2011
DOI: 10.1524/ncrs.2011.0123
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Crystal structure of N-(3-hydroxyphenyl)-5-chlorosalicylideneimine, C13H10ClNO2

Abstract: C 13 H 10 ClNO 2 ,monoclinic, P2

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“…Compared with the Schi base with electron-donating groups [4], the title compound with electron-withdrawing groups has much lesser keto-form (which is proved by the bond length of C13-O3 (1.340 Å) that is much longer than that C4-O1 (1.302 Å) in the related literature known compound [4]. The reason is that the title compound with electron-withdrawing groups decreases the electron cloud density of nitrogen atom of −C=N-, resulting in reduction of binding force with hydrogen atom.…”
Section: Discussionmentioning
confidence: 99%
“…Compared with the Schi base with electron-donating groups [4], the title compound with electron-withdrawing groups has much lesser keto-form (which is proved by the bond length of C13-O3 (1.340 Å) that is much longer than that C4-O1 (1.302 Å) in the related literature known compound [4]. The reason is that the title compound with electron-withdrawing groups decreases the electron cloud density of nitrogen atom of −C=N-, resulting in reduction of binding force with hydrogen atom.…”
Section: Discussionmentioning
confidence: 99%