IP Library Granted Patent US 10,549,255
Granted Patent B2
US 10,549,255 · App. 13/760,497 · Granted Feb 4, 2020

Functionalized chromatographic materials and methods of making and using therefor

Inventors: Yongsong Huang (Barrington, RI); Jose C. Aponte (Silver Spring, MD); Rafael Tarozo (Providence, RI); James Dillon (Pawtucket, RI)
Assignee: BROWN UNIVERSITY
B01J20/0262B01D15/38B01J20/0233B01J20/283B01J20/287B01J20/3242B01D15/10B01J20/284B01J20/285
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Quick Facts
Patent No.
US 10,549,255
App. No.
13/760,497
Granted
Feb 4, 2020
Kind
B2
Abstract

Methods, compositions, devices and kits having a novel chromatographic material are provided herein for separating and identifying organic molecules and compounds, for example molecules and compounds containing electron rich functional groups such as carbon-carbon double bonds. The methods, compositions, and kits include a metal-thiolate chromatographic medium (MTCM) with a sulfur-containing functional group or a metal-selenolate chromatographic medium (MSCM) comprising a selenium-containing functional group covalently attached to a support medium, such that the sulfur-containing functional group or selenium-containing functional group is bound to at least one metal atom. The MTCM and/or MSCM has affinity and specificity to compounds having one or more carbon-carbon double bonds, and performs a highly efficient and rapid separation of samples yielding non-overlapping peaks of purified materials compared to traditional media.

Claims (6)

1. A separation system comprising:

a silver thiolate chromatographic medium present as a stationary phase in a pipette or column, wherein the chromatographic medium comprises a sulfur-containing functional group wherein the sulfur is covalently bound to a silver atom, and

wherein the sulfur-containing functional group is linked to a support by at least one spacer selected from: a (C 1 -C 15 )alkyl, a (C 1 -C 15 )alkoxy, a (C 1 -C 15 )heteroalkyl, a (C 6 -C 10 )aryl, a (C 1 -C 9 )heteroaryl, and a (C 6 -C 10 )aryl(C 1 -C 6 )alkyl, and

a sample source coupled to the pipette or column comprising a sample to be separated, wherein the sample includes a compound having a functional group selected from the group consisting of alkenyls, alkynyls, aromatics, and amines.

2. The chromatographic medium according to claim 1 , on a support selected from the group consisting of: silica gel, alumina, polystyrene, agarose, modified polymeric resin, cellulose, magnesium silicate, dextran, and starch.

3. The chromatographic medium according to claim 1 , configured as an analytical component of a chromatographic separation system selected from: normal phase chromatography, reversed-phase chromatography, liquid chromatography, planar chromatography, column chromatography, flush chromatography, flash chromatography, thin layer chromatography, high performance liquid chromatography, gas chromatography, and solid phase extraction chromatography.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 16, 2020
From: APONTE, JOSE C.; DILLON, JAMES
To: BROWN UNIVERSITY
Reel/Frame 054073/0657 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 30, 2019
From: HUANG, YONGSONG; TAROZO, RAFAEL
To: BROWN UNIVERSITY
Reel/Frame 051386/0102 →
CONFIRMATORY LICENSE Recorded Jul 10, 2014
From: BROWN UNIVERSITY
To: NATIONAL SCIENCE FOUNDATION
Reel/Frame 033296/0020 →
Continuity (3)
Continuation PCTUS2011046810 · Aug 5, 2011
Provisional Application 61371207 · Aug 6, 2010
Related Publication 20130146542A1 · Jun 13, 2013