The synthesis of the two new phosphoramidites 5 and 8 bearing a carbostyril (¼ quinolin-2(1H)-one) chromophore used as donor entity in our recently developed new FRET (fluorescence-resonance-energy transfer) system is described (Schemes 1 and 2) The high stability of the chromophore to basic conditions enables the incorporation of the phosphoramidites directly into DNA during solid-phase synthesis (Schemes 3 and 4). Since this is also possible for the (bathophenanthroline)ruthenium(II) complex used as acceptor (Scheme 4, Steps d and e), the whole labelling procedure to insert the FRET system into synthetic DNA is straightforward and represents a major improvement to our previous strategy.Introduction. -Fluorescently labelled nucleic acids are particularly important tools in molecular biology, diagnostics, and structural studies [1] [2]. In this context, DNA with incorporated dyes representing fluorescence-resonance-energy transfer (FRET) systems have proven to be important tools for the elucidation of distance-dependent interactions on the molecular level and in real time mode. Any changes in donoracceptor distance will affect the rate of energy transfer which can be measured either by steady-state or time-resolved fluorescence studies. The latter approach requires labels with a long lifetime of their fluorescence, and this is usually achieved via the use of lanthanide chelates as acceptor in FRET systems [3] [4]. As alternative labels, we have developed, some time ago, (bathophenanthroline)ruthenium(II) complexes (bathophenanthroline ¼ 4,7-diphenyl-1,10-phenanthroline) which show, after excitation of their metal-to-ligand charge transfer, a fluorescence lifetime in the low msec range [5]. In combination with a quinolinone derivative as donor, this yielded a highly efficient and robust new FRET system, of which the feasibility was first demonstrated in peptides in the course of the development of a homogeneous assay for the serine protease thrombin [6] [7]. Later, we were also able to demonstrate the efficiency of the system in DNA [8]. In this study, both constituents, the (bathophenanthroline)ruthenium(II) complex as well as the carbostyril (¼ quinolin-2(1H)-one) chromophore were attached to aminomodified DNA after deprotection following solid-phase assembly of the oligonucleotide chain. The described method was time-consuming. Hence, we sought for possibilities to improve this labelling procedure.