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Stabilization of Near Identical Hydrogen Bonded Octameric Water Clusters in Crystal Structures of Three Distinct Non-Charged Polyamide Macrocyclic Host Molecules.


ABSTRACT: In this paper, we present a comparative analysis of the solid state structures of three well-resolved hydrates of macrocyclic host molecules 1a, 1b, and 2 containing an intrannular amide-aryl substituent (lariat arm) connected to a fixed 26-membered ring in a normal (-NHCOAr, hosts 1a and 1b) or reverse manner (-CONHAr, host 2). Despite different chemical structures, these hosts crystallize as isostructural tetrahydrates in the same P-1 space group. Moreover, their crystals exhibit identical hydrogen bond motifs resulting in a stabilization of an almost identical unusual octameric water cluster built from the cyclic tetramer core and four water molecules, attached sequentially in an "up-and-down" manner. Further analysis reveals that, among the series, the structure of host 2 provides the most suitable environment for the accommodation of this type of water cluster.

SUBMITTER: Dabrowa K 

PROVIDER: S-EPMC8125911 | biostudies-literature | 2021 May

REPOSITORIES: biostudies-literature

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Stabilization of Near Identical Hydrogen Bonded Octameric Water Clusters in Crystal Structures of Three Distinct Non-Charged Polyamide Macrocyclic Host Molecules.

Dąbrowa Kajetan K   Ceborska Magdalena M   Jurczak Janusz J  

Molecules (Basel, Switzerland) 20210509 9


In this paper, we present a comparative analysis of the solid state structures of three well-resolved hydrates of macrocyclic host molecules <b>1a</b>, <b>1b</b>, and <b>2</b> containing an intrannular amide-aryl substituent (lariat arm) connected to a fixed 26-membered ring in a normal (-NHCOAr, hosts <b>1a</b> and <b>1b</b>) or reverse manner (-CONHAr, host <b>2</b>). Despite different chemical structures, these hosts crystallize as isostructural tetrahydrates in the same <i>P</i>-1 space grou  ...[more]

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