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Studies on photodissociation dynamics of butadiene monoxide at 193 nm.

Studies on photodissociation dynamics of butadiene monoxide at 193 nm. Research Abstract Details 

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  • Studies on photodissociation dynamics of butadiene monoxide at 193 nm. Abstract Text:

    sumana senguptaSumana Sengupta,yogesh indulkarYogesh Indulkar,awadhesh kumarAwadhesh Kumar,prakash d naikPrakash D Naik,paramanand bajajParamanand Bajaj,sumana senguptaSumana Sengupta,yogesh indulkarYogesh Indulkar,awadhesh kumarAwadhesh Kumar,prakash d naikPrakash D Naik,paramanand bajajParamanand Bajaj,sumana senguptaSumana Sengupta,yogesh indulkarYogesh Indulkar,awadhesh kumarAwadhesh Kumar,prakash d naikPrakash D Naik,paramanand bajajParamanand Bajaj,

    Butadiene monoxide (BMO) undergoes the S(0)-->S(1) transition, involving the excitation of both pi and n electrons to pi(*) orbital, at 193 nm. After relaxing to the ground electronic state via internal conversion, BMO molecules undergo intramolecular rearrangement and subsequently dissociate to form unexpected OH radicals, which were detected state selectively by laser-induced fluorescence technique, and the energy state distribution was measured. OH is produced vibrationally cold, OH(nu(")=0,J(")), with the rotational population characterized by a rotational temperature of 456+/-70 K. The major portion ( approximately 60%) of the available energy is partitioned into internal degrees of the photofragments, namely, vibration and rotation. A considerable portion (25%-35%) also goes to the relative translation of the products. The Lambda doublet and spin-orbit ratios of OH were measured to be nearly unity, implying statistical distribution of these states and, hence, no preference for any of the Lambda doublet (Lambda(+) and Lambda(-)) and spin-orbit (Pi(32) and Pi(12)) states. Formation time of the nascent OH radical was measured to be <100 ns. Different products, such as crotonaldehyde and methyl vinyl ketone, were detected by gas chromatography as stable products of photodissociation. A reaction mechanism for the formation of all these photoproducts, transient and stable, is proposed. The multiple pathways by which these products can be formed have been theoretically optimized, and energies have been calculated. Absorption cross section of BMO at 193 nm was measured, and quantum yield of OH generation channel was also determined.

    Studies on photodissociation dynamics of butadiene monoxide at 193 nm. Publishing Authors By Initials

    s senguptaS Sengupta,y indulkarY Indulkar,a kumarA Kumar,pd naikPD Naik,p bajajP Bajaj,s senguptaS Sengupta,y indulkarY Indulkar,a kumarA Kumar,pd naikPD Naik,p bajajP Bajaj,s senguptaS Sengupta,y indulkarY Indulkar,a kumarA Kumar,pd naikPD Naik,p bajajP Bajaj,

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    Studies on photodissociation dynamics of butadiene monoxide at 193 nm. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: The Journal of chemical physics

    VOLUME: 128

    Page Numbers: 024309

    Journal Abbreviation:

    ISSN: 0021-9606

    DAY: 14

    MONTH: Jan

    YEAR: 2008

    Studies on photodissociation dynamics of butadiene monoxide at 193 nm. Information

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    LANGUAGE: eng

    NlmUniqueID: 375360

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    Grant and Affiliation Information for Studies on photodissociation dynamics of butadiene monoxide at 193 nm.

    AFFILIATION: Radiation and Photochemistry Division, Bhabha Atomic Research Centre, Mumbai 400085, India.

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: J Chem Phys

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