SYNTHESIS AND CHELATION PROPERTIES OF SOME NEW MANNICH CONDENSATION POLYMERS CONTAINING A SALICYLALDOXIME GROUP

2002 ◽  
Vol 39 (3) ◽  
pp. 217-229 ◽  
Author(s):  
Kais A. K. Ebraheem ◽  
Mohammad S. Mubarak ◽  
Samer I. Al-Gharabli
2021 ◽  
Vol 211 ◽  
pp. 108664
Author(s):  
Bo-Wen Liu ◽  
Hai-Bo Zhao ◽  
Lin Chen ◽  
Li Chen ◽  
Xiu-Li Wang ◽  
...  

1980 ◽  
Vol 16 (6) ◽  
pp. 611
Author(s):  
G. Caporiccio ◽  
E. Strepparola ◽  
G.A. Bargigia ◽  
G. Novaira ◽  
G. Peveri

1962 ◽  
Vol 58 (166) ◽  
pp. 611-620 ◽  
Author(s):  
E. H. Pryde ◽  
D. J. Moore ◽  
H. M. Teeter ◽  
J. C. Cowan

Author(s):  
Rubina Siddiqui ◽  
Urooj Iqbal ◽  
Zafar Saeed Saify ◽  
Shammim Akhter ◽  
Sammer Yousuf

The title compound, C31H46NO7 +·Cl−, was synthesized by a one-pot Mannich condensation reaction. In the molecule, the piperidinone ring adopts a chair conformation, and the trimethoxy-substituted benzene rings and octyl chain are arranged equatorially. In the crystal, centrosymmetric dimers are linked into layers parallel to (011) by N—H...Cl and C—H...Cl hydrogen bonds. A Hirshfeld surface analysis indicates that the most important contributions for the crystal packing are O...H (20.5%) interactions followed by C...H (7.8%), Cl...H (5.5%), C...C (1.2%), C...O (0.5%) and Cl...O (0.4%) interactions.


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