Abstract: A method of producing a pentafluorosulfanyl aromatic compound is provided. A method of producing a pentafluorosulfanyl aromatic compound represented by general formula (3): Ar—(SF5)k??(3) where Ar is a substituted or an unsubstituted aryl group or heteroaryl group, and k is an integer of 1 to 3; the method includes reacting IF5 with a halotetrafluorosulfanyl aromatic compound represented by general formula (2): Ar—(SF4Hal)k??(2) where Ar and k are defined as above; and Hal is a Cl group, a Br group, or an I group.

Abstract: A pyridine compound having a SF5 group on position-3 and position-4 of a pyridine ring is provided.

Abstract: A method of producing a pentafluorosulfanyl aromatic compound is provided. A method of producing a pentafluorosulfanyl aromatic compound represented by general formula (3): Ar—(SF5)k??(3) where Ar is a substituted or an unsubstituted aryl group or heteroaryl group, and k is an integer of 1 to 3; the method includes reacting IF5 with a halotetrafluorosulfanyl aromatic compound represented by general formula (2): Ar—(SF4Hal)k??(2) where Ar and k are defined as above; and Hal is a Cl group, a Br group, or an I group.

Abstract: A compound having a SF4 group on a pyridine ring is provided. Specifically, the compound is represented by the general formula (c): wherein k is 1 or 2; X is a hydrogen atom or a halogen atom; R1 is a hydrogen atom, a halogen atom, a substituted or unsubstituted alkyl group having 1 to 18 carbon atoms, a substituted or unsubstituted aryl group having 6 to 30 carbon atoms, or a nitro group; and R2 is a substituted or unsubstituted alkyl group having 1 to 18 carbon atoms or a substituted or unsubstituted aryl group having 6 to 30 carbon atoms.

Abstract: A pyridine compound having a SF5 group on position-3 and position-4 of a pyridine ring is provided.

Abstract: Provided is a compound that can easily introduce a 2-pentafluorosulfanylpyridyl group into a target compound. The compound is represented by General Formula (d): In the formula, k is 1 or 2, R1 is an alkyl group having 1 or 2 carbon atoms, k is an integer of 0 to 4, R2 is a linear or branched alkyl group having 1 to 4 carbon atoms, m is an integer of 0 to 5, and A? is a counter anion.

Abstract: A compound having a SF4 group on a pyridine ring is provided. Specifically, the compound is represented by the general formula (c): wherein k is 1 or 2; X is a hydrogen atom or a halogen atom; R1 is a hydrogen atom, a halogen atom, a substituted or unsubstituted alkyl group having 1 to 18 carbon atoms, a substituted or unsubstituted aryl group having 6 to 30 carbon atoms, or a nitro group; and R2 is a substituted or unsubstituted alkyl group having 1 to 18 carbon atoms or a substituted or unsubstituted aryl group having 6 to 30 carbon atoms.

Abstract: Industrial methods for producing arylsulfur pentafluorides are disclosed. Methods include reacting arylsulfur halotetrafluoride with hydrogen fluoride in the absence or presence of one or more additives selected from a group of fluoride salts, non-fluoride salts, and unsaturated organic compounds to form arylsulfur pentafluorides.

Abstract: Industrial methods for producing arylsulfur pentafluorides are disclosed. Methods include reacting arylsulfur halotetrafluoride with hydrogen fluoride in the absence or presence of one or more additives selected from a group of fluoride salts, non-fluoride salts, and unsaturated organic compounds to form arylsulfur pentafluorides.

Abstract: Industrial methods for producing arylsulfur pentafluorides are disclosed. Methods include reacting arylsulfur halotetrafluoride with hydrogen fluoride in the absence or presence of one or more additives selected from a group of fluoride salts, non-fluoride salts, and unsaturated organic compounds to form arylsulfur pentafluorides.

Abstract: Provided is a phthalocyanine derivative of the following general formula (1) which has superior solubility in organic solvents: General formula (1): (wherein M is a hydrogen atom, a metal element, a metalloid element, a metal oxide, a metalloid oxide, a metal hydroxide, a metalloid hydroxide, a metal halide, or a metalloid halide, and R is each independently a hydrogen atom, an alkyl ethyl group, an aryl ether group, an alkyl sulfide group, an aryl sulfide group, or a trifluoromethyl group).

Abstract: Industrial methods for producing arylsulfur pentafluorides are disclosed. Methods include reacting arylsulfur halotetrafluoride with hydrogen fluoride in the absence or presence of one or more additives selected from a group of fluoride salts, non-fluoride salts, and unsaturated organic compounds to form arylsulfur pentafluorides.

Abstract: Industrial methods for producing arylsulfur pentafluorides are disclosed. Methods include reacting arylsulfur halotetrafluoride with hydrogen fluoride in the absence or presence of one or more additives selected from a group of fluoride salts, non-fluoride salts, and unsaturated organic compounds to form arylsulfur pentafluorides.

Abstract: Industrial methods for producing arylsulfur pentafluorides are disclosed. Methods include reacting arylsulfur halotetrafluoride with hydrogen fluoride in the absence or presence of one or more additives selected from a group of fluoride salts, non-fluoride salts, and unsaturated organic compounds to form arylsulfur pentafluorides.

Abstract: Industrial methods for producing arylsulfur pentafluorides are disclosed. Methods include reacting arylsulfur halotetrafluoride with hydrogen fluoride in the absence or presence of one or more additives selected from a group of fluoride salts, non-fluoride salts, and unsaturated organic compounds to form arylsulfur pentafluorides.

Abstract: Provided is a compound that allows easy introduction of a pentafluorosulfanylaryl group into a compound of interest. A diaryliodonium salt is represented by the general formula (d) shown below: In this formula, k is 1 or 2, R1 is an alkyl group having 1 or 2 carbon atoms, m is an integer of 0 to 4, R2 is a straight or branched alkyl group having 1 to 4 carbon atoms, n is an integer of 0 to 5, and A? is a counter anion.

Abstract: Provided is a compound that allows easy introduction of a pentafluorosulfanylaryl group into a compound of interest. A diaryliodonium salt is represented by the general formula (d) shown below: In this formula, k is 1 or 2, R1 is an alkyl group having 1 or 2 carbon atoms, m is an integer of 0 to 4, R2 is a straight or branched alkyl group having 1 to 4 carbon atoms, n is an integer of 0 to 5, and A? is a counter anion.

Abstract: Provided is a phthalocyanine derivative of the following general formula (1) which has superior solubility in organic solvents: General formula (1): (wherein M is a hydrogen atom, a metal element, a metalloid element, a metal oxide, a metalloid oxide, a metal hydroxide, a metalloid hydroxide, a metal halide, or a metalloid halide, and R is each independently a hydrogen atom, an alkyl ethyl group, an aryl ether group, an alkyl sulfide group, an aryl sulfide group, or a trifluoromethyl group).

Abstract: Industrial methods for producing arylsulfur pentafluorides are disclosed. Methods include reacting arylsulfur halotetrafluoride with hydrogen fluoride in the absence or presence of one or more additives selected from a group of fluoride salts, non-fluoride salts, and unsaturated organic compounds to form arylsulfur pentafluorides.

Abstract: Industrial methods for producing arylsulfur pentafluorides are disclosed. Methods include reacting arylsulfur halotetrafluoride with hydrogen fluoride in the absence or presence of one or more additives selected from a group of fluoride salts, non-fluoride salts, and unsaturated organic compounds to form arylsulfur pentafluorides.