Design of novel podand-like compounds with two short diphenylphosphine oxide pendant arms
Abstract
Crystal and molecular structure of 1,3,5-benzenetris(methylenediphenylphosphine oxide) cyclohexylammonium chloride dibenzene solvate monohydrate has been determined. The overall arrangement of two diphenylphosphine oxide substituents atoms is imposed by intermolecular strong hydrogen bonds, O(water)H···O(oxide) and NH···O(oxide, water). Cyclohexylamine exists in almost ideal chair conformation and nitrogen atom is equatorial to the ring. The structure is build up from strong and weak intermolecular hydrogen bonds to form the three-dimensional infinite hydrogen bond network.
Crystal and molecular structure of 1,4-bis[(diphenylphosphineoxide)methyl] - 2,5 - bis (ethoxymethyl) benzene has been determined. The phenyl rings are inclined at 80.91(7)° within the substituent, and they are involved in weak C(phenyl)H···O(oxide) hydrogen bonds. The arrangement of diphenylphosphine oxide substituents is imposed practically only by steric effects. Two intramolecular weak hydrogen bonds exist between diphenylphosphine oxide and ethoxymethyl substituents, which can provide additional stabilization to molecule, but it has no noticeable influence on overall molecule geometry. Molecules are assembled via weak intermolecular CH···O(oxide) hydrogen bonds to the one-dimensional hydrogen-bonded chain along y axis. © 2004 Wiley Periodicals, Inc. Heteroatom Chem 15:233–240, 2004; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20008
