A structure-function relationship for the optical modulation of phenyl boronic acid-grafted, polyethylene glycol-wrapped single-walled carbon nanotubes

Journal of the American Chemical Society

Volumn 134, Issue 42, 2012, Pages 17620-17627

  Mu, Bin ^a   Mcnicholas, Thomas P ^a   Zhang, Jingqing ^a   Hilmer, Andrew J ^a   Jin, Zhong ^a   Reuel, Nigel F ^a   Kim, Jong Ho ^b   Yum, Kyungsuk ^a   Strano, Michael S ^a  

^a Massachusetts Institute of Technology Cambridge   (United States)

^b Hanyang University   (South Korea)

Author keywords

[No Author keywords available]

Indexed keywords

ALKYL GROUPS; AQUEOUS DISPERSIONS; AROMATIC RINGS; BINDING LIGANDS; BORONIC ACID; BRANCHED POLYMER; ELECTRON-DONATING GROUP; ELECTRON-WITHDRAWING SUBSTITUENTS; ELECTRONWITHDRAWING; HIGH SELECTIVITY; HOMOLOGOUS SERIES; HYDROPHILIC POLYMERS; LINEAR DIELECTRIC; NEAR-INFRARED FLUORESCENCE; NITRO GROUP; PHENYL RINGS; PHENYLBORONIC ACIDS; PHOTOLUMINESCENCE QUANTUM YIELDS; POLYMER SURFACE COVERAGE; SACCHARIDE RECOGNITION; SOLVATOCHROMIC SHIFTS; STRUCTURAL ISOMERS; STRUCTURE-FUNCTION RELATIONSHIP;

AMIDES; CONJUGATED POLYMERS; FRUCTOSE; GRAPHENE; MODULATION; OPTICAL PROPERTIES; PHOTOLUMINESCENCE; POLYETHYLENE GLYCOLS; POLYMERS; QUANTUM YIELD; SINGLE-WALLED CARBON NANOTUBES (SWCN);

ISOMERS;

2 CARBOXYPHENYLBORONIC ACID; 3 CARBOXY 5 FLUORO PHENYLBORONIC ACID; 3 CARBOXY 5 NITRO PHENYLBORONIC ACID; 3 CARBOXYPHENYLBORONIC ACID; 4 CARBOXYPHENYLBORONIC ACID; 5 BROMO 3 CARBOXY PHENYLBORONIC ACID; ALKYL GROUP; AMIDE; ARABINOSE; BORONIC ACID DERIVATIVE; CARBOHYDRATE; FRUCTOSE; MACROGOL; N (4 PHENYLBORONIC)SUCCINAMIC ACID; POLYMER; RIBOSE; SINGLE WALLED NANOTUBE; UNCLASSIFIED DRUG; XYLOSE;

ARTICLE; CHEMICAL STRUCTURE; CONTROLLED STUDY; DIELECTRIC CONSTANT; DISPERSION; ELECTRON TRANSPORT; FLUORESCENCE SPECTROSCOPY; ISOMER; MOLECULAR MODEL; MOLECULAR RECOGNITION; NEAR INFRARED SPECTROSCOPY; PHOTOLUMINESCENCE; QUANTUM YIELD; STRUCTURE ACTIVITY RELATION;

BORONIC ACIDS; MOLECULAR STRUCTURE; NANOTUBES, CARBON; OPTICAL PROCESSES; POLYETHYLENE GLYCOLS;

EID: 84867815939     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja307085h     Document Type: Article

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