@Article{Hockett2007,
  Title                    = {Complete determination of the photoionization dynamics of a polyatomic molecule. I. Experimental photoelectron angular distributions from à Au1 acetylene},
  Author                   = {Hockett, P., King, A.K., Powis, I., Reid, K.L.},
  Journal                  = {Journal of Chemical Physics},
  Year                     = {2007},
  Number                   = {15},
  Volume                   = {127},

  Abstract                 = {Angle-resolved photoelectron spectra from rotationally selected à Au1 state acetylene have been recorded using velocity-map imaging. Several Renner-Teller split vibrational bands have been observed and assigned, showing good agreement with previous zero kinetic energy photoelectron (ZEKE) work [S. T. Pratt, P. M. Dehmer, and J. L. Dehmer, J. Chem. Phys. 99, 6233 (1993); S.-J. Tang, Y.-C. Chou, J. J.-M. Lin, and Y.-C. Hsu, ibid. 125, 133201 (2006).] The extracted photoelectron angular distributions (PADs) corresponding to these bands show a strong dependence on the vibronic angular momentum projection quantum number K+. Subbands with odd K+ show PADs with maximum intensity along the polarization vector of the ionizing laser beam, while those with even K+ show PADs with maximum intensity perpendicular to this direction. Velocity-map images recorded at low photoelectron energies approach rotational resolution of the ion, and the evolution of the PADs with increasing rotational level prepared in the à Au1 state indicates the potential of a "complete" determination of the photoionization dynamics of the à Au1 state. This is further investigated in the following paper. © 2007 American Institute of Physics.},
  Affiliation              = {School of Chemistry, University of Nottingham, Nottingham NG7 2RD, United Kingdom},
  Art_number               = {154307},
  Document_type            = {Article},
  Doi                      = {10.1063/1.2790442},
  Source                   = {Scopus},
  Timestamp                = {2016.03.02},
  Url                      = {http://www.scopus.com/inward/record.url?eid=2-s2.0-39349090837&partnerID=40&md5=2c5ab209e45a44d6714b3f55db7a4fdb}
}

{"_id":"uidricTXN2fS7WXbJ","bibbaseid":"hockett-king-powis-reid-completedeterminationofthephotoionizationdynamicsofapolyatomicmoleculeiexperimentalphotoelectronangulardistributionsfromau1acetylene-2007","downloads":0,"creationDate":"2016-03-02T15:16:44.754Z","title":"Complete determination of the photoionization dynamics of a polyatomic molecule. I. Experimental photoelectron angular distributions from à Au1 acetylene","author_short":["Hockett, P.","King, A.","Powis, I.","Reid, K."],"year":2007,"bibtype":"article","biburl":"http://github.com/phockett/UQO-group/raw/main/group_ongoing.bib","bibdata":{"bibtype":"article","type":"article","title":"Complete determination of the photoionization dynamics of a polyatomic molecule. I. Experimental photoelectron angular distributions from à Au1 acetylene","author":[{"propositions":[],"lastnames":["Hockett"],"firstnames":["P."],"suffixes":[]},{"propositions":[],"lastnames":["King"],"firstnames":["A.K."],"suffixes":[]},{"propositions":[],"lastnames":["Powis"],"firstnames":["I."],"suffixes":[]},{"propositions":[],"lastnames":["Reid"],"firstnames":["K.L."],"suffixes":[]}],"journal":"Journal of Chemical Physics","year":"2007","number":"15","volume":"127","abstract":"Angle-resolved photoelectron spectra from rotationally selected à Au1 state acetylene have been recorded using velocity-map imaging. Several Renner-Teller split vibrational bands have been observed and assigned, showing good agreement with previous zero kinetic energy photoelectron (ZEKE) work [S. T. Pratt, P. M. Dehmer, and J. L. Dehmer, J. Chem. Phys. 99, 6233 (1993); S.-J. Tang, Y.-C. Chou, J. J.-M. Lin, and Y.-C. Hsu, ibid. 125, 133201 (2006).] The extracted photoelectron angular distributions (PADs) corresponding to these bands show a strong dependence on the vibronic angular momentum projection quantum number K+. Subbands with odd K+ show PADs with maximum intensity along the polarization vector of the ionizing laser beam, while those with even K+ show PADs with maximum intensity perpendicular to this direction. Velocity-map images recorded at low photoelectron energies approach rotational resolution of the ion, and the evolution of the PADs with increasing rotational level prepared in the à Au1 state indicates the potential of a \"complete\" determination of the photoionization dynamics of the à Au1 state. This is further investigated in the following paper. © 2007 American Institute of Physics.","affiliation":"School of Chemistry, University of Nottingham, Nottingham NG7 2RD, United Kingdom","art_number":"154307","document_type":"Article","doi":"10.1063/1.2790442","source":"Scopus","timestamp":"2016.03.02","url":"http://www.scopus.com/inward/record.url?eid=2-s2.0-39349090837&partnerID=40&md5=2c5ab209e45a44d6714b3f55db7a4fdb","bibtex":"@Article{Hockett2007,\n Title = {Complete determination of the photoionization dynamics of a polyatomic molecule. I. Experimental photoelectron angular distributions from à Au1 acetylene},\n Author = {Hockett, P., King, A.K., Powis, I., Reid, K.L.},\n Journal = {Journal of Chemical Physics},\n Year = {2007},\n Number = {15},\n Volume = {127},\n\n Abstract = {Angle-resolved photoelectron spectra from rotationally selected à Au1 state acetylene have been recorded using velocity-map imaging. Several Renner-Teller split vibrational bands have been observed and assigned, showing good agreement with previous zero kinetic energy photoelectron (ZEKE) work [S. T. Pratt, P. M. Dehmer, and J. L. Dehmer, J. Chem. Phys. 99, 6233 (1993); S.-J. Tang, Y.-C. Chou, J. J.-M. Lin, and Y.-C. Hsu, ibid. 125, 133201 (2006).] The extracted photoelectron angular distributions (PADs) corresponding to these bands show a strong dependence on the vibronic angular momentum projection quantum number K+. Subbands with odd K+ show PADs with maximum intensity along the polarization vector of the ionizing laser beam, while those with even K+ show PADs with maximum intensity perpendicular to this direction. Velocity-map images recorded at low photoelectron energies approach rotational resolution of the ion, and the evolution of the PADs with increasing rotational level prepared in the à Au1 state indicates the potential of a \"complete\" determination of the photoionization dynamics of the à Au1 state. This is further investigated in the following paper. © 2007 American Institute of Physics.},\n Affiliation = {School of Chemistry, University of Nottingham, Nottingham NG7 2RD, United Kingdom},\n Art_number = {154307},\n Document_type = {Article},\n Doi = {10.1063/1.2790442},\n Source = {Scopus},\n Timestamp = {2016.03.02},\n Url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-39349090837&partnerID=40&md5=2c5ab209e45a44d6714b3f55db7a4fdb}\n}\n\n","author_short":["Hockett, P.","King, A.","Powis, I.","Reid, K."],"key":"Hockett2007","id":"Hockett2007","bibbaseid":"hockett-king-powis-reid-completedeterminationofthephotoionizationdynamicsofapolyatomicmoleculeiexperimentalphotoelectronangulardistributionsfromau1acetylene-2007","role":"author","urls":{"Paper":"http://www.scopus.com/inward/record.url?eid=2-s2.0-39349090837&partnerID=40&md5=2c5ab209e45a44d6714b3f55db7a4fdb"},"metadata":{"authorlinks":{}},"downloads":0},"search_terms":["complete","determination","photoionization","dynamics","polyatomic","molecule","experimental","photoelectron","angular","distributions","au1","acetylene","hockett","king","powis","reid"],"keywords":[],"authorIDs":[],"dataSources":["6KGmJxs9RrDfHzcu8","ZeSAiiSynrZYWcdaA","74PaJ3jeYTJQFhBLi","Cyvp3egaEX9XcqyzN","YfcyZnFA2cDJDftuJ","9YtT85enAASHbgEpa","BqutdYRmHLywqGRJb"]}