Electron-Rich Three-Center Bonding: The Role of s,p
Interactions Across the p-Block

J 2002

Electron-Rich Three-Center Bonding: The Role of s,p Interactions Across the p-Block

MUNZAROVÁ, Markéta a Roald HOFFMANN

Základní údaje

Originální název

Electron-Rich Three-Center Bonding: The Role of s,p Interactions Across the p-Block

Autoři

MUNZAROVÁ, Markéta (203 Česká republika, garant) a Roald HOFFMANN (840 Spojené státy)

Vydání

J. Am. Chem. Soc. Washington, American Chemical Society, 2002, 0002-7863

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Obor

10403 Physical chemistry

Stát vydavatele

Spojené státy

Utajení

není předmětem státního či obchodního tajemství

Impakt faktor

Impact factor: 6.201

Kód RIV

RIV/00216224:14310/02:00006521

Organizační jednotka

Přírodovědecká fakulta

Klíčová slova anglicky

AB-INITIO CALCULATIONS; GAS-PHASE; POLYHALIDE ANIONS; CRYSTAL-STRUCTURE; TRIFLUORIDE ION; SOLID-STATE; ENERGY; HYPERVALENT; APPROXIMATION; STABILITY

Štítky

AB-INITIO CALCULATIONS, APPROXIMATION, CRYSTAL-STRUCTURE, energy, GAS-PHASE, HYPERVALENT, POLYHALIDE ANIONS, SOLID-STATE, stability, TRIFLUORIDE ION

Změněno: 27. 2. 2009 08:54, doc. Mgr. Markéta Munzarová, Dr. rer. nat.

Anotace

V originále

This paper analyzes the importance of s,p mixing-a necessary addition to the simplest Rundle-Pimentel picture-and periodic and group trends in electron-rich three-center bonding. Our analysis proceeds through a detailed quantum chemical study of the stability of electron-rich three-center bonding in triatomic 22-valence electron anions, To provide interpretations, a perturbational molecular orbital (MO) analysis of s,p mixing is carried out. This analysis of the orbitals and the overlap populations is then tested by density functional calculations for a number of linear trihalides, trichalcogenides, and tripnictides. The most important effect of s,p mixing on the in-line bonding is in destabilization of the 3sigma(g) orbital and is determined by the overlap between the s orbital of the central atom and the p orbital of the terminal atom. Further destabilization arises from the repulsion of p, lone pairs. Both of these antibonding effects increase with increasing negative charge of the system. The stability of isoelectronic X-3 systems thus decreases when moving from right to left in the periodic table. Interesting group trends are discerned; for instance, for the electron-rich tripnictides, the ability to accommodate a hypervalent electron count is the largest in the middle rather at the end of the roup. Particularly strong s,p mixing can reverse the bonding/antibonding character of MOs: thus MO 2sigma(u) that is responsible for bonding for trihalides and trichalcogenides is actually antibonding in N-3(7-).

Návaznosti

MSM 143100011, záměr

Název: Struktura a vazebné poměry, vlastnosti a analýza syntetických a přírodních molekulových ansamblů

Investor: Ministerstvo školství, mládeže a tělovýchovy ČR, Struktura a vazebné poměry, vlastnosti a analýza syntetických a přírodních molekulových ansamblů

Citovat

MUNZAROVÁ, Markéta a Roald HOFFMANN. Electron-Rich Three-Center Bonding: The Role of s,p Interactions Across the p-Block. J. Am. Chem. Soc. Washington: American Chemical Society, 2002, roč. 124, č. 17, s. 4787-4795. ISSN 0002-7863.

@article{405827,
   author = {Munzarová, Markéta and Hoffmann, Roald},
   article_location = {Washington},
   article_number = {17},
   keywords = {AB-INITIO CALCULATIONS; GAS-PHASE; POLYHALIDE ANIONS; CRYSTAL-STRUCTURE; TRIFLUORIDE ION; SOLID-STATE; ENERGY; HYPERVALENT; APPROXIMATION; STABILITY},
   language = {eng},
   issn = {0002-7863},
   journal = {J. Am. Chem. Soc.},
   title = {Electron-Rich Three-Center Bonding: The Role of s,p Interactions Across the p-Block},
   volume = {124},
   year = {2002}
}

TY  - JOUR
ID  - 405827
AU  - Munzarová, Markéta - Hoffmann, Roald
PY  - 2002
TI  - Electron-Rich Three-Center Bonding: The Role of s,p Interactions Across the p-Block
JF  - J. Am. Chem. Soc.
VL  - 124
IS  - 17
SP  - 4787
EP  - 4787
PB  - American Chemical Society
SN  - 00027863
KW  - AB-INITIO CALCULATIONS
KW  - GAS-PHASE
KW  - POLYHALIDE ANIONS
KW  - CRYSTAL-STRUCTURE
KW  - TRIFLUORIDE ION
KW  - SOLID-STATE
KW  - ENERGY
KW  - HYPERVALENT
KW  - APPROXIMATION
KW  - STABILITY
N2  - This paper analyzes the importance of s,p mixing-a necessary addition to the simplest Rundle-Pimentel picture-and periodic and group trends in electron-rich three-center bonding. Our analysis proceeds through a detailed quantum chemical study of the stability of electron-rich three-center bonding in triatomic 22-valence electron anions, To provide interpretations, a perturbational molecular orbital (MO) analysis of s,p mixing is carried out. This analysis of the orbitals and the overlap populations is then tested by density functional calculations for a number of linear trihalides, trichalcogenides, and tripnictides. The most important effect of s,p mixing on the in-line bonding is in destabilization of the 3sigma(g) orbital and is determined by the overlap between the s orbital of the central atom and the p orbital of the terminal atom. Further destabilization arises from the repulsion of p, lone pairs. Both of these antibonding effects increase with increasing negative charge of the system. The stability of isoelectronic X-3 systems thus decreases when moving from right to left in the periodic table. Interesting group trends are discerned; for instance, for the electron-rich tripnictides, the ability to accommodate a hypervalent electron count is the largest in the middle rather at the end of the roup. Particularly strong s,p mixing can reverse the bonding/antibonding character of MOs: thus MO 2sigma(u) that is responsible for bonding for trihalides and trichalcogenides is actually antibonding in N-3(7-).
ER  -

MUNZAROVÁ, Markéta a Roald HOFFMANN. Electron-Rich Three-Center Bonding: The Role of s,p Interactions Across the p-Block. \textit{J. Am. Chem. Soc.}. Washington: American Chemical Society, 2002, roč.~124, č.~17, s.~4787-4795. ISSN~0002-7863.

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