Abstract: Described are compounds of the structure R4-a—Si-((Sp-Y)—Zb)a, wherein “a” is an integer from 1 to 3; “b” is an integer from 0 to (3×a); “Z,” which is absent when “b”=0, is halogen, C1-6 linear or branched alkyl, alkenyl, or alkynyl, C1-6 linear or branched halo-alkyl, halo-alkenyl, or halo-alkynyl, or wherein each “R” is halogen, C1-6 linear or branched alkyl, alkenyl, or alkynyl or C1-6 linear or branched halo-alkyl, halo-alkenyl, or halo-alkynyl; each “Sp” C1-15 linear or branched alkylenyl or C1-15 linear or branched halo-alkylenyl; and each “Y” an organic polar group. Also described are electrolyte compositions containing one or more of these compounds.

Abstract: Described are compounds of the structure R4-a—Si-(Sp-Y)a—Zb, wherein “a” is an integer from 1 to 4; “b” is an integer from 0 to (3×a); “Z,” which is absent when “b”=0, is “R” or wherein each “R” is halogen, C1-6 linear or branched alkyl, alkenyl, or alkynyl or C1-6 linear or branched halo-alkyl, halo-alkenyl, or halo-alkynyl; each “Sp” C1-15 linear or branched alkylenyl or C1-15 linear or branched halo-alkylenyl; and each “Y” an organic polar group. Also described are electrolyte compositions containing one or more of these compounds.

Abstract: Described herein are liquid, organosilicon compounds that including a substituent that is a cyano (—CN), cyanate (—OCN), isocyanate (—NCO), thiocyanate (—SCN) or isothiocyanate (—NCS). The organosilicon compounds are useful in electrolyte compositions and can be used in any electrochemical device where electrolytes are conventionally used.

Abstract: Described are electrolyte compositions and electrochemical devices containing the electrolyte compositions. The compositions include an organosilicon compound, an imide salt and optionally LiPF6. The electrolytes provide improved high-temperature performance and stability and will operate at temperatures as high as 250° C.

Abstract: Described are compounds of the structure R4-a—Si-(Sp-Y)a—Zb, wherein “a” is an integer from 1 to 4; “b” is an integer from 0 to (3×a); “Z,” which is absent when “b”=0, is “R” or wherein each “R” is halogen, C1-6 linear or branched alkyl, alkenyl, or alkynyl or C1-6 linear or branched halo-alkyl, halo-alkenyl, or halo-alkynyl; each “Sp” C1-15 linear or branched alkylenyl or C1-15 linear or branched halo-alkylenyl; and each “Y” an organic polar group. Also described are electrolyte compositions containing one or more of these compounds.

Abstract: Described are compounds of the structure R4-a—Si-(Sp-Y)a—Zb, wherein “a” is integer from 1 to 4; “b” is an integer from 0 to (3×a); “Z,” which is absent when “b “R” or formula (II), wherein each “R” is halogen, C1-6 linear or branched alkyl, alkenyl, or alkynyl or C1-6 linear or branched halo-alkyl, halo-alkenyl, or halo-alkynyl; each “Sp” C1-15 linear or branched alkylenyl or CMS linear or branched halo-alkylenyl; and each “Y” an organic polar group. Also described are electrolyte compositions containing one or more of these compounds.

Abstract: Described are electrolyte compositions and electrochemical devices containing the electrolyte compositions. The compositions include an organosilicon compound, an imide salt and optionally LiPF6. The electrolytes provide improved high-temperature performance and stability and will operate at temperatures as high as 250° C.

Abstract: Described herein are liquid, organosilicon compounds that including a substituent that is a cyano (—CN), cyanate (—OCN), isocyanate (—NCO), thiocyanate (—SCN) or isothiocyanate (—NCS). The organosilicon compounds are useful in electrolyte compositions and can be used in any electrochemical device where electrolytes are conventionally used.

Abstract: Described herein are liquid, organosilicon compounds that including a substituent that is a cyano (—CN), cyanate (—OCN), isocyanate (—NCO), thiocyanate (—SCN) or isothiocyanate (—NCS). The organosilicon compounds are useful in electrolyte compositions and can be used in any electrochemical device where electrolytes are conventionally used.

Abstract: Described are electrolyte compositions and electrochemical devices containing the electrolyte compositions. The compositions include an organosilicon compound, an imide salt and optionally LiPF6. The electrolytes provide improved high-temperature performance and stability and will operate at temperatures as high as 250° C.

Abstract: Described are compounds of the structure R4—a—Si—(Sp-Y)a—Zb, wherein “a” is integer from 1 to 4; “b” is an integer from 0 to (3×a); “Z,” which is absent when “b”“R” or formula (II), wherein each “R” is halogen, C1-6 linear or branched alkyl, alkenyl, or alkynyl or C1-6 linear or branched halo-alkyl, halo-alkenyl, or halo-alkynyl; each “Sp” C1-15 linear or branched alkylenyl or CMS linear or branched halo-alkylenyl; and each “Y” an organic polar group. Also described are electrolyte compositions containing one or more of these compounds.

Abstract: Described are electrolyte compositions and electrochemical devices containing the electrolyte compositions. The compositions include an organosilicon compound, an imide salt and optionally LiPF6. The electrolytes provide improved high-temperature performance and stability and will operate at temperatures as high as 250° C.

Abstract: Described are electrolyte compositions and electrochemical devices containing them. The compositions include an organosilicon compound, an imide salt and optionally LiPF6. The electrolytes provide improved high-temperature performance and stability and will operate at temperatures as high as 250 C. An electrolyte composition comprising, in combination: an organosilicon compound and an imide salt and optionally UPF6; wherein when subjected to cyclic voltammetry at a plurality of cycles ranging from about 3V to about 5V and using a cathode current collector comprising aluminum versus Li/Lit electrodes the composition exhibits an oxidative corrosion current of about 0.10 mA/cm2 or less for a second and subsequent cycles.

Abstract: Described herein are liquid, organosilicon compounds that including a substituent that is a cyano (—CN), cyanate (—OCN), isocyanate (—NCO), thiocyanate (—SCN) or isothiocyanate (—NCS). The organosilicon compounds are useful in electrolyte compositions and can be used in any electrochemical device where electrolytes are conventionally used.

Abstract: Described are electrolyte compositions and electrochemical devices containing them. The compositions include an organosilicon compound, an imide salt and optionally LiPF6. The electrolytes provide improved high-temperature performance and stability and will operate at temperatures as high as 250 C. An electrolyte composition comprising, in combination: an organosilicon compound and an imide salt and optionally UPF6; wherein when subjected to cyclic voltammetry at a plurality of cycles ranging from about 3V to about 5V and using a cathode current collector comprising aluminum versus Li/Lit electrodes the composition exhibits an oxidative corrosion current of about 0.10 mA/cm2 or less for a second and subsequent cycles.

Abstract: Described herein are liquid, organosilicon compounds that including a substituent that is a cyano (—CN), cyanate (—OCN), isocyanate (—NCO), thiocyanate (—SCN) or isothiocyanate (—NCS). The organosilicon compounds are useful in electrolyte compositions and can be used in any electrochemical device where electrolytes are conventionally used.

Abstract: Described herein are liquid, organosilicon compounds that including a substituent that is a cyano (—CN), cyanate (—OCN), isocyanate (—NCO), thiocyanate (—SCN) or isothiocyanate (—NCS). The organosilicon compounds are useful in electrolyte compositions and can be used in any electrochemical device where electrolytes are conventionally used.

Abstract: The present invention is directed toward methods of selectively functionalizing carbon nanotubes of a specific type or range of types, based on their electronic properties, using diazonium chemistry. The present invention is also directed toward methods of separating carbon nanotubes into populations of specific types or range(s) of types via selective functionalization and electrophoresis, and also to the novel compositions generated by such separations.

Abstract: The present invention is directed toward methods of selectively functionalizing carbon nanotubes of a specific type or range of types, based on their electronic properties, using diazonium chemistry. The present invention is also directed toward methods of separating carbon nanotubes into populations of specific types or range(s) of types via selective functionalization and electrophoresis, and also to the novel compositions generated by such separations.

Abstract: The present invention is directed toward methods of selectively functionalizing carbon nanotubes of a specific type or range of types, based on their electronic properties, using diazonium chemistry. The present invention is also directed toward methods of separating carbon nanotubes into populations of specific types or range(s) of types via selective functionalization and electrophoresis, and also to the novel compositions generated by such separations.