Nucleoside monophosphate-templated green synthesis of AgNP: effects of reducing agents on the optical properties of as-synthesized AgNPs
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OpenAlex topics: Nanocluster Synthesis and Applications · Nanomaterials for catalytic reactions · Nanoparticles: synthesis and applications
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References (48)
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1. Nyabadza A, McCarthy É, Makhesana M, Heidarinassab S, Plouze A, Vazquez M, Brabazon D (2023) A review of physical, chemical and biological synthesis methods of bimetallic nanoparticles and applications in sensing, water treatment, biomedicine, catalysis and hydrogen storage. Adv Colloid Interface Sci 321:103010. https://doi.org/10.1016/J.CIS.2023.10301010.1016/J.CIS.2023.103010 ↗
2. Sharma NK, Vishwakarma J, Rai S, Alomar TS, Almasoud N, Bhattarai A (2022) Green route synthesis and characterization techniques of silver nanoparticles and their biological adeptness. ACS Omega 7:27004–27020. https://doi.org/10.1021/ACSOMEGA.2C01400/ASSET/IMAGES/LARGE/AO2C01400_0016.JPEG10.1021/ACSOMEGA.2C01400/ASSET/IMAGES/LARGE/AO2C01400_0016.JPEG ↗
3. Figat AM, Bartosewicz B, Liszewska M, Budner B, Norek M, Jankiewicz BJ (2023) α-Amino acids as reducing and capping agents in gold nanoparticles synthesis using the Turkevich method. Langmuir 39:8646–8657. https://doi.org/10.1021/ACS.LANGMUIR.3C00507/ASSET/IMAGES/LARGE/LA3C00507_0004.JPEG10.1021/ACS.LANGMUIR.3C00507/ASSET/IMAGES/LARGE/LA3C00507_0004.JPEG ↗
4. Ajitha B, Kumar Reddy YA, Reddy PS, Jeon HJ, Ahn CW (2016) Role of capping agents in controlling silver nanoparticles size, antibacterial activity and potential application as optical hydrogen peroxide sensor. RSC Adv 6:36171–36179. https://doi.org/10.1039/C6RA03766F10.1039/C6RA03766F ↗
5. Rodrigues TS, Zhao M, Yang TH, Gilroy KD, da Silva AGM, Camargo PHC, Xia Y (2018) Synthesis of colloidal metal nanocrystals: a comprehensive review on the reductants. Chem – Eur J 24:16944–16963. https://doi.org/10.1002/CHEM.20180219410.1002/CHEM.201802194 ↗
6. Jeevanandam J, Kiew SF, Boakye-Ansah S, Lau SY, Barhoum A, Danquah MK, Rodrigues J (2022) Green approaches for the synthesis of metal and metal oxide nanoparticles using microbial and plant extracts. Nanoscale 14:2534–2571. https://doi.org/10.1039/D1NR08144F10.1039/D1NR08144F ↗
7. Shirtcliffe N, Nickel U, Schneider S (1999) Reproducible preparation of silver sols with small particle size using borohydride reduction: for use as nuclei for preparation of larger particles. J Colloid Interface Sci 211:122–129. https://doi.org/10.1006/JCIS.1998.598010.1006/JCIS.1998.5980 ↗
8. Suriati G, Mariatti M, Azizan A (2014) Synthesis of silver nanoparticles by chemical reduction method: effect of reducing agent and surfactant concentration. Int J Automot Mech Eng 5:1920–1927. https://doi.org/10.15282/ijame.10.2014.9.016010.15282/ijame.10.2014.9.0160 ↗
9. Amirjani A, Firouzi F, Haghshenas DF (2020) Predicting the size of silver nanoparticles from their optical properties. Plasmonics 15:1077–1082. https://doi.org/10.1007/S11468-020-01121-X/FIGURES/310.1007/S11468-020-01121-X/FIGURES/3 ↗
10. Zhang XF, Liu ZG, Shen W, Gurunathan S (2016) Silver nanoparticles: synthesis, characterization, properties, applications, and therapeutic approaches. Int J Mol Sci 17:1534. https://doi.org/10.3390/IJMS1709153410.3390/IJMS17091534 ↗
11. Xu L, Wang YY, Huang J, Chen CY, Wang ZX, Xie H (2020) Silver nanoparticles: synthesis, medical applications and biosafety. Theranostics 10:8996–9031. https://doi.org/10.7150/THNO.4541310.7150/THNO.45413 ↗
12. Velgosova O, Mačák L, Čižmárová E, Mára V (2022) Influence of reagents on the synthesis process and shape of silver nanoparticles. Materials 15:6829. https://doi.org/10.3390/MA1519682910.3390/MA15196829 ↗
13. Dong X, Ji X, Jing J, Li M, Li J, Yang W (2010) Synthesis of triangular silver nanoprisms by stepwise reduction of sodium borohydride and trisodium citrate. J Phys Chem C 114:2070–2074. https://doi.org/10.1021/JP909964K/SUPPL_FILE/JP909964K_SI_001.PDF10.1021/JP909964K/SUPPL_FILE/JP909964K_SI_001.PDF ↗
14. Mirzaei A, Janghorban K, Hashemi B, Bonyani M, Leonardi SG, Neri G (2017) Characterization and optical studies of PVP-capped silver nanoparticles. J Nanostructure Chem 7:37–46. https://doi.org/10.1007/S40097-016-0212-3/FIGURES/1410.1007/S40097-016-0212-3/FIGURES/14 ↗
15. Agnihotri S, Mukherji S, Mukherji S (2013) Size-controlled silver nanoparticles synthesized over the range 5–100 nm using the same protocol and their antibacterial efficacy. RSC Adv 4:3974–3983. https://doi.org/10.1039/C3RA44507K10.1039/C3RA44507K ↗
16. Wu C, Zhou X, Wei J (2015) Localized surface plasmon resonance of silver nanotriangles synthesized by a versatile solution reaction. Nanoscale Res Lett 10:1–6. https://doi.org/10.1186/S11671-015-1058-1/TABLES/210.1186/S11671-015-1058-1/TABLES/2 ↗
17. Acharya D, Mohanta B, Pandey P, Singha M, Nasiri F (2017) Optical and antibacterial properties of synthesised silver nanoparticles. Micro Nano Lett 12:223–226. https://doi.org/10.1049/MNL.2016.066610.1049/MNL.2016.0666 ↗
18. Teng Y, Yang X, Han L, Wang E (2014) The relationship between DNA sequences and oligonucleotide-templated silver nanoclusters and their fluorescence properties. Chem Eur J 20:1111–1115. https://doi.org/10.1002/CHEM.20130147310.1002/CHEM.201301473 ↗
19. Ren X, Chen Z, Meng X, Chen D, Tang F (2012) Synthesis of fluorescent Ag nanoclusters and their application in α-L-fucosidase detection. Chem Comm 48:9504–9506. https://doi.org/10.1039/C2CC34112C10.1039/C2CC34112C ↗
20. Berti L, Burley GA (2008) Nucleic acid and nucleotide-mediated synthesis of inorganic nanoparticles. Nat Nanotechnol 3:81–87. https://doi.org/10.1038/NNANO.2007.46010.1038/NNANO.2007.460 ↗
21. Petty JT, Zheng J, Hud NV, Dickson RM (2004) DNA-templated Ag nanocluster formation. J Am Chem Soc 126:5207–5212. https://doi.org/10.1021/JA031931O/ASSET/IMAGES/LARGE/JA031931OF00008.JPEG10.1021/JA031931O/ASSET/IMAGES/LARGE/JA031931OF00008.JPEG ↗
22. Richards CI, Choi S, Hsiang JC, Antoku Y, Vosch T, Bongiorno A, Tzeng YL, Dickson RM (2008) Oligonucleotide-stabilized Ag nanocluster fluorophores. J Am Chem Soc 130:5038–5039. https://doi.org/10.1021/JA8005644/ASSET/IMAGES/LARGE/JA-2008-005644_0003.JPEG10.1021/JA8005644/ASSET/IMAGES/LARGE/JA-2008-005644_0003.JPEG ↗
23. Huang L, Li P, Lin C, Wu Y, Chen Z, Fu FF (2021) DNA-templated fluorescent silver nanoclusters on-off switch for specific and sensitive determination of organic mercury in seafood. Biosens Bioelectron 183:113217. https://doi.org/10.1016/J.BIOS.2021.11321710.1016/J.BIOS.2021.113217 ↗
24. Nie F, Ga L, Ai J (2019) One-pot synthesis of nucleoside-templated fluorescent silver nanoparticles and gold nanoparticles. ACS Omega 4:7643–7649. https://doi.org/10.1021/ACSOMEGA.9B00701/ASSET/IMAGES/LARGE/AO-2019-00701J_0003.JPEG10.1021/ACSOMEGA.9B00701/ASSET/IMAGES/LARGE/AO-2019-00701J_0003.JPEG ↗
25. Sharma B, Mahata A, Mandani S, Sarma TK, Pathak B (2016) Coordination polymer hydrogels through Ag(I)-mediated spontaneous self-assembly of unsubstituted nucleobases and their antimicrobial activity. RSC Adv 6:62968–62973. https://doi.org/10.1039/C6RA11137H10.1039/C6RA11137H ↗
26. New SY, Lee ST, Su XD (2016) DNA-templated silver nanoclusters: structural correlation and fluorescence modulation. Nanoscale 8:17729–17746. https://doi.org/10.1039/C6NR05872H10.1039/C6NR05872H ↗
27. Swasey SM, Leal LE, Lopez-Acevedo O, Pavlovich J, Gwinn EG (2015) Silver (I) as DNA glue: Ag+-mediated guanine pairing revealed by removing Watson-Crick constraints. Sci Rep 5:1–9. https://doi.org/10.1038/srep1016310.1038/srep10163 ↗
28. Martin RB (1985) Nucleoside sites for transition metal ion binding. Acc Chem Res 18:32–38. https://doi.org/10.1021/AR00110A001/ASSET/AR00110A001.FP.PNG_V0310.1021/AR00110A001/ASSET/AR00110A001.FP.PNG_V03 ↗
29. Sigel H (1993) Interactions of metal ions with nucleotides and nucleic acids and their constituents. Chem Soc Rev 22:255–267. https://doi.org/10.1039/CS993220025510.1039/CS9932200255 ↗
30. Sharma J, Yeh HC, Yoo H, Werner JH, Martinez JS (2010) A complementary palette of fluorescent silver nanoclusters. Chem Comm 46:3280–3282. https://doi.org/10.1039/B927268B10.1039/B927268B ↗
31. Li J, Zhu Z, Liu F, Zhu B, Ma Y, Yan J, Lin B, Ke G, Liu R, Zhou L, Tu S, Yang C (2016) DNA-mediated morphological control of silver nanoparticles. Small 12:5449–5487. https://doi.org/10.1002/SMLL.20160133810.1002/SMLL.201601338 ↗
32. Gogoi A, Mazumder N, Konwer S, Ranawat H, Chen NT, Zhuo GY (2019) Enantiomeric recognition and separation by chiral nanoparticles. Molecules 24:1007. https://doi.org/10.3390/MOLECULES2406100710.3390/MOLECULES24061007 ↗
33. Jafari M, Tashkhourian J, Absalan G (2018) Chiral recognition of tryptophan enantiomers using chitosan-capped silver nanoparticles: scanometry and spectrophotometry approaches. Talanta 178:870–878. https://doi.org/10.1016/J.TALANTA.2017.10.00510.1016/J.TALANTA.2017.10.005 ↗
34. Obaid A, Mohd Jamil AK, Saharin SM, Mohamad S (2021) L-cysteine capped silver nanoparticles as chiral recognition sensor for ketoprofen enantiomers. Chirality 33:810–823. https://doi.org/10.1002/CHIR.2335410.1002/CHIR.23354 ↗
35. Zhang M, Ye BC (2011) Colorimetric chiral recognition of enantiomers using the nucleotide-capped silver nanoparticles. Anal Chem 83:1504–1509. https://doi.org/10.1021/AC102922F/SUPPL_FILE/AC102922F_SI_001.PDF10.1021/AC102922F/SUPPL_FILE/AC102922F_SI_001.PDF ↗
36. Wang Y, Chen Y, Bian H, Sun Y, Zhu L, Xia D (2021) Highly selective and sensitive chiral recognition to deoxynucleosides by calixarene oligomers modified silver nanoparticles. Sens Actuators B Chem 341:130044. https://doi.org/10.1016/J.SNB.2021.13004410.1016/J.SNB.2021.130044 ↗
37. Liu C, Lian J, Liu Q, Xu C, Li B (2016) β-Cyclodextrin-modified silver nanoparticles as colorimetric probes for the direct visual enantioselective recognition of aromatic α-amino acids. Anal Methods 8:5794–5800. https://doi.org/10.1039/C6AY01308B10.1039/C6AY01308B ↗
38. Muhammed MAH, Aldeek F, Palui G, Trapiella-Alfonso L, Mattoussi H (2012) Growth of in situ functionalized luminescent silver nanoclusters by direct reduction and size focusing. ACS Nano 6:8950–8961. https://doi.org/10.1021/NN302954N/SUPPL_FILE/NN302954N_SI_001.PDF10.1021/NN302954N/SUPPL_FILE/NN302954N_SI_001.PDF ↗
39. Kundu S (2013) Formation of self-assembled Ag nanoparticles on DNA chains with enhanced catalytic activity. Phys Chem Chem Phys 15:14107–14119. https://doi.org/10.1039/C3CP51890F10.1039/C3CP51890F ↗
40. Fan Z, Govorov AO (2010) Plasmonic circular dichroism of chiral metal nanoparticle assemblies. Nano Lett 10:2580–2587. https://doi.org/10.1021/NL101231B/SUPPL_FILE/NL101231B_SI_001.PDF10.1021/NL101231B/SUPPL_FILE/NL101231B_SI_001.PDF ↗
41. Govorov AO, Fan Z, Hernandez P, Slocik JM, Naik RR (2010) Theory of circular dichroism of nanomaterials comprising chiral molecules and nanocrystals: plasmon enhancement, dipole interactions, and dielectric effects. Nano Lett 10:1374–1382. https://doi.org/10.1021/NL100010V/SUPPL_FILE/NL100010V_SI_001.PDF10.1021/NL100010V/SUPPL_FILE/NL100010V_SI_001.PDF ↗
42. Yoshida H, Ehara M, Priyakumar UD, Kawai T, Nakashima T (2020) Enantioseparation and chiral induction in Ag29 nanoclusters with intrinsic chirality. Chem Sci 11:2394–2400. https://doi.org/10.1039/C9SC05299B10.1039/C9SC05299B ↗
43. Maoz BM, Van Der Weegen R, Fan Z, Govorov AO, Ellestad G, Berova N, Meijer EW, Markovich G (2012) Plasmonic chiroptical response of silver nanoparticles interacting with chiral supramolecular assemblies. J Am Chem Soc 134:17807–17813. https://doi.org/10.1021/JA309016K/SUPPL_FILE/JA309016K_SI_001.PDF10.1021/JA309016K/SUPPL_FILE/JA309016K_SI_001.PDF ↗
44. Nishida N, Yao H, Kimura K (2008) Chiral functionalization of optically inactive monolayer-protected silver nanoclusters by chiral ligand-exchange reactions. Langmuir 24:2759–2766. https://doi.org/10.1021/LA703351P/SUPPL_FILE/LA703351P-FILE001.PDF10.1021/LA703351P/SUPPL_FILE/LA703351P-FILE001.PDF ↗
45. Loo K, Degtyareva N, Park J, Sengupta B, Reddish M, Rogers CC, Bryant A, Petty JT (2010) Ag+-mediated assembly of 5′-guanosine monophosphate. J Phys Chem B 114:4320–4326. https://doi.org/10.1021/JP908085S/ASSET/IMAGES/LARGE/JP-2009-08085S_0005.JPEG10.1021/JP908085S/ASSET/IMAGES/LARGE/JP-2009-08085S_0005.JPEG ↗
46. Hu Y, Xie D, Wu Y, Lin N, Song A, Hao J (2017) Hydrogels based on Ag+-modulated assembly of 5′-adenosine monophosphate for enriching biomolecules. Chem Eur J 23:15721–15728. https://doi.org/10.1002/CHEM.20170318010.1002/CHEM.201703180 ↗
47. Mu X, Wu M, Zhang B, Liu X, Xu S, Huang Y, Wang X, Song D, Ma P, Sun Y (2021) A sensitive “off-on” carbon dots-Ag nanoparticles fluorescent probe for cysteamine detection via the inner filter effect. Talanta 221:121463. https://doi.org/10.1016/J.TALANTA.2020.12146310.1016/J.TALANTA.2020.121463 ↗
48. Diamai S, Negi DPS (2019) Cysteine-stabilized silver nanoparticles as a colorimetric probe for the selective detection of cysteamine. Spectrochim Acta A Mol Biomol Spectrosc 215:203–208. https://doi.org/10.1016/J.SAA.2019.02.10110.1016/J.SAA.2019.02.101 ↗