Bibliography.bib

@article{simkin_you_2006,
	title = {Do You Sincerely Want to Be Cited? Or: Read Before You Cite},
	volume = {3},
	issn = {1740-9705, 1740-9713},
	url = {https://academic.oup.com/jrssig/article/3/4/179/7029597},
	doi = {10.1111/j.1740-9713.2006.00202.x},
	shorttitle = {Do You Sincerely Want to Be Cited?},
	abstract = {Abstract
            Do you sincerely want to be cited? Prestige depends on the number of times your academic paper gets cited. But that need not be a measure of how good it is, nor even of how many times it is actually read. Mikhail Simkin and Vwani Roychowdhury explain their theory of the unread citation.},
	pages = {179--181},
	number = {4},
	journaltitle = {Significance},
	author = {Simkin, Mikhail and Roychowdhury, Vwany},
	urldate = {2023-04-16},
	date = {2006-12-01},
	langid = {english},
	file = {Do You Sincerely Want to Be Cited? Or\: Read Before You Cite:/home/stefanom/GoogleDrive/University/Zotero/Zotero/storage/5AH8GY5J/simkin2006.pdf.pdf:application/pdf},
}

@article{blatov_applied_2014,
	title = {Applied Topological Analysis of Crystal Structures with the Program Package {ToposPro}},
	volume = {14},
	issn = {1528-7483, 1528-7505},
	url = {https://pubs.acs.org/doi/10.1021/cg500498k},
	doi = {10.1021/cg500498k},
	abstract = {Basic concepts of computer topological analysis of crystal structures realized in the current version of the program package {ToposPro} are considered. Applications of the {ToposPro} methods to various classes of chemical compoundscoordination polymers, molecular crystals, supramolecular ensembles, inorganic ionic compounds, intermetallics, fast-ion conductors, microporous materialsare illustrated by many examples. It is shown that chemically and crystallographically different structures can be automatically treated in a similar way with the {ToposPro} approaches.},
	pages = {3576--3586},
	number = {7},
	journaltitle = {Crystal Growth \& Design},
	shortjournal = {Crystal Growth \& Design},
	author = {Blatov, Vladislav A. and Shevchenko, Alexander P. and Proserpio, Davide M.},
	urldate = {2023-04-16},
	date = {2014-07-02},
	langid = {english},
	file = {applied_topological_analysis_of_crystal_structures_with_the_program_packageblatov_et_al_2014_.pdf:/home/stefanom/GoogleDrive/University/Zotero/ZotFiles/Crystal Growth & Design/2014/applied_topological_analysis_of_crystal_structures_with_the_program_packageblatov_et_al_2014_.pdf:application/pdf},
}

@article{erdman_reaction_2004,
	title = {The Reaction of Hydrazine with α‐Cyanocinnamate Esters: A Caveat},
	volume = {34},
	issn = {0039-7911, 1532-2432},
	url = {http://www.tandfonline.com/doi/abs/10.1081/SCC-120028648},
	doi = {10.1081/SCC-120028648},
	shorttitle = {The Reaction of Hydrazine with α‐Cyanocinnamate Esters},
	pages = {1163--1171},
	number = {6},
	journaltitle = {Synthetic Communications},
	shortjournal = {Synthetic Communications},
	author = {Erdman, Paul J. and Gosse, Jimmy L. and Jacobson, Jamey A. and Lewis, David E.},
	urldate = {2023-04-17},
	date = {2004-12-31},
	langid = {english},
	file = {Erdman_et_al_2004_The_Reaction_of_Hydrazine_with_α‐Cyanocinnamate_Esters.pdf:/home/stefanom/GoogleDrive/Zot/Erdman_et_al_2004_The_Reaction_of_Hydrazine_with_α‐Cyanocinnamate_Esters.pdf:application/pdf;The Reaction of Hydrazine with α‐Cyanocinnamate Esters\: A Caveat:/home/stefanom/GoogleDrive/University/Zotero/Zotero/storage/XEBGHV2I/erdman2004.pdf.pdf:application/pdf;The Reaction of Hydrazine with α‐Cyanocinnamate Esters\: A Caveat:/home/stefanom/GoogleDrive/University/Zotero/Zotero/storage/A5ATJYBF/erdman2004.pdf.pdf:application/pdf},
}

@article{smith_reactions_1968,
	title = {Reactions of hydrazines with esters and carboxylic acids},
	volume = {33},
	issn = {0022-3263, 1520-6904},
	url = {https://pubs.acs.org/doi/abs/10.1021/jo01266a085},
	doi = {10.1021/jo01266a085},
	pages = {851--855},
	number = {2},
	journaltitle = {The Journal of Organic Chemistry},
	shortjournal = {J. Org. Chem.},
	author = {Smith, Richard Frederick and Bates, Alvin C. and Battisti, Angello J. and Byrnes, Peter G. and Mroz, Christine T. and Smearing, Thomas J. and Albrecht, Frederick X.},
	urldate = {2023-04-17},
	date = {1968-02},
	langid = {english},
	file = {Reactions of hydrazines with esters and carboxylic acids:/home/stefanom/GoogleDrive/University/Zotero/Zotero/storage/QUJ78VAE/smith1968.pdf.pdf:application/pdf},
}

@article{nagpal_synthesis_2001,
	title = {{SYNTHESIS} {OF} 1, 3-{DIKETONE} {AND} {ITS} {REACTION} {WITH} {DIFFERENT} N-{NUCLEOPHILES} ({PART} I)},
	volume = {7},
	issn = {2191-0197, 0793-0283},
	url = {https://www.degruyter.com/document/doi/10.1515/HC.2001.7.6.589/html},
	doi = {10.1515/HC.2001.7.6.589},
	abstract = {Treatment of resorcinol with ethyl acetoacetate in presence of conc. sulphuric acid led to formation of 1,3-diketone 3 in several steps, which on reaction with ethylene diamine 4, phenylene diamine 5, hydroxylamine 8, phenyl hydrazine 9 and hydrazine 10 led to formation of 1,4-diazepine 3a, 1, 5-benzodiazepine 3b, isoxazole 3c and pyrazole 3d derivatives respectively.},
	number = {6},
	journaltitle = {Heterocyclic Communications},
	author = {Nagpal, Anita and Unny, Rashmy and Joshi, P. and Joshi, Y.C.},
	urldate = {2023-04-18},
	date = {2001-01},
	langid = {english},
	file = {nagpal_et_al_2001_synthesis_of_1,_3-diketone_and_its_reaction_with_different_n-nucleophiles_(part.pdf:/home/stefanom/GoogleDrive/University/Zotero/ZotFiles/Heterocyclic Communications/2001/nagpal_et_al_2001_synthesis_of_1,_3-diketone_and_its_reaction_with_different_n-nucleophiles_(part.pdf:application/pdf},
}

@article{joshi_synthesis_2004,
	title = {{SYNTHESIS} {OF} {NOVEL} {PYRAZOLE} {DERIVATIVES} {FROM} {DIARYL} 1,3-{DIKETONES} ({PART}-{II})},
	volume = {10},
	issn = {2191-0197, 0793-0283},
	url = {https://www.degruyter.com/document/doi/10.1515/HC.2004.10.2-3.249/html},
	doi = {10.1515/HC.2004.10.2-3.249},
	abstract = {Some 3,5-disubstituted pyrazoles derivatives (2a-2f) have been synthesized. Their structure were confirmed by elemental analysis, {IR}, 'H {NMR}, l3C {NMR} and {MS} spectral studies.},
	number = {2},
	journaltitle = {Heterocyclic Communications},
	author = {Joshi, Y.C. and Joshi, P. and Chauhan, Suresh Singh and Nigam, Sandeep},
	urldate = {2023-04-18},
	date = {2004-01},
	langid = {english},
	file = {10.1515_hc.2004.10.2-3.249.pdf:/home/stefanom/GoogleDrive/Zot/10.1515_hc.2004.10.2-3.249.pdf:application/pdf;joshi_et_al_2004_synthesis_of_novel_pyrazole_derivatives_from_diaryl_1,3-diketones_(part-ii).pdf:/home/stefanom/GoogleDrive/Università/Zot/Heterocyclic Communications/2004/joshi_et_al_2004_synthesis_of_novel_pyrazole_derivatives_from_diaryl_1,3-diketones_(part-ii).pdf:application/pdf;SYNTHESIS OF NOVEL PYRAZOLE DERIVATIVES FROM DIARYL 1,3-DIKETONES (PART-II):/home/stefanom/GoogleDrive/University/Zotero/Zotero/storage/W8PLL9MK/joshi2004.pdf.pdf:application/pdf},
}

@article{cinar_synthesis_2021,
	title = {Synthesis of New Pyrazole Compounds via Diketonic Michael Adducts},
	issn = {1303-5002},
	url = {https://dergipark.org.tr/en/doi/10.15671/hjbc.954044},
	doi = {10.15671/hjbc.954044},
	journaltitle = {Hacettepe Journal of Biology and Chemistry},
	author = {Çinar, Seda and Eren, Aslı},
	urldate = {2023-04-18},
	date = {2021-12-24},
	langid = {english},
	file = {synthesis_of_new_pyrazole_compounds_via_diketonic_michael_adductsçinar_et_al_2021_.pdf:/home/stefanom/GoogleDrive/University/Zotero/ZotFiles/Hacettepe Journal of Biology and Chemistry/2021/synthesis_of_new_pyrazole_compounds_via_diketonic_michael_adductsçinar_et_al_2021_.pdf:application/pdf},
}

@article{cetin_synthesis_nodate,
	title = {Synthesis of Some New Pyrazoles},
	abstract = {In this paper, firstly, 2-(2-(4-bromophenyl)hydrazino)-1-(2-(hydroxyphenyl)-3-phenylpropane-1,3-dione (1), which is a starting material, was synthesized. Then, the new substituted pyrazoles derivatives (2a-e) were obtained via the reaction-starting material and various hydrazines. The structures of newly-synthesized compounds were determined by spectroscopic methods.},
	author = {Çetin, Adnan},
	langid = {english},
}

@article{fustero_improved_2008,
	title = {Improved Regioselectivity in Pyrazole Formation through the Use of Fluorinated Alcohols as Solvents: Synthesis and Biological Activity of Fluorinated Tebufenpyrad Analogs},
	volume = {73},
	issn = {0022-3263, 1520-6904},
	url = {https://pubs.acs.org/doi/10.1021/jo800251g},
	doi = {10.1021/jo800251g},
	shorttitle = {Improved Regioselectivity in Pyrazole Formation through the Use of Fluorinated Alcohols as Solvents},
	pages = {3523--3529},
	number = {9},
	journaltitle = {The Journal of Organic Chemistry},
	shortjournal = {J. Org. Chem.},
	author = {Fustero, Santos and Román, Raquel and Sanz-Cervera, Juan F. and Simón-Fuentes, Antonio and Cuñat, Ana C. and Villanova, Salvador and Murguía, Marcelo},
	urldate = {2023-04-18},
	date = {2008-05-01},
	langid = {english},
	file = {Improved Regioselectivity in Pyrazole Formation through the Use of Fluorinated Alcohols as Solvents\: Synthesis and Biological Activity of Fluorinated Tebufenpyrad Analogs:/home/stefanom/GoogleDrive/University/Zotero/Zotero/storage/7HITF9XB/fustero2008.pdf.pdf:application/pdf},
}

@article{konkov_synthesis_2009,
	title = {Synthesis of pyrazoles and pyrazolones from 1,3- and 1,4-diketones of the adamantane series},
	volume = {45},
	issn = {1070-4280, 1608-3393},
	url = {http://link.springer.com/10.1134/S1070428009120124},
	doi = {10.1134/S1070428009120124},
	abstract = {Various pyrazole and dihydropyrazolones containing an adamantane fragment were synthesized from adamantyl-substituted 1,3- and 1,4-diketones, ethyl 4-(1-adamantyl)-2-R-4-oxobutanoates (R = {CN}, Ac), and ethyl 2-(1-adamantylcarbonyl)-4-oxo-4-phenylbutanoate.},
	pages = {1824--1828},
	number = {12},
	journaltitle = {Russian Journal of Organic Chemistry},
	shortjournal = {Russ J Org Chem},
	author = {Kon’kov, S. A. and Moiseev, I. K.},
	urldate = {2023-04-18},
	date = {2009-12},
	langid = {english},
	file = {S1070428009120124.pdf:/home/stefanom/GoogleDrive/Zot/S1070428009120124.pdf:application/pdf;Synthesis of pyrazoles and pyrazolones from 1,3- and 1,4-diketones of the adamantane series:/home/stefanom/GoogleDrive/University/Zotero/Zotero/storage/KNGVLAWP/10.1134@S1070428009120124.pdf.pdf:application/pdf;Synthesis of pyrazoles and pyrazolones from 1,3- and 1,4-diketones of the adamantane series:/home/stefanom/GoogleDrive/University/Zotero/Zotero/storage/69JEM22R/10.1134@S1070428009120124.pdf.pdf:application/pdf},
}

@article{carlucci_heterometallic_2010,
	title = {Heterometallic Modular Metal–Organic 3D Frameworks Assembled via New Tris‐β‐Diketonate Metalloligands: Nanoporous Materials for Anion Exchange and Scaffolding of Selected Anionic Guests},
	volume = {16},
	issn = {0947-6539, 1521-3765},
	url = {https://onlinelibrary.wiley.com/doi/10.1002/chem.201001256},
	doi = {10.1002/chem.201001256},
	shorttitle = {Heterometallic Modular Metal–Organic 3D Frameworks Assembled via New Tris‐β‐Diketonate Metalloligands},
	pages = {12328--12341},
	number = {41},
	journaltitle = {Chemistry – A European Journal},
	shortjournal = {Chem. Eur. J.},
	author = {Carlucci, Lucia and Ciani, Gianfranco and Maggini, Simona and Proserpio, Davide M. and Visconti, Marco},
	urldate = {2023-05-01},
	date = {2010-11-02},
	langid = {english},
	file = {carlucci_et_al_2010_heterometallic_modular_metal–organic_3d_frameworks_assembled_via_new.pdf:/home/stefanom/GoogleDrive/Università/Zot/Chemistry – A European Journal/2010/carlucci_et_al_2010_heterometallic_modular_metal–organic_3d_frameworks_assembled_via_new.pdf:application/pdf;Submitted Version:/home/stefanom/GoogleDrive/University/Zotero/Zotero/storage/E262I2HN/Carlucci et al. - 2010 - Heterometallic Modular Metal–Organic 3D Frameworks.pdf:application/pdf},
}

@article{rodriguez-villar_design_2021,
	title = {Design, Synthesis and Anticandidal Evaluation of Indazole and Pyrazole Derivatives},
	volume = {14},
	issn = {1424-8247},
	url = {https://www.mdpi.com/1424-8247/14/3/176},
	doi = {10.3390/ph14030176},
	abstract = {Candidiasis, caused by yeasts of the genus Candida, is the second cause of superficial and mucosal infections and the fourth cause of bloodstream infections. Although some antifungal drugs to treat candidiasis are available, resistant strains to current therapies are emerging. Therefore, the search for new candicidal compounds is certainly a priority. In this regard, a series of indazole and pyrazole derivatives were designed in this work, employing bioisosteric replacement, homologation, and molecular simplification as new anticandidal agents. Compounds were synthesized and evaluated against C. albicans, C. glabrata, and C. tropicalis strains. The series of 3-phenyl-1H-indazole moiety (10a–i) demonstrated to have the best broad anticandidal activity. Particularly, compound 10g, with N,N-diethylcarboxamide substituent, was the most active against C. albicans and both miconazole susceptible and resistant C. glabrata species. Therefore, the 3-phenyl-1H-indazole scaffold represents an opportunity for the development of new anticandidal agents with a new chemotype.},
	pages = {176},
	number = {3},
	journaltitle = {Pharmaceuticals},
	shortjournal = {Pharmaceuticals},
	author = {Rodríguez-Villar, Karen and Hernández-Campos, Alicia and Yépez-Mulia, Lilián and Sainz-Espuñes, Teresita del Rosario and Soria-Arteche, Olivia and Palacios-Espinosa, Juan Francisco and Cortés-Benítez, Francisco and Leyte-Lugo, Martha and Varela-Petrissans, Bárbara and Quintana-Salazar, Edgar A. and Pérez-Villanueva, Jaime},
	urldate = {2023-06-26},
	date = {2021-02-24},
	langid = {english},
	file = {design,_synthesis_and_anticandidal_evaluation_of_indazole_and_pyrazolerodríguez-villar_et_al_2021_.pdf:/home/stefanom/GoogleDrive/University/Zotero/ZotFiles/Pharmaceuticals/2021/design,_synthesis_and_anticandidal_evaluation_of_indazole_and_pyrazolerodríguez-villar_et_al_2021_.pdf:application/pdf},
}

@article{yaghi_hydrothermal_1995,
	title = {Hydrothermal Synthesis of a Metal-Organic Framework Containing Large Rectangular Channels},
	volume = {117},
	issn = {0002-7863, 1520-5126},
	url = {https://pubs.acs.org/doi/abs/10.1021/ja00146a033},
	doi = {10.1021/ja00146a033},
	pages = {10401--10402},
	number = {41},
	journaltitle = {Journal of the American Chemical Society},
	shortjournal = {J. Am. Chem. Soc.},
	author = {Yaghi, O. M. and Li, Hailian},
	urldate = {2023-07-04},
	date = {1995-10},
	langid = {english},
	file = {Hydrothermal Synthesis of a Metal-Organic Framework Containing Large Rectangular Channels:/home/stefanom/GoogleDrive/University/Zotero/Zotero/storage/4YYTUB7Y/yaghi1995.pdf.pdf:application/pdf},
}

@article{desiraju_chemistry_2001,
	title = {Chemistry beyond the molecule},
	volume = {412},
	issn = {0028-0836, 1476-4687},
	url = {https://www.nature.com/articles/35086640},
	doi = {10.1038/35086640},
	pages = {397--400},
	number = {6845},
	journaltitle = {Nature},
	shortjournal = {Nature},
	author = {Desiraju, Gautam R.},
	urldate = {2023-07-06},
	date = {2001-07},
	langid = {english},
	file = {chemistry_beyond_the_moleculedesiraju_2001_.pdf:/home/stefanom/GoogleDrive/University/Zotero/ZotFiles/Nature/2001/chemistry_beyond_the_moleculedesiraju_2001_.pdf:application/pdf},
}

@article{vigato_evolution_2009,
	title = {The evolution of β-diketone or β-diketophenol ligands and related complexes},
	volume = {253},
	issn = {00108545},
	url = {https://linkinghub.elsevier.com/retrieve/pii/S0010854508001343},
	doi = {10.1016/j.ccr.2008.07.013},
	pages = {1099--1201},
	number = {7},
	journaltitle = {Coordination Chemistry Reviews},
	shortjournal = {Coordination Chemistry Reviews},
	author = {Vigato, P. Alessandro and Peruzzo, Valentina and Tamburini, Sergio},
	urldate = {2023-07-06},
	date = {2009-04},
	langid = {english},
	file = {The evolution of β-diketone or β-diketophenol ligands and related complexes:/home/stefanom/GoogleDrive/University/Zotero/Zotero/storage/2XGM78PS/vigato2009.pdf.pdf:application/pdf;The evolution of β-diketone or β-diketophenol ligands and related complexes:/home/stefanom/GoogleDrive/University/Zotero/Zotero/storage/MJMB377U/vigato2009.pdf.pdf:application/pdf;Vigato_et_al_2009_The_evolution_of_β-diketone_or_β-diketophenol_ligands_and_related_complexes.pdf:/home/stefanom/GoogleDrive/Zot/Vigato_et_al_2009_The_evolution_of_β-diketone_or_β-diketophenol_ligands_and_related_complexes.pdf:application/pdf},
}

@article{aromi_poly_2008,
	title = {Poly beta-diketones: Prime ligands to generate supramolecular metalloclusters},
	volume = {252},
	issn = {00108545},
	url = {https://linkinghub.elsevier.com/retrieve/pii/S0010854507001488},
	doi = {10.1016/j.ccr.2007.07.008},
	shorttitle = {Poly beta-diketones},
	pages = {964--989},
	number = {8},
	journaltitle = {Coordination Chemistry Reviews},
	shortjournal = {Coordination Chemistry Reviews},
	author = {Aromí, Guillem and Gamez, Patrick and Reedijk, Jan},
	urldate = {2023-07-06},
	date = {2008-04},
	langid = {english},
	file = {poly_beta-diketonesaromí_et_al_2008_.pdf:/home/stefanom/GoogleDrive/University/Zotero/ZotFiles/Coordination Chemistry Reviews/2008/poly_beta-diketonesaromí_et_al_2008_.pdf:application/pdf},
}

@article{cong_highly_2021,
	title = {Highly Water-Permeable Metal–Organic Framework {MOF}-303 Membranes for Desalination},
	volume = {143},
	issn = {0002-7863, 1520-5126},
	url = {https://pubs.acs.org/doi/10.1021/jacs.1c10192},
	doi = {10.1021/jacs.1c10192},
	pages = {20055--20058},
	number = {48},
	journaltitle = {Journal of the American Chemical Society},
	shortjournal = {J. Am. Chem. Soc.},
	author = {Cong, Shenzhen and Yuan, Ye and Wang, Jixiao and Wang, Zhi and Kapteijn, Freek and Liu, Xinlei},
	urldate = {2023-07-07},
	date = {2021-12-08},
	langid = {english},
	file = {highly_water-permeable_metal–organic_framework_mof-303_membranes_forcong_et_al_2021_.pdf:/home/stefanom/GoogleDrive/University/Zotero/ZotFiles/Journal of the American Chemical Society/2021/highly_water-permeable_metal–organic_framework_mof-303_membranes_forcong_et_al_2021_.pdf:application/pdf},
}

@article{zheng_broadly_2022,
	title = {Broadly Tunable Atmospheric Water Harvesting in Multivariate Metal–Organic Frameworks},
	volume = {144},
	issn = {0002-7863, 1520-5126},
	url = {https://pubs.acs.org/doi/10.1021/jacs.2c09756},
	doi = {10.1021/jacs.2c09756},
	pages = {22669--22675},
	number = {49},
	journaltitle = {Journal of the American Chemical Society},
	shortjournal = {J. Am. Chem. Soc.},
	author = {Zheng, Zhiling and Hanikel, Nikita and Lyu, Hao and Yaghi, Omar M.},
	urldate = {2023-07-07},
	date = {2022-12-14},
	langid = {english},
}

@article{elgrishi_practical_2018,
	title = {A Practical Beginner’s Guide to Cyclic Voltammetry},
	volume = {95},
	issn = {0021-9584, 1938-1328},
	url = {https://pubs.acs.org/doi/10.1021/acs.jchemed.7b00361},
	doi = {10.1021/acs.jchemed.7b00361},
	pages = {197--206},
	number = {2},
	journaltitle = {Journal of Chemical Education},
	shortjournal = {J. Chem. Educ.},
	author = {Elgrishi, Noémie and Rountree, Kelley J. and {McCarthy}, Brian D. and Rountree, Eric S. and Eisenhart, Thomas T. and Dempsey, Jillian L.},
	urldate = {2023-07-09},
	date = {2018-02-13},
	langid = {english},
	file = {A Practical Beginner’s Guide to Cyclic Voltammetry:/home/stefanom/GoogleDrive/University/Zotero/Zotero/storage/PL5EPE33/elgrishi2017.pdf.pdf:application/pdf},
}

@article{pluczyk_using_2018,
	title = {Using Cyclic Voltammetry, {UV}-Vis-{NIR}, and {EPR} Spectroelectrochemistry to Analyze Organic Compounds},
	issn = {1940-087X},
	url = {https://www.jove.com/t/56656/using-cyclic-voltammetry-uv-vis-nir-epr-spectroelectrochemistry-to},
	doi = {10.3791/56656},
	pages = {56656},
	number = {140},
	journaltitle = {Journal of Visualized Experiments},
	shortjournal = {{JoVE}},
	author = {Pluczyk, Sandra and Vasylieva, Marharyta and Data, Przemyslaw},
	urldate = {2023-07-09},
	date = {2018-10-18},
	langid = {english},
	file = {Pluczyk_et_al_2018_Using_Cyclic_Voltammetry,_UV-Vis-NIR,_and_EPR_Spectroelectrochemistry_to.pdf:/home/stefanom/GoogleDrive/Zot/Pluczyk_et_al_2018_Using_Cyclic_Voltammetry,_UV-Vis-NIR,_and_EPR_Spectroelectrochemistry_to.pdf:application/pdf;Using Cyclic Voltammetry, UV-Vis-NIR, and EPR Spectroelectrochemistry to Analyze Organic Compounds:/home/stefanom/GoogleDrive/University/Zotero/Zotero/storage/W575F3HG/9f08168d823137a1be8f90d4c7782f69.pdf.pdf:application/pdf;Using Cyclic Voltammetry, UV-Vis-NIR, and EPR Spectroelectrochemistry to Analyze Organic Compounds:/home/stefanom/GoogleDrive/University/Zotero/Zotero/storage/ZVVYLHXU/9f08168d823137a1be8f90d4c7782f69.pdf.pdf:application/pdf},
}

@article{begue_fluorinated_2004,
	title = {Fluorinated Alcohols: A New Medium for Selective and Clean Reaction},
	issn = {0936-5214, 1437-2096},
	url = {http://www.thieme-connect.de/DOI/DOI?10.1055/s-2003-44973},
	doi = {10.1055/s-2003-44973},
	shorttitle = {Fluorinated Alcohols},
	pages = {18--29},
	number = {1},
	journaltitle = {Synlett},
	shortjournal = {Synlett},
	author = {Bégué, Jean-Pierre and Bonnet-Delpon, Danièle and Crousse, Benoit},
	urldate = {2023-07-10},
	date = {2004},
	langid = {english},
	file = {fluorinated_alcoholsbégué_et_al_2004_.pdf:/home/stefanom/GoogleDrive/University/Zotero/ZotFiles/Synlett/2004/fluorinated_alcoholsbégué_et_al_2004_.pdf:application/pdf},
}

@article{leavai_synthesis_2002,
	title = {Synthesis of 2-pyrazolines by the reactions of α,β-unsaturated aldehydes, ketones, and esters with diazoalkanes, nitrile imines, and hydrazines},
	volume = {39},
	issn = {0022-152X},
	doi = {10.1002/jhet.5570390101},
	pages = {1--13},
	number = {1},
	journaltitle = {Journal of heterocyclic chemistry},
	author = {Léavai, Albert},
	date = {2002},
	note = {Place: Hoboken
Publisher: Wiley-Blackwell},
	file = {Synthesis of 2-pyrazolines by the reactions of α,β-unsaturated aldehydes, ketones, and esters with diazoalkanes, nitrile imines, and hydrazines:/home/stefanom/GoogleDrive/University/Zotero/Zotero/storage/V2SD39UL/10.1002@jhet.5570390101.pdf.pdf:application/pdf},
}

@article{pimenov_interaction_2004,
	title = {Interaction of α,β-Unsaturated Ketones of the Adamantane Series with N,N'-Binucleophiles},
	volume = {40},
	issn = {1573-8353},
	url = {https://doi.org/10.1023/B:COHC.0000037312.60476.60},
	doi = {10.1023/B:COHC.0000037312.60476.60},
	abstract = {The influence has been established of the structure of the initial ketone, the reactants, and the reaction conditions on the direction of the interaction of α,β-unsaturated ketones of the adamantane series with hydrazine, phenylhydrazine, semicarbazide, thiosemicarbazide, urea, and thiourea. It was found that on interaction with hydrazine and phenylhydrazine both intermediate hydrazones and the final cyclization products, pyrazolines, were formed. Reaction with semicarbazide and thiosemicarbazide leads only to the synthesis of derivatives at the carbonyl group, semicarbazones and thiosemicarbazones, but with urea and thiourea leads to products of addition at the double bond.},
	pages = {575--581},
	number = {5},
	journaltitle = {Chemistry of Heterocyclic Compounds},
	shortjournal = {Chemistry of Heterocyclic Compounds},
	author = {Pimenov, A. A. and Makarova, N. V. and Moiseev, I. K. and Zemtsova, M. N.},
	urldate = {2023-07-12},
	date = {2004-05-01},
	langid = {english},
	keywords = {addition, hydrazones, pyrazolines, semicarbazones, thiosemicarbazones, thioureas, ureas, α,β-enones, α,β-unsaturated ketones},
	file = {Interaction of α,β-Unsaturated Ketones of the Adamantane Series with N,N'-Binucleophiles:/home/stefanom/GoogleDrive/University/Zotero/Zotero/storage/WAIKMGZ5/pimenov2004.pdf.pdf:application/pdf},
}

@article{raiford_-unsaturated_1938,
	title = {α,β-{UNSATURATED} {KETONES} {OBTAINED} {FROM} {ACETOPHENONE}, {AND} {THEIR} {REACTION} {WITH} {PHENYLHYDRAZINE}},
	volume = {03},
	issn = {0022-3263, 1520-6904},
	url = {https://pubs.acs.org/doi/abs/10.1021/jo01220a009},
	doi = {10.1021/jo01220a009},
	pages = {265--272},
	number = {3},
	journaltitle = {The Journal of Organic Chemistry},
	shortjournal = {J. Org. Chem.},
	author = {Raiford, L. Chas. and Gundy, Glen V.},
	urldate = {2023-07-12},
	date = {1938-07},
	langid = {english},
	file = {α,β-UNSATURATED KETONES OBTAINED FROM ACETOPHENONE, AND THEIR REACTION WITH PHENYLHYDRAZINE:/home/stefanom/GoogleDrive/University/Zotero/Zotero/storage/NRKBY3AW/raiford1938.pdf.pdf:application/pdf},
}

@article{priecel_advantages_2019,
	title = {Advantages and Limitations of Microwave Reactors: From Chemical Synthesis to the Catalytic Valorization of Biobased Chemicals},
	volume = {7},
	url = {https://doi.org/10.1021/acssuschemeng.8b03286},
	doi = {10.1021/acssuschemeng.8b03286},
	shorttitle = {Advantages and Limitations of Microwave Reactors},
	abstract = {This critical review examines recent scientific and patent literature in the application of microwave reactors for catalytic transformation of biomass and biomass-derived molecules with a particular emphasis on heterogeneous catalysis. Several recent reports highlight dramatic reductions in reaction time and even superior selectivity when microwaves are used. However, there are still many controversies and unexplained effects in this area that deserve attention. We critically review the available sources attempting to establish trends and elucidate the actual status of this area of research. Additionally, where possible, we discuss the potential for scale-up and commercial utilization of microwaves and impediments that currently hold back their implementation. This critical review aims at highlighting the opportunity of combining catalysis with microwave technology for biomass conversion but also to stimulate the reader to generate future understanding of the influence of the microwaves in catalytic processes in general.},
	pages = {3--21},
	number = {1},
	journaltitle = {{ACS} Sustainable Chemistry \& Engineering},
	shortjournal = {{ACS} Sustainable Chem. Eng.},
	author = {Priecel, Peter and Lopez-Sanchez, Jose Antonio},
	urldate = {2023-07-24},
	date = {2019-01-07},
	note = {Publisher: American Chemical Society},
	file = {ACS Full Text Snapshot:/home/stefanom/GoogleDrive/University/Zotero/Zotero/storage/KG3RMVI4/acssuschemeng.html:text/html;Full Text:/home/stefanom/GoogleDrive/University/Zotero/Zotero/storage/T664GDR8/Priecel and Lopez-Sanchez - 2019 - Advantages and Limitations of Microwave Reactors .pdf:application/pdf;Priecel_Lopez-Sanchez_2019_Advantages and Limitations of Microwave Reactors.pdf:/home/stefanom/GoogleDrive/Zot/Priecel_Lopez-Sanchez_2019_Advantages and Limitations of Microwave Reactors.pdf:application/pdf;Priecel_Lopez-Sanchez_2019_Advantages_and_Limitations_of_Microwave_Reactors.pdf:/home/stefanom/GoogleDrive/Zot/Priecel_Lopez-Sanchez_2019_Advantages_and_Limitations_of_Microwave_Reactors.pdf:application/pdf},
}

@article{rana_microwave_2014,
	title = {Microwave Reactors: A Brief Review on Its Fundamental Aspects and Applications},
	volume = {01},
	issn = {2333-9705, 2333-9721},
	url = {http://www.oalib.com/paper/pdf/3096250},
	doi = {10.4236/oalib.1100686},
	shorttitle = {Microwave Reactors},
	abstract = {Improved laboratory protocols for convenient and rapid transformations are highly desired in modern synthetic chemistry. Microwave irradiated reactions have received considerable attention in recent years and it is a subject of intense discussion in the scientific community. Microwave heating is more efficient in terms of the energy used, produces higher temperature homogeneity and is considerably more rapid than conventional heating methods. This technique as an alternative to conventional energy sources for introduction of energy into reactions has become a recognized practical method in various fields of chemistry. Microwave-assisted organic synthesis ({MAOS}) is known for the spectacular accelerations produced in many reactions as a consequence of the increased heating rate, a phenomenon that cannot be easily reproduced by classical heating means. As a result, higher yields, milder reaction conditions and shorter reaction times can often be attained. Its specific heating method attracts extensive interest not only because of rapid volumetric heating, but also for suppressed side reactions, energy saving, decreased environmental pollutions and safe operations. In this review, we will try to represent an overview on origin and fundamental features of microwave ovens and its usefulness in {MAOS}.},
	pages = {1--20},
	number = {6},
	journaltitle = {{OALib}},
	shortjournal = {{OALib}},
	author = {Rana, Kalyan Kumar and Rana, Suparna},
	urldate = {2023-07-24},
	date = {2014},
	langid = {english},
	file = {Rana and Rana - 2014 - Microwave Reactors A Brief Review on Its Fundamen.pdf:/home/stefanom/GoogleDrive/University/Zotero/Zotero/storage/6EVPCV69/Rana and Rana - 2014 - Microwave Reactors A Brief Review on Its Fundamen.pdf:application/pdf},
}

@article{azarifar_microwave-assisted_2003,
	title = {Microwave-Assisted Synthesis of Some 3,5-Arylated 2-Pyrazolines},
	volume = {8},
	rights = {http://creativecommons.org/licenses/by/3.0/},
	issn = {1420-3049},
	url = {https://www.mdpi.com/1420-3049/8/8/642},
	doi = {10.3390/80800642},
	abstract = {Condensation of 2-acetylnaphthalene with benzaldehydes under microwave irradiation affords chalcones which undergo facile and clean cyclizations with hydrazines {RNHNH}2 (R= H, Ph, Ac) to afford 3,5-arylated 2-pyrazolines in quantitative yields, also under microwave irradiation and in the presence of dry {AcOH} as cyclizing agent. The results obtained indicate that, unlike classical heating, microwave irradiation results in higher yields, shorter reaction times (2-12 min.) and cleaner reactions.},
	pages = {642--648},
	number = {8},
	journaltitle = {Molecules},
	author = {Azarifar, Davood and Ghasemnejad, Hassan},
	urldate = {2023-07-25},
	date = {2003-08},
	langid = {english},
	note = {Number: 8
Publisher: Molecular Diversity Preservation International},
	keywords = {pyrazolines, 3, 5-arylated-2-pyrazolines, chalcones, heterocyclic synthesis, Microwave irradiation},
	file = {Azarifar_Ghasemnejad_2003_Microwave-Assisted Synthesis of Some 3,5-Arylated 2-Pyrazolines.pdf:/home/stefanom/GoogleDrive/Zot/Azarifar_Ghasemnejad_2003_Microwave-Assisted Synthesis of Some 3,5-Arylated 2-Pyrazolines.pdf:application/pdf;Azarifar_Ghasemnejad_2003_Microwave-Assisted_Synthesis_of_Some_3,5-Arylated_2-Pyrazolines.pdf:/home/stefanom/GoogleDrive/Zot/Azarifar_Ghasemnejad_2003_Microwave-Assisted_Synthesis_of_Some_3,5-Arylated_2-Pyrazolines.pdf:application/pdf;Full Text PDF:/home/stefanom/GoogleDrive/University/Zotero/Zotero/storage/IT336RB3/Azarifar and Ghasemnejad - 2003 - Microwave-Assisted Synthesis of Some 3,5-Arylated .pdf:application/pdf},
}

@article{levai_synthesis_2006,
	title = {Synthesis of 1-substituted 3,5-diaryl-2-pyrazolines by the reaction of α,β-unsaturated ketones with hydrazines},
	volume = {43},
	issn = {0022152X, 19435193},
	url = {https://onlinelibrary.wiley.com/doi/10.1002/jhet.5570430117},
	doi = {10.1002/jhet.5570430117},
	pages = {111--115},
	number = {1},
	journaltitle = {Journal of Heterocyclic Chemistry},
	author = {Lévai, Albert and Jekö, József},
	urldate = {2023-07-26},
	date = {2006-01},
	langid = {english},
	file = {lévai_et_al_2006_synthesis_of_1-substituted_3,5-diaryl-2-pyrazolines_by_the_reaction_of.pdf:/home/stefanom/GoogleDrive/University/Zotero/ZotFiles/Journal of Heterocyclic Chemistry/2006/lévai_et_al_2006_synthesis_of_1-substituted_3,5-diaryl-2-pyrazolines_by_the_reaction_of.pdf:application/pdf},
}

@article{hoz_mechanism_2021,
	title = {The mechanism of the reaction of hydrazines with α,β-unsaturated carbonyl compounds to afford hydrazones and 2-pyrazolines (4,5-dihydro-1H-pyrazoles): Experimental and theoretical results},
	volume = {97},
	issn = {00404020},
	url = {https://linkinghub.elsevier.com/retrieve/pii/S0040402021006724},
	doi = {10.1016/j.tet.2021.132413},
	shorttitle = {The mechanism of the reaction of hydrazines with α,β-unsaturated carbonyl compounds to afford hydrazones and 2-pyrazolines (4,5-dihydro-1H-pyrazoles)},
	pages = {132413},
	journaltitle = {Tetrahedron},
	shortjournal = {Tetrahedron},
	author = {Hoz, Antonio De La and Alkorta, Ibon and Elguero, José},
	urldate = {2023-07-26},
	date = {2021-09},
	langid = {english},
	file = {hoz_et_al_2021_the_mechanism_of_the_reaction_of_hydrazines_with_α,β-unsaturated_carbonyl.pdf:/home/stefanom/GoogleDrive/Università/Zot/Tetrahedron/2021/hoz_et_al_2021_the_mechanism_of_the_reaction_of_hydrazines_with_α,β-unsaturated_carbonyl.pdf:application/pdf;The mechanism of the reaction of hydrazines with α,β-unsaturated carbonyl compounds to afford hydrazones and 2-pyrazolines (4,5-dihydro-1H-pyrazoles)\: Experimental and theoretical results:/home/stefanom/GoogleDrive/University/Zotero/Zotero/storage/AXHUDPSG/S0040402021006724.pdf.pdf:application/pdf},
}

@article{blasi_supramolecular_2022,
	title = {Supramolecular Frameworks and a Luminescent Coordination Polymer from New β-Diketone/Tetrazole Ligands},
	volume = {10},
	issn = {2304-6740},
	url = {https://www.mdpi.com/2304-6740/10/4/55},
	doi = {10.3390/inorganics10040055},
	abstract = {Mixed multidentate linkers with donor groups of different types can be fruitfully exploited in the self-assembly of coordination polymers ({CPs}) and Metal-Organic Frameworks ({MOFs}). In this work we develop new ligands containing a β-diketone chelating functionality, to better control the stereochemistry at the metal center, and tetrazolyl multidentate bridging groups, a combination not yet explored for networking with metal ions. The new ligands, 1,3-bis(4-(1H-tetrazol-5-yl)phenyl)-1,3-propanedione (H3L1) and 1-phenyl-3-(4-(1H-tetrazol-5-yl)phenyl)-1,3-propanedione (H2L2), are synthesized from the corresponding nitrile precursors by [2+3] dipolar cycloaddition of azide under metal-free catalytic conditions. Crystal structure analysis evidences the involvement of tetrazolyl fragments in multiple hydrogen bonding giving 2D and 1D supramolecular frameworks. Reactivity of the new ligands with different metal salts indicates good coordinating ability, and we report the preparation and structural characterization of the tris–chelate complex [Fe({HL}1)3]3− (1) and the homometallic 2D {CP} [{ZnL}2({DMSO})] (2). In compound 1 only the diketonate donor is used, whereas the partially deprotonated tetrazolyl groups are involved in hydrogen bonding, giving rise to a 2D supramolecular framework of (6,3){IIa} topological type. In compound 2 the ligand is completely deprotonated and uses both the diketonate donor (chelating) and the tetrazolate fragment (bridging) to coordinate the Zn({II}) ions. The resulting neutral 2D network of sql topology shows luminescence in the solid state, which is red shifted with respect to the free ligand. Interestingly, it can be easily exfoliated in water to give a luminescent colloidal solution.},
	pages = {55},
	number = {4},
	journaltitle = {Inorganics},
	shortjournal = {Inorganics},
	author = {Blasi, Delia and Mercandelli, Pierluigi and Carlucci, Lucia},
	urldate = {2023-09-18},
	date = {2022-04-18},
	langid = {english},
	file = {Blasi et al_2022_Supramolecular Frameworks and a Luminescent Coordination Polymer from New.pdf:/home/stefanom/GoogleDrive/University/Zotero/Zotero/storage/7I4XDFPH/Blasi et al_2022_Supramolecular Frameworks and a Luminescent Coordination Polymer from New.pdf:application/pdf},
}

@inproceedings{li_discussion_2023,
	location = {Guangzhou, China},
	title = {Discussion on programming language teaching of information major based on Python language},
	isbn = {978-1-5106-6130-1 978-1-5106-6131-8},
	url = {https://www.spiedigitallibrary.org/conference-proceedings-of-spie/12509/2656038/Discussion-on-programming-language-teaching-of-information-major-based-on/10.1117/12.2656038.full},
	doi = {10.1117/12.2656038},
	eventtitle = {Third International Conference on Intelligent Computing and Human-Computer Interaction ({ICHCI} 2022)},
	pages = {104},
	booktitle = {Third International Conference on Intelligent Computing and Human-Computer Interaction ({ICHCI} 2022)},
	publisher = {{SPIE}},
	author = {Li, Lu and Xue, Xiangui and Yang, Xia},
	editor = {Subramanian, Kannimuthu},
	urldate = {2023-09-19},
	date = {2023-01-13},
}

@article{hunter_matplotlib_2007,
	title = {Matplotlib: A 2D Graphics Environment},
	volume = {9},
	issn = {1521-9615},
	url = {http://ieeexplore.ieee.org/document/4160265/},
	doi = {10.1109/MCSE.2007.55},
	shorttitle = {Matplotlib},
	pages = {90--95},
	number = {3},
	journaltitle = {Computing in Science \& Engineering},
	shortjournal = {Comput. Sci. Eng.},
	author = {Hunter, John D.},
	urldate = {2023-09-19},
	date = {2007},
}

@article{gritzner_recommendations_1982,
	title = {Recommendations on reporting electrode potentials in nonaqueous solvents (Provisional)},
	volume = {54},
	issn = {1365-3075, 0033-4545},
	url = {https://www.degruyter.com/document/doi/10.1351/pac198254081527/html},
	doi = {10.1351/pac198254081527},
	abstract = {Abstract},
	pages = {1527--1532},
	number = {8},
	journaltitle = {Pure and Applied Chemistry},
	author = {Gritzner, G. and Kuta, J.},
	urldate = {2023-09-25},
	date = {1982-01-01},
	langid = {english},
	file = {Gritzner_Kuta_1982_Recommendations on reporting electrode potentials in nonaqueous solvents.pdf:/home/stefanom/GoogleDrive/University/Zotero/Zotero/storage/WHKJDID3/Gritzner_Kuta_1982_Recommendations on reporting electrode potentials in nonaqueous solvents.pdf:application/pdf},
}

@book{bard_electrochemical_2001,
	location = {New York},
	edition = {2nd ed},
	title = {Electrochemical methods: fundamentals and applications},
	isbn = {978-0-471-04372-0},
	shorttitle = {Electrochemical methods},
	pagetotal = {833},
	publisher = {Wiley},
	author = {Bard, Allen J. and Faulkner, Larry R.},
	date = {2001},
	keywords = {Electrochemistry},
}

@article{hansch_survey_1991,
	title = {A survey of Hammett substituent constants and resonance and field parameters},
	volume = {91},
	issn = {0009-2665, 1520-6890},
	url = {https://pubs.acs.org/doi/abs/10.1021/cr00002a004},
	doi = {10.1021/cr00002a004},
	pages = {165--195},
	number = {2},
	journaltitle = {Chemical Reviews},
	shortjournal = {Chem. Rev.},
	author = {Hansch, Corwin. and Leo, A. and Taft, R. W.},
	urldate = {2023-09-25},
	date = {1991-03-01},
	langid = {english},
}

@thesis{marco_visconti_new_2021,
	title = {New metal-Organic Polymeric Materials: from design to synthesis, structural characterization and properties},
	institution = {Universitá degli Studi di Milano},
	type = {phdthesis},
	author = {Marco Visconti},
	date = {2021},
}

@thesis{simone_galeazzi_nuovi_2021,
	title = {Nuovi leganti contenenti donatori all'N e all'O per la costruzione di nuovi Metal-Organic Frameworks},
	institution = {Universitá degli Studi di Milano},
	type = {Master Thesis},
	author = {Simone Galeazzi},
	date = {2021},
}