A triazine derivative with a triple‐decker sandwich conformation

A triazine derivative with a triple‐decker sandwich conformation

In dimethyl 3,3′‐[6‐methoxy‐1,3,5‐triazine‐2,4‐diyl)bis(oxy)]bis(4‐benzyloxy‐5‐methoxybenzoate), C36H33N3O11, a new triazine derivative, the benz­yloxy groups adopt an inter­esting conformation in which they are positioned above and below the triazine ring `core' of the mol­ecule to form an int...

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Veröffentlicht in:Acta crystallographica. Section E, Structure reports online Structure reports online, 2007-02, Vol.63 (2), p.o624-o626
Hauptverfasser: Peter, Xolani K., Heerden, Fanie R. van, Munro, Orde Q.
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container_title Acta crystallographica. Section E, Structure reports online
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Heerden, Fanie R. van
Munro, Orde Q.
description In dimethyl 3,3′‐[6‐methoxy‐1,3,5‐triazine‐2,4‐diyl)bis(oxy)]bis(4‐benzyloxy‐5‐methoxybenzoate), C36H33N3O11, a new triazine derivative, the benz­yloxy groups adopt an inter­esting conformation in which they are positioned above and below the triazine ring `core' of the mol­ecule to form an intra­molecular triple‐decker sandwich. The ester carbonyl O atoms of adjacent mol­ecules in the crystal structure participate in non‐conventional (alk­yl)C—H⋯O hydrogen bonds [averaging 2.45 (1)Å] about an inversion centre to give a weakly hydrogen‐bonded dimer.
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