Pre-mechanism for the Swern Oxidation: formation of chlorosulfonium chloride.

DOI: 10.14469/hpc/13151 Metadata

Created: 2023-08-25 06:41

Last modified: 2023-09-05 08:45

Author: Henry Rzepa

License: Creative Commons: Public Domain Dedication 1.0

Funding: (none given)

Description

Gaussian 16 calculations

Member of collection / collaboration

DOIDescription
10.14469/hpc/177 Computation data for Henry Rzepa's blog

Members

DOIDescription
10.14469/hpc/13159 DMSO + oxalyl chloride, TS3 for CO2/CO elimination , S-inv, G = -1699.572121 ==> Def2-TZVPP, G = -1700.501179, IRC
10.14469/hpc/13162 DMSO + oxalyl chloride, TS1 for addn/elim of sulfoxide, G = -1699.559436 Def2-TZVPP, G = -1700.487258 IRC
10.14469/hpc/13163 DMSO + oxalyl chloride, TS2 for pseudorotation to convert eq Cl to ax Cl, G = -1699.544684 ==> Def2-TZVPP, G = -1700.477737 IRC
10.14469/hpc/13165 DMSO + oxalyl chloride, TS2 for pseudorotation to convert eq Cl to ax Cl, Def2-TZVPP, G = -1700.477737 ==> oxalyl rotamer G = -1700.476097 IRC
10.14469/hpc/13166 DMSO + oxalyl chloride, TS2 for pseudorotation to convert eq Cl to ax Cl, Def2-TZVPP, G = -1700.477737 ==> oxalyl rotamer G = -1700.476097 IRC, phase(4,16)
10.14469/hpc/13126 DMSO + oxalyl chloride, TS3 for CO2/CO elimination , G =-1699.564183, IRC
10.14469/hpc/13127 DMSO + oxalyl chloride, TS3 for CO2/CO elimination , G = -1699.564183
10.14469/hpc/13128 DMSO + oxalyl chloride, TS3 for CO2/CO elimination , S-inv, G = -1699.572121
10.14469/hpc/13129 DMSO + oxalyl chloride, TS3 for CO2/CO elimination , S-inv, G = -1699.572121, IRC
10.14469/hpc/13130 DMSO + oxalyl chloride, TS3 for addn/elim of sulfoxide, G = -1699.559436
10.14469/hpc/13131 DMSO + oxalyl chloride, TS1 for addn/elim of sulfoxide, G = -1699.559436, IRC
10.14469/hpc/13152 DMSO + oxalyl chloride, TS3 for CO2/CO elimination , S-inv, G = -1699.572121 ==> Product (ax/eq) G = -1700.541813
10.14469/hpc/13132 DMSO + oxalyl chloride, TS2 for pseudorotation to convert eq Cl to ax Cl, G = -1699.544684
10.14469/hpc/13133 DMSO + oxalyl chloride, TS2 for pseudorotation to convert eq Cl to ax Cl, G = -1699.544684, IRC
10.14469/hpc/13149 DMSO + oxalyl chloride, TS3 for CO2/CO elimination , S-inv, G = -1699.572121, IRC, phase(3,4)
10.14469/hpc/13147 DMSO + oxalyl chloride, TS1 for addn/elim of sulfoxide, G = -1699.559436 Def2-TZVPP, G = -1700.487258
10.14469/hpc/13150 DMSO + oxalyl chloride, TS3 for CO2/CO elimination , S-inv, G = -1699.572121 ==> Product (ax/ax) G = -1700.562974
10.14469/hpc/13161 DMSO + oxalyl chloride, TS1 for addn/elim of sulfoxide, Def2-TZVPP, G = -1700.487258 ==> oxalyl rotamer, G = -1700.483214
10.14469/hpc/13148 DMSO + oxalyl chloride, Reactant (s-trans), G = -1700.503340 s-cis -1700.501382
10.14469/hpc/13164 DMSO + oxalyl chloride, TS1 for addn/elim of sulfoxide, Def2-TZVPP, G = -1700.487258 I ==> s-cis oxalyl rotamer, G = -1700.483214, IRC
10.14469/hpc/13160 DMSO + oxalyl chloride, TS2 for pseudorotation to convert eq Cl to ax Cl, Def2-TZVPP, G = -1700.477737 ==> s-cis oxalyl rotamer G = -1700.476097
10.14469/hpc/13135 DMSO + oxalyl chloride, TS3 for CO2/CO elimination , S-inv, Def2-TZVPP, G = -1700.501179
10.14469/hpc/13134 DMSO + oxalyl chloride, TS2 for pseudorotation to convert eq Cl to ax Cl, Def2-TZVPP, G = -1700.477737

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