COS Photoinitiated cis–trans Isomerization of 2-Butenes in the Gas Phase: A Chain Process

It is found that 2-butenes cleanly undergo cis–trans isomerization by a chain process when the gaseous mixtures of COS and cis-2-butene (or trans-2-butene) is photolyzed at 2537 Å; no intramolecular doublebond migration in 2-butenes is observed and the process is largely homogeneous. The catalytic c...

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Veröffentlicht in:The Journal of chemical physics 1969-09, Vol.51 (5), p.2024-2034
Hauptverfasser: Schmidt, Manfred W., Lee, Edward K. C.
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Lee, Edward K. C.
description It is found that 2-butenes cleanly undergo cis–trans isomerization by a chain process when the gaseous mixtures of COS and cis-2-butene (or trans-2-butene) is photolyzed at 2537 Å; no intramolecular doublebond migration in 2-butenes is observed and the process is largely homogeneous. The catalytic chain initiator is proposed to be the ground-electronic-state S atom (3P) which is produced by the photodecomposition of COS. The quantum yield of trans-2-butene resulting from the gaseous mixture of COS (1.0 torr) and cis-2-butene (2.5 torr) is (2.3 ± 0.5) × 102 at room temperature, and the chain length is estimated to be (1 − 3) × 103. The photostationary-state ratio of trans to cis, [(t-B) / (c-B)]Pss, and the initial isomerizationrate ratio, [Rc→t / Rt→c], have been determined to be 2.83 ± 0.06 and 2.8 ± 0.2, respectively. A competitive quenching study has been carried out to determine the efficiencies of various chain terminators. 1,3-Butadiene is found to be the most efficient terminator, more efficient than O2 or mono-olefins by 3 orders of magnitude.
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C.</creator><creatorcontrib>Schmidt, Manfred W. ; Lee, Edward K. C.</creatorcontrib><description>It is found that 2-butenes cleanly undergo cis–trans isomerization by a chain process when the gaseous mixtures of COS and cis-2-butene (or trans-2-butene) is photolyzed at 2537 Å; no intramolecular doublebond migration in 2-butenes is observed and the process is largely homogeneous. The catalytic chain initiator is proposed to be the ground-electronic-state S atom (3P) which is produced by the photodecomposition of COS. The quantum yield of trans-2-butene resulting from the gaseous mixture of COS (1.0 torr) and cis-2-butene (2.5 torr) is (2.3 ± 0.5) × 102 at room temperature, and the chain length is estimated to be (1 − 3) × 103. The photostationary-state ratio of trans to cis, [(t-B) / (c-B)]Pss, and the initial isomerizationrate ratio, [Rc→t / Rt→c], have been determined to be 2.83 ± 0.06 and 2.8 ± 0.2, respectively. 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C.</creatorcontrib><title>COS Photoinitiated cis–trans Isomerization of 2-Butenes in the Gas Phase: A Chain Process</title><title>The Journal of chemical physics</title><description>It is found that 2-butenes cleanly undergo cis–trans isomerization by a chain process when the gaseous mixtures of COS and cis-2-butene (or trans-2-butene) is photolyzed at 2537 Å; no intramolecular doublebond migration in 2-butenes is observed and the process is largely homogeneous. The catalytic chain initiator is proposed to be the ground-electronic-state S atom (3P) which is produced by the photodecomposition of COS. The quantum yield of trans-2-butene resulting from the gaseous mixture of COS (1.0 torr) and cis-2-butene (2.5 torr) is (2.3 ± 0.5) × 102 at room temperature, and the chain length is estimated to be (1 − 3) × 103. The photostationary-state ratio of trans to cis, [(t-B) / (c-B)]Pss, and the initial isomerizationrate ratio, [Rc→t / Rt→c], have been determined to be 2.83 ± 0.06 and 2.8 ± 0.2, respectively. 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C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>COS Photoinitiated cis–trans Isomerization of 2-Butenes in the Gas Phase: A Chain Process</atitle><jtitle>The Journal of chemical physics</jtitle><date>1969-09-01</date><risdate>1969</risdate><volume>51</volume><issue>5</issue><spage>2024</spage><epage>2034</epage><pages>2024-2034</pages><issn>0021-9606</issn><eissn>1089-7690</eissn><abstract>It is found that 2-butenes cleanly undergo cis–trans isomerization by a chain process when the gaseous mixtures of COS and cis-2-butene (or trans-2-butene) is photolyzed at 2537 Å; no intramolecular doublebond migration in 2-butenes is observed and the process is largely homogeneous. The catalytic chain initiator is proposed to be the ground-electronic-state S atom (3P) which is produced by the photodecomposition of COS. The quantum yield of trans-2-butene resulting from the gaseous mixture of COS (1.0 torr) and cis-2-butene (2.5 torr) is (2.3 ± 0.5) × 102 at room temperature, and the chain length is estimated to be (1 − 3) × 103. The photostationary-state ratio of trans to cis, [(t-B) / (c-B)]Pss, and the initial isomerizationrate ratio, [Rc→t / Rt→c], have been determined to be 2.83 ± 0.06 and 2.8 ± 0.2, respectively. A competitive quenching study has been carried out to determine the efficiencies of various chain terminators. 1,3-Butadiene is found to be the most efficient terminator, more efficient than O2 or mono-olefins by 3 orders of magnitude.</abstract><doi>10.1063/1.1672296</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record>
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title COS Photoinitiated cis–trans Isomerization of 2-Butenes in the Gas Phase: A Chain Process
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