Thiocarbonate describes a family of anions with the general chemical formula (x = 0, 1, or 2):
Like the carbonate dianion, the thiocarbonate ions are trigonal planar, with carbon atom at the center of triangle, and oxygen and sulfur atoms at the peaks of the triangle. The average bond order between C and S or O is . The state of protonation is usually not specified. These anions are good nucleophiles and good ligands.
Thiocarbonates refer to salts of those ions as well (e.g. potassium trithiocarbonate, ).
Thiocarbonates refer to esters of those ions as well (e.g. dimethyl trithiocarbonate, ). They contain trigonal planar divalent functional groups similar to these anions (x = 0, 1, or 2, R is organyl group). Esters with the formula are also called xanthates, while esters with the formula are also called thioxanthates.
Thiocarbonates also refer to salts of organyl thiocarbonate ions (e.g. sodium ethyl xanthate or SEX, ). They contain anions (x = 0, 1, or 2, R is organyl group). Anions with the formula , and their salts, are also called xanthates, while salts with the formula , and their salts, are also called thioxanthates.
Monothiocarbonate is the dianion , which has C<sub>2v</sub> symmetry. Monothiocarbonate arises by the hydrolysis of thiophosgene or the reaction of base with carbonyl sulfide:
The esters of monothiocarbonic acids are called monothiocarbonates as well (e.g. O-ethyl-S-methyl monothiocarbonate ).
Dithiocarbonate is the dianion , which has C<sub>2v</sub> symmetry. It arises from the reaction of aqueous base with carbon disulfide:
Important derivatives of dithiocarbonates are the xanthates (O-esters of dithiocarbonates), with the formula . These salts are typically prepared by the reaction of sodium alkoxides with carbon disulfide.
Another group of dithiocarbonates have the formula . They are often derived by hydrolysis of the corresponding trithiocarbonates (RS)<sub>2</sub>CS. One example is tetrathiapentalenedione, a heterocycle that consists of two dithiocarbonate groups.
Trithiocarbonate is the dianion , which has D<sub>3h</sub> symmetry. Trithiocarbonate is prepared by the reaction of sodium hydrosulfide (NaSH) with carbon disulfide:
The relatively elusive trithiocarbonic acid has been characterized by X-ray crystallography.
Esters of thiocarbonic acid, such as dimethyl trithiocarbonate () are also called thioxanthate esters. Trithiocarbonate esters inhibit the enzyme carbonic anhydrase.
Addition of sulfur to trithiocarbonate gives the perthiocarbonate anion , which contains one sulfurâÂÂsulfur bond.
Perthiocarbonic acid (or tetrathioperoxycarbonic acid / disulfanylmethanedithioic acid / CAS#13074-70-9) has never been obtained in pure form.