IP Library Granted Patent US 7,265,236
Granted Patent B2
US 7,265,236 · App. 11/063,069 · Granted Sep 4, 2007

Polypodal silanes with embedded hydrophilicity

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Quick Facts
Patent No.
US 7,265,236
App. No.
11/063,069
Granted
Sep 4, 2007
Kind
B2
Abstract

A polypodal silane compounds are provided for use as a bonded phase and which have embedded hydrophilicity. The compounds have at least two podal branches bonded via an ether linkage or alkoxy group to a hydrophilic group. Each podal branch has a silicon atom which is bonded to each podal branch through a Si—C bond and each of the podal branches is capable of bonding to a siliceous substrate through at least one hydrolyzable functional group capable of being displaced by a Si—O bond. Bonded phases using such compounds and substrates having such compounds bonded to their surface are also described, as well as a method for preparing a bonded phase.

Claims (29)

1. A polypodal silane compound for use as a bonded phase and having hydrophilicity, comprising at least two podal branches bonded via an ether linkage or alkoxy group to a hydrophilic group, wherein each podal branch has a silicon atom, the silicon atoms are bonded to each podal branch through a Si—C bond and each of the podal branches is capable of bonding to a siliceous substrate through at least one hydrolyzable functional group capable of being displaced by a Si—O bond, and wherein the compound has a structure according to Formula (I):

wherein:

R 1 is selected from hydrogen, and substituted and unsubstituted, branched and straight chain, alkyl, alkenyl, alkynyl, aryl, alkylene ether, alkenyl ether, alkynyl ether or aryl ether groups, and wherein, in R 1 , oxygen atoms are not bonded together so as to form peroxy functionality;

R 2 is selected from substituted and unsubstituted, branched and straight chain alkyl and alkylene ether groups;

R 3 is selected from substituted and unsubstituted, branched and straight chain alkyl groups, wherein each R 3 group in Formula (I) may be the same or different;

R 4 is selected from substituted and unsubstituted, branched and straight chain alkyl, alkylene, alkylene ether and alkenyl ether groups, and an ether linkage;

X is a hydrolyzable group capable of bonding to a siliceous substrate and of being displaced by a silicon-oxygen bond or a non-hydrolyzable organic functional group, wherein at least one of the X groups on each Si atom is hydrolyzable;

n is 0 or an integer which is no greater than 3;

y is 0 or an integer which is no greater than 3; and

wherein 2≦n+y≦3; and n and y are never both zero.

2. A polypodal silane compound comprising a structure according to Formula (I):

wherein:

R 1 is selected from hydrogen, and substituted and unsubstituted, branched and straight chain, alkyl, alkenyl, alkynyl, aryl, alkylene ether, alkenyl ether, alkynyl ether or aryl ether groups, and wherein, in R 1 ,oxygen atoms are not bonded together so as to form peroxy functionality;

R 2 is selected from substituted and unsubstituted, branched and straight chain alkyl and alkylene ether groups;

R 3 is selected from substituted and unsubstituted, branched and straight chain alkyl groups, wherein each R 3 group in Formula (I) may be the same or different;

R 4 is selected from substituted and unsubstituted, branched and straight chain alkyl, alkylene, alkylene ether and alkenyl ether groups, and an ether linkage;

X is a hydrolyzable group capable of bonding to a siliceous substrate and of being displaced by a silicon-oxygen bond or a non-hydrolyzable organic functional group, wherein at least one of the X groups on each Si atom is hydrolyzable;

n is 0 or an integer which is no greater than 3;

y is 0 or an integer which is no greater than 3; and

wherein 2≦n+y≦3; and n and y are never both zero.

3. The polypodal silane compound according to claim 2 , wherein X is selected from an alkoxy group, a halogen, a carboxylate, and a non-hydrolyzable organic functional group.

4. The polypodal silane compound according to claim 2 , wherein R 1 is selected from substituted and unsubstituted, branched or straight chain alkyl or alkylene ether groups of from 1 to 30 carbons.

5. The polypodal silane compound according to claim 2 , wherein R 1 is capable of interacting, binding or covalently linking to a the biological polymer selected from the group consisting of peptides, polypeptides, oligonucleotides, and proteins bonded to the oxygen attached to R 1 in Formula (I) by an ester or amide linkage.

6. The polypodal silane compound according to claim 2 , wherein each of the X groups, is hydrolyzable.

7. The polypodal silane compound according to claim 2 , wherein n is 0; y is 2; R 2 is methyl; R 3 is selected from unsubstituted, straight chain alkyl groups of from 1 to 10 carbon atoms; and X is selected from the group consisting of methoxy, ethoxy, chlorine, acetate, methyl, and isopropyl.

8. The polypodal silane compound according to claim 7 , wherein R 3 has from 3 to 5 carbon atoms.

9. The polypodal silane compound according to claim 2 , wherein n is 2; y is 0; R 2 is methyl; R 3 is selected from unsubstituted, straight chain alkyl group of from 1 to 10 carbon atoms; R 4 is selected from unsubstituted, straight chain alkylene ethers of from 1 to 10 carbon atoms having a least one terminal ether linkage which bonds R 4 to R 3 ; and X is selected from the group consisting of methoxy, ethoxy, chlorine, acetate, methyl and isopropyl.

10. The polypodal silane compound according to claim 2 , wherein n is 2; y is 0; R 2 is a straight chain alkylene ether group of from 1 to 10 carbon atoms having at least one C—O—C ether linkage; R 3 is selected from unsubstituted, straight chain alkyl groups of from 1 to 10 carbon atoms; R 4 is selected from unsubstituted, straight chain alkylene ether groups of form 1 to 10 carbon atoms having at least one terminal ether linkage which bonds R 4 to R 3 ; and X is selected from the group consisting of methoxy, ethoxy, chlorine, acetate, methyl and isopropyl.

11. The polypodal silane compound according to claim 2 , wherein at least one of the podal branches bracketed in Formula (I) has two or more ether linkages.

Assignments (5)
RELEASE OF SECURITY INTEREST Recorded Oct 1, 2020
From: ANTARES CAPITAL LP
To: GELEST BIOSYSTEMS, LLC; GELEST, INC.; GELEST TECHNOLOGIES, INC.
Reel/Frame 053946/0556 →
RELEASE OF SECURITY INTEREST Recorded Jun 24, 2019
From: WELLS FARGO BANK, NATIONAL ASSOCIATION
To: GELEST TECHNOLOGIES, INC.; GELEST, INC.; GELEST BIOSYSTEMS, LLC
Reel/Frame 049567/0194 →
PATENT SECURITY AGREEMENT Recorded Jun 21, 2019
From: GELEST, INC.; GELEST TECHNOLOGIES, INC.; GELEST BIOSYSTEMS, LLC
To: ANTARES CAPITAL LP
Reel/Frame 049557/0526 →
SECURITY INTEREST Recorded Aug 14, 2017
From: GELEST, INC.; GELEST TECHNOLOGIES, INC.; GELEST BIOSYSTEMS, LLC
To: WELLS FARGO BANK, NATIONAL ASSOCIATION
Reel/Frame 043540/0963 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 14, 2005
From: ARKLES, BARRY C.; PAN, YOULIN
To: GELEST, INC.
Reel/Frame 016472/0569 →