FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W2001020738> ?p ?o ?g. }

• W2001020738 endingPage "6020" @default.
• W2001020738 startingPage "6013" @default.
• W2001020738 abstract "The ion–ion neutralization reaction between NO+ (X 1Σ+:v″=0) and C6F−6 has been spectroscopically studied in the flowing helium afterglow. In addition to the NO(A 2Σ+–X 2Πr) emission system, which has been found in the previous studies on the NO+/NO−2 and NO+/SF−6 reactions, the NO(C 2Πr–X 2Πr, D 2Σ+–X 2Πr) emission systems are observed in the NO+/C6F−6 reaction. The relative formation rates of NO(A), NO(C), and NO(D) are evaluated to be 1.0, 0.13±0.04, and 0.24±0.04, respectively. Only the v′=0 levels of NO(A,C,D) are formed, indicating that no energy is deposited into the vibration of NO(A,C,D). The rotational distributions of NO(A:v′=0), NO(C:v′=0), and NO(D:v′=0) are expressed by single Boltzmann rotational temperature of 500±50, 300±50, and 400±50 K, respectively. The average fractions of the total available energy deposited into rotation of NO(A), NO(C), and NO(D) are evaluated to be only 1.5±0.1%, 1.4±0.2%, and 1.9±0.2%, respectively. Most of all excess energy is expected to be partitioned into translation of the products. The observed vibrational and rotational distributions are less excited than statistical prior ones, indicating that the reaction dynamics is not governed by a simple statistical theory. The excitation mechanism of NO(A,C,D) in the NO+/C6F−6 reaction is compared with those in the NO+/NO−2 and NO+/SF−6 reactions, which give only the NO(A) state." @default.
• W2001020738 created "2016-06-24" @default.
• W2001020738 creator A5028014263 @default.
• W2001020738 creator A5035412340 @default.
• W2001020738 creator A5042880630 @default.
• W2001020738 creator A5062934675 @default.
• W2001020738 date "1995-04-15" @default.
• W2001020738 modified "2023-09-26" @default.
• W2001020738 title "Formation of NO(<i>A</i> ²Σ⁺, <i>C</i> ²Π_<i>r</i>, <i>D</i> ²Σ⁺) by the ion–ion neutralization reaction between NO⁺ and C₆F₆⁻ at thermal energy" @default.
• W2001020738 cites W1965606852 @default.
• W2001020738 cites W1976459753 @default.
• W2001020738 cites W1977417621 @default.
• W2001020738 cites W1978946489 @default.
• W2001020738 cites W1998196772 @default.
• W2001020738 cites W2004470270 @default.
• W2001020738 cites W2015543253 @default.
• W2001020738 cites W2016235943 @default.
• W2001020738 cites W2029235894 @default.
• W2001020738 cites W2031596920 @default.
• W2001020738 cites W2039080011 @default.
• W2001020738 cites W2040532696 @default.
• W2001020738 cites W2042037982 @default.
• W2001020738 cites W2051022195 @default.
• W2001020738 cites W2054713188 @default.
• W2001020738 cites W2057093331 @default.
• W2001020738 cites W2068131167 @default.
• W2001020738 cites W2070343044 @default.
• W2001020738 cites W2071917344 @default.
• W2001020738 cites W2073460876 @default.
• W2001020738 cites W2086471812 @default.
• W2001020738 cites W2090660701 @default.
• W2001020738 cites W2091418955 @default.
• W2001020738 cites W2135986533 @default.
• W2001020738 cites W2141302852 @default.
• W2001020738 cites W2176599823 @default.
• W2001020738 cites W1995225098 @default.
• W2001020738 doi "https://doi.org/10.1063/1.469335" @default.
• W2001020738 hasPublicationYear "1995" @default.
• W2001020738 type Work @default.
• W2001020738 sameAs 2001020738 @default.
• W2001020738 citedByCount "10" @default.
• W2001020738 crossrefType "journal-article" @default.
• W2001020738 hasAuthorship W2001020738A5028014263 @default.
• W2001020738 hasAuthorship W2001020738A5035412340 @default.
• W2001020738 hasAuthorship W2001020738A5042880630 @default.
• W2001020738 hasAuthorship W2001020738A5062934675 @default.
• W2001020738 hasConcept C113196181 @default.
• W2001020738 hasConcept C121332964 @default.
• W2001020738 hasConcept C145148216 @default.
• W2001020738 hasConcept C148898269 @default.
• W2001020738 hasConcept C178790620 @default.
• W2001020738 hasConcept C181500209 @default.
• W2001020738 hasConcept C184779094 @default.
• W2001020738 hasConcept C185592680 @default.
• W2001020738 hasConcept C36663273 @default.
• W2001020738 hasConcept C43617362 @default.
• W2001020738 hasConcept C546029482 @default.
• W2001020738 hasConcept C62520636 @default.
• W2001020738 hasConcept C83581075 @default.
• W2001020738 hasConceptScore W2001020738C113196181 @default.
• W2001020738 hasConceptScore W2001020738C121332964 @default.
• W2001020738 hasConceptScore W2001020738C145148216 @default.
• W2001020738 hasConceptScore W2001020738C148898269 @default.
• W2001020738 hasConceptScore W2001020738C178790620 @default.
• W2001020738 hasConceptScore W2001020738C181500209 @default.
• W2001020738 hasConceptScore W2001020738C184779094 @default.
• W2001020738 hasConceptScore W2001020738C185592680 @default.
• W2001020738 hasConceptScore W2001020738C36663273 @default.
• W2001020738 hasConceptScore W2001020738C43617362 @default.
• W2001020738 hasConceptScore W2001020738C546029482 @default.
• W2001020738 hasConceptScore W2001020738C62520636 @default.
• W2001020738 hasConceptScore W2001020738C83581075 @default.
• W2001020738 hasIssue "15" @default.
• W2001020738 hasLocation W20010207381 @default.
• W2001020738 hasOpenAccess W2001020738 @default.
• W2001020738 hasPrimaryLocation W20010207381 @default.
• W2001020738 hasRelatedWork W1966240944 @default.
• W2001020738 hasRelatedWork W1983093236 @default.
• W2001020738 hasRelatedWork W1986040275 @default.
• W2001020738 hasRelatedWork W1994470540 @default.
• W2001020738 hasRelatedWork W2016535033 @default.
• W2001020738 hasRelatedWork W2030746443 @default.
• W2001020738 hasRelatedWork W2057490834 @default.
• W2001020738 hasRelatedWork W2066684722 @default.
• W2001020738 hasRelatedWork W2521421757 @default.
• W2001020738 hasRelatedWork W4239962552 @default.
• W2001020738 hasVolume "102" @default.
• W2001020738 isParatext "false" @default.
• W2001020738 isRetracted "false" @default.
• W2001020738 magId "2001020738" @default.
• W2001020738 workType "article" @default.