Binding and photodissociation of CO in iron(II) complexes for application in positron emission tomography (PET) radiolabelling

被引:16
作者
Child, Chloe R. [1 ,2 ]
Kealey, Steven [2 ]
Jones, Harriet [3 ]
Miller, Philip W. [1 ]
White, Andrew J. P. [1 ]
Gee, Anthony D. [4 ]
Long, Nicholas J. [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Chem, London SW7 2AZ, England
[2] Hammersmith Hosp, GlaxoSmithKline Clin Imaging Ctr, London W12 0NN, England
[3] Abbey Sch, Reading RG1 5DZ, Berks, England
[4] Kings Coll London, Rayne Inst, St Thomas Hosp, London SE1 7EH, England
基金
英国工程与自然科学研究理事会;
关键词
REACTIVITY; MONOXIDE;
D O I
10.1039/c0dt01614d
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
(R-DAB)FeI(2) complexes containing bidentate diimide ligands (R-DAB = RN=CH-CH=NR; R = (i)Pr, c-C(6)H(11)) have been investigated for their ability to react with carbon monoxide to form iron(II) dicarbonyl complexes, (R-DAB)FeI(2)(CO)(2). Solution IR spectroscopy revealed two vCO stretches between 2000 and 2040 cm(-1) corresponding to a cis-arrangement of the carbonyl ligands around the iron. Photochemical decarbonylation was achieved by UV irradiation (365 nm), which occurred within 5 min as evidenced by solution IR spectroscopy. (c-C(6)H(11)-DAB)FeI(2) has been characterised by X-ray crystallography. Reactions using (11)C-labelled carbon monoxide were investigated and revealed that both (R-DAB)FeI(2) species were not effective as trapping complexes due to the low concentrations of [(11)C] CO used in these experiments. A Fe(TPP)(THF)(x) (TPP = tetraphenylporphyrin) complex was investigated with unlabelled CO and the monocarbonyl adduct Fe(TPP)(THF) CO was formed in situ as identified by IR spectroscopy (vCO = 1966 cm(-1)) yet was stable to CO loss upon UV irradiation. Carbonylation reactions of in situ-generated Fe(TPP)(THF)(x) using [(11)C] CO revealed that 97% of the [(11)C] CO stream could be trapped in one pass of the gas at room temperature and at atmospheric pressure.
引用
收藏
页码:6210 / 6215
页数:6
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