Some scientific research about 61-82-5

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I found the field of Chemistry very interesting. Saw the article Preparation and application of a novel supported 3-(3-sulfamic acid imidazolium trifluoroacetate)propyl triethoxysilane on magnetic nanoparticles as a new magnetic ionic liquid for the synthesis of triazole quinazolinones and fused pyrimidines published in 2020.0. HPLC of Formula: C2H4N4, Reprint Addresses Basirat, N (corresponding author), Payame Noor Univ PNU, Dept Chem, Tehran, Iran.. The CAS is 61-82-5. Through research, I have a further understanding and discovery of 1H-1,2,4-Triazol-5-amine

Supported 3-(3-sulfamic acid imidazolium trifluoroacetate)propyl triethoxysilane on magnetic nanoparticles as a novel nanocatalyst was synthesized and characterized by FT-IR, XRD, TGA, SEM, TEM and VSM techniques. The catalytic activity of the magnetic catalyst was studied through one-pot synthesis of triazole quinazolinones and fused pyrimidine derivatives via one-pot multi-component reactions under thermal conditions. This catalyst demonstrated excellent catalytic properties with high percentage in short reaction times, low cost and easily separated using an external magnet and reusable without significant loss of its catalytic efficiency. [GRAPHICS] .

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Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

Archives for Chemistry Experiments of 1H-1,2,4-Triazol-5-amine

Formula: C2H4N4. Bye, fridends, I hope you can learn more about C2H4N4, If you have any questions, you can browse other blog as well. See you lster.

Formula: C2H4N4. Authors Kubo, A; Kimachi, T; Haginaka, J in ELSEVIER published article about in [Kubo, Arisa; Kimachi, Tetsutaro] Mukogawa Womens Univ, Sch Pharm & Pharmaceut Sci, 11-68 Koshien Kyuban Cho, Nishinomiya, Hyogo 6638179, Japan; [Haginaka, Jun] Mukogawa Womens Univ, Inst Biosci, 11-68 Koshien Kyuban Cho, Nishinomiya, Hyogo 6638179, Japan in 2021.0, Cited 31.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5

Monodisperse molecularly imprinted polymers (MIPs) for warfarin (WF), 4′-chlorowarfarin (CWF), (S)-CWF and (R)-CWF (MIPWF, MIPCWF, MIP(S)-CWF and MIP(R)-CWF, respectively) were prepared using 4-vinylpyridine (4-VPY) and ethylene glycol dimethacrylate (EDMA) as a functional monomer and a crosslinker, respectively, by multi-step swelling and polymerization. The molar ratio of a template molecule, 4-VPY to EDMA was 6:18:25 or 4:18:25. The retention and molecular recognition properties of MIPWF and MIPCWF were evaluated using a mixture of sodium phosphate buffer or ammonium formate and acetonitrile in reversed-phase LC. WF and CWF on these MIPs gave the maximal retentions at mobile phase pH 7, and those retentions were decreased with an increase of acetonitrile content. The retention and imprinting factors were in the order of WF < CWF < 4'-bromowarfarin (BWF) on MIPWF and MIPCWF in neutral mobile phases. On the other hands, in acidic mobile phases the retention factors were in the same order with those in neutral mobile phases, while the imprinting factors of WF and CWF were higher on the respective MIPs. These results suggest that ionic or hydrogen bonding interactions, hydrophobic interactions and pi-pi interactions could work for the retention and molecular recognition of WF, CWF and BWF on these MIPs in a reversed-phase mode. Furthermore, MIP(S)-CWF and MIP(R)-CWF could separate WF, CWF and BWF enantiomers in acidic mobile phases. (C) 2021 Elsevier B.V. All rights reserved. Formula: C2H4N4. Bye, fridends, I hope you can learn more about C2H4N4, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

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Name: 1H-1,2,4-Triazol-5-amine. Bye, fridends, I hope you can learn more about C2H4N4, If you have any questions, you can browse other blog as well. See you lster.

An article A Stable Zn-Based Metal-Organic Framework as an Efficient Catalyst for Carbon Dioxide Cycloaddition and Alcoholysis at Mild Conditions WOS:000499226600003 published article about CHEMICAL FIXATION; CO2; PERFORMANCE; SEPARATION; POLYMER; MOF; MG in [Luo, Zhiqiang; Wang, Jun; He, Yanqing; Ao, Qiong; Deng, Qiang; Zeng, Zheling] Nanchang Univ, Minist Educ, Key Lab Poyang Environm & Resource Utilizat, Nanchang 330031, Jiangxi, Peoples R China; [Luo, Zhiqiang; Wang, Jun; He, Yanqing; Ao, Qiong; Deng, Qiang; Zeng, Zheling] Nanchang Univ, Sch Resource Environm & Chem Engn, Nanchang 330031, Jiangxi, Peoples R China; [Wang, Hongming] Nanchang Univ, Inst Adv Study, Nanchang 330031, Jiangxi, Peoples R China; [Deng, Shuguang] Arizona State Univ, Sch Engn Matter Transport & Energy, 551 E Tyler Mall, Tempe, AZ 85287 USA in 2020.0, Cited 31.0. Name: 1H-1,2,4-Triazol-5-amine. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5

Developing highly efficient heterogeneous catalysts for cycloaddition of CO2 and epoxides to produce cyclic carbonates is promising but challenging. In this work, a novel three-dimensional metal organic framework (MOF) with cylinder pore systems and unsaturated Zn sites has been demonstrated as potent candidate in CO2 fixation at mild and solvent-free conditions. The Zn(atz)(bdc)(0.5), where atz = aminotriazole and H(2)bdc = terephthalic, exhibits microporous nature that can regulate the catalytic interaction of active centers and substrates. The structure stability has been systematically investigated and proven to be sufficient for practical application. Furthermore, the cooperative effects of porosity, CO2 binding affinity, activation centers, and synergism with co-catalyst have been deeply investigated. Moreover, high propylene epoxide conversion (97%) and selectivity (> 99%) have been achieved at mild conditions (60 degrees C and 1 MPa) with excellent cycle stability. Owing to the well-defined pore system, an obvious substrates selectivity has been clearly observed. A possible catalytic mechanism has been proposed and verified by DFT calculations. Furthermore, the prepared Zn-MOF can also be used as an efficient heterogeneous catalyst for the reaction of epoxides with alcohols to produce beta-alkoxy alcohol. [GRAPHICS] .

Name: 1H-1,2,4-Triazol-5-amine. Bye, fridends, I hope you can learn more about C2H4N4, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

Our Top Choice Compound:1H-1,2,4-Triazol-5-amine

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COA of Formula: C2H4N4. In 2020.0 BIOMACROMOLECULES published article about MEDIATED DELIVERY; CELLULAR UPTAKE; DRUG-DELIVERY; NANOCARRIERS; PEPTIDES; PROBES; FUTURE; RGD in [Ding, Zexuan; Liu, Guhuan; Hu, Jinming] Univ Sci & Technol China, Dept Polymer Sci & Engn, CAS Key Lab Soft Matter Chem, Hefei Natl Lab Phys Sci Microscale, Hefei 230026, Anhui, Peoples R China in 2020.0, Cited 56.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5.

Visualization of intracellular transport pathways is crucial to investigate the internalization mechanism and understand the intracellular behavior of nanomaterials. Herein, we rationalized the design of micellar nanopartides (NPs for ratiometric fluorescent mapping of intracellular pH and glutathione (GSH), two essential parameters for maintaining normal cellular functions. Specifically, pH-sensitive naphthalimide-based probe (NPI) and pH-inert rhodamine B (RhB) were covalently labeled to double hydrophilic block copolymers (DHBCs) using the thiolactone chemistry, enabling the covalent attachment of NPI and RhB to one molecule with a redox-responsive disulfide linkage. The dually labeled DHBCs exhibited blue/orange dual emissions in acidic pH, which was further converted into green/orange dual emissions in neutral pH because of the deprotonation of NPI moieties and the sole green emission in the presence of GSH at neutral pH because of the decreased Forster resonance energy transfer efficiency between an NPI donor and an RhB acceptor as a result of GSH-mediated cleavage of disulfide bonds. These remarkable ratiometric fluorescence changes allowed for not only the simultaneous mapping of the intracellular pH and GSH but also the intracellular transport pathways of internalized NPs.

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Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

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An article An efficient green synthesis of novel 1H-imidazo[1,2-a]imidazole-3-amine and imidazo[2,1-c][1,2,4]triazole-5-amine derivatives via Strecker reaction under controlled microwave heating WOS:000459811200036 published article about ALPHA-AMINO NITRILES; MULTICOMPONENT REACTIONS; NATURAL-PRODUCTS; IMIDAZOLES; ALDEHYDES in [Sadek, Kamal Usef; Abdel-Hameed, Afaf Mohamed; Abdelnabi, Hisham A.; Meleigy, Yasser] Menia Univ, Fac Sci, Chem Dept, Al Minya 61519, Egypt in 2019.0, Cited 28.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5. Safety of 1H-1,2,4-Triazol-5-amine

A highly efficient multi-component one-pot synthesis of novel 1H-imidazo[1,2-a]imidazole-3-amine and imidazo[2,1-c][1,2,4]triazole-5-amine derivatives has been developed through the reaction of easily available aromatic aldehydes, benzoyl cyanide and either 2-aminoimidazole-4,5-dicarbonitrile or 3-amino-1,2,4-triazole in pyridine under controlled microwave heating. The process is environmentally friendly, is operationally simple, with short reaction time and with high yields.

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Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

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Recently I am researching about IN-VITRO; ENHANCED ANTIOXIDANT; ANTIBACTERIAL; COMPLEXES, Saw an article supported by the Natural Science Foundation of Shandong Province Science and Technology Development Plan [2019GHY112010]; National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [41576156]; Natural Science Foundation of Shandong Province of ChinaNatural Science Foundation of Shandong Province [ZR2017BD015, ZR2019BD064]. Published in WILEY-V C H VERLAG GMBH in WEINHEIM ,Authors: Zhang, JJ; Mi, YQ; Sun, XQ; Chen, Y; Miao, Q; Tan, WQ; Li, Q; Dong, F; Guo, ZY. The CAS is 61-82-5. Through research, I have a further understanding and discovery of 1H-1,2,4-Triazol-5-amine. Application In Synthesis of 1H-1,2,4-Triazol-5-amine

Eight novel chitosan derivatives bearing urea groups are designed and synthesized. Fourier transform infrared spectroscopy, H-1 nuclear magnetic resonance spectrometer, and elemental analysis are performed to confirm the structural characteristics of chitosan derivatives. The antioxidant activities, including superoxide radicals’ scavenging activity, 1,1-diphenyl-2-picrylhydrazyl radicals’ scavenging activity, and hydroxyl radical’ scavenging activity, of the derivatives are explored within different concentrations in the reaction system. In vitro fungicidal activity of these compounds is further tested against Fusarium oxysporum f. sp. niveum, Phomopsis asparagus, F. oxysporum f. sp. cucumebrium Owen, and Botrytis cinerea, respectively, particularly compounds exhibit significant control effect at 1.0 mg mL(-1). The experimental results indicate that the products bearing urea groups show enhanced antifungal property and antioxidant activity compared with pristine chitosan. Meanwhile, their bioactivities follow some regularity on the whole, that is, they are related to the electron-withdrawing property of the different substituted groups of urea. Derivatives with stronger electron-withdrawing property will have higher biological activities. L929 cells are used to carry out cytotoxicity test of chitosan and chitosan derivatives by Cell Counting Kit-8 assay. The results indicate that some of the samples show low cytotoxicity. This research will be helpful to broaden the application of chitosan in materials.

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Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

Final Thoughts on Chemistry for C2H4N4

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Hulin, M; Leroux, C; Mathieu, A; Gouzy, A; Berthet, A; Boivin, A; Bonicelli, B; Chubilleau, C; Hulin, A; Garziandia, EL; Mamy, L; Millet, M; Pernot, P; Quivet, E; Scelo, AL; Merlo, M; Ruelle, B; Bedos, C in [Hulin, Marion; Leroux, Carole; Mathieu, Aurelie; Merlo, Mathilde] ANSES, Risk Assessment Dept, 14 Rue Pierre & Marie Curie, F-94701 Maisons Alfort, France; [Gouzy, Aurelien; Garziandia, Eva Leoz] INERIS, Parc Technol ALATA BP2, F-60550 Verneuil En Halatte, France; [Berthet, Aurelie] Univ Lausanne, Ctr Primary Care & Publ Hlth Unisante, Lausanne, Switzerland; [Boivin, Arnaud; Scelo, Anne-Laure] ANSES, Regulated Prod Assessment Dept, 14 Rue Pierre & Marie Curie, F-94701 Maisons Alfort, France; [Bonicelli, Bernard; Ruelle, Bernadette] INRAE UMR ITAP, 361 Rue Jean Francois Breton, F-34196 Montpellier, France; [Chubilleau, Catherine] Ctr Hosp Niort, Serv Hyg Hosp, F-79000 Niort, France; [Hulin, Agnes] ATMO Nouvelle Aquitaine, F-17180 La Rochelle, Perigny, France; [Garziandia, Eva Leoz] LCSQA, F-60550 Verneuil En Halatte, France; [Mamy, Laure; Bedos, Carole] Univ Paris Saclay, UMR ECOSYS, AgroParisTech, INRAE, F-78850 Thiverval Grignon, France; [Millet, Maurice] Univ Strasbourg, EPEES UMR 7515 CNRS, 25 Rue Becquerel, F-67087 Strasbourg 2, France; [Pernot, Pierre] AirParif, 7 Rue Crillon, F-75005 Paris, France; [Quivet, Etienne] Aix Marseille Univ, LCE, CNRS, Marseille, France published Monitoring of pesticides in ambient air: Prioritization of substances in 2021.0, Cited 26.0. Product Details of 61-82-5. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5.

Despite the richness of data collected on pesticide concentrations in ambient air in France, knowledge on this topic remains partial and heterogeneous in the absence of specific regulations. The population exposure remains thus difficult to estimate; therefore it was necessary to define modalities for implementing national monitoring of pesticides in ambient air in metropolitan France and in the overseas territories. The objective of this work was to identify which active substances (a.s.) have to be monitored in priority. As part of a collective expertise, a group of multidisciplinary experts has developed a method to rank active substances authorised as plant protection products, biocides and antiparasitic agents, which were available on the French market in 2015. A 3-steps approach has been developed. The first step consisted of a theoretical approach based on a hierarchy of substances according to four criteria: (a) national uses, (b) emission potential to the air, (c) persistence in the air, and (d) chronic toxicity. The three first criteria give information on their potential to be present in the atmosphere, and the fourth criterion allows to consider their potential of hazard. The second step was an observational approach based on existing database on pesticide air measurements in France. In the third step, both approaches were combined using decision trees to select priority pesticides. Among the 1316 a.s. first identified from the EU Pesticides database, 90 were selected, among which 43 required metrological and/or analytical development. The experts recommended confirming the relevance of performing a longer term monitoring of these a.s. after a one-year exploratory campaign. The proposed method is reproduceable, transparent, easy to update (e.g. in the light of a change in product authorization), and can be adapted to other agricultural and geographical conditions, and objectives (e.g. monitoring of the ecotoxicological effects of pesticides). (C) 2020 Published by Elsevier B.V.

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Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

The Best Chemistry compound:C2H4N4

Welcome to talk about 61-82-5, If you have any questions, you can contact Shahnavaz, Z; Khaligh, NG; Mihankhah, T; Johan, MR or send Email.. Formula: C2H4N4

An article Design, synthesis, characterization, and physical property determination of a new ionic liquid: the preparation of triazolo-pyrimidines at room temperature under metal-free conditions WOS:000557222500001 published article about AGENTS; ACID in [Shahnavaz, Zohreh; Khaligh, Nader Ghaffari; Johan, Mohd Rafie] Univ Malaya, Nanotechnol & Catalysis Res Ctr, Inst Postgrad Studies, Kuala Lumpur 50603, Malaysia; [Mihankhah, Taraneh] Iran Univ Sci & Technol, Sch Civil Engn, Dept Water & Environm Engn, Environm Res Lab, Tehran 16765163, Iran in 2020.0, Cited 19.0. Formula: C2H4N4. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5

A new ionic liquid is synthesized, and its chemical structure is characterized by FTIR, 1D NMR and 2D NMR, and mass analyses. The thermal behavior and thermal stability of this ionic liquid are investigated. The results approved the formation of 4,4MODIFIER LETTER PRIME-trimethylene-N,NMODIFIER LETTER PRIME-dipiperidinium sulfate instead of 4,4MODIFIER LETTER PRIME-trimethylene-N,NMODIFIER LETTER PRIME-dipiperidinium hydrogen sulfate. Moreover, the synthesis of triazolo-pyrimidine derivatives was successfully conducted in the presence of new ionic liquid at room temperature under metal-free conditions, which demonstrated the catalytic efficiency of this ionic liquid. The workup was carried out without the utilization of high-cost column chromatography. After extraction of desired products, the residual ionic liquid could be recycled and reused in the next runs. New ionic liquid exhibited high catalytic activity even after fifth run with no significant change in the chemical structure.

Welcome to talk about 61-82-5, If you have any questions, you can contact Shahnavaz, Z; Khaligh, NG; Mihankhah, T; Johan, MR or send Email.. Formula: C2H4N4

Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

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Category: Triazoles. Bye, fridends, I hope you can learn more about C2H4N4, If you have any questions, you can browse other blog as well. See you lster.

I found the field of Chemistry very interesting. Saw the article Synthesis of highly functionalised 5-membered ring fused pyrimidine derivatives using an isocyanide-based one-pot, three component reaction published in 2020.0. Category: Triazoles, Reprint Addresses Coyanis, EM (corresponding author), MINTEK, Adv Mat Div, Private Bag X3015, ZA-2125 Randburg, South Africa.; Bode, ML (corresponding author), Univ Witwatersrand, Sch Chem, Mol Sci Inst, PO Wits, ZA-2050 Johannesburg, South Africa.. The CAS is 61-82-5. Through research, I have a further understanding and discovery of 1H-1,2,4-Triazol-5-amine

A one-pot reaction of the zwitterion formed from an isocyanide and an acetylenedicarboxylate with different five-membered rings containing both an acidic proton and a suitable nucleophile resulted in the preparation of novel 5-membered ring fused pyrimidine derivatives in yields ranging from 18 to 87%. (C) 2020 Elsevier Ltd. All rights reserved.

Category: Triazoles. Bye, fridends, I hope you can learn more about C2H4N4, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

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Quality Control of 1H-1,2,4-Triazol-5-amine. Welcome to talk about 61-82-5, If you have any questions, you can contact Tang, YZ; Huang, HL; Peng, B; Chang, YJ; Li, Y; Zhong, CL or send Email.

Authors Tang, YZ; Huang, HL; Peng, B; Chang, YJ; Li, Y; Zhong, CL in ROYAL SOC CHEMISTRY published article about METAL-ORGANIC FRAMEWORK; FLUORESCENT-PROBE; IONIC LIQUIDS; ANILINE; LUMINESCENT; BENZOTHIADIAZOLE; ADSORPTION; MOLECULES; REMOVAL; CAPTURE in [Tang, Yuanzhe; Huang, Hongliang; Peng, Ben; Chang, Yanjiao; Li, Yang; Zhong, Chongli] Tiangong Univ, State Key Lab Separat Membranes & Membrane Proc, Tianjin 300387, Peoples R China; [Tang, Yuanzhe; Huang, Hongliang; Peng, Ben; Chang, Yanjiao; Li, Yang; Zhong, Chongli] Tiangong Univ, Sch Chem & Chem Engn, Tianjin 300387, Peoples R China; [Zhong, Chongli] Beijing Univ Chem Technol, Coll Chem Engn, Beijing 100029, Peoples R China in 2020.0, Cited 53.0. Quality Control of 1H-1,2,4-Triazol-5-amine. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5

Primary aromatic amines (PAAs), as a class of persistent and highly toxic organic pollutants, have been posing a great threat to human health and the environment. Therefore, the design and preparation of a highly sensitive and selective luminescent probe to detect PAAs among various amines are important but challenging. In this work, by introducing electron-deficient monomer 4,4 ‘-(benzo[c][1,2,5]thiadiazole-4,7-diyl)dibenzaldehyde (BTDD) with an aggregation-caused quenching behavior into the 2D framework, fluorescent ultrathin covalent triazine framework (F-CTF) nanosheets were constructed. Compared with the aggregated BTDD monomer, the obtained F-CTF-3 nanosheet shows much higher fluorescence quantum yield due to the BTDD fragment being well dispersed in the 2D framework. The F-CTF-3 nanosheet exhibits high stability, high porosity, and high fluorescence performance and has a rich electron-deficient unit in the pore channel, making it an ideal platform for sensing electron-rich PAA molecules. In fact, the F-CTF-3 nanosheet shows high sensitivity and selectivity for PAA detection by fluorescence quenching, among various amines, covering some classic aliphatic amines, heterocyclic amines, secondary aromatic amines and tertiary aromatic amines. To the best of our knowledge, it is the first reported fluorescent sensor for selective sensing of PAAs among various amines. Moreover, F-CTF-3 exhibits unprecedented low detection limits of 11.7 and 1.47 nM toward phenylamine (PA) andp-phenylenediamine (PDA), respectively, surpassing all the reported fluorescent sensors. The combination of experimental analysis and density functional theory (DFT) calculations demonstrates that the unique PAA detection performance of F-CTF-3 can be attributed to the static quenching process, which is confirmed by the formation of a ground-state fluorescence-quenched complex on account of the hydrogen bonding interactions between F-CTF-3 and PAAs. This work not only provides a thiadiazole-based 2D fluorescent organic framework nanosheet, but also an excellent fluorescent sensor with unexpected sensitivity and selectivity for PAA detection.

Quality Control of 1H-1,2,4-Triazol-5-amine. Welcome to talk about 61-82-5, If you have any questions, you can contact Tang, YZ; Huang, HL; Peng, B; Chang, YJ; Li, Y; Zhong, CL or send Email.

Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics