Investigation of β-cyclodextrin complex formation with 2,2′-dipyridine in ground and excited triplet states
العنوان: | Investigation of β-cyclodextrin complex formation with 2,2′-dipyridine in ground and excited triplet states |
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المؤلفون: | Simon V. Babenko, Yuri P. Tsentalovich, Alexander I. Kruppa |
المصدر: | Journal of Inclusion Phenomena and Macrocyclic Chemistry. 89:117-125 |
بيانات النشر: | Springer Science and Business Media LLC, 2017. |
سنة النشر: | 2017 |
مصطلحات موضوعية: | chemistry.chemical_classification, Annihilation, Cyclodextrin, medicine.diagnostic_test, 010405 organic chemistry, Chemistry, General Chemistry, 010402 general chemistry, Condensed Matter Physics, 01 natural sciences, 0104 chemical sciences, Crystallography, Reaction rate constant, Computational chemistry, Yield (chemistry), Excited state, Spectrophotometry, medicine, Ground state, Constant (mathematics), Food Science |
الوصف: | It was found that 2,2′-dipyridine ( $$DP$$ ) forms inclusion complex with beta-cyclodextrin ( $$CD$$ ) in basic water solution by using NMR and spectrophotometry. Complex formation does not have an effect on the yield of triplet excited 2,2′-dipyridine. Triplet excited 2,2′-dipyridine $$({}^{3}DP)$$ also forms inclusion complex with beta-cyclodextrin and the value of complex formation constant is close to that for $$DP$$ in the ground state. The electron transfer rate constant between the inclusion complex of $${}^{3}DP$$ with $$CD$$ and N-acetyl-l-tyrosine ( $$TyrOH$$ ) is about ten times less than between $${}^{3}DP$$ in free (non complexed) state and $$TyrOH$$ in basic (pH 11) solution. Also it was found that inclusion complex formation of $${}^{3}DP$$ with $$CD$$ slightly decreases the rate constant of triplet–triplet annihilation process. |
تدمد: | 1573-1111 1388-3127 |
DOI: | 10.1007/s10847-017-0736-2 |
URL الوصول: | https://explore.openaire.eu/search/publication?articleId=doi_________::4e733b4ce38f54e625a2f559b06506ed https://doi.org/10.1007/s10847-017-0736-2 |
Rights: | CLOSED |
رقم الانضمام: | edsair.doi...........4e733b4ce38f54e625a2f559b06506ed |
قاعدة البيانات: | OpenAIRE |
تدمد: | 15731111 13883127 |
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DOI: | 10.1007/s10847-017-0736-2 |