Baysal, AkınDurap, FeyyazGümgüm, BahattinYıldırım, Leyla T.Ülkü, DinçerBoğa, Ayşe DilekÖzkar, Saim2024-04-242024-04-242007Baysal, A., Durap, F., Gümgüm, B., Yıldırım, L. T., Ülkü, D., Boğa, A. D. ve diğerleri. (2007). Synthesis, characterization, crystal and molecular structure of 1,5-Dihydro-2H-cyclopenta[1,2-b:5,4-b′]dipyridin-2-imine, Helvetica Chimica Acta, 90(6), 1211-1217.0018-019Xhttps://doi.org/10.1002/hlca.200790120https://hdl.handle.net/11468/14041https://onlinelibrary.wiley.com/doi/epdf/10.1002/hlca.200790120The reaction of 1,5-diliydro-2H-cyclopenta[1,2-b:5,4-b'ldipyridin-2-one (3) with an alkylamine (butvlamine, hexylamine or ethylenediamine) yields, quite unexpectedly and in the absence of catalyst, the novel compound 1,5-dihydro-2H-cyclopentafl,2-b:5.4-b']dipyridin-2-imine (4) as the sole, analytically pure, solid product, which was fully characterized. The structure of 4 was unequivocally solved by single-crystal X-ray-diffraction analysis. The compound crystallizes in a monoclinic cell (space group P 2(1/c)). with two molecules in the asymmetric unit. held together by intermolecular H-bonds. Compound 4 could be interesting as a bi- or even tridentate ligand, and exhibits a strong fluorescence upon excitation at 310 nm. A mechanism, based on the observed C-N bond cleavage, is proposed.eninfo:eu-repo/semantics/closedAccess[No Keyword]Synthesis, Characterization, Crystal and Molecular Structure of 1,5-Dihydro-2H-cyclopenta[1,2-b:5,4-b′]dipyridin-2-imineSynthesis, Characterization, Crystal and Molecular Structure of 1,5-Dihydro-2H-cyclopenta[1,2-b:5,4-b?]dipyridin-2-imineArticle90612111217WOS:0002476906000162-s2.0-3444732728410.1002/hlca.200790120Q3Q2