Matches in SemOpenAlex for { <https://semopenalex.org/work/W2276249767> ?p ?o ?g. }
- W2276249767 abstract "Products and rates of the reactions of 1,1,1-Trichlorethane, Isobutylchloride, Di-t-Butyl-Peroxide, t-Butyl-Peroxy-Pivalate and Dimethoxymethane with Fluorine atoms are examined in the gas phase in an isothermal flow reactor with continuous molecular beam sampling and mass spectrometric analysis at pressure of 1-2 mbar. The radicals Methyl, Ethyl, Allyl, 1-Propyl, 2-Propyl, 1-Butyl, 2-Butyl, Isobutyl, t-Butyl, t-Butyl, c-Pentadienyl, c-Pentyl, c-Hexyl, c-Heptyl, c-Heptyl, c-Octyl, Methoxymethyl and 2-Chlor-2-Methyl-Propyl are formed by Hydrogen atom abstraction at their corresponding precursor molecules in the gas phase at pressure of 1 - 2 mbar. They are specifically detected by resonance enhanced multi photon ionization (REMPI) in the wavelength region of 335-540 nm and coupled time of flight mass spectrometer (TOF). In this way for some of the mentioned radicals the usage of partially deuterated compounds is necessary. The 1,1,1-Trichlorethyl radical is generated by H-atom abstraction at 1,1,1-Trichlorethan. It is detected by electron impact ionization (EI) in a sector field mass spectrometer. The kinetics of the reactions of the radicals Methyl, Allyl, 1-Propyl, 2-Propyl, 1-Butyl, 2-Butyl, Isobutyl, t-Butyl, c-Pentadienyl, c-Pentyl, c-Heptyl, c-Octyl, Methoxymethyl, 2-Chlor-2-Methyl-Propyl and 1,1,1-Trichlorethyl with Oxygen atoms at room temperature is determined. The temperature dependence of the reaction of c-Octyl with O-atoms is measured in the interval 278 K - 363 K, that of the reaction of Trichlorethyl with O-atoms in interval 243 K - 363 K. The rates of the reactions Methyl + O and Ethyl + O are examined on an isotopic effect. The products of the reaction t-Butyl + O are investigated in a static photolysis cell by FTIR-detection. The kinetics of the reactions of the radicals t-Butyl, c-Pentadienyl, c-Heptyl, c-Octyl and 2-Chlor-2-Methyl-Propyl with oxygen molecules is determined at room temperature. For the reaction of c-Octyl with molecular oxygen the temperature dependence is determined in the interval 278 K - 363 K, for the reaction of t-Butyl with oxygen molecules in the interval 243 K - 363 K. The products of the reaction of t-Butyl with molecular oxygen are examined in a static photolysis cell with FTIR-detection. The kinetics of the reactions of the radicals t-Butyl, c-Heptyl, c-Heptyl, c-Octyl and 2-Chlor-2-Methyl-Propyl with ozone is determined at room temperature. The rate of the reactions of the radicals t-Butyl and Allyl with Nitrogen Monoxide is determined in the range 243 - 363 K. The kinetics of the reactions of the radicals Allyl, 2-Propyl, 2-Butyl, t-Butyl, c-Heptyl, c-Heptyl, c-Oktyl and 2-Chlor-2-Methyl-Propyl with Hydrogen atoms is determined at room temperature." @default.
- W2276249767 created "2016-06-24" @default.
- W2276249767 creator A5054467422 @default.
- W2276249767 date "2022-02-20" @default.
- W2276249767 modified "2023-09-25" @default.
- W2276249767 title "Erzeugung, Nachweis und Reaktionen reiner, teiloxidierter und substituierter Kohlenwasserstoffradikale in der Gasphase" @default.
- W2276249767 cites W1484666425 @default.
- W2276249767 cites W1508997538 @default.
- W2276249767 cites W1523080548 @default.
- W2276249767 cites W1571932167 @default.
- W2276249767 cites W1579893055 @default.
- W2276249767 cites W19445716 @default.
- W2276249767 cites W1963531569 @default.
- W2276249767 cites W1967540856 @default.
- W2276249767 cites W1969277811 @default.
- W2276249767 cites W1969763843 @default.
- W2276249767 cites W1970906886 @default.
- W2276249767 cites W1971715420 @default.
- W2276249767 cites W1978956851 @default.
- W2276249767 cites W1980369915 @default.
- W2276249767 cites W1981343038 @default.
- W2276249767 cites W1984768821 @default.
- W2276249767 cites W1987139981 @default.
- W2276249767 cites W1988774814 @default.
- W2276249767 cites W1996575155 @default.
- W2276249767 cites W1996818420 @default.
- W2276249767 cites W1997939981 @default.
- W2276249767 cites W2001177810 @default.
- W2276249767 cites W2001526405 @default.
- W2276249767 cites W2003615030 @default.
- W2276249767 cites W2003806445 @default.
- W2276249767 cites W2006875375 @default.
- W2276249767 cites W2007666980 @default.
- W2276249767 cites W2012293080 @default.
- W2276249767 cites W2013380444 @default.
- W2276249767 cites W2017399690 @default.
- W2276249767 cites W2018538924 @default.
- W2276249767 cites W2019450622 @default.
- W2276249767 cites W2024772571 @default.
- W2276249767 cites W2025632142 @default.
- W2276249767 cites W2029549258 @default.
- W2276249767 cites W2034974857 @default.
- W2276249767 cites W2039205486 @default.
- W2276249767 cites W2039495070 @default.
- W2276249767 cites W2041036478 @default.
- W2276249767 cites W2046087805 @default.
- W2276249767 cites W2048164660 @default.
- W2276249767 cites W2051554285 @default.
- W2276249767 cites W2053994687 @default.
- W2276249767 cites W2054914927 @default.
- W2276249767 cites W2056402632 @default.
- W2276249767 cites W2059203928 @default.
- W2276249767 cites W2066205058 @default.
- W2276249767 cites W2066803754 @default.
- W2276249767 cites W2067375542 @default.
- W2276249767 cites W2068199294 @default.
- W2276249767 cites W2068220576 @default.
- W2276249767 cites W2068816490 @default.
- W2276249767 cites W2069693907 @default.
- W2276249767 cites W2069844808 @default.
- W2276249767 cites W2075083733 @default.
- W2276249767 cites W2078898278 @default.
- W2276249767 cites W2080468070 @default.
- W2276249767 cites W2082284887 @default.
- W2276249767 cites W2085612992 @default.
- W2276249767 cites W2086548102 @default.
- W2276249767 cites W2113983700 @default.
- W2276249767 cites W2133967581 @default.
- W2276249767 cites W2172158857 @default.
- W2276249767 cites W2185840994 @default.
- W2276249767 cites W2478147674 @default.
- W2276249767 cites W2482852015 @default.
- W2276249767 cites W2949305622 @default.
- W2276249767 cites W299877977 @default.
- W2276249767 cites W3022998099 @default.
- W2276249767 cites W918323433 @default.
- W2276249767 doi "https://doi.org/10.53846/goediss-2137" @default.
- W2276249767 hasPublicationYear "2022" @default.
- W2276249767 type Work @default.
- W2276249767 sameAs 2276249767 @default.
- W2276249767 citedByCount "1" @default.
- W2276249767 countsByYear W22762497672022 @default.
- W2276249767 crossrefType "dissertation" @default.
- W2276249767 hasAuthorship W2276249767A5054467422 @default.
- W2276249767 hasBestOaLocation W22762497671 @default.
- W2276249767 hasConcept C121332964 @default.
- W2276249767 hasConcept C139066938 @default.
- W2276249767 hasConcept C145148216 @default.
- W2276249767 hasConcept C147789679 @default.
- W2276249767 hasConcept C155647269 @default.
- W2276249767 hasConcept C162356407 @default.
- W2276249767 hasConcept C178790620 @default.
- W2276249767 hasConcept C185592680 @default.
- W2276249767 hasConcept C198291218 @default.
- W2276249767 hasConcept C205759337 @default.
- W2276249767 hasConcept C43617362 @default.
- W2276249767 hasConcept C58364064 @default.
- W2276249767 hasConcept C62520636 @default.
- W2276249767 hasConcept C75473681 @default.
- W2276249767 hasConcept C81022585 @default.