US2023104413A1PendingUtilityA1
Nanoparticles for chemiresistor sensors
Est. expiryOct 6, 2041(~15.2 yrs left)· nominal 20-yr term from priority
G01N 33/0047G01N 27/127B82Y 15/00
54
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Claims
Abstract
A nanoparticle characterized by sensitivity to an analyte of interest, and comprising a conductive core in contact with a plurality of ligands bound to the conductive core is disclosed. Additionally, a chemiresistor sensor comprising the nanoparticles of the invention and a method of using thereof such as for detection of an analyte of interest in a gaseous sample are disclosed.
Claims
exact text as granted — not AI-modified1 . A nanoparticle, comprising a conductive core in contact with a plurality of ligands bound to said core, wherein:
wherein the ligand comprises an alkyl-aryl moiety comprising at least 2 aliphatic carbon atoms and the plurality of ligands are assembled to form a shell on top of said core; and wherein said nanoparticle is characterized by sensitivity to an analyte of interest.
2 . The nanoparticle of claim 1 , wherein each of the plurality of ligands is bound to the core via a covalent bond and wherein the covalent bond comprises a coordinative bond.
3 . The nanoparticle of claim 1 , wherein each core independently comprises a transitional metal, optionally wherein the transitional metal is substantially in an elemental state within said core.
4 . The nanoparticle of claim 1 , wherein the ligand is represented by Formula 1:
wherein:
R represents an additional moiety covalently bound to said core;
each R1 independently represents a substituent or H;
each X and X1 independently represents a heteroatom, —CHR1-, —CR1R1-, or is absent;
A represents an optionally substituted aryl, an optionally substituted heteroaryl, a polycyclic aryl or any combination thereof;
n and k are integers each independently ranging from 0 to 5; and
m is an integer ranging from 1 to 5.
5 . The nanoparticle of claim 4 , wherein said heteroatom is selected from the group consisting of O, S, NH, NR1, PH and PR1 or a combination thereof; and if X1 represents the heteroatom then k ranges between 1 and 5.
6 . The nanoparticle of claim 4 , wherein the additional moiety comprises thio, carboxy, carbonyl, amino, hydroxy, amide, optionally substituted disulfide, silyl, diazo, heteroaryl, an olefin, phosphate, silyl, phosphine, including any salts, any derivative or any combination thereof.
7 . The nanoparticle of claim 4 , wherein said additional moiety comprises thio or thiolate, and wherein the alkyl-aryl moiety is represented by Formula 2:
wherein:
each R1 independently represents a substituent or H;
each X and X1 independently represents a heteroatom, or is absent;
A represents an optionally substituted aryl, an optionally substituted heteroaryl, or any combination thereof the dashed line represents an attachment point to the additional moiety;
the heteroatom is selected from the group consisting of O, S, NH, and NR1, or a combination thereof;
n is an integer each independently being 0 or 1;
k is an integer ranging from 0 to 5;
m is an integer ranging from 1 to 5; and if X1 represents the heteroatom then k ranges between 1 and 5.
8 . The nanoparticle of claim 7 , wherein m and k each independently is 1 or 2.
9 . The nanoparticle of claim 1 , wherein the alkyl-aryl moiety comprises an aryl substituted in meta-, or in para-position.
10 . The nanoparticle of claim 1 , wherein the alkyl-aryl moiety is represented by Formula 3:
wherein m is 2, and wherein k is between 1 and 3.
11 . The nanoparticle of claim 1 , wherein the ligand comprises at least one of:
wherein L comprises ethyl or butyl.
12 . The nanoparticle of claim 7 , wherein said substituted comprises one or more substituents, each independently selected from the group consisting of: C 1 -C 6 alkyl, halo, —NO 2 , —CN, —OH, —NH 2 , carbonyl, —CONH 2 , —CONR′2, —CNNR 2 , —CSNR 2 , —CONH—OH, —CONH—NH 2 , —NHCOR′, —NHCSR′, —NHCNR′, —NC(═O)OR′, —NC(═O)NR′, —NC(═S)OR′, —NC(═S)NR′, —SO 2 R′, —SOR′, —SR′, —SO 2 OR′, —SO 2 N(R′) 2 , —NHNR′ 2 , —NNR′, —NH(C 1 -C 6 alkyl), —N(C 1 -C 6 alkyl) 2 , C 1 -C 6 alkoxy, C 1 -C 6 haloalkoxy, hydroxy(C 1 -C 6 alkyl), hydroxy(C 1 -C 6 alkoxy), alkoxy(C 1 -C 6 alkyl), alkoxy(C 1 -C 6 alkoxy), amino(C 1 -C 6 alkyl), —CONH(C 1 -C 6 alkyl), —CON(C 1 -C 6 alkyl) 2 , —CO 2 H, —CO 2 R′, —OCOR′, —OCOR′, —OC(═O)OR′, —OC(═O)NR′, —OC(═S)OR′, —OC(═S)NR′, a heteroatom, an optionally substituted cycloalkyl, an optionally substituted heterocyclyl, or a combination thereof, wherein each R′ is independently selected from hydrogen, alkyl, alkenyl, aryl, heteroaryl a heteroatom, an optionally substituted cycloalkyl, an optionally substituted heterocyclyl, or any combination thereof.
13 . The nanoparticle of claim 1 , wherein said analyte of interest is a volatile organic compound (VOC) selected from an optionally unsaturated C1-C20 aldehyde, and an optionally unsaturated C1-C20alkane, or both.
14 . A chemiresistor sensor comprising:
at least two electrodes; and a sensing element electrically connected to the two electrodes and comprising a structure made from a plurality of nanoparticles, wherein: each nanoparticle comprises a metal core in contact with a plurality of ligands bound to said core; each ligand comprises an alkyl-aryl moiety; and the plurality of ligands are assembled to form a shell on top of said core;
15 . The chemiresistor sensor of claim 14 , wherein each ligand is covalently bound to said core via an additional moiety and wherein the alkyl-aryl moiety is represented by Formula 2:
wherein:
each R1 independently represents a substituent or H;
each X and X1 independently represents a heteroatom, or is absent;
A represents an optionally substituted aryl, an optionally substituted heteroaryl, or any combination thereof; the dashed line represents an attachment point to the additional moiety;
the heteroatom is selected from the group consisting of O, S, NH, and NR1, or a combination thereof;
n is an integer each independently being 0 or 1;
k is an integer ranging from 0 to 5;
m is an integer ranging from 1 to 5; and if X1 represents the heteroatom then k ranges between 1 and 5.
16 . The chemiresistor sensor of claim 15 , wherein the additional moiety comprises thio or thiolate.
17 . The chemiresistor sensor of claim 14 , wherein the ligand comprises at least one of:
wherein L comprises ethyl or butyl.
18 . The chemiresistor sensor of claim 14 , wherein the sensor is configured for selective detection of the analyte of interest within a gaseous sample, wherein a concentration of the analyte of interest within the sample is between 1 ppb and 1 ppm.
19 . A method for detection of an analyte of interest in a gaseous sample, comprising:
a. exposing the chemiresistor sensor of claim 14 to the sample comprises a plurality of VOCs; b. providing electricity to the sensor, so as to obtain a plurality of values generated by the sensor, wherein the plurality of values are selected from: conductivity, resistivity, capacity, impedance, current and voltage of the sensor; and c. analyzing said values, thereby determining the presence of the analyte of interest within said sample, wherein the analyte of interest comprises a VOC selected from an aldehyde, an alkane or both.
20 . The method of claim 19 , wherein the analyzing step further comprises determining a concentration of the analyte of interest within the sample, and wherein a concentration of the analyte of interest within the sample is between 1 ppb and 1 ppm.Cited by (0)
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