HIGHLY FLUORESCENT MATERIALS WITH PYRROLO - DIAZINE SKELETON

Valeur B. Molecular Fluorescence, Willey-VCH, Weinheim, 2002. DOI: 10.1002/3527600248

Popovici L., Amarandei R.M., Mangalagiu I.I., Mangalagiu V., Danac, R. Synthesis, molecular modelling and anticancer evaluation of new pyrrolo[1,2-b]pyridazine and pyrrolo[2,1-a]phthalazine derivatives, J. Enzyme Inhib. Med. Chem., 34, pp 230-243, 2019, DOI: 10.1080/14756366.2018.1550085

Olaru A., Vasilache V., Danac R., Mangalagiu I.I. Antimycobacterial activity of nitrogen heterocycles derivatives: 7-(pyridine-4-yl)- indolizine derivatives, J. Enzyme Inhib. Med. Chem., 32, pp 1291-1298, 2017, DOI: 10.1080/14756366.2017.1375483

Tucaliuc R.A., Mangalagiu V., Mangalagiu I.I. Pyridazinic Bioisosteres with Potential Applications in Medicinal Chemistry and Agriculture, Processes, 11, 2306, 2023, DOI: 10.3390/pr11082306

Zbancioc G., Bejan, V., Risca M., Moldoveanu, C., Mangalagiu I.I. Microwave assisted reactions of new azaheterocyles compounds, Molecules, 14, pp 403-411, 2009, DOI: 10.3390/molecules14010403

Kim T., Kim J. Color-Tunable Indolizine-Based Fluorophores and Fluorescent pH Sensor, Molecules, 27, 12, 2022, DOI: 10.3390/molecules27010012

Mangalagiu I.I., Baban C., Mardare D., Rusu G.I. On the electrical properties of some new stable disubstituted ylides in thin films, Appl. Surf. Sci., 108, pp 205-210, 1997, DOI: 10.1016/S0169-4332(97)80017-7

Yi S., Kim D., Cho W., Lee J.H., Kwon J.H., Kim J., Park S.B. Rational Design of Pyrido[3,2-b]indolizine as a Tunable Fluorescent Scaffold for Fluorogenic Bioimaging, JACS AU, 4, pp 2896-2906, 2024, DOI: 10.1021/jacsau.4c00135

Badaro J.S.A., Wrzosek A., Morawski O., Szewczyk A., Deperasinska, I., Gryko D.T. Strongly fluorescent indolizine-based coumarin analogs, Org. Chem. Front. 11(23), pp 6627-6641, 2024, DOI: 10.1039/D4QO01216J

Pohl R., Montes V.A., Shinar J., Anzenbacher P. Red-green-blue emission from tris(5-aryl-8-quinolinolate)Al(III) complexes, J. Org. Chem., 69(5), pp.1723-1725, 2024, DOI: 10.1021/jo035602q

Li Z., Askim J.R., Suslick K.S. The Optoelectronic Nose: Colorimetric and Fluorometric Sensor Arrays, Chem. Rev., 119, pp 231�292, 2019, DOI: 10.1021/acs.chemrev.8b00226

Gasiorski P., Matusiewicz M., Gondek E., Pokladko-Kowar M., Armatys P., Wojtasik K., Danel A., Uchacz T., Kityk A.V. Efficient green electroluminescence from 1,3-diphenyl-1H-pyrazolo[3,4-b]quinoxaline dyes in dye-doped polymer based electroluminescent devices, Dyes Pigm., 151, pp 380�384, https://doi.org/ 10.1016 /j.dyepig.2018.01.002 DOI: 10.1016/j.dyepig.2018.01.002

Fu Y., Finney N.S. Small-molecule fluorescent probes and their design, RSC Adv., 8, pp 29051�29061, 2018, DOI: 10.1039/C8RA02297F

Wu L., Qu X. Cancer Biomarker Detection: Recent Achievements and Challenges, Chem. Soc. Rev., 44, pp 2963�2997, 2025, DOI: 10.1039/C4CS00370E

Mitsumori T., Craig I.M., Martini I.B., Schwartz B.J., Wudl F. Synthesis and Color Tuning Properties of Blue Highly Fluorescent Vinyl Polymers Containing a Pendant Pyrrolopyridazine, Macromolecules, 38, pp 4698-4704, 2005, DOI: 10.1021/ma048091y

Mitsumori T., Bendikov M., Dautel O., Wudl F., Shioya T., Sato H., Sato Y. Synthesis and Properties of Highly Fluorescent Indolizino[3,4,5-ab]isoindoles. J. Am. Chem. Soc., 126, pp 16793-16803, 2004, DOI: 10.1021/ja049214x

Mitsumori T., Bendikov M., Sedo� J., Wudl, F. Synthesis and Properties of Novel Highly Fluorescent Pyrrolopyridazine Derivatives, Chem. Mater., 15, pp 3759-3768, 2003, DOI: 10.1021/cm0340532

Cheng Y., Ma B., Wudl, F. Synthesis and optical properties of a series of pyrrolopyridazine derivatives: deep blue organic luminophors for electroluminescent devices, J. Mater. Chem., 9, pp 2183-2188, 1999, DOI: 10.1039/A903025E

Zbancioc G., Mangalagiu I.I. Microwave-Assisted Synthesis of Highly Fluorescent Pyrrolopyridazine Derivatives, Synlett, 5, pp 804-806, 2006, DOI: 10.1055/s-2006-932459