Literature DB >> 12860429

A new crystal form of beta-cyclodextrin-ethanol inclusion complex: channel-type structure without long guest molecules.

Thammarat Aree1, Narongsak Chaichit.   

Abstract

A new crystal form of beta-cyclodextrin (beta-CD)[bond]ethanol[bond]dodecahydrate inclusion complex [(C(6)H(10)O(5))(7).0.3C(2)H(5)OH.12H(2)O] belongs to monoclinic space group C2 (form II) with unit cell constants a=19.292(1), b=24.691(1), c=15.884(1) A, beta=109.35(1) degrees. The beta-CD macrocycle is more circular than that of the complex in space group P2(1) [form I: J. Am. Chem. Soc. 113 (1991) 5676]. In form II, a disordered ethanol molecule (occupancy 0.3) is placed in the upper part of beta-CD cavity (above the O-4 plane) and is sustained by hydrogen bonding to water site W-2. In form I, an ethanol molecule located below the O-4-plane is well ordered because it hydrogen bonds to surrounding O-3[bond]H, O-6[bond]H groups of the symmetry-related beta-CD molecules. In the crystal lattice of form I, beta-CD macrocycles are stacked in a typical herringbone cage structure. By contrast, the packing structure of form II is a head-to-head channel that is stabilized at both O-2/O-3 and O-6 sides of each beta-CD by direct O(CD)...O(CD) and indirect O(CD)...O(W)...(O(W))...O(CD) hydrogen bonds. The 12 water molecules are disordered in 18 positions both inside the channel-like cavity of beta-CD dimer (W-1[bond]W-6) and in the interstices between the beta-CD macrocycles (W-7[bond]W-18). The latter forms a cluster that is hydrogen bonded together and to the neighboring beta-CD O[bond]H groups.

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Year:  2003        PMID: 12860429     DOI: 10.1016/s0008-6215(03)00220-9

Source DB:  PubMed          Journal:  Carbohydr Res        ISSN: 0008-6215            Impact factor:   2.104


  3 in total

1.  Dissolution behavior of β-cyclodextrin molecular inclusion complexes of aceclofenac.

Authors:  Kamal Dua; Kavita Pabreja; M V Ramana; Vinny Lather
Journal:  J Pharm Bioallied Sci       Date:  2011-07

2.  Co-solvation effect on the binding mode of the α-mangostin/β-cyclodextrin inclusion complex.

Authors:  Thanyada Rungrotmongkol; Uracha Ruktanonchai; Chompoonut Rungnim; Sarunya Phunpee; Manaschai Kunaseth; Supawadee Namuangruk; Kanin Rungsardthong
Journal:  Beilstein J Org Chem       Date:  2015-11-25       Impact factor: 2.883

Review 3.  Grinding as Solvent-Free Green Chemistry Approach for Cyclodextrin Inclusion Complex Preparation in the Solid State.

Authors:  Mario Jug; Paola Angela Mura
Journal:  Pharmaceutics       Date:  2018-10-16       Impact factor: 6.321

  3 in total

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