Radical routes to interstellar glycolaldehyde. The possibility of stereoselectivity in gas-phase polymerization reactions involving CH₂O and·CH₂OH

dc.contributor.authorWang, T.
dc.contributor.authorBowie, J.
dc.date.issued2010
dc.description.abstractA previous report that the interstellar molecule glycolaldehyde (HOCH₂CHO) can be made from hydroxymethylene (HOCH:) and formaldehyde has been revisited at the CCSD(T)/6-311++G(3df,2p)//MP2/6-311++G(3df,2p) level of theory. This reaction competes with the formation of acetic acid and methylformate, molecules which have also been detected in interstellar clouds. Other possible modes of formation of glycolaldehyde by radical/radical reactions have been shown to be viable theoretically as follows: HO• + •CH₂CHO→HOCH₂CHO [ΔGr(298 K) = -303 kJ mol⁻ ¹] HOCH₂• + •CHO→HOCH₂CHO (-259 kJ mol⁻¹). The species in these two processes are known interstellar molecules. Key radicals •CH₂CHO and •CH₂OH in these sequences have been shown to be stable for the microsecond duration of neutralization/reionization experiments in the dual collision cells of a VG ZAB 2HF mass spectrometer. The polymerization reaction HOCH₂CH•OH + nCH₂O→HOCH₂[CH(OH)]n •CHOH (n = 1 to 3) has been studied theoretically and shown to be energetically feasible, as is the cyclization reaction of HOCH₂[(CH₂OH)₄] •CHOH (in the presence of one molecule of water at the reacting centre) to form glucose. The probability of such a reaction sequence is small even if polymerization were to occur in interstellar ice containing a significant concentration of CH₂O. The large number of stereoisomers produced by such a reaction sequence makes the formation of a particular sugar, again for example glucose, an inefficient synthesis. The possibility of stereoselectivity occurring during the polymerization was investigated for two diastereoisomers of HOCH₂[(CHOH)]₂ •CHOH. No significant difference was found in the transition state energies for addition of CH₂O to these two diastereoisomers, but a barrier difference of 12 kJ mol⁻¹ was found for the H transfer reactions •OCH₂[(CHOH)]₂CH₂OH→HOCH₂[(CHOH)₂ •CHOH of the two diastereoisomers.
dc.description.statementofresponsibilityTianfang Wang and John H. Bowie
dc.identifier.citationOrganic and Biomolecular Chemistry, 2010; 8(20):4757-4766
dc.identifier.doi10.1039/C0OB00125B
dc.identifier.issn1477-0520
dc.identifier.issn1477-0539
dc.identifier.urihttp://hdl.handle.net/2440/62189
dc.language.isoen
dc.publisherRoyal Soc Chemistry
dc.relation.grantARC
dc.rightsThis journal is © The Royal Society of Chemistry 2010
dc.source.urihttps://doi.org/10.1039/c0ob00125b
dc.subjectHydroxyl Radical
dc.subjectAcetaldehyde
dc.subjectEthylenes
dc.subjectKinetics
dc.subjectThermodynamics
dc.subjectPolymerization
dc.titleRadical routes to interstellar glycolaldehyde. The possibility of stereoselectivity in gas-phase polymerization reactions involving CH₂O and·CH₂OH
dc.title.alternativeRadical routes to interstellar glycolaldehyde. The possibility of stereoselectivity in gas-phase polymerization reactions involving CH(2)O and (.)CH(2)OH
dc.typeJournal article
pubs.publication-statusPublished

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