Strategic Synthesis and Supramolecular Organization of Arylenebis(aryliodonium) Salts; Journal of Organic Chemistry; Vol. 90, iss.44

Sonraí bibleagrafaíochta
Parent link:Journal of Organic Chemistry.— .— Washington: American Chemical Society
Vol. 90, iss.44.— 2025.— P. 15542-15554
Rannpháirtithe: Knyazeva E. V. Elizaveta Vyacheslavovna, Soldatova N. S. Nataliya Sergeevna, Abramov P. A. Pavel Aleksandrovich, Ivanov D. M. Daniil Mikhaylovich, Burykina Ju. V. Julia, Radzhabov A. D. Amirbek Dzhurabekovich, Yusubov M. S. Mekhman Suleiman-Ogly (Suleimanovich), Resnati D. P. Dzhuzeppe Paolo, Kukushkin V. Yu. Vadim Yurjevich, Postnikov P. S. Pavel Sergeevich
Achoimre:Title screen
A comprehensive synthetic toolkit was developed for the preparation of arylenebis(aryliodonium) salts from diiodoarenes via m-CPBA oxidation. The methodology offers versatile approaches that can be adapted based on the solubility of reaction intermediates, enabling either one-pot or two-stage synthesis pathways. Four distinct synthetic methods were established, accommodating a wide range of arenes and diiodoarenes, including sterically hindered and electron-deficient substrates. The resulting bis(iodonium) salts were isolated in good to excellent yields (up to 99%). X-ray crystallographic analysis of these compounds revealed intriguing supramolecular organization in the solid state, with the formation of 1D chains through halogen bonding interactions. These self-assembled architectures demonstrate the potential of bis(iodonium) cations as valuable building blocks for applications in crystal engineering
Текстовый файл
Teanga:Béarla
Foilsithe / Cruthaithe: 2025
Ábhair:
Rochtain ar líne:https://doi.org/10.1021/acs.joc.5c01508
Formáid: Leictreonach Caibidil leabhair
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=683111

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330 |a A comprehensive synthetic toolkit was developed for the preparation of arylenebis(aryliodonium) salts from diiodoarenes via m-CPBA oxidation. The methodology offers versatile approaches that can be adapted based on the solubility of reaction intermediates, enabling either one-pot or two-stage synthesis pathways. Four distinct synthetic methods were established, accommodating a wide range of arenes and diiodoarenes, including sterically hindered and electron-deficient substrates. The resulting bis(iodonium) salts were isolated in good to excellent yields (up to 99%). X-ray crystallographic analysis of these compounds revealed intriguing supramolecular organization in the solid state, with the formation of 1D chains through halogen bonding interactions. These self-assembled architectures demonstrate the potential of bis(iodonium) cations as valuable building blocks for applications in crystal engineering 
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461 1 |t Journal of Organic Chemistry  |c Washington  |n American Chemical Society 
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701 1 |a Knyazeva  |b E. V.  |g Elizaveta Vyacheslavovna  |f 2001-  |c chemist  |c laboratory assistant of Tomsk Polytechnic University  |y Tomsk  |7 ba  |8 eng  |9 89036 
701 1 |a Soldatova  |b N. S.  |c organic chemist  |c engineer of Tomsk Polytechnic University  |f 1992-  |g Nataliya Sergeevna  |9 19363 
701 1 |a Abramov  |b P. A.  |c chemist  |c professor, senior researcher at Tomsk Polytechnic University, Doctor of Chemical Sciences  |f 1985-  |g Pavel Aleksandrovich  |9 88582 
701 1 |a Ivanov  |b D. M.  |c Chemist  |c Senior researcher of Tomsk Polytechnic University, Candidate of chemical sciences  |f 1992-  |g Daniil Mikhaylovich  |9 22632 
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701 1 |a Kukushkin  |b V. Yu.  |g Vadim Yurjevich 
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