Synthesis of SERS active nanoparticles for detection of biomolecules

Tetrahedron

Volumn 68, Issue 4, 2012, Pages 1230-1240

  Wrzesien, Joanna ^a   Graham, Duncan ^a  

^a UNIVERSITY OF STRATHCLYDE   (United Kingdom)

Author keywords

DNA; Linker; Nanoparticle; SERS

Indexed keywords

1 [9 [5 [5 (1,2 DITHIOLAN 3 YL)PENTANAMIDO] 2 (ETHOXYCARBONYL)PHENYL] 3 OXO 3H XANTHEN 6 YLOXY] 2 OXO 6,9,12 TRIOXA 3 AZAPENTADECAN 15 OIC ACID; 2 [9 [5 AMINO 2 (ETHOXYCARBONYL)PHENYL] 3 OXO 3H XANTHEN 6 YLOXY]ACETIC ACID; 4 (4,6 DIMETHOXY 1,3,5 TRIAZIN 2 YL) 4 METHYLMORPHOLINIUM CHLORIDE; 6 AMINOFLUORESCEIN; BENZOIC ACID DERIVATIVE; CARBOXYL GROUP; CITRATE EDETIC ACID; CITRIC ACID; DNA; ETHYL 2 (6 HYDROXY 3 OXO 3H XANTHEN 9 YL)BENZOATE; ETHYL 2 [6 (2 TERT BUTOXY 2 OXOETHOXY) 3 OXO 3H XANTHEN 9 YL]BENZOATE; ETHYL 4 AMINO 2 (6 HYDROXY 3 OXO 3H XANTHEN 9 YL)BENZOATE; ETHYL 4 AMINO 2 [(6 TERT BUTOXY 2 OXOETHOXY) 3 OXO 3H XANTHEN 9 YL]BENZOATE; FLUORESCEIN; FLUORESCENT DYE; GOLD CITRATE; MACROGOL; N HYDROXYSULFOSUCCINIMIDE; N(3 DIMETHYLAMINOPROPYL)N' ETHYLCARBODIIMIDE HYDROCHLORIDE; NANOPARTICLE; OLIGONUCLEOTIDE; SILVER CITRATE; TERT BUTYL 1 [9 [5 (1,2 DITHIOLAN 3 YL)PENTANAMIDO] 2 [(ETHOXYCARBONYL)PHENYL] 3 OXO 3H XANTHEN 6 YLOXY] 2 OXO 6,9,12 TRIOXA 3 AZAPENTADECAN 15 OATE; TERT BUTYL 1 [[9 (5 AMINO 2 ETHOXYCARBONYL)PHENYL] 3 OXO 3H XANTHEN 6 YLOXY] 2 OXO 6,9,12 TRIOXA 3 AZAPENTADECAN 15 OATE; TERT BUTYL 10 [[(9H FLUOREN 9 YL)METHOXY]CARBONYLAMINO] 2,2 DIMETHYL 4,11 DIOXO 3,5,18,21 TETRAOXA 5,12 DIAZATETRACOSAN 24 OATE; TERT BUTYL 15 AMINO 25 (1,2 DITHIOLAN 3 YL) 14,21 DIOXO 4,7,10 TRIOXA 13,20 DIAZAPENTACOSAN 1 OATE; TERT BUTYL 5 (4 AMINOBUTYL) 1 (9H FLUOREN 9 YL) 3,6 DIOXO 2,10,13,16 TETRAOXA 4,7 DIAZANONADECAN 19 OATE; TETRAMETHYLRHODAMINE; THIOCTIC ACID; UNCLASSIFIED DRUG; UNINDEXED DRUG;

ARTICLE; CHEMICAL ANALYSIS; DNA SEQUENCE; DNA SYNTHESIS; DRUG CONJUGATION; DRUG STABILITY; FLUORESCENCE; LASER; PRIORITY JOURNAL; RAMAN SPECTROMETRY; SURFACE PROPERTY; ZETA POTENTIAL;

EID: 84855453282     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2011.11.053     Document Type: Article

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