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An Unprecedented Class of Benzoyldiazenido‐Functionalized Polyoxometalates with Enhanced Antitumour Activities
Author(s) -
Wang Longsheng,
Yin Panchao,
Zhang Jin,
Xiao Fengping,
Fang Zhikun,
Fu Weiwei,
Wei Yongge,
Xue Shijia
Publication year - 2017
Publication title -
european journal of inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 1434-1948
DOI - 10.1002/ejic.201700990
Subject(s) - chemistry , natural bond orbital , acetonitrile , hydrazide , cyclic voltammetry , medicinal chemistry , inorganic chemistry , single crystal , crystallography , organic chemistry , electrochemistry , molecule , electrode
An unprecedented class of benzoyldiazenido‐functionalized polyoxometalates, [Bu 4 N] 3 [Mo 6 O 18 (=N=NCOAr)] (Ar=Ph, 1 ; Ph‐ o ‐Cl, 2 ; Ph‐ m ‐Cl, 3 ; Ph‐ p ‐Cl, 4 ; Ph‐ o , p ‐Cl 2 , 5 ; Ph‐ p ‐Br, 6 ; Ph‐ m ‐NO 2 , 7 ; Ph‐ p ‐NO 2 , 8 ; Ph‐ p ‐OMe, 9 ), are prepared through the reactions of α‐octamolybdate and the corresponding hydrazides in dry acetonitrile under reflux with dicyclohexylcarbodiimide (DCC) as a dehydrating agent. Single‐crystal X‐ray diffraction structural analysis reveals that their anions demonstrate the typical structural features of monofunctionalized hexamolybdates with different organic substituents. 1 H NMR spectroscopy indicates that the [Mo 6 O 18 (NN)] fragments in these compounds are electron‐donating groups rather than electron‐withdrawing groups, and this behaviour was further validated by the calculation of the atomic‐charge distributions [natural bond orbital (NBO) and Mülliken]. Cyclic voltammetry (CV) indicates that they are more difficult to reduce than hexamolybdate and its organoimido derivatives. Antitumour activity tests against K562 show that most of the hybrid compounds have enhanced inhibitory activities compared with those of hexamolybdate and the corresponding hydrazide ligands.