New type of charge-transfer complex from an antiaromatic electron donor. Possible radical cation stabilization by the captodative effect

1991 ◽  
Vol 113 (15) ◽  
pp. 5910-5911 ◽  
Author(s):  
David J. R. Brook ◽  
R. Curtis Haltiwanger ◽  
Tad H. Koch
Keyword(s):  
Charge Transfer ◽  
Radical Cation ◽  
Electron Donor ◽  
Charge Transfer Complex ◽  
New Type

scholarly journals Anion-enhanced excited state charge separation in a spiro-locked N-heterocycle-fused push-pull zinc porphyrin

2021 ◽  
Author(s):  
Mandeep K. Chahal ◽  
Anuradha Liyanage ◽  
Ajyal Z. Alsaleh ◽  
Paul A. Karr ◽  
Jonathan P. Hill ◽  
...  
Keyword(s):  
Excited State ◽  
Charge Transfer ◽  
Charge Separation ◽  
Charge Transfer Complex ◽  
Zinc Porphyrin ◽  
New Type ◽  
State Charge

A new type of push–pull charge transfer complex, viz., a spiro-locked N-heterocycle-fused zinc porphyrin, ZnP-SQ, is shown to undergo excited state charge separation, which is enhanced by axial F− binding to the Zn center.

Photochemical Nitration by Tetranitromethane. XVII. The Regiochemistry of Adduct Formation in the Photochemical Reaction of 1-Methylnaphthalene and Tetranitromethane

1994 ◽  
Vol 47 (8) ◽  
pp. 1591 ◽  
Author(s):  
JL Calvert ◽  
L Eberson ◽  
MP Hartshorn ◽  
n Maclaga ◽  
WT Robinson
Keyword(s):  
Crystal Structure ◽  
Charge Transfer ◽  
Radical Cation ◽  
Photochemical Reaction ◽  
Charge Transfer Complex ◽  
Adduct Formation ◽  
X Ray ◽  
Analogous Manner ◽  
Structure Determinations ◽  
Ion Recombination

Photolysis of the 1-methylnaphthalene/tetranitromethane charge-transfer complex yields the triad of 1-methylnaphthalene radical cation, nitrogen dioxide and trinitromethanide ion. Recombination of this triad gives predominantly 4-methyl-t-2-nitro-r-1-trinitromethyl-1,2- dihydronaphthalene (1), the epimeric 1-methyl-1-nitro-4-trinitromethyl-1,4-dihydronaphtha-lenes (2) and (3), 8-methyl-c-4-trinitromethyl-1,4-dihydronaphthalen-r-l-ol (4), nitro cyclo -adduct (5), 8-methyl-c-4-trinitromethyl-1,4-dihydronaphthalen-r-l-ol (6), hydroxy cyclo-adduct (7) and 4-methyl-t-1-trinitromethyl-1,2-dihydronaphthalen-r-2-ol (8). Adducts (1)- (3), (5), (7) and (8) are formed by attack of the trinitromethanide ion at C4 of the 1-methylnaphthalene radical cation, while adducts (4) and (6) are formed by corresponding attack at C5. Adduct (1) undergoes thermal cycloaddition to give the nitro cycloadduct (5) and it is assumed that the hydroxy cycloadduct (7) is formed in analogous manner from 4-methyl-t-1-trinitromethyl-1,2-dihydronaphthalen-r-2-ol (8). X-Ray crystal structure determinations are reported for adducts (1), (3)-(5) and (7).

scholarly journals Photopolymerization of Dialkylfumarates with Electron Donor Monomers via Charge-Transfer Complex.

1999 ◽  
Vol 12 (1) ◽  
pp. 107-113 ◽  
Author(s):  
Shigeki Katogi ◽  
Chris W. Miller ◽  
Charles E. Hoyle ◽  
Mikael Johansson ◽  
Sonny JÖnsson
Keyword(s):  
Charge Transfer ◽  
Electron Donor ◽  
Charge Transfer Complex

Photochemical Nitration by Tetranitromethane. XIV. The Formation of 1,3-Dipolar Nitro Addition Products From the Photochemical Reaction of 1,2-Dimethylnaphthalene and Tetranitromethane

1994 ◽  
Vol 47 (6) ◽  
pp. 1087 ◽  
Author(s):  
CP Butts ◽  
JL Calvert ◽  
L Eberson ◽  
MP Hartshorn ◽  
n Maclaga ◽  
...  
Keyword(s):  
Charge Transfer ◽  
Nitrogen Dioxide ◽  
Radical Cation ◽  
Photochemical Reaction ◽  
Charge Transfer Complex ◽  
Ion Recombination

Photolysis of the 1,2-dimethylnaphthalene/tetranitromethane charge-transfer complex yields the triad of 1,2-dimethylnaphthalene radical cation, nitrogen dioxide, and trinitromethanide ion. Recombination of this triad gives predominantly the adducts (13)-(16), each of which is formed by attack of the trinitromethanide ion at C4 of the 1,2-dimethylnaphthalene radical cation. Thermal cycloaddition in adducts (13) and (16) gives the cycloadducts (12) and (17) respectively.

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