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# b3lyp/6-31+g(d,p) opt(readfc,Z-matrix,maxcycle=200) # freq=Noraman t
est geom=allcheck guSample TextSample Textess=read
Êý¾Ý£¨RC£©£º
Zero-point correction        0.390102        0.389708
Thermal correction to Energy        0.417702        0.417416
Thermal correction to Enthalpy        0.418646        0.418360
Thermal correction to Gibbs Free Energy        0.323077        0.322155
Sum of electronic and zero-point Energies        -1201.663854        -1201.658909
Sum of electronic and thermal Energies        -1201.636254        -1201.631201
Sum of electronic and thermal Enthalpies        -1201.635310        -1201.630257
Sum of electronic and thermal Free Energies        -1201.730879        -1201.726462
E(RB+HF-LYP)        -1202.05395564        -1202.04861701
2¡¢        ÔÚÈܼÁÖР              
# MP2/6-31++G(d,p) SCRF(CPCM,Solvent=Chloroform) # scf=tight test density=current
Êý¾Ý£¨RC_S£©£º
SCF Done:  E(RHF) =  -1194.80632735     A.U. after   20 cycles
             Convg  =    0.8303D-08             -V/T =  2.0029
             S**2   =   0.0000
--------------------------------------------------------------------
Variational C-PCM results
=========================
                     (a.u.) =   -1194.778048
                     (a.u.) =   -1194.806327
Total free energy in solution:
  with all non electrostatic terms            (a.u.) =   -1194.780618
--------------------------------------------------------------------
(Polarized solute)-Solvent               (kcal/mol) =     -17.75
--------------------------------------------------------------------
Cavitation energy                        (kcal/mol) =      37.47
Dispersion energy                        (kcal/mol) =     -22.59
Repulsion energy                         (kcal/mol) =       1.26
Total non electrostatic                  (kcal/mol) =      16.13
Table1.Electronic£¨¦¤Ees£© and non-electrostatic terms £¨cavitation energy £¬¦¤ecav;dispersion energy ,¦¤Edisp£»repulsion energy ,¦¤Erep£©in solvent effects £¨kcal/mol),relative to the separated reactants
        Electrostatic        Non-electrostatic £¨¦¤Enon-es£©        ¦¤¦¤Esola
        £¨¦¤Ees£©        ¦¤Ecav        ¦¤Edisp        ¦¤Erep       
P1-RC_1                                       
P1-TS_1                                       
P1-PC_1                                       

Table 2.Relative electronic £¨¦¤Egas£©and Gibbs free energies £¨¦¤Ggas£©to the separated reactants £¨kcal/mol £©
        B3LYP                CPCM-MP2
        ¦¤Egas        ¦¤Ggas                ¦¤Esol        ¦¤Gsola
P1-RC                                       
P1-TS                                       
P1-PC                                       


Table S1. Relative energies a (kcal/mol) for all relevant structures in the gas phase and in chloroform.


        In the gas phaseb        In chloroformc
        ∆Eelec        ∆E(T)        ∆G(T)        ∆Eelec        ∆E(T)        ∆G(T)
Path A
PA_RC        -2.73        -1.97        6.87        2.69        -3.76        12.31
PA_TS        20.25        21.86        34.05        27.98        10.28        28.80
PA_PC        -12.84        -11.53        -2.35        -10.63        -16.45        0.34
                                               
Çë¸÷λ°ïæ¿´¿´ÈÜÒºÖеÄ∆Eelec        £¬∆E(T)        £¬∆G(T)£¬¦¤Esol        £¬¦¤GsolaÔõô¼ÆË㣿£¿£¿£¿
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