Electronic Influences on the Stability and Kinetics of Cp* Rhodium(III) Azide Complexes in the iClick Reaction with Electron‐Poor Alkynes
Electronic Influences on the Stability and Kinetics of Cp* Rhodium(III) Azide Complexes in the iClick Reaction with Electron‐Poor Alkynes
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电子对贫电子炔烃 iClick 反应中 Cp* 铑 (III) 叠氮化物配合物稳定性和动力学的影响
DOI:
10.1002/ejic.201700199
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发表时间:
2017
影响因子:
2.3
通讯作者:
U. Schatzschneider
中科院分区:
文献类型:
--
作者:
L. Hiersch;J. Mößeler;U. Schatzschneider
Rhodium(III) azide half‐sandwich complexes of general formula [Rh(Cp*)(N3)(bpyR,R)]CF3SO3with R = H, OCH3were prepared in three steps in an overall yield of 55–65 %. Their stability strongly depends on the 4,4′‐substituent on the 2,2′‐bipyridine (bpy) ligand and increases in the order COOCH3< H < OCH3. Consequently, no stable product could be isolated for the complex with the methyl ester substituent. The title compounds easily underwent cycloaddition reactions with ethyl 4,4,4‐trifluoro‐2‐butynoate in acetonitrile at room temperature in the absence of catalyst. The resulting triazolate products were simply isolated by precipitation in 65–75 % yield. The trifluoromethyl group enabled facile monitoring of the reaction by19F NMR spectroscopy. Kinetic studies with solution IR spectroscopy revealed pseudo‐first‐order rate constants of 2.4 to 3.8 × 10–3s–1, and the reactions were accelerated by the presence of electron‐donating groups at the 4,4′‐position of the bpy coligand. These values are of a similar magnitude as those for the Staudinger ligation utilized for bio(macro)molecule functionalization.
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影响因子:
46.2
作者:
Jewett JC;Bertozzi CR
通讯作者:
Bertozzi CR
影响因子:
--
作者:
Yuri Tulchinsky;S. Kozuch;P. Saha;Assaf Mauda;G. Nisnevich;M. Botoshansky;L. Shimon;Mark Gandelman
通讯作者:
Yuri Tulchinsky;S. Kozuch;P. Saha;Assaf Mauda;G. Nisnevich;M. Botoshansky;L. Shimon;Mark Gandelman
影响因子:
2.3
作者:
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通讯作者:
S. Pai;K. Radacki;U. Schatzschneider
DOI:
--
发表时间:
1981
期刊:
影响因子:
--
作者:
A. Nutton;P. M. Bailey;P. Maitlis
通讯作者:
P. Maitlis
影响因子:
4
作者:
A. R. Powers;I. Ghiviriga;K. Abboud;A. Veige
通讯作者:
A. Veige