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    ChemInform Abstract: Hg(OTf)2Catalyzed Intramolecular 1,4-Addition of Donor-Acceptor Cyclopropenesto Arenes.
    ChemInform (2016)
    Yongming DengChangcheng JingPeter Y. ZavalijMichael P. Doyle
    The title reaction is described to yield bicyclo[3.2.2]nonatriene derivatives (II) and (V) as sole or main products.
    Acceptor
    Citations (0)
    Heavy-atom-free charge transfer photosensitizers: Tuning the efficiency of BODIPY in singlet oxygen generation via intramolecular electron donor-acceptor interaction
    Dyes and Pigments (2019)
    Wenbin HuYanhe LinXian‐Fu ZhangMingna FengSiwen Zhao
    BODIPY
    Quantum yield
    Acceptor
    Flash photolysis
    Electron donor
    Electron acceptor
    Citations (42)
    Intramolecular charge transfer promoted fluorescence transfer: A demonstration of re-absorption of the donor fluorescence by the acceptor
    Journal of Molecular Liquids (2010)
    Debanjana GhoshDeboleena SarkarNitin Chattopadhyay
    Acceptor
    Cationic polymerization
    Citations (15)
    Self-correcting energy transfer Diels-Alder adduct dyes
    Dyes and Pigments (2022)
    Haonan XuBin LeiXin Zhang
    Acceptor
    Citations (2)
    Highly activated Michael acceptor by an intramolecular hydrogen bond as a fluorescence turn-on probe for cyanide
    Chemical Communications (2010)
    Seokan ParkHae-Jo Kim
    An activated Michael acceptor type of probe by an intramolecular hydrogen bond has shown a selective fluorescence turn-on response to cyanide through a conjugated addition of the nucleophilic anion to the enone probe with a 1300-fold increase in its fluorescence intensity.
    Acceptor
    Michael reaction
    Turn (biochemistry)
    Citations (141)
    ChemInform Abstract: Intramolecular Donor‐Acceptor Interactions in λ4P(V) Compounds. ‐ Phosphorus(V) Derivatives of N,N,N′‐Trimethylethylenediamine.
    ChemInform (1990)
    Wilfried BeckerPeter G. JonesDietmar SchomburgReinhard Schmutzler
    Abstract The chlorophosphino derivative (I) of trimethylethylenediamine is oxidized by DMSO or S8 to give the corresponding phosphonamidic chlorides (II) and (III), respectively.
    Acceptor
    Derivative (finance)
    Citations (0)
    ChemInform Abstract: A STUDY OF INTRAMOLECULAR ENERGY TRANSFER IN CONFORMATIONALLY RIGID MOLECULES WITH STEREOISOMERICALLY ORIENTED DONOR AND ACCEPTOR GROUPS
    Chemischer Informationsdienst (1975)
    Walter AmreinKurt Schaffner
    Abstract Es wird gezeigt, daß die endo‐ und exo‐Isomeren der Indanononaphthalino‐Verbindungen (I) und (II) bei Einstrahlung in die (1)Lb‐Bande (315 nm) und den n → π* ‐Übergang (>340 nm) in EPA bei 77 K keine Fluoreszenz des Naphthalin‐Molekülteils und keine Phosphoreszenz der Indanon‐Molekülteils, jedoch Phosphoreszenz des Naphthalin‐Molekülteils liefern.
    Acceptor
    Citations (0)
    Fluorescence properties of bichromophoric molecules
    Spectrochimica Acta Part A Molecular Spectroscopy (1992)
    Etelka FarkasMichael HilbertI. KetskemétyL. Gáti
    Acceptor
    Citations (6)
    A Study of Intramolecular Energy Transfer in Conformationally Rigid molecules with stereoisomerically oriented donor and acceptor groups
    Helvetica Chimica Acta (1975)
    Walter AmreinKurt Schaffner
    Abstract The indanono naphthaleno compounds 1 , 3 , 5 and 7 exhibit, on both irradiation in the 1 L b band (315 nm) and the n → π* transition (> 340 nm) in EPA at 77° K, neither fluorescence from naphthalene nor phosphorescence from indanone, but exclusively phosphorescence from naphthalene, and quenching in liquid solution with 1,3‐pentadiene results in triplet energy transfer from the naphthaleno group only. The naphthalene phosphorescence exhibited by the ketones ( 1 , 3 , 5 , 7 ) has an enhanced quantum efficiency with respect to that on direct excitation of the corresponding hydrocarbons ( 2 , 4 , 6 , 8 ) and more strongly in the exo than in the endo orientation. In order to account for the energy wasting in the intramolecular triplet energy transfer in the endo compounds, a transfer route via a weak triplet donor‐acceptor exciplex, specific to through‐space interaction in the endo configuration (providing for additional radiationless T → S energy dissipation through vibrational coupling), competing with an efficient through‐σ‐bond exchange transfer mechanism operative in both configurations is proposed.
    Acceptor
    Excimer
    Biphenyl
    Citations (19)
    Long-lived charge separated state and thermally activated delayed fluorescence in anthraquinone-phenoxazine electron donor–acceptor dyads
    Chemical Communications (2022)
    Xiaoyu ZhaoJianzhang Zhao
    Long-lived charge separated (CS) triplet state (2.6 μs) and thermally activated delayed fluorescence (TADF) [τ = 282 ns (90.4%)/2.4 μs (9.6%)] were observed in an anthraquinone-phenoxazine electron donor-acceptor dyad via the electron spin control method, and emissive 1CS and non-emissive 3CS states were discriminated via nanosecond transient absorption spectroscopy and global analysis.
    Phenoxazine
    Anthraquinones
    Acceptor
    Electron acceptor
    Electron donor
    Citations (20)