The classification of three-center two-electron (3c2e) bonds into supported (closed) or unsupported (open) was proposed by Lipscomb in his work on boranes and extended to transition metal complexes by Bau and co-workers. The species in which the interactions of the terminal atoms are negligible are called “unsupported bonds.” Examples of chemical species that are said to exhibit such bonds are Li2H+, Na2H+, B2H7, Al2(CH3)7, and [(μ2-H)Cr2(CO)10] although the general criterion for distinguishing these types of bonds is somewhat qualitative. Besides providing a unifying view of the nature of the chemical bond, in terms of quantum interference among electronic states, the Generalized Product Function Energy Partitioning method through the Interference Energy Analysis (IEA) is also potentially capable of providing a rigorous ground to the concept of supported bonds by looking at the specific interference energies between the orbital pairs associated with the bond. The IEA was performed in the species Li2H+, Na2H+, B2H7, C2H7, Al2H7, and [(μ2-H)Cr2(CO)10], as well as along the reaction path Li2H+ → Li2+ + H. The results shown that in all studied A–B–C bonds, the A–C interactions are as important as the A–B/B–C ones, leading to the conclusion that all studied 3c2e bonds are “supported,” in the sense that the A–C interaction is not negligible. The particularity of those species in preferring linear geometry is completely explained by quasi-classical effects, more specifically, by minimization of the electron–electron and nucleus–nucleus repulsions.

1.
W. H.
Eberhardt
,
B.
Crawford
, and
W. N.
Lipscomb
,
J. Chem. Phys.
22
,
989
(
1954
).
2.
R.
Bau
,
R. G.
Teller
,
S. W.
Kirtley
, and
T. F.
Koetzle
,
Acc. Chem. Res.
12
,
176
(
1979
).
3.
R. L.
DeKock
and
W. B.
Bosma
,
J. Chem. Educ.
65
,
194
(
1988
).
4.
J. E.
McMurry
and
T.
Lectka
,
Acc. Chem. Res.
25
,
47
(
1992
).
5.
T. M.
Cardozo
and
M. A. C.
Nascimento
,
J. Chem. Phys.
130
,
104102
(
2009
).
6.
K.
Ruedenberg
,
Rev. Mod. Phys.
34
,
326
(
1962
).
7.
F.
Fantuzzi
,
D. W. O.
de Sousa
, and
M. A. C.
Nascimento
,
ChemistrySelect
2
,
604
(
2017
).
8.
F.
Fantuzzi
,
T. M.
Cardozo
, and
M. A. C.
Nascimento
,
Phys. Chem. Chem. Phys.
19
,
19352
(
2017
).
9.
D. W. O. d.
Sousa
and
M. A. C.
Nascimento
,
Acc. Chem. Res.
50
,
2264
(
2017
).
10.
D. W.
Oliveira de Sousa
and
M. A. C.
Nascimento
,
J. Phys. Chem. A
122
,
1406
(
2018
).
11.
D. W. O.
de Sousa
and
M. A. C.
Nascimento
,
Phys. Chem. Chem. Phys.
21
,
13319
(
2019
).
12.
F.
Fantuzzi
,
W.
Wolff
,
H. M.
Quitián-Lara
,
H. M.
Boechat-Roberty
,
G.
Hilgers
,
B.
Rudek
, and
M. A. C.
Nascimento
,
Phys. Chem. Chem. Phys.
21
,
24984
(
2019
).
13.
D. W. O.
de Sousa
and
M. A. C.
Nascimento
,
Theor. Chem. Acc.
139
,
140
(
2020
).
14.
D. W. O.
de Sousa
and
M. A. C.
Nascimento
,
J. Phys. Chem. A
125
,
4558
(
2021
).
15.
D. W. O.
de Sousa
and
M. A. C.
Nascimento
,
Phys. Chem. Chem. Phys.
24
,
15958
(
2022
).
16.
D. W. O.
de Sousa
and
M. A. C.
Nascimento
,
J. Chem. Theory Comput.
12
,
2234
(
2016
).
17.
S.
Shaik
,
D.
Danovich
,
W.
Wu
,
P.
Su
,
H. S.
Rzepa
, and
P. C.
Hiberty
,
Nat. Chem.
4
,
195
(
2012
).
18.
M.-E.
Moret
,
L.
Zhang
, and
J. C.
Peters
,
J. Am. Chem. Soc.
135
,
3792
(
2013
).
19.
L. B.
Handy
,
P. M.
Treichel
,
L. F.
Dahl
, and
R. G.
Hayter
,
J. Am. Chem. Soc.
88
,
366
(
1966
).
20.
L. B.
Handy
,
J. K.
Ruff
, and
L. F.
Dahl
,
J. Am. Chem. Soc.
92
,
7312
(
1970
).
21.
J.
Roziere
,
J. M.
Williams
,
R. P.
Stewart
,
J. L.
Petersen
, and
L. F.
Dahl
,
J. Am. Chem. Soc.
99
,
4497
(
1977
).
22.
R. D.
Wilson
,
S. A.
Graham
, and
R.
Bau
,
J. Organomet. Chem.
91
,
C49
(
1975
).
23.
J. H.
Hall
,
D. S.
Marynick
, and
W. N.
Lipscomb
,
Inorg. Chem.
11
,
3126
(
1972
).
24.
C.
Hoheisel
and
W.
Kutzelnigg
,
J. Am. Chem. Soc.
97
,
6970
(
1975
).
25.
S. G.
Shore
,
S. H.
Lawrence
,
M. I.
Watkins
, and
R.
Bau
,
J. Am. Chem. Soc.
104
,
7669
(
1982
).
26.
S. I.
Khan
,
M. Y.
Chiang
,
R.
Bau
,
T. F.
Koetzle
,
S. G.
Shore
, and
S. H.
Lawrence
,
J. Chem. Soc., Dalton Trans.
1986
,
1753
.
27.
K.
Raghavachari
,
P. v. R.
Schleyer
, and
G. W.
Spitznagel
,
J. Am. Chem. Soc.
105
,
5917
(
1983
).
28.
A. M.
Sapse
and
L.
Osorio
,
Inorg. Chem.
23
,
627
(
1984
).
29.
K.
Raghavachari
,
R. A.
Whiteside
,
J. A.
Pople
, and
P. V. R.
Schleyer
,
J. Am. Chem. Soc.
103
,
5649
(
1981
).
30.
L. I.
Yeh
,
J. M.
Price
, and
Y. T.
Lee
,
J. Am. Chem. Soc.
111
,
5597
(
1989
).
31.
J. L.
Atwood
,
D. C.
Hrncir
,
R. D.
Rogers
, and
J. A. K.
Howard
,
J. Am. Chem. Soc.
103
,
6787
(
1981
).
32.
R. A.
Chiles
and
C. E.
Dykstra
,
Chem. Phys. Lett.
92
,
471
(
1982
).
33.
O.
Charkin
,
M.
McKee
, and
P. V. R.
Schleyer
,
Russ. J. Inorg. Chem.
41
,
1973
(
1996
), see https://www.researchgate.net/publication/286548381.
34.
R. C.
Raffenetti
and
K.
Ruedenberg
,
J. Chem. Phys.
59
,
5978
(
1973
).
35.
A. D.
Walsh
,
J. Chem. Soc. Resumed
1953
,
2260
.
36.
R. S.
Mulliken
,
J. Am. Chem. Soc.
77
,
887
(
1955
).
37.
G. C.
Pimentel
,
J. Chem. Phys.
19
,
446
(
1951
).
38.
R. F. W.
Bader
and
H.
Essén
,
J. Chem. Phys.
80
,
1943
(
1984
).
39.
W. V.
Hicks
,
L. J.
Schaad
, and
K. K.
Innes
,
J. Chem. Phys.
65
,
463
(
1976
).
40.
R.
McWeeny
,
Proc. R. Soc. Math. Phys. Eng. Sci.
253
,
242
(
1959
).
41.
W. A.
Goddard
,
Phys. Rev.
157
,
73
(
1967
).
42.
J.
Gerratt
and
W. N.
Lipscomb
,
Proc. Natl. Acad. Sci.
59
,
332
(
1968
).
43.
M. A. C.
Nascimento
,
Int. J. Quantum Chem.
119
,
e25765
(
2019
).
44.
M. A. C.
Nascimento
,
Molecules
26
,
4524
(
2021
).
45.
P. B.
Karadakov
,
D. L.
Cooper
,
B. J.
Duke
, and
J.
Li
,
J. Phys. Chem. A
116
,
7238
(
2012
).
46.
T. M.
Cardozo
and
M. A. C.
Nascimento
,
J. Phys. Chem. A
113
,
12541
(
2009
).
47.
M. W.
Schmidt
,
K. K.
Baldridge
,
J. A.
Boatz
,
S. T.
Elbert
,
M. S.
Gordon
,
J. H.
Jensen
,
S.
Koseki
,
N.
Matsunaga
,
K. A.
Nguyen
,
S.
Su
,
T. L.
Windus
,
M.
Dupuis
, and
J. A.
Montgomery
,
J. Comput. Chem.
14
,
1347
(
1993
).
48.
J.
Li
and
R.
McWeeny
,
Int. J. Quantum Chem.
89
,
208
(
2002
).
49.
B. M.
Bode
and
M. S.
Gordon
,
J. Mol. Graphics Modell.
16
,
133
(
1998
).
50.
D. W. O.
de Sousa
, GPFPlot,
2021
.
51.
A. G. H.
Barbosa
and
J. G. S.
Monteiro
,
Theor. Chem. Acc.
131
,
1297
(
2012
).
52.
G.
Herzberg
and
K. P.
Huber
,
Constants of Diatomic Molecules
(
Springer
,
1979
).
53.
A. D.
Buckingham
and
T. W.
Rowlands
,
J. Chem. Educ.
68
,
282
(
1991
).
54.
H.-Y.
Huang
,
T.-L.
Lu
,
T.-J.
Whang
,
Y.-Y.
Chang
, and
C.-C.
Tsai
,
J. Chem. Phys.
133
,
044301
(
2010
).
55.
R. D.
Johnson
, NIST Computational Chemistry Comparison and Benchmark Database. http://cccbdb.nist.gov (
2022
).
56.
F. P.
Fleming
,
A. G. H.
Barbosa
, and
P. M.
Esteves
,
J. Phys. Chem. A
110
,
11903
(
2006
).
57.
E. P. L.
Hunter
and
S. G.
Lias
,
J. Phys. Chem. Ref. Data
27
,
413
(
1998
).
58.
G. G.
Meisels
,
W. H.
Hamill
, and
R. R.
Williams
,
J. Phys. Chem.
61
,
1456
(
1957
).
59.
K.
Hiraoka
and
P.
Kebarle
,
J. Am. Chem. Soc.
98
,
6119
(
1976
).
60.
J. W. d. M.
Carneiro
,
P. v. R.
Schleyer
,
M.
Saunders
,
R.
Remington
,
H. F.
Schaefer
,
A.
Rauk
, and
T. S.
Sorensen
,
J. Am. Chem. Soc.
116
,
3483
(
1994
).
61.
A. L. L.
East
,
Z. F.
Liu
,
C.
McCague
,
K.
Cheng
, and
J. S.
Tse
,
J. Phys. Chem. A
102
,
10903
(
1998
).
62.
J. J.
Fisher
,
G. K.
Koyanagi
, and
T. B.
McMahon
,
Int. J. Mass Spectrom.
195-196
,
491
(
2000
).
63.
H.
Borrmann
,
A. M.
Pirani
, and
G. J.
Schrobilgen
,
Acta Crystallogr., Sect. C: Struct. Chem.
53
,
19
(
1997
).
64.
M. Y.
Darensbourg
,
R.
Bau
,
M. W.
Marks
,
R. R.
Burch
,
J. C.
Deaton
, and
S.
Slater
,
J. Am. Chem. Soc.
104
,
6961
(
1982
).
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