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<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">zhps</journal-id><journal-title-group><journal-title xml:lang="ru">Журнал прикладной спектроскопии</journal-title><trans-title-group xml:lang="en"><trans-title>Zhurnal Prikladnoii Spektroskopii</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">0514-7506</issn><publisher><publisher-name>B. I. Stepanov Institute of Physics of the National Academy of Sciences</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">zhps-898</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>Статьи</subject></subj-group></article-categories><title-group><article-title>Дуальная флуоресценция 10-гидроксипроизводного акридин(1,8)диона в полярных растворителях</article-title><trans-title-group xml:lang="en"><trans-title>Dual Fluorescence of 10-Hydroxi Acridine(1,8)Dione Derivative in Polar Solvents</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Бондарев</surname><given-names>С. Л.</given-names></name><name name-style="western" xml:lang="en"><surname>Bondarev</surname><given-names>S. L.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Минск</p></bio><bio xml:lang="en"><p>Minsk</p></bio><email xlink:type="simple">stan.bond.1944@gmail.com</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Пырко</surname><given-names>А. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Pirko</surname><given-names>A. N.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Минск</p></bio><bio xml:lang="en"><p>Minsk</p></bio><email xlink:type="simple">pyrko1950@mail.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Райченок</surname><given-names>Т. Ф.</given-names></name><name name-style="western" xml:lang="en"><surname>Raichenok</surname><given-names>T. F.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Минск</p></bio><bio xml:lang="en"><p>Minsk</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Пилипович</surname><given-names>А. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Pilipovich</surname><given-names>A. S.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Минск</p></bio><bio xml:lang="en"><p>Minsk</p></bio><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Институт физики НАН Беларуси</institution></aff><aff xml:lang="en"><institution>B. I. Stepanov Institute of Physics of the National Academy of Sciences of Belarus</institution></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Международный государственный институт имени А. Д. Сахарова Белорусского государственного университета</institution></aff><aff xml:lang="en"><institution>A. D. Saharov International State Institute of Belarusian State University</institution></aff></aff-alternatives><pub-date pub-type="collection"><year>2021</year></pub-date><pub-date pub-type="epub"><day>09</day><month>10</month><year>2021</year></pub-date><volume>88</volume><issue>5</issue><fpage>694</fpage><lpage>700</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Бондарев С.Л., Пырко А.Н., Райченок Т.Ф., Пилипович А.С., 2021</copyright-statement><copyright-year>2021</copyright-year><copyright-holder xml:lang="ru">Бондарев С.Л., Пырко А.Н., Райченок Т.Ф., Пилипович А.С.</copyright-holder><copyright-holder xml:lang="en">Bondarev S.L., Pirko A.N., Raichenok T.F., Pilipovich A.S.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://zhps.ejournal.by/jour/article/view/898">https://zhps.ejournal.by/jour/article/view/898</self-uri><abstract><p>Методами стационарной люминесценции и импульсной флуорометрии исследованы спектрально-кинетические и фотофизические свойства 9-метилпроизводного 10-гидрокси-акридин(1,8)дионового красителя в полярных (протонных и апротонных) растворителях при 293 и 77 К. Впервые в полярных протонных (метаноле, этаноле, изопропаноле) и апротонных (N,N-диметилформамиде, диметилсульфоксиде) растворителях при комнатной температуре в длинноволновой области 670—710 нм обнаружена новая полоса флуоресценции (длинноволновая флуоресценция (ДФ)). Она образуется из более высоко лежащего (в диапазоне 460–490 нм) синглетно возбужденного состояния, ответственного за полосу коротковолновой флуоресценции (КФ). ДФ не обнаруживается в малополярном (хлористом метилене), полярном апротонном (ацетонитриле) и высоковязком протонном (глицерине) растворителях при 293 К, а также в этаноле при 77 К. Она возникает в результате депротонирования молекулы в возбужденном состоянии и высвечивания образующегося аниона в длинноволновой области. На основании анализа спектральных и кинетических данных затухания КФ и разгорания ДФ предлагаются механизм образования аниона красителя в зависимости от основности полярного растворителя, а также возможные практические применения обнаруженного спектрального эффекта в биологии, медицине и аналитической химии.</p></abstract><trans-abstract xml:lang="en"><p>Using stationary luminescence and pulse fluorometry methods, spectral-kinetic and photophysical properties of 9 methyl-10-hydroxi acridine(1,8)dione derivative dye (9,10-ACD) in polar (protonic and nonprotonic) solvents at 293 and 77 K have been investigated. For the first time, a new long-wavelength fluorescence band (LF, 670–710 nm) in polar protonic (methanol, ethanol) and nonprotonic (N,N-dimethylformamide, dimethylsulfoxide) at room temperature was revealed. This band has been formed from the high lying (in the range of 460–490 nm) singlet excited state responsible for the short-wavelength fluorescence band (SF). The LF is not revealed in low polar (methylene chloride), polar nonprotonic (acetonitrile) and high viscose protonic (glycerol) solvents at 293 K, as well as at 77 K in ethanol. It arises as a result of deprotonation of a molecule in an excited state and emission of the resulting anion in the long-wavelength region. Based on the analysis of the spectral and kinetic data of the SF decay and the LF rise, a mechanism for the dye anion formation depending on the basicity of the polar solvent is proposed. Possible practical applications of the revealed spectral effect in biology, medicine and analytical chemistry are proposed.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>акридин(1</kwd><kwd>8)дионовые красители</kwd><kwd>полярные растворители</kwd><kwd>дуальная флуоресценция</kwd><kwd>депротонирование</kwd></kwd-group><kwd-group xml:lang="en"><kwd>acridine(1</kwd><kwd>8)dione dyes</kwd><kwd>polar solvents</kwd><kwd>dual fluorescence</kwd><kwd>deprotonation</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">P. Shanmugasundaram, K. J. Prabahar, V. T. Ramakrishnan. J. Heterocycl. Chem., 30 (1993) 1003-1007</mixed-citation><mixed-citation xml:lang="en">P. Shanmugasundaram, K. J. Prabahar, V. T. Ramakrishnan. J. Heterocycl. Chem., 30 (1993) 1003-1007</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">G. K. Thorat, R. P. Tayade, N. Sekar. Opt. Mater., 62 (2016) 306-319</mixed-citation><mixed-citation xml:lang="en">G. K. Thorat, R. P. Tayade, N. Sekar. Opt. Mater., 62 (2016) 306-319</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">N. Sahiba, A. Sethiya, J. Soni, S. Agarwal. Chem. Sel., 6 (2021) 2210-2251</mixed-citation><mixed-citation xml:lang="en">N. Sahiba, A. Sethiya, J. Soni, S. Agarwal. Chem. Sel., 6 (2021) 2210-2251</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">J. P. Foussier, F. Morlet-Savary, J. Lalevee, C. Ley. Materials, 3 (2010) 5130-5442</mixed-citation><mixed-citation xml:lang="en">J. P. Foussier, F. Morlet-Savary, J. Lalevee, C. Ley. Materials, 3 (2010) 5130-5442</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">P. A. Kumar, V. T. Ramakrishnan, P. Ramamurthy. J. Phys. Chem. A, 115 (2011) 14292-14300</mixed-citation><mixed-citation xml:lang="en">P. A. Kumar, V. T. Ramakrishnan, P. Ramamurthy. J. Phys. Chem. A, 115 (2011) 14292-14300</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">A. P. de Silva, H. Q. N. Gunaratne, T. E. Rice. Chem. Rev., 97 (1997) 1515-1566</mixed-citation><mixed-citation xml:lang="en">A. P. de Silva, H. Q. N. Gunaratne, T. E. Rice. Chem. Rev., 97 (1997) 1515-1566</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">L. Stryer. Biochemistry, 4th ed., Freeman, New York (1995)</mixed-citation><mixed-citation xml:lang="en">L. Stryer. Biochemistry, 4th ed., Freeman, New York (1995)</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">R. Kumaran, P. Ramamurthy. J. Lumin., 130 (2010) 1203-1210</mixed-citation><mixed-citation xml:lang="en">R. Kumaran, P. Ramamurthy. J. Lumin., 130 (2010) 1203-1210</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">C. Seivaraju, P. Ramamarthy. Chem. Eur. J., 10 (2004) 2253-2262</mixed-citation><mixed-citation xml:lang="en">C. Seivaraju, P. Ramamarthy. Chem. Eur. J., 10 (2004) 2253-2262</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">R. Kumaran, M. Vanjinathan, P. Ramamurthy. J. Lumin., 164 (2015) 146-153</mixed-citation><mixed-citation xml:lang="en">R. Kumaran, M. Vanjinathan, P. Ramamurthy. J. Lumin., 164 (2015) 146-153</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">K. Anju, S. Gayathri, A. Sumita, P. Ramamurthy, R. Kumaran. J. Lumin., 199 (2018) 352-362</mixed-citation><mixed-citation xml:lang="en">K. Anju, S. Gayathri, A. Sumita, P. Ramamurthy, R. Kumaran. J. Lumin., 199 (2018) 352-362</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">V. Thiagarajan, C. Selvaraja, E. J. P. Malar, P. Ramamurthy. ChemPhysChem., 5 (2004) 1200-1209</mixed-citation><mixed-citation xml:lang="en">V. Thiagarajan, C. Selvaraja, E. J. P. Malar, P. Ramamurthy. ChemPhysChem., 5 (2004) 1200-1209</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">А. Н. Пырко. Журн. орг. химии, 44 (2008) 1227-1236</mixed-citation><mixed-citation xml:lang="en">А. Н. Пырко. Журн. орг. химии, 44 (2008) 1227-1236</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">J. Catalan, C. Diaz, V. Lopez, P. Perez, J.-L. G.dePaz, J. G. Rodriguez. Liebigs Ann. (1996) 1785-1794</mixed-citation><mixed-citation xml:lang="en">J. Catalan, C. Diaz, V. Lopez, P. Perez, J.-L. G.dePaz, J. G. Rodriguez. Liebigs Ann. (1996) 1785-1794</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">А. Гордон, Р. Форд. Спутник химика, Москва, Мир (1976) 437-445</mixed-citation><mixed-citation xml:lang="en">А. Гордон, Р. Форд. Спутник химика, Москва, Мир (1976) 437-445</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">J. N. Demas, G. A. Crosby. J. Chem. Phys., 75 (1971) 991-1012</mixed-citation><mixed-citation xml:lang="en">J. N. Demas, G. A. Crosby. J. Chem. Phys., 75 (1971) 991-1012</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">V. Karunakaran, P. Ramamurthu, T. Rosephrajan, V. T. Ramakrishnan. Spectrochim. Acta A, 58 (2002) 1443-1451</mixed-citation><mixed-citation xml:lang="en">V. Karunakaran, P. Ramamurthu, T. Rosephrajan, V. T. Ramakrishnan. Spectrochim. Acta A, 58 (2002) 1443-1451</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Б. С. Непорент, Н. Г. Бахшиев. Опт. и спектр., 5 (1958) 634-645</mixed-citation><mixed-citation xml:lang="en">Б. С. Непорент, Н. Г. Бахшиев. Опт. и спектр., 5 (1958) 634-645</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Б. И. Степанов, Л. П. Казаченко. Журн. прикл. спектр., 14 (1971) 819-825</mixed-citation><mixed-citation xml:lang="en">Б. И. Степанов, Л. П. Казаченко. Журн. прикл. спектр., 14 (1971) 819-825</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
