146 research outputs found

    Excited state dynamics of Michler's ketone: a laser flash photolysis study

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    Steady state absorption and fluorescence as well as the time resolved absorption studies in the pico and subpicosecond time domain have been performed to characterize the excited singlet and triplet states of Michler's ketone (MK). The nature of the lowest excited singlet (S1) and triplet (T1) states depends on the polarity of the solvent - in nonpolar solvents they have either pure nπ∗ character or mixed character of π ∗ and π π ∗ states but in more polar solvents the states have CT character. Concentration dependence of the shapes of the fluorescence as well the excited singlet and triplet absorption spectra provide the evidence for the association of the MK molecules in the ground state

    Solvatochromism, aggregation and photochemical properties of Fullerenes, C<SUB>60</SUB> and C<SUB>70</SUB>, in solution

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    Fullerenes, C60 and C70, display interesting physicochemical properties in solutions, especially due to their unique chemical structures and their good electron accepting abilities. Solubility of fullerenes in different organic solvents and their unusual solvatochromic behavior, the ability of the fullerenes to form aggregates in solutions, and their electron transfer and charge transfer interactions with variety of electron donors, are the subjects of extensive research activities for more than one decade. Many research groups including ours have contributed substantially in the understanding of the solvatochromism, aggregation behavior, and the photoinduced electron transfer and charge transfer chemistry of fullerenes, in condensed phase. Present article is aimed to summarize the important results reported on the above aspects of fullerenes, subsequent to the earlier report from our group. (D.K. Palit and J.P. Mittal, Full. Sci. &amp; Tech. 3, 1995, 643-659)

    Laser-induced fluorescence study of the hydrogen atom formation dynamics in the 248 nm gas-phase photodissociation of vibrational state selected water (H<SUB>2</SUB>O (|04<SUP>-</SUP>&gt;))

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    The vibrationally-mediated H2O gas-phase photodissociation was studied at a photolysis wavelength of 248 nm. Single rotational states of the |03-&gt;|2&gt; and |04.&gt; H2O overtone vibrations were prepared by laser photoexcitation around 720 nm. H atoms formed in the photodissociation of the H2O (|04-&gt;J'KaKc = 313) were detected by Lyman-&#945; laser-induced fluorescence spectroscopy with sub-Doppler resolution to determine their translational energy. The present result confirms that in the dissociation process the major part (ca. 93%) of the available energy is released as relative translational energy of the nascent H + OH photofragments, in agreement with earlier complementary measurements (R. L. Vander Wal, J. L. Scott and F. F. Crim, J. Chem. Phys. 94, 1859 (1991)), where the internal excitation of the OH product radical was investigated at different photolysis wavelengths

    Later Photochemietry of UF6

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    Excited states and electron transfer reactions of C<sub>60</sub>(OH)<sub>18</sub> in aqueous solution

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    Dynamic light scattering of fullerenol solutions [C60(OH)18] reveals evidence for the formation of fullerene aggregates at high solute concentration (up to 3.85×10-2 mol dm-3). This hydrophilic fullerene derivative emits very weak fluorescence regardless of its concentration. Photolysis (35 ps; &#955;ex=355 nm) of C60(OH)18 in aqueous solution yields the immediate formation of a transient singlet excited state with broad absorption in the 550–800 nm region with &#949;670nm=2130 d mol-1 cm-1. The energetically higher-lying singlet excited state transforms via intersystem crossing (i.e., with &#964;1/2=500 ps) to the also broadly absorbing (550-800 nm), triplet excited state. In contrast, at low solute concentration, the features of the (&#8727;T1&#8594;&#8727;Tn) absorption differ significantly exhibiting an absorption maximum at 650 nm concomitant to a shoulder at 570 nm. The &#960;-radical anion of fullerenol, [C60(OH)18]&#183;&#8722;, generated by electron transfer from hydrated electrons and (CH3)2C(OH) radicals, absorbs with &#955;max at 870, 980 and 1050 nm. Based on electron transfer studies with suitable electron donor/acceptor substrates, the reduction potential of the C60(OH)18/[C60(OH)18]&#183;&#8722; couple was estimated to be in the range between -0.358 and -0.465 V vs. NHE

    What do we know about chronic kidney disease in India: first report of the Indian CKD registry

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    <p>Abstract</p> <p>Background</p> <p>There are no national data on the magnitude and pattern of chronic kidney disease (CKD) in India. The Indian CKD Registry documents the demographics, etiological spectrum, practice patterns, variations and special characteristics.</p> <p>Methods</p> <p>Data was collected for this cross-sectional study in a standardized format according to predetermined criteria. Of the 52,273 adult patients, 35.5%, 27.9%, 25.6% and 11% patients came from South, North, West and East zones respectively.</p> <p>Results</p> <p>The mean age was 50.1 ± 14.6 years, with M:F ratio of 70:30. Patients from North Zone were younger and those from the East Zone older. Diabetic nephropathy was the commonest cause (31%), followed by CKD of undetermined etiology (16%), chronic glomerulonephritis (14%) and hypertensive nephrosclerosis (13%). About 48% cases presented in Stage V; they were younger than those in Stages III-IV. Diabetic nephropathy patients were older, more likely to present in earlier stages of CKD and had a higher frequency of males; whereas those with CKD of unexplained etiology were younger, had more females and more frequently presented in Stage V. Patients in lower income groups had more advanced CKD at presentation. Patients presenting to public sector hospitals were poorer, younger, and more frequently had CKD of unknown etiology.</p> <p>Conclusions</p> <p>This report confirms the emergence of diabetic nephropathy as the pre-eminent cause in India. Patients with CKD of unknown etiology are younger, poorer and more likely to present with advanced CKD. There were some geographic variations.</p

    Development of the PSYCHS: Positive SYmptoms and Diagnostic Criteria for the CAARMS Harmonized with the SIPS

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    Aim: To harmonize two ascertainment and severity rating instruments commonly used for the clinical high risk syndrome for psychosis (CHR-P): the Structured Interview for Psychosis-risk Syndromes (SIPS) and the Comprehensive Assessment of At-Risk Mental States (CAARMS). Methods: The initial workshop is described in the companion report from Addington et al. After the workshop, lead experts for each instrument continued harmonizing attenuated positive symptoms and criteria for psychosis and CHR-P through an intensive series of joint videoconferences. Results: Full harmonization was achieved for attenuated positive symptom ratings and psychosis criteria, and modest harmonization for CHR-P criteria. The semi-structured interview, named Positive SYmptoms and Diagnostic Criteria for the CAARMS Harmonized with the SIPS (PSYCHS), generates CHR-P criteria and severity scores for both CAARMS and SIPS. Conclusions: Using the PSYCHS for CHR-P ascertainment, conversion determination, and attenuated positive symptom severity rating will help in comparing findings across studies and in meta-analyses
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