Nothing Special   »   [go: up one dir, main page]

Perepichka et al., 2000 - Google Patents

Electron Acceptors of the Fluorene Series. 10.1 Novel Acceptors Containing Butylsulfanyl, Butylsulfinyl, and Butylsulfonyl Substituents: Synthesis, Cyclic Voltammetry …

Perepichka et al., 2000

View PDF
Document ID
13366504487988053271
Author
Perepichka I
Popov A
Orekhova T
Bryce M
Andrievskii A
Batsanov A
Howard J
Sokolov N
Publication year
Publication venue
The Journal of Organic Chemistry

External Links

Snippet

2, 4, 5, 7-Tetranitro-9-fluorenone (1b) reacts readily with n-butanethiol in dipolar aprotic solvents with selective substitution of nitro groups by butylsulfanyl groups in positions 2 and 7 (2, 3); the 2, 5-isomer 4 was formed only as a minor product (< 1%). Condensation of …
Continue reading at www.academia.edu (PDF) (other versions)

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D333/00Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulfur
    • C07D333/26Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulfur with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D333/30Hetero atoms other than halogen
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic 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
    • C07D213/02Heterocyclic 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
    • C07D213/04Heterocyclic 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
    • C07D213/06Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D333/00Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulfur
    • C07D333/06Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulfur with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
    • C07D333/22Radicals substituted by doubly bound hetero atoms, or by two hetero atoms other than halogen singly bound to the same carbon atom
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic 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
    • C07D213/02Heterocyclic 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
    • C07D213/04Heterocyclic 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
    • C07D213/24Heterocyclic 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 with substituted hydrocarbon radicals attached to ring carbon atoms

Similar Documents

Publication Publication Date Title
Perepichka et al. Electron Acceptors of the Fluorene Series. 10.1 Novel Acceptors Containing Butylsulfanyl, Butylsulfinyl, and Butylsulfonyl Substituents: Synthesis, Cyclic Voltammetry, Charge-Transfer Complexation with Anthracene in Solution, and X-ray Crystal Structures of Two Tetrathiafulvalene Complexes
Klikar et al. Dipolar NLO chromophores bearing diazine rings as π-conjugated linkers
James et al. Photophysical and theoretical investigations of oligo (p-phenyleneethynylene) s: Effect of alkoxy substitution and alkyne− aryl bond rotations
González et al. Tetrathiafulvalene derivatives as NLO-phores: Synthesis, electrochemistry, Raman spectroscopy, theoretical calculations, and NLO properties of novel TTF-derived donor-π-acceptor dyads
Ahrens et al. Sulfur‐Bridged BODIPY DYEmers
Zhou et al. Push–pull tetraene chromophores derived from dialkylaminophenyl, tetrahydroquinolinyl and julolidinyl moieties: optimization of second-order optical nonlinearity by fine-tuning the strength of electron-donating groups
Shi et al. Ultra-high-response, multiply twisted electro-optic chromophores: influence of π-system elongation and interplanar torsion on hyperpolarizability
Xuan et al. Synthesis and spectroscopic investigation of a series of push–pull boron dipyrromethenes (BODIPYs)
Pan et al. A Novel and Perfectly Aligned Highly Electro− Optic Organic Cocrystal of a Merocyanine Dye and 2, 4-Dihydroxybenzaldehyde
Barnsley et al. Benzo [c][1, 2, 5] thiadiazole donor–acceptor dyes: A synthetic, spectroscopic, and computational study
Maslak et al. Optical properties of spiroconjugated charge-transfer dyes
Wu et al. Near-infrared colorimetric and fluorescent Cu2+ sensors based on indoline–benzothiadiazole derivatives via formation of radical cations
Giguère et al. Cruciform Alkynylated Anthanthrene Derivatives: A Structure–Properties Relationship Case Study
Perepichka et al. A (π-extended tetrathiafulvalene)− fluorene conjugate. Unusual electrochemistry and charge transfer properties: the first observation of a covalent D2+− σ− A•-Redox State1
Mysyk et al. Electron Acceptors of the Fluorene Series. 9.1 Derivatives of 9-(1, 2-Dithiol-3-ylidene)-, 9-(1, 3-Dithiol-2-ylidene)-, and 9-(1, 3-Selenathiol-2-ylidene) fluorenes: Synthesis, Intramolecular Charge Transfer, and Redox Properties
Perepichka et al. Electron Acceptors of the Fluorene Series. 7.1 2, 7-Dicyano-4, 5-dinitro-9-X-fluorenes: Synthesis, Cyclic Voltammetry, Charge Transfer Complexation with N-Propylcarbazole in Solution, and X-ray Crystal Structures of Two Tetrathiafulvalene Complexes
Munoz et al. Synthesis and properties of subphthalocyanine–tetracyanobutadiene–ferrocene triads
Lv et al. Polybrominated BOPHY dyes: synthesis, reactivity, and properties
Giguere et al. Synthesis and optoelectronic properties of 6, 12-bis (amino) anthanthrene derivatives
Yang et al. Effect of ground-state twisting on the trans→ cis photoisomerization and TICT state formation of aminostilbenes
van Haare et al. π-Dimers of prototype high-spin polaronic oligomers
Ye et al. Regulation of the molecular architectures on second-order nonlinear optical response and thermally activated delayed fluorescence property: homoconjugation and twisted donor–acceptor
Giguere et al. Super extended tetrathiafulvalene: synthesis, optoelectronic properties, fullerenes complexation, and photooxidation study
Breiten et al. Donor-substituted octacyano [4] dendralenes: investigation of π-electron delocalization in their radical ions
Skabara et al. Toward Controlled Donor− Acceptor Interactions in Noncomposite Polymeric Materials: Synthesis and Characterization of a Novel Polythiophene Incorporating π-Conjugated 1, 3-Dithiole-2-ylidenefluorene Units as Strong D− A Components