rifporphyrin.bib

@article{silva_porphyrins_2006,
	title = {Porphyrins in 1,3-{Dipolar} {Cycloaddition} {Reactions}. {Synthesis} of {New} {Porphyrin}−{Chlorin} and {Porphyrin}−{Tetraazachlorin} {Dyads}},
	volume = {71},
	issn = {0022-3263, 1520-6904},
	url = {https://pubs.acs.org/doi/10.1021/jo0611770},
	doi = {10.1021/jo0611770},
	language = {en},
	number = {22},
	urldate = {2022-03-31},
	journal = {The Journal of Organic Chemistry},
	author = {Silva, Ana M. G. and Lacerda, Paula S. S. and Tomé, Augusto C. and Neves, Maria G. P. M. S. and Silva, Artur M. S. and Cavaleiro, José A. S. and Makarova, Elena A. and Lukyanets, Evgeny A.},
	month = oct,
	year = {2006},
	keywords = {prof},
	pages = {8352--8356},
	file = {Silva et al. - 2006 - Porphyrins in 1,3-Dipolar Cycloaddition Reactions..pdf:C\:\\Users\\finco\\Zotero\\storage\\LM22VCDY\\Silva et al. - 2006 - Porphyrins in 1,3-Dipolar Cycloaddition Reactions..pdf:application/pdf},
}

@article{johnson_four-atom-linked_1996,
	title = {Four-{Atom}-{Linked} {Capped} {Porphyrins}: {Synthesis} and {Characterization}},
	volume = {61},
	issn = {0022-3263, 1520-6904},
	shorttitle = {Four-{Atom}-{Linked} {Capped} {Porphyrins}},
	url = {https://pubs.acs.org/doi/10.1021/jo9521615},
	doi = {10.1021/jo9521615},
	language = {en},
	number = {10},
	urldate = {2022-03-31},
	journal = {The Journal of Organic Chemistry},
	author = {Johnson, Martin R. and Seok, Won K. and Ma, Wuping and Slebodnick, Carla and Wilcoxen, Keith M. and Ibers, James A.},
	month = jan,
	year = {1996},
	keywords = {prof},
	pages = {3298--3303},
	file = {Johnson et al. - 1996 - Four-Atom-Linked Capped Porphyrins Synthesis and .pdf:C\:\\Users\\finco\\Zotero\\storage\\6E72LFBG\\Johnson et al. - 1996 - Four-Atom-Linked Capped Porphyrins Synthesis and .pdf:application/pdf},
}

@article{carofiglio_one-pot_2004,
	title = {One-{Pot} {Synthesis} of {Cyanuric} {Acid}-{Bridged} {Porphyrin}−{Porphyrin} {Dyads}},
	volume = {69},
	issn = {0022-3263, 1520-6904},
	url = {https://pubs.acs.org/doi/10.1021/jo048713d},
	doi = {10.1021/jo048713d},
	abstract = {Stepwise amination of cyanuric chloride (1) with 5-(4-aminophenyl)-10,15,20-triphenylporphyrin (2) and/or its zinc(II) complex (3) enables the synthesis of porphyrin-porphyrin dyads with predetermined free base-free base forms or free base-zinc and zinc-zinc metalation states. Furthermore, the use of aminopropyl-silanized silica gel as a scavenger for unwanted byproducts allowed the one-pot synthesis of title porphyrin compounds in high yield and purity with minimum use of preparative column chromatography.},
	language = {en},
	number = {23},
	urldate = {2022-03-31},
	journal = {The Journal of Organic Chemistry},
	author = {Carofiglio, Tommaso and Varotto, Alessandro and Tonellato, Umberto},
	month = nov,
	year = {2004},
	keywords = {prof},
	pages = {8121--8124},
	file = {Carofiglio et al. - 2004 - One-Pot Synthesis of Cyanuric Acid-Bridged Porphyr.pdf:C\:\\Users\\finco\\Zotero\\storage\\HVUZPTDP\\Carofiglio et al. - 2004 - One-Pot Synthesis of Cyanuric Acid-Bridged Porphyr.pdf:application/pdf},
}

@article{rothemund_new_1936,
	title = {A {New} {Porphyrin} {Synthesis}. {The} {Synthesis} of {Porphin} $^{\textrm{1}}$},
	volume = {58},
	issn = {0002-7863, 1520-5126},
	url = {https://pubs.acs.org/doi/abs/10.1021/ja01295a027},
	doi = {10.1021/ja01295a027},
	language = {en},
	number = {4},
	urldate = {2022-03-31},
	journal = {Journal of the American Chemical Society},
	author = {Rothemund, Paul},
	month = apr,
	year = {1936},
	keywords = {prof},
	pages = {625--627},
	file = {Rothemund - 1936 - A New Porphyrin Synthesis. The Synthesis of Porphi.pdf:C\:\\Users\\finco\\Zotero\\storage\\LVDSEBCJ\\Rothemund - 1936 - A New Porphyrin Synthesis. The Synthesis of Porphi.pdf:application/pdf},
}

@article{huang_novel_2005,
	title = {Novel spectral and electrochemical characteristics of triphenylamine-bound zinc porphyrins and their intramolecular energy and electron transfer},
	issn = {1477-9226, 1477-9234},
	url = {http://xlink.rsc.org/?DOI=b503683f},
	doi = {10.1039/b503683f},
	language = {en},
	number = {14},
	urldate = {2022-03-31},
	journal = {Dalton Transactions},
	author = {Huang, Chih-Wei and Yuan Chiu, Kuo and Cheng, Shu-Hua},
	year = {2005},
	keywords = {prof},
	pages = {2417},
	file = {Huang et al. - 2005 - Novel spectral and electrochemical characteristics.pdf:C\:\\Users\\finco\\Zotero\\storage\\M6BVHMTB\\Huang et al. - 2005 - Novel spectral and electrochemical characteristics.pdf:application/pdf},
}

@article{dolphin_porphyrinogens_1970,
	title = {Porphyrinogens and porphodimethenes, intermediates in the synthesis of \textit{meso} -tetraphenylporphins from pyrroles and benzaldehyde},
	volume = {7},
	issn = {0022152X, 19435193},
	url = {https://onlinelibrary.wiley.com/doi/10.1002/jhet.5570070205},
	doi = {10.1002/jhet.5570070205},
	language = {en},
	number = {2},
	urldate = {2022-03-31},
	journal = {Journal of Heterocyclic Chemistry},
	author = {Dolphin, D.},
	month = apr,
	year = {1970},
	keywords = {prof},
	pages = {275--283},
	file = {Dolphin - 1970 - Porphyrinogens and porphodimethenes, intermediates.pdf:C\:\\Users\\finco\\Zotero\\storage\\ZIKF9YBA\\Dolphin - 1970 - Porphyrinogens and porphodimethenes, intermediates.pdf:application/pdf},
}

@article{thamyongkit_swallowtail_2004,
	title = {Swallowtail {Porphyrins}: {Synthesis}, {Characterization} and {Incorporation} into {Porphyrin} {Dyads}},
	volume = {69},
	issn = {0022-3263, 1520-6904},
	shorttitle = {Swallowtail {Porphyrins}},
	url = {https://pubs.acs.org/doi/10.1021/jo049860e},
	doi = {10.1021/jo049860e},
	language = {en},
	number = {11},
	urldate = {2022-03-31},
	journal = {The Journal of Organic Chemistry},
	author = {Thamyongkit, Patchanita and Speckbacher, Markus and Diers, James R. and Kee, Hooi Ling and Kirmaier, Christine and Holten, Dewey and Bocian, David F. and Lindsey, Jonathan S.},
	month = may,
	year = {2004},
	keywords = {prof},
	pages = {3700--3710},
	file = {Thamyongkit et al. - 2004 - Swallowtail Porphyrins Synthesis, Characterizatio.pdf:C\:\\Users\\finco\\Zotero\\storage\\PNLZQ2Q4\\Thamyongkit et al. - 2004 - Swallowtail Porphyrins Synthesis, Characterizatio.pdf:application/pdf},
}

@article{diev_porphyrins_2012,
	title = {Porphyrins {Fused} with {Unactivated} {Polycyclic} {Aromatic} {Hydrocarbons}},
	volume = {77},
	issn = {0022-3263, 1520-6904},
	url = {https://pubs.acs.org/doi/10.1021/jo201490y},
	doi = {10.1021/jo201490y},
	abstract = {A systematic study of the preparation of porphyrins with extended conjugation by meso,β-fusion with polycyclic aromatic hydrocarbons (PAHs) is reported. The meso-positions of 5,15-unsubstituted porphyrins were readily functionalized with PAHs. Ring fusion using standard Scholl reaction conditions (FeCl3, dichloromethane) occurs for perylene-substituted porphyrins to give a porphyrin β,meso annulated with perylene rings (0.7:1 ratio of syn and anti isomers). The naphthalene, pyrene, and coronene derivatives do not react under Scholl conditions but are fused using thermal cyclodehydrogenation at high temperatures, giving mixtures of syn and anti isomers of the meso,β-fused porphyrins. For pyrenylsubstituted porphyrins, a thermal method gives synthetically acceptable yields ({\textgreater}30\%). Absorption spectra of the fused porphyrins undergo a progressive bathochromic shift in a series of naphthyl (λmax = 730 nm), coronenyl (λmax = 780 nm), pyrenyl (λmax = 815 nm), and perylenyl (λmax = 900 nm) annulated porphyrins. Despite being conjugated with unsubstituted fused PAHs, the β,mesofused porphyrins are more soluble and processable than the parent nonfused precursors. Pyrenyl-fused porphyrins exhibit strong fluorescence in the near-infrared (NIR) spectral region, with a progressive improvement in luminescent efficiency (up to 13\% with λmax = 829 nm) with increasing degree of fusion. Fused pyrenyl-porphyrins have been used as broadband absorption donor materials in photovoltaic cells, leading to devices that show comparatively high photovoltaic efficiencies.},
	language = {en},
	number = {1},
	urldate = {2022-03-31},
	journal = {The Journal of Organic Chemistry},
	author = {Diev, Vyacheslav V. and Schlenker, Cody W. and Hanson, Kenneth and Zhong, Qiwen and Zimmerman, Jeramy D. and Forrest, Stephen R. and Thompson, Mark E.},
	month = jan,
	year = {2012},
	keywords = {prof},
	pages = {143--159},
	file = {Diev et al. - 2012 - Porphyrins Fused with Unactivated Polycyclic Aroma.pdf:C\:\\Users\\finco\\Zotero\\storage\\RQA8HJRT\\Diev et al. - 2012 - Porphyrins Fused with Unactivated Polycyclic Aroma.pdf:application/pdf},
}

@article{shi_3-cyclobutenyl-12-dione-substituted_2000,
	title = {3-{Cyclobutenyl}-1,2-dione-{Substituted} {Porphyrins}. {A} {General} and {Efficient} {Entry} to {Porphyrin}−{Quinone} and {Quinone}−{Porphyrin}−{Quinone} {Architectures}},
	volume = {65},
	issn = {0022-3263, 1520-6904},
	url = {https://pubs.acs.org/doi/10.1021/jo9912799},
	doi = {10.1021/jo9912799},
	language = {en},
	number = {6},
	urldate = {2022-03-31},
	journal = {The Journal of Organic Chemistry},
	author = {Shi, Xianglin and Amin, Sk. Rasidul and Liebeskind, Lanny S.},
	month = mar,
	year = {2000},
	keywords = {prof},
	pages = {1650--1664},
	file = {Shi et al. - 2000 - 3-Cyclobutenyl-1,2-dione-Substituted Porphyrins. A.pdf:C\:\\Users\\finco\\Zotero\\storage\\CZGSUEFS\\Shi et al. - 2000 - 3-Cyclobutenyl-1,2-dione-Substituted Porphyrins. A.pdf:application/pdf},
}

@article{hardison_evolution_2012,
	title = {Evolution of {Hemoglobin} and {Its} {Genes}},
	volume = {2},
	issn = {2157-1422},
	url = {http://perspectivesinmedicine.cshlp.org/lookup/doi/10.1101/cshperspect.a011627},
	doi = {10.1101/cshperspect.a011627},
	language = {en},
	number = {12},
	urldate = {2022-04-03},
	journal = {Cold Spring Harbor Perspectives in Medicine},
	author = {Hardison, R. C.},
	month = dec,
	year = {2012},
	pages = {a011627--a011627},
	file = {Full Text:C\:\\Users\\finco\\Zotero\\storage\\NICCNFJW\\Hardison - 2012 - Evolution of Hemoglobin and Its Genes.pdf:application/pdf},
}

@article{kendrew_three-dimensional_1958,
	title = {A {Three}-{Dimensional} {Model} of the {Myoglobin} {Molecule} {Obtained} by {X}-{Ray} {Analysis}},
	volume = {181},
	issn = {0028-0836, 1476-4687},
	url = {https://www.nature.com/articles/181662a0},
	doi = {10.1038/181662a0},
	language = {en},
	number = {4610},
	urldate = {2022-04-03},
	journal = {Nature},
	author = {Kendrew, J. C. and Bodo, G. and Dintzis, H. M. and Parrish, R. G. and Wyckoff, H. and Phillips, D. C.},
	month = mar,
	year = {1958},
	pages = {662--666},
}

@article{keilin_cytochrome_1925,
	title = {On {Cytochrome}, a {Respiratory} {Pigment}, {Common} to {Animals}, {Yeast}, and {Higher} {Plants}},
	volume = {98},
	issn = {0080-46490962-8452},
	url = {https://ui.adsabs.harvard.edu/abs/1925RSPSB..98..312K},
	urldate = {2022-04-03},
	journal = {Proceedings of the Royal Society of London Series B},
	author = {Keilin, D.},
	month = aug,
	year = {1925},
	note = {ADS Bibcode: 1925RSPSB..98..312K},
	pages = {312--339},
}

@article{liang_porphyrin-based_2021,
	title = {Porphyrin-based frameworks for oxygen electrocatalysis and catalytic reduction of carbon dioxide},
	volume = {50},
	issn = {0306-0012, 1460-4744},
	url = {http://xlink.rsc.org/?DOI=D0CS01482F},
	doi = {10.1039/D0CS01482F},
	abstract = {The recent progress made on porphyrin-based frameworks and their applications in energy-related conversion technologies (
              e.g.
              , ORR, OER and CO
              2
              RR) and storage technologies (
              e.g.
              , Zn–air batteries).
            
          , 
            
              Porphyrin-based frameworks, as specific kinds of metal–organic frameworks (MOFs) and covalent organic frameworks (COFs), have been widely used in energy-related conversion processes, including the oxygen reduction reaction (ORR), oxygen evolution reaction (OER) and CO
              2
              reduction reaction (CO
              2
              RR), and also in energy-related storage technologies such as rechargeable Zn–air batteries. This review starts by summarizing typical crystal structures, molecular building blocks, and common synthetic procedures of various porphyrin-based frameworks used in energy-related technologies. Then, a brief introduction is provided and representative applications of porphyrin-based frameworks in ORR, OER, Zn–air batteries, and CO
              2
              RR are discussed. The performance comparison of these porphyrin-based frameworks in each field is also summarized and discussed, which pinpoints a clear structure–activity relationship. In addition to utilizing highly active porphyrin units for catalytic conversions, regulating the porous structures of porphyrin-based frameworks will enhance mass transfer and growing porphyrin-based frameworks on conductive supports will accelerate electron transfer, which will result in the improvement of the electrocatalytic performance. This review is therefore valuable for the rational design of more efficient porphyrin-based framework catalytic systems in energy-related conversion and storage technologies.},
	language = {en},
	number = {4},
	urldate = {2022-04-03},
	journal = {Chemical Society Reviews},
	author = {Liang, Zuozhong and Wang, Hong-Yan and Zheng, Haoquan and Zhang, Wei and Cao, Rui},
	year = {2021},
	pages = {2540--2581},
}

@article{facchin_oxygen_2021,
	title = {Oxygen {Reduction} {Reaction} at {Single}‐{Site} {Catalysts}: {A} {Combined} {Electrochemical} {Scanning} {Tunnelling} {Microscopy} and {DFT} {Investigation} on {Iron} {Octaethylporphyrin} {Chloride} on {HOPG}**},
	volume = {8},
	issn = {2196-0216, 2196-0216},
	shorttitle = {Oxygen {Reduction} {Reaction} at {Single}‐{Site} {Catalysts}},
	url = {https://onlinelibrary.wiley.com/doi/10.1002/celc.202100543},
	doi = {10.1002/celc.202100543},
	language = {en},
	number = {15},
	urldate = {2022-04-03},
	journal = {ChemElectroChem},
	author = {Facchin, Alessandro and Zerbetto, Mirco and Gennaro, Armando and Vittadini, Andrea and Forrer, Daniel and Durante, Christian},
	month = aug,
	year = {2021},
	pages = {2825--2835},
	file = {Full Text:C\:\\Users\\finco\\Zotero\\storage\\RA4YU4IB\\Facchin et al. - 2021 - Oxygen Reduction Reaction at Single‐Site Catalysts.pdf:application/pdf},
}

@article{wang_recent_2021,
	title = {Recent advances in porphyrin-based {MOFs} for cancer therapy and diagnosis therapy},
	volume = {439},
	issn = {00108545},
	url = {https://linkinghub.elsevier.com/retrieve/pii/S0010854521002198},
	doi = {10.1016/j.ccr.2021.213945},
	language = {en},
	urldate = {2022-04-03},
	journal = {Coordination Chemistry Reviews},
	author = {Wang, Zhao and Sun, Qianqian and Liu, Bin and Kuang, Ye and Gulzar, Arif and He, Fei and Gai, Shili and Yang, Piaoping and Lin, Jun},
	month = jul,
	year = {2021},
	pages = {213945},
}

@article{anjali_zinc-tetraphenylporphyrin_2020,
	title = {Zinc-tetraphenylporphyrin grafted on functionalised mesoporous {SBA}-15: synthesis and utilisation for nitroaldol condensation},
	volume = {27},
	issn = {1380-2224, 1573-4854},
	shorttitle = {Zinc-tetraphenylporphyrin grafted on functionalised mesoporous {SBA}-15},
	url = {https://link.springer.com/10.1007/s10934-020-00890-4},
	doi = {10.1007/s10934-020-00890-4},
	language = {en},
	number = {4},
	urldate = {2022-04-27},
	journal = {Journal of Porous Materials},
	author = {Anjali, Kaiprathu and Nishana, L. K. and Christopher, Jayaraj and Sakthivel, Ayyamperumal},
	month = aug,
	year = {2020},
	keywords = {NMR characterization, to be mentioned},
	pages = {1191--1201},
	annote = {Description of the 1H NMR of H2TPP
There are 4 main signals. The most shielded at -2.713 ppm is attributed to NH protons, due to the electronrich character of the pyrrolic ring. In addition, its absence of multiplicity suggests the absence of hydrogen atoms in neighbouring positions, a condition that is only verified by NH protons in the structure of the target TPP. 
The remaining peaks are all placed in the aromatic reagion. The attributions indicated are based on the idea that the proximity to the porphyrinic ring provides shielding, in order to distinguish b and c positions, and that vinylic protons are more shielded than phenylic ones, in order to attribute the d position.
Finally, it is noted that TMS is found in very close proximity to its expected shift of 0.
Description of the 1H NMR of Zn-TPP
Absence of the NH proton.
},
}

@article{matamala-cea_efficient_2020,
	title = {Efficient preparation of 5,10,15,20-tetrakis(4-bromophenyl)porphyrin. {Microwave} assisted v/s conventional synthetic method, {X}-ray and hirshfeld surface structural analysis},
	volume = {1201},
	issn = {00222860},
	url = {https://linkinghub.elsevier.com/retrieve/pii/S0022286019312487},
	doi = {10.1016/j.molstruc.2019.127139},
	language = {en},
	urldate = {2022-04-28},
	journal = {Journal of Molecular Structure},
	author = {Matamala-Cea, Edison and Valenzuela-Godoy, Fabián and González, Déborah and Arancibia, Rodrigo and Dorcet, Vincent and Hamon, Jean-René and Novoa, Néstor},
	month = feb,
	year = {2020},
	keywords = {summary},
	pages = {127139},
	file = {Submitted Version:C\:\\Users\\finco\\Zotero\\storage\\RLCXJE6E\\Matamala-Cea et al. - 2020 - Efficient preparation of 5,10,15,20-tetrakis(4-bro.pdf:application/pdf},
}

@article{al_mousawi_zinc_2017,
	title = {Zinc {Tetraphenylporphyrin} as {High} {Performance} {Visible} {Light} {Photoinitiator} of {Cationic} {Photosensitive} {Resins} for {LED} {Projector} {3D} {Printing} {Applications}},
	volume = {50},
	issn = {0024-9297, 1520-5835},
	url = {https://pubs.acs.org/doi/10.1021/acs.macromol.6b02596},
	doi = {10.1021/acs.macromol.6b02596},
	language = {en},
	number = {3},
	urldate = {2022-04-29},
	journal = {Macromolecules},
	author = {Al Mousawi, Assi and Poriel, Cyril and Dumur, Frédéric and Toufaily, Joumana and Hamieh, Tayssir and Fouassier, Jean Pierre and Lalevée, Jacques},
	month = feb,
	year = {2017},
	pages = {746--753},
}