Chemical bonding
Chemical
bonding is the permanent attraction between atoms, ions, or molecules that
enables the formation of chemical compounds. This bond can be derived from
attractive electrical energy by splitting electrons into electrically charged ions,
such as ionic bonds or covalent bonds. The strength of chemical bonding varies
considerably; there are "strong bonds" or "primary bonds"
like covalent, ionic, and metallic bonds and "weak bonds" or
"secondary bonds" like dipole-dipole interactions, and hydrogen
bonds. In general, strong chemical bonding is involved in the electronic sharing
or transfer between participating atoms. Atoms of molecules, crystals, metals, and diatomic gases are present in most of the physical environment around us.
These are held together by chemical bonding, which indicates the structure and
bulk properties of the material.
Chemical bonding has three main features
i.
Atoms interact with each other to form aggregates such as molecules, compounds,
and crystals because doing so reduces the total energy of the system; That is,
aggregates are more stable than isolated atoms.
ii.
Energy is required to separate bonded atoms or ions into isolated atoms or
ions. For ionic solids, where ions form a three-dimensional array called a
lattice, this force is called lattice energy (U), the enthalpy change occurs
when a solid ionic compound is converted into gaseous ions. For covalent
compounds, this energy is called bond energy, which is the enthalpy change that
occurs when the bond given to the gaseous molecule breaks.
iii.
Each chemical bonding is characterized by a special optimal interstitial distance
called a bond distance (r0).
Types of chemical bonding
Ionic bonding
Ionic
bonding is the electrical interaction between a type of atom that has a large
difference in electrical dynamics. There is no exact value for separating ionic
form from covalent bonds, but an electromotive difference greater than 1.7 is
likely to be ionic, and a difference less than 1.7 is likely to be auxiliary.
Ionic bonds lead to individual positive and negative ions. Ionic charges
usually range from −3e to + 3e. Ionic bonding usually occurs in metallic salts
such as sodium chloride. A feature of ionic bonds is that species take the form
of ionic crystals, where no ion is uniquely attached to any other ion in a
specific directional bond. Instead, each species of ions is surrounded by ions
of reverse charge, and each of the reversely charged ions near it is the same
for the same type of surrounding atoms. So it is no longer possible to attach
an ion to a specific single ionized atom near it. This is not the case with
covalent crystals, where the covalent bonds between specific atoms measured by
techniques such as X-ray scattering still differ from the short distances
between them.
Covalent bond
The covalent bond is a chemical bonding that involves sharing of electronic pairs into
atoms. These electron pairs are known as shared pairs or bond pairs, and the
stable balance of attractive and hostile energies between atoms, when they share
electrons, is known as a covalent bond. For many molecules, the splitting of
the electrons allows each atom to achieve the equivalent of a complete valence
shell according to a static electronic configuration. In organic chemistry,
covalent bonds are much more common than ionic bonds. Covalent bonds include
many types of interactions, including σ-bonds, π-bonds, metal-to-metal bonds,
agnostic interactions, bent bonds, three-center two-electron bonds, and
three-center four-electronic bonds.
Metallic bond
Metallic
bonding is a type of chemical bonding that arises from the electron gravitational
force between the conduction electron and the positively charged metal ions. It
can be identified as the sharing of free electrons into a structure of
positively charged ions (cations). Metal bonding accounts for many of the
physical properties of metals such as strength, flexibility, heat and
electrical resistance and conductivity, opacity, and luster. Even pure
substances, metallic bonds are not only chemical bonds of any kind, which can
exhibit metals. For example, the primary gallium is composed of parallelly
bound atoms in both liquid and solid states - these pairs form a crystal
structure with a metal bond between them. Another example of metal-metal
covalent bonds is mercurous ions (Hg2+).
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The
atoms of metals have a strong attractive force. It takes a lot of energy to
overcome it. Therefore, metals often have high boiling points, with tungsten
(5828 K) being extremely high. A notable exception is the components of the
zinc group: Zn, Cd, and Hg. Their electron configurations end in ... ns2,
which resembles a great gas configuration like helium, spend more time going
down in the periodic table because the energy difference with the empty np
orbitals is even greater. These metals are therefore relatively volatile and
are avoided in ultra-high vacuum systems. Otherwise, the metal bond can be very
strong even in molten metals like gallium. Although gallium will melt from the
heat of one's hand just above room temperature, its heating point is not too
far away. Molten gallium is therefore a much-uninterrupted liquid thanks to its
strong metallic bond.
Hydrogen bonding
The hydrogen bond is the primary force of attraction between the hydrogen (H) atoms
that binds to one more electron atom or group and another electron atom that
carries a lone pair of electrons - the hydrogen bond acceptor (Ac). Such an
interactive system is usually referred to as Dn - H ··· Ac, where the solid
line refers to a polar covalent bond and the dotted or dashed line refers to
hydrogen bonding. The most frequent donor and receptor atoms are the second row
of nitrogen (N), oxygen (O), and fluorine (F).
Hydrogen
bonds can be intermolecular or intramolecular, the strength of hydrogen bonds
can vary from 1 to 40 kcal/mol depending on the bonds of donor and acceptor
atoms, their geometry, and the nature of the environment structure. This makes
them somewhat stronger than the van der Waals interactions and weaker than the
complete covalent or ionic bonds. This type of bond can occur in inorganic
molecules like water and in organic molecules like DNA and proteins. Hydrogen
bonds such as paper and felted wool are held together and are responsible for
sticking separate sheets of paper together after getting wet and subsequently
drying.
Pi bond
In
chemistry, pi bonds are covalent chemical bonding where two lobes in the upper
orbit of an atom overlap two lobes in an orbit over another atom, and this
overlap eventually occurs. Each of these atomic orbits carries two bonded
nuclei and has a zero electron density in a shared nodal plane. The same bond
is the nodal plane for the molecular orbit of the pi bond. Pi bonds can form in
double and triple bonds but in most cases not in single bonds.
The
Greek letters π in their name refer to the p orbital as the symmetry of the pi
bond orbital is equal to the p orbital as seen in the bond axis. One of the
most common forms of this type of bond involves p orbitals, although d orbitals
involve pi bonds. This subsequent mode forms part of the base for multiple bonding
of metal-metal. Pi bonds are generally weaker than sigma bonds. The bond
strength of a C-C double bond consisting of a sigma and a pi bond is less than
twice that of a C-C single bond, indicating that the stability added by a pi
bond is less than that of a sigma bond.
Sigma bond
A single bond is a sigma bond when multiple bonds are formed by sigma bonds together with pi or other bonds. A double bond has a sigma plus a pi bond, and a triple bond has a sigma plus two pi bonds. In chemistry, sigma bonds (σ bonds) are the strongest forms of covalent chemical bonding. These are formed by head-on overlapping between atomic orbitals. Sigma bonding is most defined for diatomic molecules using the languages and tools of symmetry groups. In this formal method, an σ-bond is symmetrical about the rotation of the bond axis. According to this definition, the most common forms of sigma bonds are s + s, pz + pz, s + pz, and dz2 + dz2. Quantum theory also suggests that molecular orbitals (MO) of uniform symmetry are actually mixed or hybridized. The practical consequence of this mixture of diatomic molecules is that wave-related s + s and pz + pz molecular orbits are blended. The degree of this hybridization depends on the relative strength of the symmetrical MOs as preferred.
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