Abstract: Method for storing and/or transporting GaCl3 involving the step of adding an aluminium compounds of the formula R3-xAlClx, wherein R is a linear or branched alkyl group with 1-8 carbon atoms and x is 0 or 1, to said GaCl3 in an Al/Ga molar ratio of at least 0.2, thereby forming a liquid formulation, followed by introducing said liquid formulation in a container.

Abstract: Method for storing and/or transporting GaCl3 involving the step of adding an aluminium compounds of the formula R3-xAlClx, wherein R is a linear or branched alkyl group with 1-8 carbon atoms and x is 0 or 1, to said GaCl3 in an Al/Ga molar ratio of at least 0.2, thereby forming a liquid formulation, followed by introducing said liquid formulation in a container.

Abstract: Process for the preparation of a trimethyl metal compound with the formula M(CH3)3, said process comprising the step of reacting a trialkyl metal compound of the formula M(R)3 with trimethyl aluminium [AI(CH3)3] to form said trimethyl metal compound with the formula M(CH3)3, wherein M is selected from the group consisting of Ga and In, and R is a linear or branched alkyl group with 2 to 8 carbon atoms.

Abstract: The present invention relates to a process to prepare alkylaluminoxanes by reaction of alkylaluminium with methacrylic acid or a conjugated unsaturated carbonyl-functional compound of the formula (I) wherein each R1 and R2 independently are an aliphatic hydrocarbon group, and R3 independently is the same hydrocarbon group as R1 and R2 or a hydrogen atom, and R4 isanaliphatic hydrocarbon group, a hydroxyl group or a hydrogen atom in the presence of an inert organic solvent. Additionally, it relates to the alkylaluminoxanes obtainable by the above process and their use.

Abstract: Process for the production of a trimethyl metal compound with the formula M(CH3)3, said process comprising the steps of (i) reacting a metal trihalide MX3 with a trialkyl aluminium compound AI(R)3 to form a trialkyl metal compound M(R)3 and a dialkyl aluminium halide AI(R)2X, and (ii) reacting said trialkyl metal compound M(R)3 with either trimethyl aluminium [AI(CH3)3] or dimethylaluminium halide [AI(CH3)2X] to form said trimethyl metal compound M(CH3)3, wherein M is selected from the group consisting of Ga and In, X is a halogen, and R is a linear or branched alkyl group with 2 to 8 carbon atoms.

Abstract: Process for the production of a trimethyl metal compound with the formula M(CH3)3, said process comprising the steps of (i) reacting a metal trihalide MX3 with a trialkyl aluminium compound AI(R)3 to form a trialkyl metal compound M(R)3 and a dialkyl aluminium halide AI(R)2X, and (ii) reacting said trialkyl metal compound M(R)3 with either trimethyl aluminium [AI(CH3)3] or dimethylaluminium halide [AI(CH3)2X] to form said trimethyl metal compound M(CH3)3, wherein M is selected from the group consisting of Ga and In, X is a halogen, and R is a linear or branched alkyl group with 2 to 8 carbon atoms.

Abstract: The present invention relates to a process to prepare alkylaluminoxanes by reaction of alkylaluminium with methacrylic acid or a conjugated unsaturated carbonyl-functional compound of the formula (I) wherein each R1 and R2 independently are an aliphatic hydrocarbon group, and R3 independently is the same hydrocarbon group as R1 and R2 or a hydrogen atom, and R4 isanaliphatic hydrocarbon group, a hydroxyl group or a hydrogen atom in the presence of an inert organic solvent. Additionally, it relates to the alkylaluminoxanes obtainable by the above process and their use.

Abstract: The present invention relates to a process to prepare alkylaluminoxanes by reaction of alkylaluminium with a substituted allylic alcohol of the formula wherein each R1 and R2 independently are an aliphatic or aromatic hydrocarbon group, and R3, R4, and R5 each independently may be the same hydrocarbon group as R1 and R2 or a hydrogen atom in the presence of an inert organic solvent. Additionally, it relates to the alkylaluminoxanes obtainable by the above process and their use.

Abstract: The present invention relates to a process to prepare alkylaluminoxanes by reaction of alkylaluminium with a substituted allylic alcohol of the formula wherein each R1 and R2 independently are an aliphatic or aromatic hydrocarbon group, and R3, R4, and R5 each independently may be the same hydrocarbon group as R1 and R2 or a hydrogen atom in the presence of an inert organic solvent. Additionally, it relates to the alkylaluminoxanes obtainable by the above process and their use.

Abstract: The present invention relates to a process for the catalytic halogenation of an organic compound comprising at least one vicinal diol moiety, said process comprising a step of bringing the organic compound comprising at least one vicinal diol moiety into contact with a hydrogen halide in the presence of a catalyst, characterized in that the catalyst is an organic compound comprising a ?-diketone moiety or a ?-keto aldehyde moiety.

Abstract: The present invention relates to a process for the catalytic halogenation of an organic compound comprising at least one vicinal diol moiety, said process comprising a step of bringing the organic compound comprising at least one vicinal diol moiety into contact with a hydrogen halide in the presence of a catalyst, characterized in that the catalyst is an organic compound comprising a ?-diketone moiety or a ?-keto aldehyde moiety.

Abstract: The present invention relates to a process for preparing 1-indanones of formula I: and isomers thereof, wherein R1, R2, R3, R4, R5, and R6 independently represent H or a C1-C20 hydrocarbon group or R1 and R2 or R2 and R3 or R3 and R4 and/or R5 and R6 together with the carbon atoms to which they are attached form a saturated or unsaturated 5- or 6-membered ring, said hydrocarbon group and/or said ring optionally containing one or more hetero atoms, said ring optionally being substituted with a C1-C4 hydrocarbon group, said process comprising reacting a compound of formula II: wherein R1, R2, R3, R4, R5, and R6 have the same meaning as defined above, with a chlorinating agent, followed by reaction with a Friedel-Crafts catalyst. The invention further relates to the preparation of the corresponding indenes.

Abstract: The present invention relates to a process for preparing bisindenylalkanes of formula I: wherein R1, R2, R3, and R4 independently represent H or a C1-C6 hydrocarbon group or R1 and R2 or R1 and R3 or R3 and R4 together with the carbon atoms to which they are attached form a saturated or unsaturated 5- or 6-membered ring, said ring being optionally substituted with a C1-C4 hydrocarbon group, and R5 represents a C1-C6 hydrocarbon group, comprising reacting, at a temperature which does not exceed about 5° C., a metallated indene of formula II with a disubstituted hydrocarbon of formula III: wherein R1, R2, R3, R4, and R5 have the same meaning as defined above, M represents a metal ion, and X independently represents a suitable leaving group, in a suitable reaction medium wherein the molar ratio of II to III is 2.05 or higher. The process is particularly suitable for preparing bisindenylethane, i.e., R1-R4 represent H and R5 represents an ethylene group.

Abstract: The present invention relates to a process for preparing 1-indanones of formula I: 1

Abstract: The invention pertains to a cross-linkable fluorinated polymer comprising the carbonate moiety having formula (I) wherein n=1-10 and m=0-9. Preferably, the polymer further comprises a cross-linkable moiety derived from a diol selected from (II) and (III) wherein A, A1, and A2 are independently a bond or C1-12 alkylene, or together with the carbon atoms to which they are bonded form a 5- or 6-membered ring; B is independently O or C1-4 alkyl; Q is —CO—C(=E)D, wherein D is H or C1-4 alkyl, and E is C1-6 alkylidene; and each of the alkyl, alkylene, and alkylidene groups may be halogenated. The polymers of the invention can be used in cladding layers or waveguides, in particular for thermo-optical devices.

Abstract: The present invention relates to a process for preparing bisindenylalkanes of formula I: 1

Abstract: The invention pertains to a cross-linker of the formula wherein n is 0 or 1; m is 0 or 1; R is and R1 is independently OH or —CO—O(hydroxyphenyl), or of the formula with the proviso that 3,4-dihydroxyphenylmaleimide is excluded. The invention further pertains to cross-linked optical polycarbonate and optical articles obtainable by cross-linking a polycarbonate with this cross-linker or with 3,4-dihydroxyphenylmaleimide.

Abstract: The invention relates to a process of preparing a 2-alkyl-2,3-dihydro-1H-benz?e!indene-1-one derivative, preferably 2,3-dihydro-2-methyl-benz?e!indene-1-one, characterized in that a naphthalene derivative is condensed with an active ester of 2-alkyl-2-propenoic acid, preferably with 2-methyl-2-propenoyl chloride. The product which is obtained in high yield and substantially free from its isomer is an intermediate in the preparation of rac-dimethyl bis(2-alkyl-1H-benz?e!indenyl)silandiyl zirconium dichloride complex.

Abstract: The present invention is in the field of optical polymers, more particularly, optical polycarbonates for use in optical components.The present invention provides a cross-linkable or cross-linked optical polycarbonate built up from a monomer mixture comprising:compounds according to formula 1: ##STR1## wherein: P stands for --Cl, O--R, an imidazole group or --O--Ph, Q stands for --Cl, O--R, an imidazole group or --O--Ph,R stands for an alkylene group having 1-6 carbon atoms,Ph stands for phenyl,A stands for --Ph--, halogenated --Ph--, (halo)alkyl substituted --Ph, --Ph--Ph--, halogenated --Ph--Ph, --Ph--C(CH.sub.3).sub.2 --Ph--, --Ph--SO.sub.2 --Ph--, --Ph--C(CF.sub.3)--Ph--, halogenated --Ph--C(CH.sub.3).sub.2 --Ph, halogenated --Ph--C(CF.sub.3).sub.2 --Ph, phenolphtalein, --Ph--C(Ph).sub.2 --Ph,m is an integer from 0 to 5, with the A-groups being the same or different,optionally, diols, optionally, a dihydroxy-functionalised NLO-compound, and 2,3 dihydroxy propyl methacrylate as a crosslinker.

Abstract: The invention relates to non-linear optically active (NLO) polycarbonates and to NLO active waveguides containing these polycarbonates. Waveguides containing these NLO polycarbonates have a low loss of signal, a high glass transition temperature and good polability and a high stability of the Pockel's coefficient.