IP Library Granted Patent US 11,933,748
Granted Patent B2
US 11,933,748 · App. 17/767,068 · Granted Mar 19, 2024

Method of determining the three-dimensional structure of molecules in crystalline inclusion complexes

Inventors: Clemens Richert (Stuttgart, DE); Felix Krupp (Stuttgart, DE); Wolfgang Frey (Stuttgart, DE)
Assignee: BRUKER AXS GmbH
G01N23/207C30B7/06C30B29/54G16C20/20G01N2223/604
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Quick Facts
Patent No.
US 11,933,748
App. No.
17/767,068
Granted
Mar 19, 2024
Kind
B2
Abstract

The invention is directed to a method for elucidating the three-dimensional structure of compounds by X-ray diffraction (X-ray SCD) characterized in that the compound is co-analyte crystallized with tetraaryladamantanes according to general formula I Wherein R and R′ are identical or different residues selected from the group consisting of O—R1, S—R1, NHR1, NR1R2, F, Cl, Br or I and R1, R2 stand for identical or different, substituted on not substituted aliphatic or aromatic residues having 1 to 25 carbon atoms and the the three-dimensional structure of the compound is obtained by X-ray diffraction (X-ray SCD).

Claims (13)

1. A method for elucidating the three-dimensional structure of a compounds by X-ray diffraction (X-ray SCD) characterized in that the compound is co-crystallized with tetraaryladamantes according to general formula I

Wherein R and R′ are identical or different residues selected from the group consisting of O—R1, S—R1, NHR1, NR1R2, F, Cl, Br or I and R1, R2 stand for identical or different, substituted on not substituted aliphatic or aromatic residues having 1 to 25 carbon atoms and the three-dimensional structure of the compound is obtained by X-ray diffraction (X-ray SCD) and wherein in the compound is a chiral molecule, and the absolute configuration or relative configuration of the compound is obtained.

2. The method according to claim 1 characterized in that the compound is co-crystallized with tetraaryladamantes into a single-crystal.

3. The method according to claim 1 , characterized in that the compound to be co-crystallized has a molecular weight of less than 500 g/mol.

4. The method according to claim 1 , characterized in that the compound to be co-crystallized is a liquid.

5. The method according to claim 1 , characterized in that the compound and the tetraaryladamantanes are co-crystallized in the absence of a solvent.

6. The method according to claim 1 , characterized in that the compound and the tetraaryladamantanes are co-crystallized by providing a mixture of the compound, the tetraaryladamantanes and a solvent and subsequent evaporation of the solvent followed by heating or incubation at room temperature.

7. The method according to claim 1 , characterized in that the compound is a mixture of enantiomers or a mixture of diastereomers.

8. A method for elucidating the absolute or relative three dimensional configuration of a chiral compound, comprising:

co crystallizing the compound with tetraaryladamantes according to general formula I

wherein R and R′ are identical or different residues selected from the group consisting of O—R1, S—R1, NHR1, NR1R2, F, Cl, Br or I and R1, R2 stand for

identical or different, substituted on not substituted aliphatic or aromatic residues having 1 to 25 carbon atoms; and

obtaining the absolute or relative three dimensional configuration of the compound by X-ray diffraction (X-ray SCD).

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 17, 2025
From: BRUKER AXS GMBH
To: BRUKER AXS SE
Reel/Frame 071437/0901 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 20, 2025
From: RICHERT, CLEMENS; KRUPP, FELIX; FREY, WOLFGANG
To: BRUKER AXS GMBH
Reel/Frame 071325/0598 →
Priority Claims (1)
DE 10 2019 007 099.2 · Oct 10, 2019 · national
Continuity (1)
Related Publication 20220373482A1 · Nov 24, 2022