Abstract: Briefly stated, the present invention encompasses a new class of rhenium 1,1-dithioacid complexes and their method of preparation. The complexes have the general formula [L.sub.2 Re(.mu.-S)].sub.2 wherein L is a dithioacid or similar ligand, and .mu. denotes the fact that the sulfur atoms in the core of the complex bridge the two rhenium atoms in the complex. Thus, the core structure for such typical compounds is generally of the form: ##STR1## where the dangling valences are associated with the sulfur atoms of a 1,1-dithioacid, L.

Abstract: This invention relates to a process for the preparation of promoted molybdenum and tungsten sulfide catalysts, the catalysts prepared by such process, and to the use of such catalysts for hydroprocessing processes, particularly hydrotreating. More particularly, this invention relates to the preparation and use of promoted catalysts useful for hydroprocessing processes such as hydrotreating wherein said catalysts are formed by treating molybdenum and tungsten sulfide-containing material (which may be supported) with a low valence promoter metal selected from transition metals particularly the group of Fe, Co, Ni.

Abstract: Broadly stated, the present invention encompasses tetranuclear sulfide-bridged complexes of Cr(III) having bridging organo-carboxylate ligands. Indeed, in one embodiment, the present invention is directed toward a novel composition of matter having a complex cation of the general formula Cr.sub.4 S(RCO.sub.2).sub.8 (L).sub.4.sup.2+, wherein R represents alkyl groups having from 1 to 12 carbon atoms, L represents a ligand or ligands containing a donor atom selected from oxygen, nitrogen, carbon, and sulfur. In the complex of the present invention, the four Cr(III) atoms are bound to a central tetrahedral sulfur atom. The chromium atoms also are octahedrally coordinated with bridging carboxylates and the ligand molecule. Also, the bridging carboxylates, RCO.sub.2 of the above formula, are the same or different carboxylates.

Abstract: This invention relates to heterometallic thiocubane compositions containing the M.sub.2.sup.1 M.sub.2.sup.2 S.sub.4 cluster core and methods of making them wherein M.sup.1 is Re, V, Mo or W and M.sup.2 is Co, Cr, Cu, Ni or Fe but preferably Co. More particularly, the invention relates to compositions of the formula M.sub.2.sup.2 M.sub.2.sup.2 S.sub.4 L.sub.2.sup.1 L.sub.2.sup.2 L.sub.2.sup.3 wherein M.sup.1 and M.sup.2 are as above, L.sup.1 is a bidentate sulfur or nitrogen bearing ligand (most preferably a dialkyldithiocarbamate), L.sup.2 is optional but may be an O, N, P or S-containing monodentate donor ligand, and L.sup.3 may be CO, a monodentate anion ligand such as a halide (preferably C1), mercaptide or alkoxide, or another O, N, P, or S containing monodentate donor ligand. The compositions are suitable for making active hydrotreating catalysts.

Abstract: This invention relates to neutral complexes of dithioacid vanadium sulfide dimer and to a method of producing the complexes. The 1,1-dithioacid may be a dithiocarbamate, xanthate, dithiophosphate, dithiophosphinate or other similar ligand. The structure is generally of the form ##STR1## where L is a 1,1-dithioacid. The preferred dithioacid is dithiocarbamate. The compositions are suitable for producing hydrotreating catalysts or as a lubricant additive.

Abstract: An improved hydroconversion process for carbonaceous materials wherein an ammonium or hydrocarbyl substituted ammonium salt of a metal-sulfur analog of cubane having an anion with a core structure of M.sub.4 S.sub.4 is used as a catalyst precursor. In the general formula, M may be the same or a different metal having hydrogenation catalytic activity when used as a sulfide and capable of occupying one or more vertices in a cubane structure. The metal may also have the capability of bridging one or more such structures. The improved process is effective for both normally solid and normally liquid carbonaceous materials and for carbonaceous materials which are either solid or liquid at the conversion conditions. The hydroconversion will be accomplished at a temperature within the range from about 500.degree. to about 900.degree. F., at a total pressure within the range from about 500 to about 7000 psig and at a hydrogen partial pressure within the range from about 400 to about 5000 psig.

Abstract: This invention relates to (disulfido)tris(N,N-substituted dithiocarbamato)Mo(V) complexes. More particularly, this invention relates to compounds of the formula MoS.sub.2 (S.sub.2 CNR.sub.2).sub.3 which are mononuclear, eight-coordinate, neutral Mo(V) complexes containing only eight sulfur atoms in the Mo coordination sphere. R is hydrogen, an alkyl, aryl, cycloalkyl group or mixture thereof. Preferably all of the R's are the same and are alkyl groups. These compounds are useful as lubricant additives.

Abstract: This invention relates to sulfido(disulfido)bis(N,N-substituted dithiocarbamato)W(VI) complexes, their preparation and use. More particularly, this invention relates to compounds of the formula WS(S.sub.2) (S.sub.2 CNR.sub.2).sub.2 which are mononuclear, seven-coordinate, neutral W(VI) complexes containing only seven sulfur atoms in the Mo coordination sphere. R is hydrogen, an alkyl, aryl, cycloalkyl group or mixture thereof. Preferably all of the R's are the same and are alkyl groups. These compounds are useful as catalysts or catalyst precursors for removing sulfur from sulfur containing hydrocarbons.

Abstract: Hydrocarbon feeds are upgraded by contacting same, at elevated temperature and in the presence of hydrogen, with a self-promoted catalyst formed by heating one or more carbon-containing, bis(tetrathiometallate) catalyst precursor salts selected from the group consisting of (NR.sub.4).sub.2 [M(WS.sub.4).sub.2 ], (NR.sub.4).sub.x [M(MoS.sub.4).sub.2 ] and mixtures thereof wherein R is one or more alkyl groups, aryl groups or mixture thereof, wherein promoter metal M is covalently bound in the anion and is Ni, Co or Fe and wherein x is 2 if M is Ni and x is 3 if M is Co or Fe composite in a non-oxidizing atmosphere in the presence of sulfur, hydrogen, and a hydrocarbon to form said supported catalyst.

Abstract: Compositions of the formula [(Cat.sup.n)].sub.3/n [Co(MoS.sub.4).sub.2 ] wherein Cat is a mono, di or trivalent cation and n is 1, 2 or 3, respectively, have been prepared in non-aqueous media. The [Co(MoS.sub.4).sub.2 ].sup.3- anion has the general structure ##STR1## Cat is preferably an alkyl substituted quaternary ammonium compound.

Abstract: Self-promoted molybdenum and tungsten sulfide hydrotreating catalyst are formed by heating one or more carbon-containing, bis(tetrathiometallate) catalyst precursor hydrogen with a supported, self-promoted catalyst salts selected from the group consisting of (NR.sub.4).sub.2 [M(WS.sub.4).sub.2 ], (NR.sub.4).sub.x [M(MoS.sub.4).sub.2 ] and mixtures thereof wherein R is one or more alkyl groups, aryl groups or mixture thereof, wherein promoter metal M is convalently bound in the anion and is Ni, Co or Fe and wherein x is 2 if M is Ni and x is 3 if M is Co or Fe in a non-oxidizing atmosphere in the presence of sulfur hydrogen, and hydrocarbon.