In
chemistry, π backbonding, also called π backdonation, is when
electron
The electron ( or ) is a subatomic particle with a negative one elementary electric charge. Electrons belong to the first generation of the lepton particle family,
and are generally thought to be elementary particles because they have no ...
s move from an
atomic orbital
In atomic theory and quantum mechanics, an atomic orbital is a function describing the location and wave-like behavior of an electron in an atom. This function can be used to calculate the probability of finding any electron of an atom in an ...
on one atom to an appropriate symmetry
antibonding orbital
In chemical bonding theory, an antibonding orbital is a type of molecular orbital that weakens the chemical bond between two atoms and helps to raise the energy of the molecule relative to the separated atoms. Such an orbital has one or more no ...
on a ''π-acceptor
ligand
In coordination chemistry, a ligand is an ion or molecule ( functional group) that binds to a central metal atom to form a coordination complex. The bonding with the metal generally involves formal donation of one or more of the ligand's elec ...
''. It is especially common in the
organometallic chemistry of
transition metal
In chemistry, a transition metal (or transition element) is a chemical element in the d-block of the periodic table (groups 3 to 12), though the elements of group 12 (and less often group 3) are sometimes excluded. They are the elements that ca ...
s with multi-atomic ligands such as
carbon monoxide
Carbon monoxide (chemical formula CO) is a colorless, poisonous, odorless, tasteless, flammable gas that is slightly less dense than air. Carbon monoxide consists of one carbon atom and one oxygen atom connected by a triple bond. It is the simple ...
,
ethylene or the
nitrosonium cation. Electrons from the metal are used to bond to the ligand, in the process relieving the metal of excess negative
charge
Charge or charged may refer to:
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Music
* ''Charge'' (David Ford album)
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. Compounds where π backbonding occurs include
Ni(CO)4 and
Zeise's salt
Zeise's salt, potassium trichloro(ethylene)platinate(II), is the chemical compound with the formula K platinum">PtCl3(C2H4).html" ;"title="platinum.html" ;"title="/nowiki>PtCl3(C2H4)">platinum.html"_;"title="/nowiki>platinum">PtCl3(C2H4)H2O.__Th ...
.
IUPAC
The International Union of Pure and Applied Chemistry (IUPAC ) is an international federation of National Adhering Organizations working for the advancement of the chemical sciences, especially by developing nomenclature and terminology. It is ...
offers the following definition for backbonding:
A description of the bonding of π-conjugated ligands to a transition metal which involves a synergic
Synergy is an interaction or cooperation giving rise to a whole that is greater than the simple sum of its parts. The term ''synergy'' comes from the Attic Greek word συνεργία ' from ', , meaning "working together".
History
In Christian ...
process with donation of electrons from the filled π-orbital or lone electron pair orbital of the ligand into an empty orbital of the metal (donor–acceptor bond), together with release (back donation) of electrons from an ''n''d orbital of the metal (which is of π-symmetry with respect to the metal–ligand axis) into the empty π*- antibonding orbital of the ligand.
Metal carbonyls, nitrosyls, and isocyanides
The electrons are partially transferred from a d-orbital of the metal to anti-bonding molecular orbitals of CO (and its analogues). This electron-transfer (i) strengthens the metal–C bond and (ii) weakens the C–O bond. The strengthening of the M–CO bond is reflected in increases of the vibrational frequencies for the M–C bond (often outside of the range for the usual IR spectrophotometers). Furthermore, the M–CO bond length is shortened. The weakening of the C–O bond is indicated by a decrease in the wavenumber of the ''ν''
CO band(s) from that for free CO (2143 cm
−1), for example to 2060 cm
−1 in Ni(CO)
4 and 1981 cm
−1 in Cr(CO)
6, and 1790 cm
−1 in the anion
4">e(CO)4sup>2−. For this reason,
IR spectroscopy
Infrared spectroscopy (IR spectroscopy or vibrational spectroscopy) is the measurement of the interaction of infrared radiation with matter by absorption, emission, or reflection. It is used to study and identify chemical substances or function ...
is an important diagnostic technique in
metal–carbonyl chemistry. The article
infrared spectroscopy of metal carbonyls
Metal carbonyls are coordination complexes of transition metals with carbon monoxide ligands. Metal carbonyls are useful in organic synthesis and as catalysts or catalyst precursors in homogeneous catalysis, such as hydroformylation and Reppe ch ...
discusses this in detail.
Many ligands other than CO are strong "backbonders". Nitric oxide is an even stronger π-acceptor than is CO and ν
NO is a diagnostic tool in
metal–nitrosyl chemistry.
Isocyanides, RNC, are another class of ligands that are capable of π-backbonding. In contrast with CO, the σ-donor lone pair on the C atom of isocyanides is antibonding in nature and upon complexation the CN bond is strengthened and the ν
CN increased. At the same time, π-backbonding lowers the ''ν''
CN. Depending on the balance of σ-bonding versus π-backbonding, the ν
CN can either be raised (for example, upon complexation with weak π-donor metals, such as Pt(II)) or lowered (for example, upon complexation with strong π-donor metals, such as Ni(0)). For the isocyanides, an additional parameter is the MC=N–C angle, which deviates from 180° in highly electron-rich systems. Other ligands have weak π-backbonding abilities, which creates a labilization effect of CO, which is described by the
''cis'' effect.
Metal–alkene and metal–alkyne complexes
As in metal–carbonyls, electrons are partially transferred from a d-orbital of the metal to antibonding molecular orbitals of the alkenes and alkynes. This electron transfer (i) strengthens the metal–ligand bond and (ii) weakens the C–C bonds within the ligand. In the case of metal-alkenes and alkynes, the strengthening of the M–C
2R
4 and M–C
2R
2 bond is reflected in bending of the C–C–R angles which assume greater sp
3 and sp
2 character, respectively. Thus strong π backbonding causes a metal-alkene
complex
Complex commonly refers to:
* Complexity, the behaviour of a system whose components interact in multiple ways so possible interactions are difficult to describe
** Complex system, a system composed of many components which may interact with each ...
to assume the character of a metallacyclopropane. Electronegative substituents exhibit greater π backbonding. Thus, strong π backbonding ligands are
tetrafluoroethylene
Tetrafluoroethylene (TFE) is a fluorocarbon with the chemical formula C2 F4. It is the simplest perfluorinated alkene. This gaseous species is used primarily in the industrial preparation of fluoropolymers.
Properties
Tetrafluoroethylene is a ...
,
tetracyanoethylene
Tetracyanoethylene (TCNE) is organic compound with the formula . It is a colorless solid, although samples are often off-white. It is an important member of the cyanocarbons.
Synthesis and reactions
TCNE is prepared by brominating malononitri ...
, and
hexafluoro-2-butyne
Hexafluoro-2-butyne (HFB) is a fluorocarbon with the chemical structure CF3C≡CCF3. HFB is a particularly electrophilic acetylene derivative, and hence a potent dienophile for Diels–Alder reactions.
HFB is prepared by the action of sulfur t ...
.
Metal-phosphine complexes
Phosphines accept electron density from metal p or d orbitals into combinations of P–C σ* antibonding orbitals that have π symmetry. When phosphines bond to electron-rich metal atoms, backbonding would be expected to lengthen P–C bonds as P–C σ* orbitals become populated by electrons. The expected lengthening of the P–C distance is often hidden by an opposing effect: as the phosphorus lone pair is donated to the metal, P(lone pair)–R(bonding pair) repulsions decrease, which acts to shorten the P–C bond. The two effects have been deconvoluted by comparing the structures of pairs of metal-phosphine complexes that differ only by one electron. Oxidation of R
3P–M complexes results in longer M–P bonds and shorter P–C bonds, consistent with π-backbonding. In early work, phosphine ligands were thought to utilize 3d orbitals to form M–P pi-bonding, but it is now accepted that d-orbitals on phosphorus are not involved in bonding as they are too high in energy.
See also
*
Bridging carbonyl
*
Dewar–Chatt–Duncanson model
The Dewar–Chatt–Duncanson model is a model in organometallic chemistry that explains the chemical bonding in transition metal alkene complexes. The model is named after Michael J. S. Dewar, Joseph Chatt and L. A. Duncanson.
The alkene donat ...
*
18-electron rule
*
Ligand field theory
Ligand field theory (LFT) describes the bonding, orbital arrangement, and other characteristics of coordination complexes. It represents an application of molecular orbital theory to transition metal complexes. A transition metal ion has nine valen ...
*
Pi-donor ligands
References
{{DEFAULTSORT:Pi backbonding
Chemical bonding
Coordination chemistry
Organometallic chemistry