Chromatographic materials for the separation of unsaturated molecules

Patent metadata

Field	Value
Publication number	US-12083498-B2
Application number	US-202016926102-A
Country	US
Kind code	B2
Filing date	Jul 10, 2020
Priority date	May 15, 2012
Publication date	Sep 10, 2024
Grant date	Sep 10, 2024

Abstract

The present disclosure relates to a method of separating a compound of interest, particularly unsaturated compound(s) of interest, from a mixture. The compound is separated using a column having a chromatographic stationary phase material for various different modes of chromatography containing a first substituent and a second substituent. The first substituent minimizes compound retention variation over time under chromatographic conditions. The second substituent chromatographically and selectively retains the compound by incorporating one or more aromatic, polyaromatic, heterocyclic aromatic, or polyheterocyclic aromatic hydrocarbon groups, each group being optionally substituted with an aliphatic group. In some examples, the present disclosure can include a chromatographic system having a chromatographic column having a stationary phase with a chromatographic substrate containing silica, metal oxide, an inorganic-organic hybrid material, a group of block copolymers, or a combination thereof.

First claim

The invention claimed is:

1. A chromatographic stationary phase having the following structure (i):
[X](W) a (Q) b (T) c   (i)

wherein:
X is a chromatographic substrate comprising a surface and containing silica, metal oxide, an inorganic-organic hybrid material, a group of block copolymers, or combinations thereof;

W is selected from the group consisting of hydrogen and hydroxyl, wherein W is bound to the surface of X;
Q is:

T is represented by one of the following structures:

a is zero or a positive number;
b is a positive number;
c is a positive number;
wherein a ratio of b/c is greater than or equal to 0.05 and less than or equal to 100; and
Z is independently selected for each instance from:
(a) a surface attachment group having the formula (B 1 ) x (R 5 ) y (R 6 ) z Si—, wherein x is an integer from 1-3, y is an integer from 0-2, z is an integer from 0-2, and x+y+Z=3, R 5 and R 6 are each independently selected from the group consisting of methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, tert-butyl, substituted or unsubstituted aryl, cyclic alkyl, branched alkyl, lower alkyl, a protected or deprotected alcohol, a zwitterion group and a siloxane bond, and B 1 is a siloxane bond;
(b) an attachment to a surface organofunctional hybrid group through a direct carbon-carbon bond or through a heteroatom, ester, ether, thioether, amine, amide, imide, urea, carbonate, carbamate, heterocycle, triazole, or urethane linkage; or
(c) an adsorbed surface group that is not covalently attached to the surface of X.

2. The stationary phase of claim 1 , wherein the surface of X is subject to alkoxylation by a chromatographic mobile phase under chromatographic conditions.

3. The stationary phase of claim 2 , wherein a substantial portion of the surface of X does not undergo alkoxylation by a chromatographic mobile phase under chromatographic conditions.

4. The stationary phase of claim 1 , wherein the chromatographic stationary phase is adapted for supercritical fluid chromatography.

5. The stationary phase of claim 1 , wherein the chromatographic stationary phase is adapted for carbon dioxide based chromatography.

6. A column, capillary column, microfluidic device or apparatus for normal phase chromatography, high-pressure liquid chromatography, solvated gas chromatography, supercritical fluid chromatography, sub-critical fluid chromatography, carbon dioxide based chromatography, hydrophilic interaction liquid chromatography or hydrophobic interaction liquid chromatography comprising:
a housing having at least one wall defining a chamber having an entrance and an exit, and a stationary phase according to claim 1 disposed therein, wherein the housing and stationary phase are adapted for normal phase chromatography, high-pressure liquid chromatography, solvated gas chromatography, supercritical fluid chromatography, sub-critical fluid chromatography, carbon dioxide based chromatography, hydrophilic interaction liquid chromatography or hydrophobic interaction liquid chromatography.

7. A kit for normal phase chromatography, high-pressure liquid chromatography, solvated gas chromatography, supercritical fluid chromatography, sub-critical fluid chromatography, carbon dioxide based chromatography, hydrophilic interaction liquid chromatography or hydrophobic interaction liquid chromatography comprising:
a housing having at least one wall defining a chamber having an entrance and an exit, and a stationary phase according to claim 1 disposed therein, wherein the housing and stationary phase are adapted for normal phase chromatography, high-pressure liquid chromatography, solvated gas chromatography, supercritical fluid chromatography, sub-critical fluid chromatography, carbon dioxide based chromatography, hydrophilic interaction liquid chromatography or hydrophobic interaction liquid chromatography; and
instructions for performing normal phase chromatography, high-pressure liquid chromatography, solvated gas chromatography, supercritical fluid chromatography, sub-critical fluid chromatography, carbon dioxide based chromatography, hydrophilic interaction liquid chromatography or hydrophobic interaction liquid chromatography with the housing and stationary phase.

8. A method for preparing a stationary phase according to claim 1 , the method comprising:
reacting a chromatographic substrate with a silane coupling agent having a pendant reactive group;
reacting with the pendant reactive group a second chemical agent selected from 1-aminoanthracene, 2-aminoanthracene, and 9-aminoanthracene; and
neutralizing any remaining unreacted pendant reactive groups;
thereby producing a stationary phase according to claim 1 .

9. A method for preparing a stationary phase according to claim 1 , the method comprising:
oligomerizing a silane coupling agent having a pendant reactive group;
reacting a core surface with the oligomerized silane coupling agent;
reacting with the pendant reactive group a second chemical agent selected from 1-aminoanthracene, 2-aminoanthracene, and 9-aminoanthracene; and
neutralizing any remaining unreacted pendant reactive groups,
thereby producing a stationary phase according to claim 1 .

10. A method for mitigating or preventing retention drift in normal phase chromatography, high-pressure liquid chromatography, solvated gas chromatography, supercritical fluid chromatography, sub-critical fluid chromatography, carbon dioxide based chromatography, hydrophilic interaction liquid chromatography or hydrophobic interaction liquid chromatography comprising:
chromatographically separating a sample using a chromatographic device comprising a chromatographic stationary phase according to claim 1 , thereby mitigating or preventing retention drift.

Assignees

• Waters Technologies Corp

Inventors

• Brousmiche Darryl W
• Fairchild Jacob N
• Hill Jason F
• Isaac Giorgis
• Morris Michael F
• Wyndham Kevin D

Classifications

• B01J2220/54

  Sorbents specially adapted for analytical or investigative chromatography · CPC title

• B01J20/3085

  Chemical treatments not covered by groups B01J20/3007 - B01J20/3078 · CPC title

• B01J20/28042

  Shaped bodies; Monolithic structures · CPC title

• B01J20/28016

  Particle form · CPC title

• B01J20/28004

  Sorbent size or size distribution, e.g. particle size · CPC title