Crystal Structure of an Ionic Charge-Transfer Complex of DAP-F4TCNQ (DAP = 1,6-Diaminopyrene, F4TCNQ = 2,3,5,6-Tetrafluoro-7,7,8,8-tetracyano-p-quinodimethane)

2000 ◽  
Vol 73 (10) ◽  
pp. 2231-2235
Author(s):  
Koichi Matsushima ◽  
Megumi Ogaki ◽  
Toshio Naito ◽  
Tamotsu Inabe
2021 ◽  
Author(s):  
Hosea M. Nelson ◽  
Juno C. Siu ◽  
Ambarneil Saha ◽  
Duilio Cascio ◽  
Samantha N. MacMillan ◽  
...  

Author(s):  
Hosea Nelson ◽  
Juno Siu ◽  
Ambarniel Saha ◽  
Duilio Cascio ◽  
Song-Bai Wu ◽  
...  

Recent advances in radical-based catalytic reactions have created an increasing demand for the understanding of their mechanistic underpinnings. Structural elucidation of transient reactive intermediates via diffraction techniques, though rarely possible, is one of the most decisive ways to support such mechanistic hypotheses. Here we present the isolation, structural elucidation, and theoretical analysis of an electrochemically generated and catalytically relevant charge-transfer species formed between the azidyl radical and (2,2,6,6-tetramethylpiperidin-1-yl)oxyl (TEMPO). The unusual bent N–N–N angle and the pancake bonding between these two fragments highlight the weak bonding interactions present in this complex. This X-ray structure validates computational predictions as well as mechanistic proposals of TEMPO-mediated radical azidation reactions.


2015 ◽  
Vol 7 (36) ◽  
pp. 20280-20284 ◽  
Author(s):  
Tsz-Wai Ng ◽  
Hrisheekesh Thachoth Chandran ◽  
Chiu-Yee Chan ◽  
Ming-Fai Lo ◽  
Chun-Sing Lee

2001 ◽  
pp. 1398-1399 ◽  
Author(s):  
Hirofumi Yoshikawa ◽  
Shin-ichi Nishikiori ◽  
Kinga Suwinska ◽  
Roman Luboradzki ◽  
Janusz Lipkowski

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