3‐(2,2′:6′,2′′‐Terpyridin‐4′‐yloxy)propyl toluene‐4‐sulfonate | Zendy

Hoogenboom Richard | Zendy; Nakahashi Akiko | Zendy; Kickelbick Guido | Zendy; Chujo Yoshiki | Zendy; Schubert Ulrich S. | Zendy

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3‐(2,2′:6′,2′′‐Terpyridin‐4′‐yloxy)propyl toluene‐4‐sulfonate

Author(s) -

Hoogenboom Richard,

Nakahashi Akiko,

Kickelbick Guido,

Chujo Yoshiki,

Schubert Ulrich S.

Publication year - 2007

Publication title -

acta crystallographica section e

Language(s) - English

Resource type - Journals

ISSN - 1600-5368

DOI - 10.1107/s1600536807017229

Subject(s) - dihedral angle , substituent , stacking , pyridine , hydrogen bond , ring (chemistry) , toluene , chemistry , sulfonate , aromaticity , crystallography , crystal (programming language) , tosyl , crystal structure , stereochemistry , medicinal chemistry , molecule , organic chemistry , sodium , computer science , programming language

The title compound, C 25 H 23 N 3 O 4 S, was synthesized by tosylation of 3‐(2,2′;6′,2′′‐terpyridin‐4′‐yloxy)propan‐1‐ol. The dihedral angles formed by the substituent pyridine rings with the central ring are 4.27 (4) and 17.27 (5)°. The crystal packing is stabilized by intermolecular C—H...O hydrogen‐bond interactions, with no stacking interaction between the aromatic rings.

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