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Sulfur dioxide can bind to metal ions as a ligand to form metal sulfur dioxide complexes, typically where the transition metal is in oxidation state 0 or +1. Many different bonding modes (geometries) are recognized, but in most cases, the ligand is monodentate, attached to the metal through sulfur, which can be either planar and pyramidal η 1 ...
Sulfur–sulfur bonds are a structural component used to stiffen rubber, similar to the disulfide bridges that rigidify proteins (see biological below). In the most common type of industrial "curing" or hardening and strengthening of natural rubber , elemental sulfur is heated with the rubber to the point that chemical reactions form disulfide ...
Molecular geometries can be specified in terms of 'bond lengths', 'bond angles' and 'torsional angles'. The bond length is defined to be the average distance between the nuclei of two atoms bonded together in any given molecule. A bond angle is the angle formed between three atoms across at least two bonds.
Cu 2 S reacts with oxygen to form SO 2: [6] 2 Cu 2 S + 3 O 2 → 2 Cu 2 O + 2 SO 2. The production of copper from chalcocite is a typical process in extracting the metal from ores. Usually, the conversion involves roasting, to give Cu 2 O and sulfur dioxide: [6] Cu 2 S + O 2 → 2 Cu + SO 2. Cuprous oxide readily converts to copper metal upon ...
Sulfuric(IV) acid (United Kingdom spelling: sulphuric(IV) acid), also known as sulfurous (UK: sulphurous) acid and thionic acid, [citation needed] is the chemical compound with the formula H 2 SO 3. Raman spectra of solutions of sulfur dioxide in water show only signals due to the SO 2 molecule and the bisulfite ion, HSO − 3. [2]
Dimethyldisulfide has the chemical binding CH 3 –S–S–CH 3, whereas carbon disulfide has no S–S bond, being S=C=S (linear molecule analog to CO 2). Most often in sulfur chemistry and in biochemistry, the disulfide term is commonly ascribed to the sulfur analogue of the peroxide –O–O– bond.
Cystine is composed of two cysteines linked by a disulfide bond (shown here in its neutral form). Disulfide bonds in proteins are formed between the thiol groups of cysteine residues by the process of oxidative folding. The other sulfur-containing amino acid, methionine, cannot form disulfide bonds.
In organic chemistry, a sulfone is a organosulfur compound containing a sulfonyl (R−S(=O) 2 −R’) functional group attached to two carbon atoms. The central hexavalent sulfur atom is double-bonded to each of two oxygen atoms and has a single bond to each of two carbon atoms, usually in two separate hydrocarbon substituents. [1]