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US 2015/0375180 A1Published application
Separation of nanoparticles
AssigneeYeda Research and Development Co. Ltd.
InventorsBoris RYBTCHINSKI, Elisha M. KRIEG, Haim WEISSMAN, Shira ALBECK, Yaron TlDHAR, Erez COHEN
Life of this patent
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Abstract
This invention is directed to separation, optimization and purification of nano-materials using self-assembled perylene diimide membranes, wherein said perylene diimide membrane is recyclable.
Claims18
Noncovalent self-assembled porous membrane comprising a perylene diimide supramolecular structure, which provides a chromatography medium for size-selective separation of nano-material;
- wherein said perylene diimide supramolecular structure comprises a mixture of perylene diimide compounds, wherein each perylene diimide compound is a monomeric unit represented by the structure of formula I:
- wherein
- R1 and R1′ are each independently [(CH2)qO]rCH3, [(CH2)qO]rH [(CH2)qC(O)O]rCH3, [(CH2)qC(O)NH]rCH3, [(CH2)qCH2═CH2]rCH3, [(CH2)qCH≡CH]rCH3, [(CH2)qNH]rCH3, [(alkylene)qO]rCH3, [(alkylene)qC(O)O]rCH3, [(alkylene)qC(O)NH]rCH3, [(alkylene)qCH2═CH2]rCH3, [(alkylene)qCH≡CH]rCH3, [(alkylene)qNH]rCH3, (C1-C32)alkyl, (C3-C8)cycloalkyl, aryl, heteroaryl, chiral group, (C1-C32)alkyl-COOH, (C1-C32)alkyl-Si-A, or [C(O)CHR3NH]pH wherein said aryl or heteroaryl groups are optionally substituted by 1-3 groups comprising halide, CN, CO2H, OH, SH, NH2, CO2—(C1-C6 alkyl) or O—(C1-C6 alkyl);
- wherein A comprises three same or different of the following substituents Cl, Br, I, O(C1-C8)alkyl or (C1-C8)alkyl;
- and wherein R3 in said [C(O)CHR3NH]pH is an alkyl, haloalkyl, hydroxyalkyl, hydroxyl, aryl, phenyl, alkylphenyl, alkylamino and independently the same or different when p is larger than 1;
- R2 and R2′ are each independently [(CH2)qO]rCH3, [(CH2)qC(O)O]rCH3, [(CH2)qC(O)NH]rCH3, [(CH2)qCH2═CH2]rCH3, [(CH2)qCH≡CH]rCH3, [(CH2)qNH]rCH3, [(alkylene)qO]rCH3, [(alkylene)qC(O)O]rCH3, [(alkylene)qC(O)NH]rCH3, [(alkylene)qCH2═CH2]rCH3, [(alkylene)qCH≡CH]rCH3, [(alkylene)qNH]rCH3, (C1-C32)alkyl, (C3-C8)cycloalkyl, aryl, heteroaryl, chiral group, (C1-C32)alkyl-COOH, (C1-C32)alkyl-Si-A, or [C(O)CHR4NH]5H wherein said aryl or heteroaryl groups are optionally substituted by 1-3 groups comprising halide, CN, CO2H, OH, SH, NH2, CO2—(C1-C6 alkyl) or O—(C1-C6 alkyl);
- wherein A comprises three same or different of the following substituents Cl, Br, I, O(C1-C8)alkyl or (C1-C8)alkyl;
- and wherein R4 in said [C(O)CHR4NH]5H is an alkyl, haloalkyl, hydroxyalkyl, hydroxyl, aryl, phenyl, alkylphenyl, alkylamino and independently the same or different when s is larger than 1;
- R5 and R5′ are each independently R5 and R5′ are each independently H, —ORx where Rx is C1-C6 alkyl, [(CH2)nO]oCH3 or [(CH2)nO]oH;
- [(CH2)nC(O)O]oCH3, [(CH2)nC(O)NH]oCH3, [(CH2)nCH2═CH2]oCH3, [(CH2)nCH≡CH]oCH3, [(CH2)nNH]oCH3, [(alkylene)nO]oCH3, [(alkylene)nC(O)O]oCH3, [(alkylene)nC(O)NH]oCH3, [(alkylene)nCH2═CH2]oCH3, [(alkylene)nCH≡CH]oCH3, [(alkylene)nNH]oCH3, aryl, heteroaryl, C≡C—R7, CH═CR8R9, NR10R11, chiral group, amino acid, peptide or a saturated carbocyclic or heterocyclic ring wherein said saturated heterocyclic ring or heteroaryl contains at least one nitrogen atom and R5 or R5′ are connected via the nitrogen atom and wherein said saturated carbocyclic ring, heterocyclic ring, aryl and heteroaryl groups are optionally substituted by 1-3 groups comprising halide, aryl, heteroaryl, CN, CO2H, OH, SH, NH2, CO2—(C1-C6 alkyl) or O—(C1-C6 alkyl);
- R7 is H, halo, (C1-C32)alkyl, aryl, NH2, alkyl-amino, COOH, C(O)H, alkyl-COOH heteroaryl, Si(H)3 or Si[(C1-C8)alkyl]3 wherein said aryl or heteroaryl groups are optionally substituted by 1-3 groups comprising halide, aryl, heteroaryl, CN, CO2H, OH, SH, NH2, CO2—(C1-C6 alkyl) or O—(C1-C6 alkyl);
- R8, R9, R10 and R11 are each independently H, (C1-C32)alkyl, aryl, NH2, alkyl-amino, COOH, C(O)H, alkyl-COOH or heteroaryl wherein said aryl or heteroaryl groups are optionally substituted by 1-3 groups comprising halide, CN, CO2H, OH, SH, NH2, CO2—(C1-C6 alkyl) or O—(C1-C6 alkyl);
- L is a linker;
- n is an integer from 1-5;
- o is an integer from 1-100;
- p is an integer from 1-100;
- q is an integer from 1-5;
- r is an integer from 1-100;
- and
- s is an integer from 1-100;
- wherein if R5 and/or R5′ are chiral;
- said membrane will form a chiral membrane;
- wherein said mixture comprises between 2 to 10 different perylene diimide compounds of formula I.
20 more elements
The method of claim 17, wherein said recycling comprises;
- (a) washing said solid support with the noncovalent selfassembled perylene diimide based membrane and the retentate deposited thereon, with a solution of alcohol and water;
- (b) extracting said perylene diimide structure from said solution with an organic solvent;
- and (c) isolating said perylene diimide from said organic solvent.
- The method of claim 18, wherein said isolated perylene diimide can be further used to form a noncovalent selfassembled perylene diimide based membrane in aqueous conditions.
1 more element
Dependencies are inferred from the claim text.