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Artykuły w czasopismach na temat „Azine linker”

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Autor: Grafiati

Data publikacji: 4 czerwca 2021

Data aktualizacji: 21 lutego 2023

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1

Parshamoni, Srinivasulu, Jyothi Telangae i Sanjit Konar. "Regulation of the pore size by shifting the coordination sites of ligands in two MOFs: enhancement of CO2 uptake and selective sensing of nitrobenzene". Dalton Transactions 44, nr 48 (2015): 20926–35. http://dx.doi.org/10.1039/c5dt01976a.

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Two MOFs were constructed using azine functionalized and pyridyl based neutral ligands along with a V-shaped sdb linker, and exhibit highly efficient luminescence sensing for nitrobenzene and sorption selectivity for CO₂ over CH₄.

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2

Singh, Sandhya, Ross W. Hogue, Humphrey L. C. Feltham i Sally Brooker. "Dinuclear helicate and tetranuclear cage assembly using appropriately designed ditopic triazole-azine ligands". Dalton Transactions 48, nr 41 (2019): 15435–44. http://dx.doi.org/10.1039/c9dt01890e.

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3

Rakshagan, Vikraman, Ranganathan Ajay, Arul Queenalice, Sengottaiyan Vinothkumar, Paulpandian Saravanadinesh i Thillaigovindan Ranjani. "Portraiture and Double Bond Conversion of a Monomethacrylate-based Oral Prosthetic Resin Substituted with a Novel Tri(azine-acrylate) Cross-linker". Journal of Contemporary Dental Practice 23, nr 4 (11.07.2022): 425–30. http://dx.doi.org/10.5005/jp-journals-10024-3287.

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4

Göbel, Dominik, Marius Friedrich, Enno Lork i Boris J. Nachtsheim. "Clickable azide-functionalized bromoarylaldehydes – synthesis and photophysical characterization". Beilstein Journal of Organic Chemistry 16 (14.07.2020): 1683–92. http://dx.doi.org/10.3762/bjoc.16.139.

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Herein, we present a facile synthesis of three azide-functionalized fluorophores and their covalent attachment as triazoles in Huisgen-type cycloadditions with model alkynes. Besides two ortho- and para-bromo-substituted benzaldehydes, the azide functionalization of a fluorene-based structure will be presented. The copper(I)-catalyzed azide–alkyne cycloaddition (CuAAC) of the so-synthesized azide-functionalized bromocarbaldehydes with terminal alkynes, exhibiting different degrees of steric demand, was performed in high efficiency. Finally, we investigated the photophysical properties of the azide-functionalized arenes and their covalently linked triazole derivatives to gain deeper insight towards the effect of these covalent linkers on the emission behavior.

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5

Bahrin, Lucian Gabriel, Alina Nicolescu, Sergiu Shova, Narcisa Laura Marangoci, Lucian Mihail Birsa i Laura Gabriela Sarbu. "Nitrogen-Based Linkers with a Mesitylene Core: Synthesis and Characterization". Molecules 26, nr 19 (30.09.2021): 5952. http://dx.doi.org/10.3390/molecules26195952.

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Mesitylene was used as a core in seven new tritopic nitrogen containing linkers. Three of the linkers, each containing three nitrile groups, were obtained through Suzuki, Sonogashira and Heck-type coupling reactions. Next, these were converted to tetrazol-5-yl moieties by the cycloaddition of sodium azide to the nitrile functionalities. The last linker, containing three 1,2,3-triazol-4-yl moieties, was synthesized by the Huisgen cycloaddition of phenyl azide to the corresponding alkyne. The latter was obtained via a Corey–Fuchs reaction sequence from the previously reported formyl derivative. As the proof of concept for their potential in MOF design, one of the nitriles was used to build an Ag-based network.

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6

Dalapati, Sasanka, Shangbin Jin, Jia Gao, Yanhong Xu, Atsushi Nagai i Donglin Jiang. "An Azine-Linked Covalent Organic Framework". Journal of the American Chemical Society 135, nr 46 (5.11.2013): 17310–13. http://dx.doi.org/10.1021/ja4103293.

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7

Tsao, Kelvin K., Ann C. Lee, Karl É. Racine i Jeffrey W. Keillor. "Site-Specific Fluorogenic Protein Labelling Agent for Bioconjugation". Biomolecules 10, nr 3 (28.02.2020): 369. http://dx.doi.org/10.3390/biom10030369.

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Many clinically relevant therapeutic agents are formed from the conjugation of small molecules to biomolecules through conjugating linkers. In this study, two novel conjugating linkers were prepared, comprising a central coumarin core, functionalized with a dimaleimide moiety at one end and a terminal alkyne at the other. In our first design, we developed a protein labelling method that site-specifically introduces an alkyne functional group to a dicysteine target peptide tag that was genetically fused to a protein of interest. This method allows for the subsequent attachment of azide-functionalized cargo in the facile synthesis of novel protein-cargo conjugates. However, the fluorogenic aspect of the reaction between the linker and the target peptide was less than we desired. To address this shortcoming, a second linker reagent was prepared. This new design also allowed for the site-specific introduction of an alkyne functional group onto the target peptide, but in a highly fluorogenic and rapid manner. The site-specific addition of an alkyne group to a protein of interest was thus monitored in situ by fluorescence increase, prior to the attachment of azide-functionalized cargo. Finally, we also demonstrated that the cargo can also be attached first, in an azide/alkyne cycloaddition reaction, prior to fluorogenic conjugation with the target peptide-fused protein.

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8

Li, Wen-Juan, i Hong-Fei Han. "Crystal structure of (E,E)-2′,4′-dihydroxyacetophenone azine dimethylformamide disolvate". Acta Crystallographica Section E Crystallographic Communications 72, nr 4 (8.03.2016): 467–69. http://dx.doi.org/10.1107/s2056989016003686.

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In the title compound {systematic name: 4,4′-[1,1′-(hydrazinediylidene)bis(ethan-1-yl-1-ylidene)]bis(benzene-1,3-diol)}, C16H16N2O4·2C3H7NO, the (E,E)-2′,4′-dihydroxyacetophenone azine molecule is centrosymmetric, the mid-point of the N—N bond being located on an inversion centre. All the non-H atoms of the azine molecule are approximately coplanar, the maximum deviation being 0.017 (2) Å. An intramolecular O—H...N hydrogen bond occurs between the azine N atom and the hydroxy group. In the crystal, azine and dimethylformamide solvent molecules are linked by O—H...O hydrogen bonds.

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9

Truong, Thuy Thu. "SYNTHESIS OF AN AZIDE–THIOL LINKER FOR HETEROGENEOUS POLYMER FUNCTIONALIZATION VIA THE “CLICK” REACTION". Vietnam Journal of Science and Technology 55, nr 1B (23.03.2018): 152. http://dx.doi.org/10.15625/2525-2518/55/1b/12103.

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In this study, the synthesis of a telechelic linker bearing both azide and thiol functional groups was described. The reaction conditions were investigated to optimize the reaction yield. The product was analyzed using thin layer chromatography (TLC) and proton nuclear magnetic resonance (1H NMR). The employment of the obtained azide–thiol linker in heterogeneous polymer “click” functionalization was demonstrated for the first time, which was monitored by an online FT–IR method. The obtained telechelic azide–thiol linker is envisioned to be useful chemical tools to link macromolecular chains via orthogonal click reactions.

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10

Han, Minsu, Mithrabinda K. Poduval, Haijin Shin, Nobuyuki Tamaoki, Taiho Park, Yuna Kim i Eunkyoung Kim. "Programmable dual electrochromism in azine linked conjugated polymer". Optical Materials Express 7, nr 6 (31.05.2017): 2117. http://dx.doi.org/10.1364/ome.7.002117.

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11

Alahakoon, Sampath B., Christina M. Thompson, Amy X. Nguyen, Gino Occhialini, Gregory T. McCandless i Ronald A. Smaldone. "An azine-linked hexaphenylbenzene based covalent organic framework". Chemical Communications 52, nr 13 (2016): 2843–45. http://dx.doi.org/10.1039/c5cc10408d.

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We report an azine linked covalent organic framework based on hexaphenylbenzene monomer functionalized with aldehyde groups (“HEX-COF 1”, avg. pore size = 1 nm, surface area >1200 m² g⁻¹, sorption capability at 273 K, 1 atm = 20 wt% for CO² and 2.3 wt% for CH₄).

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12

Hochegger, Patrick, Johanna Dolensky, Werner Seebacher, Robert Saf, Marcel Kaiser, Pascal Mäser i Robert Weis. "8-Amino-6-Methoxyquinoline—Tetrazole Hybrids: Impact of Linkers on Antiplasmodial Activity". Molecules 26, nr 18 (12.09.2021): 5530. http://dx.doi.org/10.3390/molecules26185530.

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A new series of compounds was prepared from 6-methoxyquinolin-8-amine or its N-(2-aminoethyl) analogue via Ugi-azide reaction. Their linkers between the quinoline and the tert-butyltetrazole moieties differ in chain length, basicity and substitution. Compounds were tested for their antiplasmodial activity against Plasmodium falciparum NF54 as well as their cytotoxicity against L-6-cells. The activity and the cytotoxicity were strongly influenced by the linker and its substitution. The most active compounds showed good activity and promising selectivity.

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13

Li, Zhongping, Xiao Feng, Yongcun Zou, Yuwei Zhang, Hong Xia, Xiaoming Liu i Ying Mu. "A 2D azine-linked covalent organic framework for gas storage applications". Chem. Commun. 50, nr 89 (2014): 13825–28. http://dx.doi.org/10.1039/c4cc05665e.

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A highly crystalline and porous azine-linked covalent organic framework exhibits excellent CO₂ uptake (17.7 wt%, 273 K and 1 bar) and high selectivity towards CO₂ over N₂ and CH₄.

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14

Guan, Pengxin, Jikuan Qiu, Yuling Zhao, Huiyong Wang, Zhiyong Li, Yunlei Shi i Jianji Wang. "A novel crystalline azine-linked three-dimensional covalent organic framework for CO2 capture and conversion". Chemical Communications 55, nr 83 (2019): 12459–62. http://dx.doi.org/10.1039/c9cc05710b.

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15

Pathigoolla, Atchutarao, i Kana M. Sureshan. "The topochemical synthesis of triazole-linked homobasic DNA". Chemical Communications 52, nr 5 (2016): 886–88. http://dx.doi.org/10.1039/c5cc08834h.

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Triazolyl-DNA (^TLDNA), DNA wherein phosphodiester units are replaced by triazole units, is of great interest. By adopting Topochemical Azide–Alkyne Cycloaddition (TAAC) reaction, we have synthesized homobasic ^TLDNA oligomers. 5′-ethynyl-3′-azido-2′,3′,5′-tri-deoxycytosine, which crystallized with proximal placement of azide and alkyne units of adjacent molecules, underwent TAAC reaction to ^TLDNA oligomers.

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16

Li, Xing, Yue Qi, Guozong Yue, Qianxun Wu, Yang Li, Meicheng Zhang, Xinghua Guo, Xiaofeng Li, Lijian Ma i Shoujian Li. "Solvent- and catalyst-free synthesis of an azine-linked covalent organic framework and the induced tautomerization in the adsorption of U(vi) and Hg(ii)". Green Chemistry 21, nr 3 (2019): 649–57. http://dx.doi.org/10.1039/c8gc03295e.

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17

Zhai, Wenlei, Brette M. Chapin, Akina Yoshizawa, Hui-Chen Wang, Stephen A. Hodge, Tony D. James, Eric V. Anslyn i John S. Fossey. "“Click-fluors”: triazole-linked saccharide sensors". Organic Chemistry Frontiers 3, nr 8 (2016): 918–28. http://dx.doi.org/10.1039/c6qo00171h.

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18

Alahakoon, Sampath B., Gino Occhialini, Gregory T. McCandless, Arosha A. K. Karunathilake, Steven O. Nielsen i Ronald A. Smaldone. "Experimental and theoretical insight into the effect of fluorine substituents on the properties of azine linked covalent organic frameworks". CrystEngComm 19, nr 33 (2017): 4882–85. http://dx.doi.org/10.1039/c7ce00598a.

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19

Poduval, Mithrabinda K., Iratxe Arrechea-Marcos, M. Carmen Ruiz Delgado, Taiho Park, J. Teodomiro López Navarrete, Rocío Ponce Ortiz i Tae-Hyun Kim. "Stereoisomers of an azine-linked donor–acceptor conjugated polymer: the impact of molecular conformation on electrical performance". RSC Advances 6, nr 50 (2016): 44272–78. http://dx.doi.org/10.1039/c6ra07389a.

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20

Fan, Hongwei, Alexander Mundstock, Jiahui Gu, Hong Meng i Jürgen Caro. "An azine-linked covalent organic framework ACOF-1 membrane for highly selective CO2/CH4 separation". Journal of Materials Chemistry A 6, nr 35 (2018): 16849–53. http://dx.doi.org/10.1039/c8ta05641b.

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21

Eisink, Niek N. H. M., Jonas Lohse, Martin D. Witte i Adriaan J. Minnaard. "Regioselective oxidation of unprotected 1,4 linked glucans". Organic & Biomolecular Chemistry 14, nr 21 (2016): 4859–64. http://dx.doi.org/10.1039/c6ob00608f.

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22

Li, Zhongping, Yuwei Zhang, Hong Xia, Ying Mu i Xiaoming Liu. "A robust and luminescent covalent organic framework as a highly sensitive and selective sensor for the detection of Cu2+ions". Chemical Communications 52, nr 39 (2016): 6613–16. http://dx.doi.org/10.1039/c6cc01476c.

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A highly crystalline and porous azine-linked covalent organic framework possesses excellent stability and luminescence properties with high quantum yield. It can serve as a promising luminescent probe for selectively sensing copper ions.

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23

Knall, Astrid-Caroline, Manuel Hollauf, Robert Saf i Christian Slugovc. "A trifunctional linker suitable for conducting three orthogonal click chemistries in one pot". Organic & Biomolecular Chemistry 14, nr 45 (2016): 10576–80. http://dx.doi.org/10.1039/c6ob02182d.

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24

Dietzgen, Ralf G., Evamarie Sander, Jürgen Christner i Günther Jung. "Examination of a New Cross-Linker in Monoclonal Antibody Reaction Against the C-Terminus of Tobacco Mosaic Virus Coat Protein". Zeitschrift für Naturforschung B 42, nr 4 (1.04.1987): 441–53. http://dx.doi.org/10.1515/znb-1987-0410.

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The C-terminal tetrapeptide Gly-Pro-Ala-Thr of TMV coat protein was linked to poly- (L-lysine) of 37,300 and 80,000 daltons and to human serum albumin using different ratios of tetrapeptide to carrier. The new hydrazidosuccinyl HSc cross-linker effected the specific amino terminal attachment of the tetrapeptide by azide coupling. The synthetic peptide and its conjugates were controlled by various methods including 13C NMR and CD. Using a conjugate containing 74 tetrapeptide residues linked to poly(L-lysine) of 80,000 daltons for screening of monoclonal antibody by ELISA, 5.8 fmol of peptide were detectable. The serological and biological properties of the monoclonal antibody were assayed by indirect ELISA and by quantitative determination of virus neutralization. This neutralization could be reversed by the poly(L-lysine)-tetrapeptide conjugate but not by the free tetrapeptide.

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25

Siboro, Sonita A. P., Sabrina Aufar Salma, Hyeung-Rak Kim, Yeon Tae Jeong, Yeong-Soon Gal i Kwon Taek Lim. "Diselenide Core Cross-Linked Micelles of Poly(Ethylene Oxide)-b-Poly(Glycidyl Methacrylate) Prepared through Alkyne-Azide Click Chemistry as a Near-Infrared Controlled Drug Delivery System". Materials 13, nr 12 (25.06.2020): 2846. http://dx.doi.org/10.3390/ma13122846.

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In this article, a drug delivery system with a near-infrared (NIR) light-responsive feature was successfully prepared using a block copolymer poly(ethylene oxide)-b-poly(glycidyl methacrylate)-azide (PEO-b-PGMA-N3) and a cross-linker containing a Se-Se bond through “click” chemistry. Doxorubicin (DOX) was loaded into the core-cross-linked (CCL) micelles of the block copolymer along with indocyanine green (ICG) as a generator of reactive oxygen species (ROS). During NIR light exposure, ROS were generated by ICG and attacked the Se-Se bond of the cross-linker, leading to de-crosslinking of the CCL micelles. After NIR irradiation, the CCL micelles were continuously disrupted, which can be a good indication for effective drug release. Photothermal analysis showed that the temperature elevation during NIR exposure was negligible, thus safe for normal cells. In vitro drug release tests demonstrated that the drug release from diselenide CCL micelles could be controlled by NIR irradiation and affected by the acidity of the environment.

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26

Kotnik, Tomaž, Gregor Žerjav, Albin Pintar, Ema Žagar i Sebastijan Kovačič. "Azine- and imine-linked conjugated polyHIPEs through Schiff-base condensation reaction". Polymer Chemistry 13, nr 4 (2022): 474–78. http://dx.doi.org/10.1039/d1py01467f.

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27

Mascal, Mark, John L. Richardson, Alexander J. Blake i Wan-Sheung Li. "Synthesis and Structural Characterization of an S-linked Calix[3]azine". Tetrahedron Letters 38, nr 43 (październik 1997): 7639–40. http://dx.doi.org/10.1016/s0040-4039(97)01814-5.

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28

Palframan, Matthew J., Rima D. Alharthy, Paulina K. Powalowska i Christopher J. Hayes. "Synthesis of triazole-linked morpholino oligonucleotides via CuI catalysed cycloaddition". Organic & Biomolecular Chemistry 14, nr 11 (2016): 3112–19. http://dx.doi.org/10.1039/c6ob00007j.

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29

Fluch, Ulrike, Brian D. McCarthy i Sascha Ott. "Post synthetic exchange enables orthogonal click chemistry in a metal organic framework". Dalton Transactions 48, nr 1 (2019): 45–49. http://dx.doi.org/10.1039/c8dt04563a.

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30

Schneider, Jérémy P., Stefano Tommasone, Paolo Della Sala, Carmine Gaeta, Carmen Talotta, Céline Tarnus, Placido Neri, Anne Bodlenner i Philippe Compain. "Synthesis and Glycosidase Inhibition Properties of Calix[8]arene-Based Iminosugar Click Clusters". Pharmaceuticals 13, nr 11 (5.11.2020): 366. http://dx.doi.org/10.3390/ph13110366.

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A set of 6- to 24-valent clusters was constructed with terminal deoxynojirimycin (DNJ) inhibitory heads through C6 or C9 linkers by way of Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC) reactions between mono- or trivalent azido-armed iminosugars and calix[8]arene scaffolds differing in their valency and their rigidity but not in their size. The power of multivalency to upgrade the inhibition potency of the weak DNJ inhibitor (monovalent DNJ Ki being at 322 and 188 µM for C6 or C9 linkers, respectively) was evaluated on the model glycosidase Jack Bean α-mannosidase (JBα-man). Although for the clusters with the shorter C6 linker the rigidity of the scaffold was essential, these parameters had no influence for clusters with C9 chains: all of them showed rather good relative affinity enhancements per inhibitory epitopes between 70 and 160 highlighting the sound combination of the calix[8]arene core and the long alkyl arms. Preliminary docking studies were performed to get insights into the preferred binding modes.

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31

Dadhwal, Sumit, Jessica M. Fairhall, Sarah Hook i Allan B. Gamble. "Tetrafluoroaryl azide as an N-terminal capping group for click-to-dissolve diphenylalanine hydrogels". RSC Advances 10, nr 16 (2020): 9234–44. http://dx.doi.org/10.1039/d0ra01013h.

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A tetrafluoroaryl azide group attached to diphenylalanine via a carbamate linker provides a strong and stable hydrogel that undergoes a gel-to-solution transition following a rapid bioorthogonal 1,3,-dipolar cycloaddition.

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32

Ramírez-Villalva, Alejandra, Davir González-Calderón, Roxana I. Rojas-García, Carlos González-Romero, Joaquín Tamaríz-Mascarúa, Macario Morales-Rodríguez, Nieves Zavala-Segovia i Aydeé Fuentes-Benítes. "Synthesis and antifungal activity of novel oxazolidin-2-one-linked 1,2,3-triazole derivatives". MedChemComm 8, nr 12 (2017): 2258–62. http://dx.doi.org/10.1039/c7md00442g.

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33

Liu, Decheng, Kai Li, Min Li, Zheng Wang, Meixia Shan i Yatao Zhang. "Moderately Crystalline Azine-Linked Covalent Organic Framework Membrane for Ultrafast Molecular Sieving". ACS Applied Materials & Interfaces 13, nr 31 (28.07.2021): 37775–84. http://dx.doi.org/10.1021/acsami.1c06891.

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34

Li, Zhongping, Yongfeng Zhi, Xiao Feng, Xuesong Ding, Yongcun Zou, Xiaoming Liu i Ying Mu. "An Azine-Linked Covalent Organic Framework: Synthesis, Characterization and Efficient Gas Storage". Chemistry - A European Journal 21, nr 34 (14.07.2015): 12079–84. http://dx.doi.org/10.1002/chem.201501206.

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35

Ivanov, A. V., A. T. Kopylov, V. G. Zgoda, I. Yu Toropygin, E. V. Khrjapova i Yu D. Ivanov. "Mass-spectrometric identification of interaction sites for cytochrome P450 2b4/nadph cytochrome P450 reductase". Biomeditsinskaya Khimiya 56, nr 1 (styczeń 2010): 40–54. http://dx.doi.org/10.18097/pbmc20105601040.

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We determined the interaction sites of the cytochrome P450's protein-partners: 2B4 (d-2B4) and NADPH-cytochrome P450 of reductase (d-Fp). While in operation, these proteins are forming the complexes. We used 4-4'-dithio(bisphenyl)azide linker for non-specific covalent coupling of d-2B4 complexes with d-Fp in Emulgen-913 - monomerized system. Covalently-linked peptides in this complex were identified with ESI-MS/MS. Several sites of these proteins' binding with each other were revealed. Based on them, a model of intermolecular protein interactions was created. The model includes 5 cross-linker-stabilized contact sites of d-2B4 with d-Fp involving the following peptides of d-2B4 and d-Fp: 1) d-2B4423-433 и d-Fp 102-109; 2) d-2B4324-336 и d-Fp570-585; 3) d-2B4327-336 и d-Fp452-464; 4) d-2B4 192-197 и d-Fp456-464; 5) d-2B4 134-139 и d-Fp406-425.Herein, in the latter two cases, the peptides of d-Fp are located in their inter-domain slit and stabilize protein-protein complex via nanoprobe cross-linker; therefore, the formation of d-2B4/d-Fp complexes in these sites may involve aminoacid residues d-Fp456-464 and d-Fp406-425 surrounding inter-domain slit.

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36

Mautner, Franz A., Harald Krischner i Christoph Kratky. "Die Kristallstruktur von [Ca(N3)2(H2O)2] · C6H14N4 bei 100 K /The Crystal Structure of [Ca(N3)2(H2O)2] · C6H14N4 at 100 K". Zeitschrift für Naturforschung B 44, nr 2 (1.02.1989): 135–38. http://dx.doi.org/10.1515/znb-1989-0207.

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Abstract The crystal structure of calcium azide dihydrate trans-bicyclo-[4.4.0]-1,4,6.9-tetraazadecane has been determined by single crystal X-ray diffraction at 100 K. [Ca(N3)2(H2O)2 (C6H14N4 crystallizes in the orthorhombic space group Pnma, Z = 4. with a - 1396.6(5), b = 1407.1(5), c = 712.2(2) pm. Calcium is hexacoordinated to four azide groups and two water molecules. The elongated octahedra are linked via μ(1,3)-bridging azide ions to form monolayers parallel to the ac-plane. The C6H14N4 molecules are arranged between these layers.

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37

Liu, Hou-Ting, i Jing Lu. "An azide-bridged copper(II) complex: poly[piperazine-1,4-dium [tetra-μ3-azido-κ12N1:N1:N1-hexa-μ2-azido-κ12N1:N1-di-μ2-azido-κ4N1:N3-pentacopper(II)] tetrahydrate]". Acta Crystallographica Section C Structural Chemistry 70, nr 11 (24.10.2014): 1083–87. http://dx.doi.org/10.1107/s2053229614022190.

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A new CuII–azide complex, {(C4H12N2)[Cu5(N3)12]·4H2O}n, has been synthesized by the reaction of piperazine, Cu(OAc)2·2H2O (OAc is acetate) and NaN3. In the structure, μ2-1,1- and μ3-1,1,1-azide anions bridge five CuIIcations to form a linear pentanuclear cluster unit, which is further linked by μ2-1,1- and μ2-1,3-azide anions to form a two-dimensional condensed [Cu5(N3)12]nlayer. The diprotonated piperazine and the solvent water molecules are hydrogen bonded to the coordination layers to form a three-dimensional supramolecular network.

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38

Karlinskii, Bogdan, Leonid Romashov, Konstantin Galkin, Pavel Kislitsyn i Valentine Ananikov. "Synthesis of 2-Azidomethyl-5-ethynylfuran: A New Bio-Derived Self-Clickable Building Block". Synthesis 51, nr 05 (8.01.2019): 1235–42. http://dx.doi.org/10.1055/s-0037-1610414.

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2-Azidomethyl-5-ethynylfuran, a new ambivalent compound with both azide and alkyne moieties that can be used as a self-clickable monomer, is synthesized starting directly from renewable biomass. The reactivity of the azide group linked to furfural is tested via the efficient preparation of a broad range of furfural-containing triazoles in good to excellent yields using a ‘green’ copper(I)-catalyzed azide–alkyne cycloaddition procedure. Access to new bio-based chemicals and oligomeric materials via a click-chemistry approach is also demonstrated using this bio-derived building block.

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39

Singh, Gurleen, Ather Majeed, Riddima Singh, Nancy George, Gurjaspreet Singh, Sofia Gupta, Harminder Singh, Gurpreet Kaur i Jandeep Singh. "CuAAC ensembled 1,2,3-triazole linked nanogels for targeted drug delivery: a review". RSC Advances 13, nr 5 (2023): 2912–36. http://dx.doi.org/10.1039/d2ra05592a.

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Copper(i) catalyzed alkyne azide cycloaddition is the quintessential example of ‘Click Chemistry’, provides an adaptable platform for the synthesis of nanogels for sustained drug release at targeted sites owing to their better biocompatibility.

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40

Fareghi-Alamdari, Reza, Najmeh Jafari, Mansour Shahidzadeh i Negar Zekri. "Reactive Plasticizers Covalently Linked to Glycidyl Azide Polymer via Catalyst-Free Huisgen Azide-Alkyne Cycloaddition". Propellants, Explosives, Pyrotechnics 43, nr 9 (24.07.2018): 893–97. http://dx.doi.org/10.1002/prep.201800013.

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Kalmár, László, Károly Ágoston, Zoltán Szurmai, Boglárka Döncző i János Kerékgyártó. "Synthesis of FullyO-BenzylatedN-Linked Core Pentasaccharide Glycosyl Azide". Journal of Carbohydrate Chemistry 31, nr 3 (marzec 2012): 203–19. http://dx.doi.org/10.1080/07328303.2011.642433.

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42

Yang, En-Che, Han-Sheng Huang, Shao-Yun Huang, Shi-Yi Huang, Yu-Ying Chang, Gene-Hsiang Lee, Hwo-Shuenn Sheu i Chung-Kai Chang. "A one dimensional coordination polymer composed of antiferromagnetically coupled disk-like [Mn7] units". CrystEngComm 20, nr 43 (2018): 6963–69. http://dx.doi.org/10.1039/c8ce01374h.

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Shan, Meixia, Beatriz Seoane, Elena Rozhko, Alla Dikhtiarenko, Guillaume Clet, Freek Kapteijn i Jorge Gascon. "Azine-Linked Covalent Organic Framework (COF)-Based Mixed-Matrix Membranes for CO2/CH4Separation". Chemistry - A European Journal 22, nr 41 (18.08.2016): 14467–70. http://dx.doi.org/10.1002/chem.201602999.

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Ursuegui, Sylvain, Jérémy P. Schneider, Claire Imbs, Florian Lauvoisard, Marta Dudek, Michel Mosser i Alain Wagner. "Expedient synthesis of trifunctional oligoethyleneglycol-amine linkers and their use in the preparation of PEG-based branched platforms". Organic & Biomolecular Chemistry 16, nr 44 (2018): 8579–84. http://dx.doi.org/10.1039/c8ob02097c.

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45

Mao, Wei, Song Rae Kim i Hyuk Sang Yoo. "Surface-decorated nanoparticles clicked into nanoparticle clusters for oligonucleotide encapsulation". RSC Advances 10, nr 61 (2020): 37040–49. http://dx.doi.org/10.1039/d0ra06622b.

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AuNPs with bPEI and azide modification are loaded with CpG and self-assembled to AuNCs by click chemistry using an alkyne-terminated MMP-2 cleavable peptide as a linker. The clusters are dissembled by MMP-2 to release CpG in a stimuli-responsive manner.

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46

Chan, Ka Keung, Qiaoshi Lei, Jinshan Tang i Xue-Long Sun. "Synthesis of aryl azide chain-end functionalized N-linked glycan polymers and their photo-labelling of specific protein". RSC Advances 10, nr 63 (2020): 38561–65. http://dx.doi.org/10.1039/d0ra08400j.

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47

Yadav, Dolly, Nem Singh, Tae Wu Kim, Jae Young Kim, No-Joong Park i Jin-Ook Baeg. "Highly regioselective and sustainable solar click reaction: a new post-synthetic modified triazole organic polymer as a recyclable photocatalyst for regioselective azide–alkyne cycloaddition reaction". Green Chemistry 21, nr 10 (2019): 2677–85. http://dx.doi.org/10.1039/c9gc00894b.

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Sustainable and highly regioselective solar light-assisted approach for the azide–alkyne cycloaddition reaction using a perylene-derived post-synthetic modified triazole-linked organic polymer photocatalyst.

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48

Mangova, M., i G. Rachovska. "Technological characteristics of newly developed mutant common winter wheat lines". Plant, Soil and Environment 50, No. 2 (21.11.2011): 84–87. http://dx.doi.org/10.17221/3686-pse.

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Fifteen hybrid-mutant lines and two direct mutant lines were studied in terms to their technological quality in 2000 and 2001 vegetation years. The hybrid-mutant lines were produced using chemical mutagen sodium azide at a concentration of 1mM on F<sub>2</sub> seeds. For parent cultivars, promising and well adapted Bulgarian and foreign common winter wheat cultivars were used. The direct mutant lines were obtained by gamma-irradiation and sodium azide treatment of dry seed from cultivars. The differences of the following three characteristics: quality index, softening of dough and energy for dough deformation (W) of MX 77/14 compared to the total mean value are positive and statistically significant. Crude protein, softening of dough, and energy for dough deformation (W) of MX 84/37 are also significantly different in relation to the total mean value. Both wheat lines refer to the group of common winter wheat with very good technological quality. This fact was confirmed of higher values of energy for dough deformation (W), than strong wheat cultivar Pobeda.

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Reddington, Samuel, Peter Watson, Pierre Rizkallah, Eric Tippmann i D. Dafydd Jones. "Genetically encoding phenyl azide chemistry: new uses and ideas for classical biochemistry". Biochemical Society Transactions 41, nr 5 (23.09.2013): 1177–82. http://dx.doi.org/10.1042/bst20130094.

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Introducing new physicochemical properties into proteins through genetically encoded Uaa (unnatural amino acid) incorporation can lead to the generation of proteins with novel properties not normally accessible with the 20 natural amino acids. Phenyl azide chemistry represents one such useful addition to the protein repertoire. Classically used in biochemistry as a non-specific photochemical protein cross-linker, genetically encoding phenyl azide chemistry at selected residues provides more powerful routes to post-translationally modify protein function in situ. The two main routes are modulation by light (optogenetics) and site-specific bio-orthogonal modification (bioconjugation) via Click chemistry. In the present article, we discuss both approaches and their influence on protein function.

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Atanasova, Petia, Maofeng Dou, Shravan R. Kousik, Joachim Bill i Maria Fyta. "Adsorption of azide-functionalized thiol linkers on zinc oxide surfaces". RSC Advances 11, nr 10 (2021): 5466–78. http://dx.doi.org/10.1039/d0ra05127f.

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Studying the interaction between organic molecules and metal oxide surfaces is key to the development and modification of organic–inorganic hybrids for application in heterogeneous catalysis, biomedical implants, and functional nanoporous matrices.

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