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In chemistry, polyvalency (or polyvalence, multivalency) is the property of molecules and larger species, such as antibodies, medical drugs, and even nanoparticles surface-functionalized with ligands, like spherical nucleic acids, that exhibit more than one supramolecular interaction.
Molecular binding is an attractive interaction between two molecules that results in a stable association in which the molecules are in close proximity to each other. It is formed when atoms or molecules bind together by sharing of electrons.
The electron density of these two bonding electrons in the region between the two atoms increases from the density of two non-interacting H atoms. Two p-orbitals forming a pi-bond. A double bond has two shared pairs of electrons, one in a sigma bond and one in a pi bond with electron density concentrated on two opposite sides of the ...
The valence is the combining capacity of an atom of a given element, determined by the number of hydrogen atoms that it combines with. In methane, carbon has a valence of 4; in ammonia, nitrogen has a valence of 3; in water, oxygen has a valence of 2; and in hydrogen chloride, chlorine has a valence of 1.
The electron binding energy derives from the electromagnetic interaction of the electron with the nucleus and the other electrons of the atom, molecule or solid and is mediated by photons. Among the chemical elements, the range of ionization energies is from 3.8939 eV for the outermost electron in an atom of caesium to 11.567617 keV for the ...
σ bond between two atoms: localization of electron density Two p-orbitals forming a π-bond. The overlapping atomic orbitals can differ. The two types of overlapping orbitals are sigma and pi. Sigma bonds occur when the orbitals of two shared electrons overlap head-to-head, with the electron density most concentrated between nuclei.
In complexes of metals with these d-electron configurations, the non-bonding and anti-bonding molecular orbitals can be filled in two ways: one in which as many electrons as possible are put in the non-bonding orbitals before filling the anti-bonding orbitals, and one in which as many unpaired electrons as possible are put in. The former case ...
The structures (left) are verified using small angle X-ray scattering (middle) and electron microscopy (right). Due to cooperative effects stemming from polyvalency (chemistry), a polyvalent SNA-nanoparticle conjugate binds tighter to a complementary free linear strand than does the same sequence of DNA free in solution. [9]