Abstract: A metal complex of formula (III) wherein: M is a transition metal and A1, A2, X, X?, Y, L1?, R1? and R2? are as defined herein, is useful in medical imaging and therapy.
Type:
Grant
Filed:
July 5, 2006
Date of Patent:
October 30, 2012
Assignee:
Isis Innovation Limited
Inventors:
Jonathan Robin Dilworth, Josephine Mary Peach, Julia May Heslop, Paul Stephen Donnelly
Abstract: Synthesis of small quantities of compounds such as methanol from reagents, especially radio-labelled reagents such as .sup.11 C oxides, in a carrier gas by a catalytic reaction using a catalyst that has been pre-conditioned for the reaction by previous use for the desired reaction and has then been passivated, or has been maintained in the pre-conditioned state, until contacted with said carrier gas. Where the product is adsorbed by the catalyst, it may be desorbed by heating or displaced by contacting the catalyst with a material, e.g. a catalyst poison that is more strongly adsorbed. Such a more strongly adsorbed material may react with the adsorbed catalytic product to produce a desired product.
Type:
Grant
Filed:
July 22, 1996
Date of Patent:
January 12, 1999
Assignee:
Imperial Chemical Industries, PLC
Inventors:
Samuel David Jackson, Frederick Ernest Hancock, Bernard John Crewdson
Abstract: The present invention relates to perfluoroalkyl substituted sulfates and salts thereof of the formulas(R.sub.f X CH.sub.2).sub.x C(CH.sub.2 OH).sub.y (CH.sub.2 OSO.sub.3 -M+).sub.z (I)or(R.sub.f E X CH.sub.2).sub.x C(CH.sub.2 OH).sub.y (CH.sub.2 OSO.sub.3 -M+).sub.z(II)wherein R.sub.f is a straight or branched chain perfluoroalkyl of 1 to 18 carbon atoms or said perfluoroalkyl substituted by perfluoroalkoxy of 2 to 6 carbon atoms,E is branched or straight chain alkylene of 1 to 10 carbon atoms or said alkylene interrupted by one to three groups selected from the group consisting of --NR--, --O--, --S--, --SO.sub.2 --, --COO--, --OOC--, --CONR--, --NRCO--, --SO.sub.2 NR-- and NRSO.sub.2 -- or terminated at the R.sub.f end with --CONR-- or --SO.sub.2 NR--, where R.sub.f is attached to the carbon or sulfur atom, and for formula II, X is --S--, --O--, --SO.sub.2 --, or --NR--, and for formula I, X is --CONR-- or --SO.sub.2 NR--, where R.sub.