Crystal structure of 1'-ethyl­spiro[chroman-4,4'-imidazolidine]-2',5'-dione: a hydantoine derivative
نوع المنشور
بحث أصيل
المؤلفون
النص الكامل
تحميل

The title compound, C13H13N2O3, a hydantoin derivative, crystallized with two molecules (A and B) in an asymmetric unit. In molecule A, the imidazolidine ring is twisted about the C—N bond involving the spiro C atom, while in molecule B this ring is flat (r.m.s. deviation = 0.010 A˚ ). The pyran rings in both molecules have distorted half-chair conformations. The mean plane of the imidazolidine ring is inclined to the aromatic ring of the chroman unit by 79.71 (11) in molecule A and 82.83 (12) in molecule B. In the crystal, pairs of N— HO hydrogen bonds link the individual molecules to form A–A and B–B inversion dimers. The dimers are linked via N— HO and C—HO hydrogen bonds, forming sheets lying parallel to the bc plane, viz. (011). Within the sheets, the A and B molecules are linked by C—H interactions.

المجلة
العنوان
Acta Crystallographica Section E
الناشر
Crystallographic Communications
بلد الناشر
المملكة المتحدة
Indexing
Thomson Reuters
معامل التأثير
0,5
نوع المنشور
مطبوع فقط
المجلد
71
السنة
2015
الصفحات
2