One-Pot Synthesis of a Cyclic Pyrene Octamer from Two Bifunctionalized Pyrene Monomers

Synthesis ◽  
2020 ◽  
Vol 53 (02) ◽  
pp. 344-347
Author(s):  
Hiroko Yamada ◽  
Naoki Aratani ◽  
Peifeng Mei ◽  
Ryo Kurosaki ◽  
Akinobu Matsumoto

AbstractA 2,2′-tert-butyl-5,9-6′,8′-cyclooctameric pyrenylene ([8]CP) was synthesized by a one-pot Suzuki–Miyaura cross-coupling reaction from two kinds of bifunctionalized monomers, as a rare example of a cyclic octamer. The octameric molecular structure of [8]CP was revealed by single-crystal X-ray diffraction analysis.

ChemInform ◽  
2016 ◽  
Vol 47 (2) ◽  
Author(s):  
Akari Ikeda ◽  
Masaaki Omote ◽  
Kana Kusumoto ◽  
Atsushi Tarui ◽  
Kazuyuki Sato ◽  
...  

CrystEngComm ◽  
2021 ◽  
Author(s):  
Ying Wang ◽  
Yao-mei Fu ◽  
Si-qi You ◽  
xuexin Li ◽  
Xinlong Wang ◽  
...  

Two new zirconium−based heterometal−organic frameworks, Zr3CP3−Mn (1) and Zr3CP3−Ni (2) constructed from [Cp3Zr3(μ3−O)(μ2−OH)3(IN)3] secondary building units and transition metal cations, were successfully synthesized through one−pot method. Single-crystal X-ray diffraction analysis...


Synlett ◽  
2017 ◽  
Vol 28 (17) ◽  
pp. 2262-2266 ◽  
Author(s):  
Ashutosh Bedekar ◽  
Blessy Rajan

An efficient protocol for the synthesis of unsymmetrical aza[7]helicenes has been developed. The bis-styryl-type substrates for regiospecific photodehydrogenative oxidative double cyclization to give helicenes were prepared by a one-pot Wittig–Heck sequence as well as a stepwise procedure. The derivatives were characterized by single-crystal X-ray diffraction analysis and fluorescence spectroscopy.


Synlett ◽  
2010 ◽  
Vol 2010 (16) ◽  
pp. 2461-2464 ◽  
Author(s):  
Masayuki Hoshi ◽  
Hirokazu Yamazaki ◽  
Mitsuhiro Okimoto

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