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Relative enthalpies of isomers - Comparison of 298.15K enthalpies (kJ mol-1)

Isomers of C2H4N4

index Species CAS number Name Relative experimental enthalpy (kJ mol-1) sketch
a C2H4N4 4076362 1H-Tetrazole, 5-methyl- 0.0 sketch of 1H-Tetrazole, 5-methyl-
b C2H4N4 16681779 1H-Tetrazole, 1-methyl- 42.2 sketch of 1H-Tetrazole, 1-methyl-
c C2H4N4 16681780 2H-Tetrazole, 2-methyl- 47.7 sketch of 2H-Tetrazole, 2-methyl-
The calculated enthalpies include the calculated and scaled vibrational zero-point energy.
Methods with predefined basis sets
semi-empirical AM1 0.0 a
56.6 b
74.9 c
PM3 0.0 a
PM6 0.0 a
37.3 b
36.0 c
MNDOd 0.0 a
37.8 b
50.2 c
composite G1 0.0 a
28.6 b
12.8 c
G2MP2 0.0 a
28.2 b
13.4 c
G2 0.0 a
14.2 c
G3 0.0 a
15.7 c
G3B3 0.0 a
30.1 b
16.3 c
G3MP2 0.0 a
30.0 b
15.2 c
G4 0.0 a
-169.8 b
14.8 c
molecular mechanics MM3 0.0 a
39.6 b

Methods with standard basis sets
STO-3G 3-21G 3-21G* 6-31G 6-31G* 6-31G** 6-31+G** 6-311G* 6-311G** 6-31G(2df,p) 6-311+G(3df,2p) cc-pVDZ cc-pVTZ aug-cc-pVDZ aug-cc-pVTZ cc-pV(T+d)Z
hartree fock HF 0.0 a
15.7 b
10.0 c
0.0 a
29.6 c
0.0 a
29.6 c
0.0 a
26.9 c
  0.0 a
17.9 c
  0.0 a
13.4 c
0.0 a
31.4 b
16.5 c
0.0 a
31.6 b
19.0 c
0.0 a
32.1 b
19.1 c
0.0 a
15.0 c
0.0 a
18.9 c
0.0 a
20.9 c
0.0 a
19.8 c
0.0 a
32.1 b
18.9 c
density functional LSDA 0.0 a
13.9 b
5.6 c
0.0 a
34.4 b
22.9 c
0.0 a
34.4 b
22.9 c
0.0 a
35.3 b
17.4 c
0.0 a
25.2 b
5.1 c
0.0 a
30.3 b
10.5 c
0.0 a
33.3 b
12.1 c
0.0 a
30.4 b
8.8 c
0.0 a
33.1 b
11.8 c
0.0 a
29.7 b
11.4 c
  0.0 a
30.5 b
9.3 c
0.0 a
33.4 b
13.8 c
0.0 a
33.7 b
14.4 c
  0.0 a
33.4 b
13.8 c
BLYP 0.0 a
6.5 b
0.5 c
0.0 a
25.4 b
18.9 c

NC
0.0 a
16.9 c
  0.0 a
9.8 c
0.0 a
11.5 c
  0.0 a
27.4 b
11.0 c
0.0 a
24.4 b
10.6 c
  0.0 a
9.0 c
0.0 a
12.8 c
0.0 a
29.3 b
14.6 c
  0.0 a
12.8 c
B1B95 0.0 a
13.1 b
5.2 c
0.0 a
31.5 b
23.1 c
0.0 a
31.5 b
23.1 c
0.0 a
34.3 b
19.2 c
0.0 a
25.2 b
6.8 c
0.0 a
30.3 b
12.1 c
0.0 a
31.9 b
13.1 c
0.0 a
28.3 b
9.1 c
0.0 a
31.3 b
12.3 c
0.0 a
29.8 b
13.1 c
  0.0 a
30.3 b
10.8 c
0.0 a
31.9 b
14.5 c
0.0 a
33.5 b
16.1 c
  0.0 a
31.9 b
14.5 c
B3LYP 0.0 a
9.9 b
3.2 c
0.0 a
28.8 b
21.3 c
0.0 a
21.3 c
0.0 a
18.4 c
0.0 a
22.5 b
5.6 c
0.0 a
27.8 b
11.0 c
0.0 a
12.3 c
0.0 a
8.5 c
0.0 a
29.3 b
11.6 c
0.0 a
11.8 c
0.0 a
29.9 b
14.1 c
0.0 a
28.2 b
9.9 c
0.0 a
13.5 c
0.0 a
31.1 b
15.2 c
  0.0 a
29.8 b
13.5 c
B3LYPultrafine         0.0 a
22.5 b
5.6 c
                     
B3PW91 0.0 a
13.3 b
5.4 c
0.0 a
25.0 c
0.0 a
25.0 c
0.0 a
20.2 c
0.0 a
7.5 c
0.0 a
13.1 c
0.0 a
32.4 b
13.9 c
0.0 a
10.0 c
0.0 a
31.9 b
13.1 c
0.0 a
30.5 b
14.0 c
  0.0 a
11.5 c
0.0 a
15.4 c
0.0 a
33.5 b
16.6 c
  0.0 a
32.6 b
15.4 c
mPW1PW91 0.0 a
14.0 b
5.9 c
0.0 a
25.0 c
0.0 a
33.6 b
25.1 c
0.0 a
35.6 b
20.4 c
0.0 a
7.7 c
0.0 a
13.3 c
0.0 a
14.2 c
0.0 a
10.0 c
0.0 a
32.2 b
13.3 c
0.0 a
31.0 b
14.3 c
  0.0 a
11.5 c
0.0 a
38.0 b
15.7 c
0.0 a
34.0 b
16.9 c
  0.0 a
38.0 b
15.7 c
PBEPBE 0.0 a
11.1 b
3.2 c
0.0 a
30.3 b
22.4 c
0.0 a
30.3 b
22.4 c
0.0 a
33.1 b
19.2 c
0.0 a
24.0 b
6.8 c
0.0 a
29.3 b
12.3 c
0.0 a
31.7 b
13.7 c
0.0 a
28.1 b
9.8 c
0.0 a
31.1 b
13.0 c
0.0 a
28.8 b
13.2 c
0.0 a
32.1 b
15.7 c
0.0 a
29.5 b
11.0 c
0.0 a
31.6 b
15.0 c
0.0 a
32.8 b
16.5 c
  0.0 a
31.6 b
15.0 c
PBEPBEultrafine         0.0 a
24.0 b
6.8 c
                     
STO-3G 3-21G 3-21G* 6-31G 6-31G* 6-31G** 6-31+G** 6-311G* 6-311G** 6-31G(2df,p) 6-311+G(3df,2p) cc-pVDZ cc-pVTZ aug-cc-pVDZ aug-cc-pVTZ cc-pV(T+d)Z
Moller Plesset perturbation MP2 0.0 a
3.6 b
-4.8 c
0.0 a
18.0 c
0.0 a
18.0 c
0.0 a
15.2 c
  0.0 a
2.6 c
    0.0 a
4.0 c
0.0 a
25.8 b
3.8 c
  0.0 a
25.9 b
1.5 c

  b

NC
 
NC
MP2=FULL  
NC

NC

NC
0.0 a
21.5 b
-0.9 c

NC

NC
0.0 a
2.7 c
0.0 a
4.3 c
   
NC

NC
   
NC
MP3         0.0 a
10.3 c
                     
MP4  
NC
                           
Configuration interaction CID  
NC
   
NC
   
NC
               
CISD  
NC
   
NC
                     
STO-3G 3-21G 3-21G* 6-31G 6-31G* 6-31G** 6-31+G** 6-311G* 6-311G** 6-31G(2df,p) 6-311+G(3df,2p) cc-pVDZ cc-pVTZ aug-cc-pVDZ aug-cc-pVTZ cc-pV(T+d)Z
Quadratic configuration interaction QCISD  
NC

NC

NC

NC

NC
                   
Coupled Cluster CCD  
NC

NC
 
NC

NC

NC

NC
               
STO-3G 3-21G 3-21G* 6-31G 6-31G* 6-31G** 6-31+G** 6-311G* 6-311G** 6-31G(2df,p) 6-311+G(3df,2p) cc-pVDZ cc-pVTZ aug-cc-pVDZ aug-cc-pVTZ cc-pV(T+d)Z

Methods with effective core potentials (select basis sets)
CEP-31G CEP-31G* CEP-121G CEP-121G* LANL2DZ SDD
hartree fock HF 0.0 a
21.6 c
0.0 a
10.0 c
0.0 a
26.2 c
0.0 a
12.8 c
0.0 a
30.3 c
0.0 a
30.6 c
density functional B1B95 0.0 a
35.0 b
16.6 c
0.0 a
25.1 b
5.5 c
       
B3LYP 0.0 a
15.6 c
0.0 a
4.5 c
0.0 a
17.4 c
0.0 a
6.2 c
0.0 a
20.9 c
0.0 a
20.9 c
Moller Plesset perturbation MP2 0.0 a
8.3 c
0.0 a
-3.0 c
0.0 a
10.1 c

NC
0.0 a
13.6 c
0.0 a
13.7 c

Single point energy calculations (select basis sets)
cc-pVDZ cc-pVTZ aug-cc-pVDZ cc-pV(T+d)Z
Moller Plesset perturbation MP2FC// HF/6-31G* 0.0 a
29.6 b
93.4 c
0.0 a
28.0 b
81.8 c
  0.0 a
28.0 b
81.8 c
MP2FC// B3LYP/6-31G* 0.0 a
26.4 b
1.4 c
     
MP2FC// MP2FC/6-31G*   0.0 a 0.0 a
27.3 b
5.9 c
0.0 a
Coupled Cluster CCSD// HF/6-31G*   0.0 a
31.4 b
  0.0 a
31.4 b
CCSD(T)// HF/6-31G*   0.0 a
30.4 b
  0.0 a
30.4 b
NC = not calculated
For descriptions of the methods (AM1, HF, MP2, ...) and basis sets (3-21G, 3-21G*, 6-31G, ...) see the glossary in section I.C. Predefined means the basis set used is determined by the method.
gaw refers to the group additivity method implemeted in the NIST Chemistry Webbook.
See section Calculated; Vibrations; Scale Factors; Scale factors to list vibrational scaling factors.
See section Calculated; Vibrations; Scale Factors; Calculate a scale factor to calculate a vibrational scaling factor for a given set of molecules.