Macroheterocycles最新文献

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Liquid-Phase Hydrogenation of the Nickel Complex with Tetra(4-tert-butyl-5-nitro)phthalocyanine 镍配合物与四(4-叔丁基-5-硝基)酞菁的液相加氢反应
IF 1.4 4区 化学
Macroheterocycles Pub Date : 2021-01-01 DOI: 10.6060/mhc211247k
M. V. Klyuev, N. A. Magdalinova, M. E. Klyueva, T. Tikhomirova, V. Maizlish
{"title":"Liquid-Phase Hydrogenation of the Nickel Complex with Tetra(4-tert-butyl-5-nitro)phthalocyanine","authors":"M. V. Klyuev, N. A. Magdalinova, M. E. Klyueva, T. Tikhomirova, V. Maizlish","doi":"10.6060/mhc211247k","DOIUrl":"https://doi.org/10.6060/mhc211247k","url":null,"abstract":"","PeriodicalId":18090,"journal":{"name":"Macroheterocycles","volume":null,"pages":null},"PeriodicalIF":1.4,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"71167243","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Synthesis of Porphyrin-Containing Hydrogels under Microwave Radiation Conditions 微波辐射条件下含卟啉水凝胶的合成
IF 1.4 4区 化学
Macroheterocycles Pub Date : 2021-01-01 DOI: 10.6060/mhc214076p
N. L. Pechnikova, A. Smirnov, I. Shilov, A. Lyubimtsev, Marina N. Mileeva, T. A. Ageeva
{"title":"Synthesis of Porphyrin-Containing Hydrogels under Microwave Radiation Conditions","authors":"N. L. Pechnikova, A. Smirnov, I. Shilov, A. Lyubimtsev, Marina N. Mileeva, T. A. Ageeva","doi":"10.6060/mhc214076p","DOIUrl":"https://doi.org/10.6060/mhc214076p","url":null,"abstract":"","PeriodicalId":18090,"journal":{"name":"Macroheterocycles","volume":null,"pages":null},"PeriodicalIF":1.4,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"71167967","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The p-Metal Porphyrins: from Specificity of Properties to Application in Medicine, Catalysis, and Optoelectronics p-金属卟啉:从性质的专一性到在医学、催化和光电子领域的应用
IF 1.4 4区 化学
Macroheterocycles Pub Date : 2021-01-01 DOI: 10.6060/mhc224201l
T. Lomova
{"title":"The p-Metal Porphyrins: from Specificity of Properties to Application in Medicine, Catalysis, and Optoelectronics","authors":"T. Lomova","doi":"10.6060/mhc224201l","DOIUrl":"https://doi.org/10.6060/mhc224201l","url":null,"abstract":"","PeriodicalId":18090,"journal":{"name":"Macroheterocycles","volume":null,"pages":null},"PeriodicalIF":1.4,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"71168203","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
In Memoriam – Brilliant Chemist, Professor Larisa Tomilova 纪念-杰出的化学家,拉里萨·托米洛娃教授
IF 1.4 4区 化学
Macroheterocycles Pub Date : 2021-01-01 DOI: 10.6060/mhc210104g
Yulia G. Gorbunova
{"title":"In Memoriam – Brilliant Chemist, Professor Larisa Tomilova","authors":"Yulia G. Gorbunova","doi":"10.6060/mhc210104g","DOIUrl":"https://doi.org/10.6060/mhc210104g","url":null,"abstract":"","PeriodicalId":18090,"journal":{"name":"Macroheterocycles","volume":null,"pages":null},"PeriodicalIF":1.4,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"71166089","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Proton Exchange of Intracyclic NH Groups of Deuteroporphyrin IX Dimethyl Ester and Water Molecules according to the Data of Exchange Spectroscopy (EXSY) 根据交换光谱(EXSY)数据,重卟啉IX二甲酯与水分子环内NH基团的质子交换
IF 1.4 4区 化学
Macroheterocycles Pub Date : 2021-01-01 DOI: 10.6060/mhc210129b
A. L. Stolypko, D. V. Belykh
{"title":"Proton Exchange of Intracyclic NH Groups of Deuteroporphyrin IX Dimethyl Ester and Water Molecules according to the Data of Exchange Spectroscopy (EXSY)","authors":"A. L. Stolypko, D. V. Belykh","doi":"10.6060/mhc210129b","DOIUrl":"https://doi.org/10.6060/mhc210129b","url":null,"abstract":"In this work, the EХSY method was used to measure the proton exchange rate constant with the participation of water molecules and intracyclic NH groups of dimethyl ester of deuteroporphyrin IX, taking into account the contribution of cross-relaxation. Comparison with the similar measurements by the DOSY method makes it possible to construct a more complete picture of exchange processes for dimethyl ester of deuteroporphyrin IX, to point out the main limiting stages, and determine the corresponding rate constants.","PeriodicalId":18090,"journal":{"name":"Macroheterocycles","volume":null,"pages":null},"PeriodicalIF":1.4,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"71166869","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Synthesis of β-Octaethylporphyrin Conjugates with Nitrogen and Sulfur Containing Heterocycles 含氮、含硫杂环β-辛乙基卟啉偶联物的合成
IF 1.4 4区 化学
Macroheterocycles Pub Date : 2021-01-01 DOI: 10.6060/mhc211046z
A. O. Shkirdova, E. Orlova, G. Ponomarev, V. Tyurin, I. A. Zamilatskov, A. Buryak
{"title":"Synthesis of β-Octaethylporphyrin Conjugates with Nitrogen and Sulfur Containing Heterocycles","authors":"A. O. Shkirdova, E. Orlova, G. Ponomarev, V. Tyurin, I. A. Zamilatskov, A. Buryak","doi":"10.6060/mhc211046z","DOIUrl":"https://doi.org/10.6060/mhc211046z","url":null,"abstract":"","PeriodicalId":18090,"journal":{"name":"Macroheterocycles","volume":null,"pages":null},"PeriodicalIF":1.4,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"71167201","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Modification of β-Octaethylporphyrin via Insertion of Amino and Azino Groups into meso-Positions 氨基和氮基插入介位修饰β-辛基卟啉
IF 1.4 4区 化学
Macroheterocycles Pub Date : 2021-01-01 DOI: 10.6060/mhc213990z
Valeriia D. Andreeva, Geliy V. Ponomarev, A. O. Shkirdova, V. Tyurin, I. A. Zamilatskov
{"title":"Modification of β-Octaethylporphyrin via Insertion of Amino and Azino Groups into meso-Positions","authors":"Valeriia D. Andreeva, Geliy V. Ponomarev, A. O. Shkirdova, V. Tyurin, I. A. Zamilatskov","doi":"10.6060/mhc213990z","DOIUrl":"https://doi.org/10.6060/mhc213990z","url":null,"abstract":"The functionalization of Ni(II) β-octaethylporphyrin was performed by introducing various amino and azino groups into meso-positions. Amino, n-propylamino, and trifluoromethylacetylamino groups were used as electron donor substituents, while azino group was inserted as an electron acceptor. The azine fragment was inserted through formylation followed by reaction with hydrazine and then with aromatic aldehydes, and the corresponding azine derivatives of p-nitrophenylbenzaldehyde and methyl pyropheophorbide d were obtained. It was found that under the conditions of formylation of meso-(trifluoroacetamido)-β-octaethylporphyrin, the amide fragment was oxidized to form hydroxamic acid. As a result of substitution of meso-positions of β-octaethylporphyrin, new functionalized porphyrin derivatives with significantly altered electron-optical properties were obtained. In particular, the azine bridged conjugate of β-octaethylporphyrin with methyl pyropheophorbide d was synthesized, the electronic absorption spectrum of which contains bathochromically shifted long-wavelength bands. The resulting compounds could be of interest as potential photosensitizers, sensor dyes and biologically active compounds. in vacuum. The residue was puri fied by the column chromatography with eluent CH 2 Cl 2 - n -hexane (1 : 1) yielding 15 mg (65 %) of the compound 5 (R f = 0.55). 1 H NMR (600 MHz, CDCl 3 , 303 K) d ppm: 1.77 (24H, m, CH 2 C H 3 ), 3.86 (16H, m, C H 2 CH 3 ), 9.56 (3H, m, 10, 15, 20-CH), 9.90 (1H, s, NH). UV-Vis (CH 2 Cl 2 ) l max (A rel ) nm: 400 (1.00), 526 (0.06), 563 (0.13). LDI TOF m/z : found 702.48, calc. for [M+H] + C 38 H 45 F 3 N 5 NiO 702.29. General procedure of insertion of azine group into Ni(II) β-octaethylporphyrin. Ni(II) 5-((trifluoromethylacetyl)amino)-2,3,7,8,12,13,17,18-octaethylporphyrin ( 5 ) (40 mg, 0.057 mmol) was dissolved in 15 mL of CH 2 Cl 2 , then Vilsmeier reagent (freshly prepared from DMF (0.7 mL, 9.06 mmol) and POCl 3 (0.7 mL, 7.51 mmol)) was added dropwise to the solution, and the reaction mixture was stirred for 1 hour at reflux. Then","PeriodicalId":18090,"journal":{"name":"Macroheterocycles","volume":null,"pages":null},"PeriodicalIF":1.4,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"71167381","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Photodynamic Therapy of Experimental Tumors of Laboratory Animals with a New Photosensitizer Heliochlorin 新型光敏剂Heliochlorin光动力治疗实验动物的实验性肿瘤
IF 1.4 4区 化学
Macroheterocycles Pub Date : 2021-01-01 DOI: 10.6060/mhc224208a
O. Abramova, V. V. Drozhzhina, Ekatherina A. Kozlovtseva, T. P. Sivovolova, M. A. Kaplan
{"title":"Photodynamic Therapy of Experimental Tumors of Laboratory Animals with a New Photosensitizer Heliochlorin","authors":"O. Abramova, V. V. Drozhzhina, Ekatherina A. Kozlovtseva, T. P. Sivovolova, M. A. Kaplan","doi":"10.6060/mhc224208a","DOIUrl":"https://doi.org/10.6060/mhc224208a","url":null,"abstract":"","PeriodicalId":18090,"journal":{"name":"Macroheterocycles","volume":null,"pages":null},"PeriodicalIF":1.4,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"71168322","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Conjugates of Zinc Tetramethylpyridylporphyrinate with Colloidal Gold Nanoparticles Stabilized with Citrate 四甲基吡啶卟啉酸锌与柠檬酸稳定胶体金纳米粒子的缀合物
IF 1.4 4区 化学
Macroheterocycles Pub Date : 2021-01-01 DOI: 10.6060/mhc200501s
O. Kulikova, V. Sheinin, O. Koifman
{"title":"Conjugates of Zinc Tetramethylpyridylporphyrinate with Colloidal Gold Nanoparticles Stabilized with Citrate","authors":"O. Kulikova, V. Sheinin, O. Koifman","doi":"10.6060/mhc200501s","DOIUrl":"https://doi.org/10.6060/mhc200501s","url":null,"abstract":"Due to electrostatic interaction of Au 30900 /Cit colloidal nanoparticles with 5,10,15,20-tetrakis(4’-N-methylpyridyl) porphine complex with zinc two different nanoconjugates of constant composition are formed one after another, the UV-Vis spectra of which differ from those of initial reagents. The formation of the first, more stable, compound is accompanied by a decrease in intensity and a red shift of the Soret bands and surface plasmon resonance (SPR) band of the conjugated reagents, which retain their spectral identity. The formation of the second conjugate is accompanied by an increase in the intensity of the Soret band while the SPR band is not changed significantly. It has been suggested that the first to form is a nanoconjugate with only one tetracation, which reduces the ability of the nanoparticle to further conjugation.","PeriodicalId":18090,"journal":{"name":"Macroheterocycles","volume":null,"pages":null},"PeriodicalIF":1.4,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"71166410","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Photoinactivation of S. Aureus by Сationic meso-Arylporphyrin and Its Zn(II) Complex Сationic介芳基卟啉及其Zn(II)配合物对金黄色葡萄球菌的光失活作用
IF 1.4 4区 化学
Macroheterocycles Pub Date : 2021-01-01 DOI: 10.6060/mhc210130z
I. O. Savelyeva, Yulia S. Bortnevskaya, A. Y. Usanev, N. A. Bragina, A. Mironov, A. Ignatova, A. Feofanov, K. A. Zhdanova
{"title":"Photoinactivation of S. Aureus by Сationic meso-Arylporphyrin and Its Zn(II) Complex","authors":"I. O. Savelyeva, Yulia S. Bortnevskaya, A. Y. Usanev, N. A. Bragina, A. Mironov, A. Ignatova, A. Feofanov, K. A. Zhdanova","doi":"10.6060/mhc210130z","DOIUrl":"https://doi.org/10.6060/mhc210130z","url":null,"abstract":"In this work, cationic meso-arylsubstituted porphyrin and its Zn(II) complex were synthesized. The compounds were characterized by multinuclear NMR spectroscopy, electronic spectroscopy and ESI-mass spectrometry. The photodynamic activity of the porphyrins was studied in relation to S. aureus bacteria and their biofilms. Application of polymeric micelles of Pluronic F-127 as nanosized delivery vehicles supports high antimicrobial photodynamic activity of the synthesized porphyrins. The influence of the central metal atom on the dark and light-induced toxicity of the synthesized compounds was revealed. non-irradiated control plate. Statistics . The results were considered statistically signifi cant with a 95 % confidence level. All experiments were repeated at least 3 times with comparable results. Statistical analysis was performed using the Student’s coefficient. Results are presented as mean ± SD.","PeriodicalId":18090,"journal":{"name":"Macroheterocycles","volume":null,"pages":null},"PeriodicalIF":1.4,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"71166625","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
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