[go: up one dir, main page]

Chen et al., 2012 - Google Patents

Synthesis and physicochemical properties of metallobacteriochlorins

Chen et al., 2012

Document ID
8509306280765616861
Author
Chen C
Sun E
Fan D
Taniguchi M
McDowell B
Yang E
Diers J
Bocian D
Holten D
Lindsey J
Publication year
Publication venue
Inorganic chemistry

External Links

Snippet

Access to metallobacteriochlorins is essential for investigation of a wide variety of fundamental photochemical processes, yet relatively few synthetic metallobacteriochlorins have been prepared. Members of a set of synthetic bacteriochlorins bearing 0–4 carbonyl …
Continue reading at pubs.acs.org (other versions)

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by C07D451/00 - C07D477/00
    • C07D487/22—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by C07D451/00 - C07D477/00 in which the condensed system contains four or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by C07D451/00 - C07D477/00
    • C07D487/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by C07D451/00 - C07D477/00 in which the condensed system contains three hetero rings
    • C07D487/14—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/06—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom containing only hydrogen and carbon atoms in addition to the ring nitrogen atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members

Similar Documents

Publication Publication Date Title
Chen et al. Synthesis and physicochemical properties of metallobacteriochlorins
Kim et al. De novo synthesis of stable tetrahydroporphyrinic macrocycles: bacteriochlorins and a tetradehydrocorrin
Krayer et al. Expanded scope of synthetic bacteriochlorins via improved acid catalysis conditions and diverse dihydrodipyrrin-acetals
Matano Synthesis of aza-, oxa-, and thiaporphyrins and related compounds
Yu et al. Excited-state energy-transfer dynamics in self-assembled triads composed of two porphyrins and an intervening bis (dipyrrinato) metal complex
Barata et al. Strategies for corrole functionalization
Anguera et al. Porphycenes and related isomers: synthetic aspects
Richeter et al. Syntheses and optical and electrochemical properties of porphyrin dimers linked by metal ions
Jasat et al. Expanded porphyrins and their heterologs
Giribabu et al. “Axial-bonding”-type hybrid porphyrin arrays: Synthesis, spectroscopy, electrochemistry, and singlet state properties
Kozyrev et al. Characterization of porphyrins, chlorins, and bacteriochlorins formed via allomerization of bacteriochlorophyll a. Synthesis of highly stable bacteriopurpurinimides and their metal complexes
Hyland et al. Meso-tetrakis (pentafluorophenyl) porphyrin-derived chromene-annulated chlorins
Richeter et al. Synthesis of new porphyrins with peripheral conjugated chelates and their use for the preparation of porphyrin dimers linked by metal ions
Filatov et al. Synthesis of 5, 15-diaryltetrabenzoporphyrins
Kozyrev et al. Synthesis, photophysical and electrochemistry of near-IR absorbing bacteriochlorins related to bacteriochlorophyll a
Taniguchi et al. Synthesis and electronic properties of regioisomerically pure oxochlorins
Potocny et al. Electrochemical, spectroscopic, and 1O2 sensitization characteristics of synthetically accessible linear tetrapyrrole complexes of palladium and platinum
Krayer et al. Synthesis and photophysical characterization of stable indium bacteriochlorins
Chaudhri et al. Versatile synthetic route for β-functionalized chlorins and porphyrins by varying the size of michael donors: Syntheses, photophysical, and electrochemical redox properties
Pistner et al. Electrochemical, spectroscopic, and 1O2 sensitization characteristics of 10, 10-dimethylbiladiene complexes of zinc and copper
Lash et al. Synthesis of indenoporphyrins, highly modified porphyrins with reduced diatropic characteristics
Mandoj et al. β-Pyrazino-fused tetrarylporphyrins
Chaudhri et al. Nickel-Induced Skeletal Rearrangement of Free Base trans-Chlorins into Monofused NiII-Porphyrins: Synthesis, Structural, Spectral, and Electrochemical Redox Properties
Martin et al. Synthesis, Redox, and Spectroscopic Properties of Pd (II) 10, 10-Dimethylisocorrole Complexes Prepared via Bromination of Dimethylbiladiene Oligotetrapyrroles
Casanova et al. Structural and photophysical characterization of multichromophoric pyridylporphyrin-rhenium (I) conjugates