for Forms α and β increase to 0.67 and ≤0.57, respectively. The changes in the φ(T) values are associated with the intramolecular charge transfer (ICT) state. The potential barrier height between the S(1)-keto and S(1)-ICT states is significantly lower for Form β than for Form α. At 77 K the S(1)-keto → S(1)-ICT process followed by S(1)-ICT → S(0)-keto internal conversion is significantly suppressed in Form β. We compare difference in the dynamics between Forms α and β in the electronic ground and excited states.

This study was conducted to assess the bacteriological quality of alternative drinking water supply options in southwest coastal areas of Bangladesh. A total of 90 water samples were collected during both dry and wet seasons from household based rainwater harvesting systems (RWHSs), community based rain water harvesting systems (CRWHSs), pond-sand filters (PSFs) and ponds. The samples were evaluated for faecal coliform, Escherichia coli and Heterotrophic Plate Count, as well as Vibrio cholerae, Salmonella spp., Shigella spp. and Pseudomonas spp. Physico-chemical parameters (pH, electrical conductivity, and color) were also examined. In addition, sanitary inspections were conducted to identify faecal contamination sources. All options showed varying degrees of indicator bacterial contamination. The median E. coli concentrations measured for RWHSs, CRWHSs, PSFs, and ponds were 16, 7, 11, and 488 cfu/100 ml during the wet season, respectively. Vibrio cholerae O1/O139, Salmonella and Shigella spp. were not found in any samples. However, Vibrio cholerae Non-O1/Non-O139 and Pseudomonas spp. were isolated from 74.4% and 91.1% of the water samples collected during the wet season. A maximum pH of 10.4 was found in CRWHSs. Estimation of the disease burden for all options in disability adjusted life years (DALYs) showed an increased disease burden during the wet season. According to sanitary inspections, poor maintenance and unprotected ponds were responsible for rainwater and PSF water contamination, respectively.The findings of the present study suggest that alternative drinking water supply options available in southwest coastal Bangladesh pose a substantial risk to public health.

Photoreaction mechanisms of 6-hydroxyquinoline (6-HQ) and 7-hydroxyquinoline (7-HQ) in low-temperature argon matrixes have been investigated by Fourier transform infrared (IR) spectroscopy and density-functional-theory (DFT) calculations. A comparison of the observed IR spectra of reactants with the corresponding calculated spectral patterns obtained by the DFT method led to the conclusion that the hydrogen atoms in the O-H group of 6-HQ and in that of 7-HQ are selectively located at the outer position against the quinoline ring. When the matrix samples were irradiated upon UV light around 300 nm, IR spectra of unknown chemical species were observed; they were assigned to the photoreaction intermediates, quinolinoxyl radicals and ketene compounds, produced by eliminations of a hydrogen atom and a hydrogen molecule, respectively. In the photoreaction of 7-HQ, a small amount of keto form was also produced by intramolecular hydrogen-atom transfer from oxygen to nitrogen in an argon cage. Kinetic analyses were made by assuming that 5-ketene and 6-ketene were produced from 6-HQ, while 6-ketene and 7-ketene were produced from 7-HQ. The effective rate constants estimated from the absorbance changes of IR bands against irradiation time revealed that the reaction pathway to produce 6-ketene was minor in both HQs, leading to the conclusion that the conformation of reactants, HQs, plays an important role in the photoproduction of ketenes through biradicals in the Wolff rearrangement.

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