Processes for producing a N,N-dialkyl perfluoroalkyl-sulfonamide product of the formula R.sub.f—S(O).sub.2—NR.sub.aR.sub.b (I) in which R.sub.f represents fully or partially fluorinated alkyl groups with carbon 1 to 12 and R.sub.a and R.sub.b represents linear or branched or cyclic alkyl, alkene or alkyne groups with carbon 1 to 12, wherein R.sub.a=R.sub.b or R.sub.a≠R.sub.b. In some embodiments, a reaction proceeds by contacting a perfluoroalkylsulfonyl halide of the formula: X—S(O).sub.2—R.sub.f, (II), in which X represents F, Cl, Br or I, with dialkylamine of the formula HNR.sub.aR.sub.b, under conditions sufficient to produce the desired N,N-dialkyl perfluoroalkylsulfonamide product of Formula I. In some embodiments, the reaction is carried out using a solvent of Formula I.

The present invention relates to new one-photon or two-photon absorbing fluorophores, a method for preparing the same, and a method for cellular imaging using the same, and more particularly, to new two-photon absorbing fluorophores having higher fluorescence quantum yield and two-photon absorption cross-section value than those of the conventional two-photon absorbing fluorophore, acedan, and thus are promisingly applicable in bioimaging. The design strategy and the compounds according to the present invention may practically utilized for developing new D-π-A fluorophores.

The present invention relates to new one-photon or two-photon absorbing fluorophores, a method for preparing the same, and a method for cellular imaging using the same, and more particularly, to new two-photon absorbing fluorophores having higher fluorescence quantum yield and two-photon absorption cross-section value than those of the conventional two-photon absorbing fluorophore, acedan, and thus are promisingly applicable in bioimaging. The design strategy and the compounds according to the present invention may practically utilized for developing new D-π-A fluorophores.

Disclosed are methods for the preparation of ligands for complexes, methods for preparing complexes and complexes having those ligands. Also provided is the use of a complex as a catalyst in a method of synthesis.

Disclosed are methods for the preparation of ligands for complexes, methods for preparing complexes and complexes having those ligands. Also provided is the use of a complex as a catalyst in a method of synthesis.

A multi-acid polymer disclosed herein has the formula

##STR00001##

wherein R is one or more units of a non-SOF.sub.2 or non-SO.sub.2Cl portion of a polymer precursor in sulfonyl fluoride or sulfonyl chloride form, X is a non-sulfonyl halide group of a multi-sulfonyl halide compound having a minimum of two acid giving groups, and Y is remaining sulfonyl halide groups of the multi-sulfonyl halide compound.

A multi-acid polymer disclosed herein has the formula

##STR00001##

wherein R is one or more units of a non-SOF.sub.2 or non-SO.sub.2Cl portion of a polymer precursor in sulfonyl fluoride or sulfonyl chloride form, X is a non-sulfonyl halide group of a multi-sulfonyl halide compound having a minimum of two acid giving groups, and Y is remaining sulfonyl halide groups of the multi-sulfonyl halide compound.

The preparation is described of a compound of formula (I) comprising an —SO.sub.2F function by reacting a compound of formula (II) with a fluorinating agent selected from hydrofluoric acid and an ionic fluoride of a monovalent or divalent cation:
R—SO.sub.2F  (I)
R′—SO.sub.2X  (II)
where R is selected from the groups R1, R2 and R3: R1=—C.sub.nH.sub.aF.sub.b with n=1-10, a+b=2n+1, b≧1; R2=—C.sub.xH.sub.yF.sub.z—SO.sub.2F with x=1-10, y+z=2x and z≧1; R3=φ-C.sub.cH.sub.hF.sub.f with c=1-10; h+f=2c and f≧1;
where R′ is selected from the following groups R′1, R′2 and R′3: R′1=—C.sub.nH.sub.aX.sub.b with n=1-10, a+b=2n+1, b≧1; R′2=—C.sub.xH.sub.yX.sub.z—SO.sub.2X with x=1-10, y+z=2x and z≧1; R′3=φ-C.sub.cH.sub.hX.sub.f with c=1-10; h+f=2c and f≧1; φ denoting a phenyl group; X═Cl, Br.

The preparation is described of a compound of formula (I) comprising an —SO.sub.2F function by reacting a compound of formula (II) with a fluorinating agent selected from hydrofluoric acid and an ionic fluoride of a monovalent or divalent cation:
R—SO.sub.2F  (I)
R′—SO.sub.2X  (II)
where R is selected from the groups R1, R2 and R3: R1=—C.sub.nH.sub.aF.sub.b with n=1-10, a+b=2n+1, b≧1; R2=—C.sub.xH.sub.yF.sub.z—SO.sub.2F with x=1-10, y+z=2x and z≧1; R3=φ-C.sub.cH.sub.hF.sub.f with c=1-10; h+f=2c and f≧1;
where R′ is selected from the following groups R′1, R′2 and R′3: R′1=—C.sub.nH.sub.aX.sub.b with n=1-10, a+b=2n+1, b≧1; R′2=—C.sub.xH.sub.yX.sub.z—SO.sub.2X with x=1-10, y+z=2x and z≧1; R′3=φ-C.sub.cH.sub.hX.sub.f with c=1-10; h+f=2c and f≧1; φ denoting a phenyl group; X═Cl, Br.

The preparation is described of a compound of formula (I) comprising an —SO.sub.2F function by reacting a compound of formula (II) with a fluorinating agent selected from hydrofluoric acid and an ionic fluoride of a monovalent or divalent cation:
R—SO.sub.2F  (I)
R′—SO.sub.2X  (II)
where R is selected from the groups R1, R2 and R3: R1=—C.sub.nH.sub.aF.sub.b with n=1-10, a+b=2n+1, b≧1; R2=—C.sub.xH.sub.yF.sub.z—SO.sub.2F with x=1-10, y+z=2x and z≧1; R3=φ-C.sub.cH.sub.hF.sub.f with c=1-10; h+f=2c and f≧1;
where R′ is selected from the following groups R′1, R′2 and R′3: R′1=—C.sub.nH.sub.aX.sub.b with n=1-10, a+b=2n+1, b≧1; R′2=—C.sub.xH.sub.yX.sub.z—SO.sub.2X with x=1-10, y+z=2x and z≧1; R′3=φ-C.sub.cH.sub.hX.sub.f with c=1-10; h+f=2c and f≧1; φ denoting a phenyl group; X═Cl, Br.