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Beryllium fluoride has distinctive optical properties. In the form of fluoroberyllate glass, it has the lowest refractive index for a solid at room temperature of 1.275. Its dispersive power is the lowest for a solid at 0.0093, and the nonlinear coefficient is also the lowest at 2 × 10 −14.
Boron trifluoride reacts with water to give boric acid and fluoroboric acid. The reaction commences with the formation of the aquo adduct, H 2 O−BF 3, which then loses HF that gives fluoroboric acid with boron trifluoride. [22] 4 BF 3 + 3 H 2 O → 3 H[BF 4] + B(OH) 3
In the diamond-like structure, called cubic boron nitride (tradename Borazon), boron atoms exist in the tetrahedral structure of carbon atoms in diamond, but one in every four B-N bonds can be viewed as a coordinate covalent bond, wherein two electrons are donated by the nitrogen atom which acts as the Lewis base to a bond to the Lewis acidic ...
The fluorine–fluorine bond of the difluorine molecule is relatively weak when compared to the bonds of heavier dihalogen molecules. The bond energy is significantly weaker than those of Cl 2 or Br 2 molecules and similar to the easily cleaved oxygen–oxygen bonds of peroxides or nitrogen–nitrogen bonds of hydrazines. [8]
Supramolecular chemistry refers to the branch of chemistry concerning chemical systems composed of a discrete number of molecules.The strength of the forces responsible for spatial organization of the system range from weak intermolecular forces, electrostatic charge, or hydrogen bonding to strong covalent bonding, provided that the electronic coupling strength remains small relative to the ...
In coordination chemistry, a coordinate covalent bond, [1] also known as a dative bond, [2] dipolar bond, [1] or coordinate bond [3] is a kind of two-center, two-electron covalent bond in which the two electrons derive from the same atom. The bonding of metal ions to ligands involves this kind of interaction. [4]
In organic chemistry, a Schiff base (named after Hugo Schiff) is a compound with the general structure R 1 R 2 C=NR 3 (R 3 = alkyl or aryl, but not hydrogen). [ 1 ] [ 2 ] They can be considered a sub-class of imines , being either secondary ketimines or secondary aldimines depending on their structure.
In water, by altering the autoionization equilibrium, bases yield solutions in which the hydrogen ion activity is lower than it is in pure water, i.e., the water has a pH higher than 7.0 at standard conditions. A soluble base is called an alkali if it contains and releases OH − ions quantitatively.