275
Devi LB, Mandal AB (2013) Self-assembly of Ag nanoparticles using hydroxypropyl cyclodextrin: synthesis, characterisation and application for the catalytic reduction of p-nitrophenol.
RSC Adv 3:5238–5253. https://doi.org/10.1039/C3RA23014G
Ferreira M, Jérôme F, Bricout H, Menuel S, Landy D, Fourmentin S, Tilloy S, Monflier E (2015)
Rhodium catalyzed hydroformylation of 1-decene in low melting mixtures based on various
cyclodextrins and N,N′-dimethylurea. Catal Commun 63:62–65. https://doi.org/10.1016/j.
catcom.2014.11.001
Francisco M, van den Bruinhorst A, Kroon MC (2013) Low-transition-temperature mixtures
(LTTMs): a new generation of designer solvents. Angew Chem Int Ed Engl 52:3074–3085.
https://doi.org/10.1002/anie.201207548
Gannimani R, Ramesh M, Mtambo S, Pillay K, Soliman ME, Govender P (2016) γ-Cyclodextrin
capped silver nanoparticles for molecular recognition and enhancement of antibacterial activity of chloramphenicol. J Inorg Biochem 157:15–24. https://doi.org/10.1016/j.
jinorgbio.2016.01.008
Girish YR, Sharath Kumar KS, Thimmaiah KN, Rangappa KS, Shashikanth S (2015) ZrO 2 -βcyclodextrin catalyzed synthesis of 2,4,5-trisubstituted imidazoles and 1,2-disubstituted benzimidazoles under solvent free conditions and evaluation of their antibacterial study. RSC Adv
5:75533–75546. https://doi.org/10.1039/C5RA13891D
Gopalan AI, Lee K-P, Manesh KM, Santhosh P, Kim JH (2006) Gold nanoparticles dispersed into
poly(aminothiophenol) as a novel electrocatalyst – fabrication of modified electrode and evaluation of electrocatalytic activities for dioxygen reduction. J Mol Catal A Chem 256:335–345.
https://doi.org/10.1016/j.molcata.2006.05.027
Guerrero M, Coppel Y, Chau NTT, Rucoux A, Denicourt-Nowicki A, Monflier E, Bricout H,
Lecante P, Philippot K (2013) Efficient ruthenium nanocatalysts in liquid-liquid biphasic
hydrogenation catalysis: towards a supramolecular control through a sulfonated diphosphinecyclodextrin smart combination. ChemCatChem 5:3802–3811. https://doi.org/10.1002/
cctc.201300467
Guerrero M, Chau NTT, Roucoux A, Nowicki-Denicourt A, Monflier E, Bricout H, Philippot K
(2014) Organometallic synthesis of water-soluble ruthenium nanoparticles in the presence of
sulfonated diphosphines and cyclodextrins. Mater Res Soc Symp Proc 1675:219–225. https://
doi.org/10.1557/opl.2014.888
Haldar KK, Kundu S, Patra A (2014) Core-size-dependent catalytic properties of bimetallic Au/Ag
core-shell nanoparticles. ACS Appl Mater Interfaces 6:21946–21953. https://doi.org/10.1021/
am507391d
Haw C, Chiu W, Khanis NH, Rahman SA, Khiew P, Radiman S, Abd-Shukor R, Abdul Hamid
MA (2016) Tin stearate organometallic precursor prepared SnO 2 quantum dots nanopowder
for aqueous- and non-aqueous medium photocatalytic hydrogen gas evolution. J Energy Chem
25:691–701. https://doi.org/10.1016/j.jechem.2016.04.006
Herbois R, Noël S, Léger B, Bai L, Roucoux A, Monflier E, Ponchel A (2012) Cyclodextrins as
growth controlling agents for enhancing the catalytic activity of PVP-stabilized Ru(0) nanoparticles. Chem Commun 48:3451–3453. https://doi.org/10.1039/c2cc17355g
Herbois R, Noël S, Léger B, Tilloy S, Menuel S, Addad A, Martel B, Ponchel A, Monflier E
(2015) Ruthenium-containing β-cyclodextrin polymer globules for the catalytic hydrogenation
of biomass-derived furanic compounds. Green Chem 17:2444–2454. https://doi.org/10.1039/
c5gc00005j
Hirano K, Takano S, Tsukuda T (2019) Asymmetric aerobic oxidation of secondary alcohols
catalyzed by poly(N-vinyl-2-pyrrolidone)-stabilized gold clusters modified with cyclodextrin
derivatives. Chem Commun 55:15033–15036. https://doi.org/10.1039/C9CC06770A
Huang T, Meng F, Qi L (2009) Facile synthesis and one-dimensional assembly of cyclodextrincapped gold nanoparticles and their applications in catalysis and surface-enhanced Raman
scattering. J Phys Chem C 113:13636–13642. https://doi.org/10.1021/jp903405y
5 Metal Nanoparticles and Cyclodextrins for Catalytic Applications
Devi LB, Mandal AB (2013) Self-assembly of Ag nanoparticles using hydroxypropyl cyclodextrin: synthesis, characterisation and application for the catalytic reduction of p-nitrophenol.
RSC Adv 3:5238–5253. https://doi.org/10.1039/C3RA23014G
Ferreira M, Jérôme F, Bricout H, Menuel S, Landy D, Fourmentin S, Tilloy S, Monflier E (2015)
Rhodium catalyzed hydroformylation of 1-decene in low melting mixtures based on various
cyclodextrins and N,N′-dimethylurea. Catal Commun 63:62–65. https://doi.org/10.1016/j.
catcom.2014.11.001
Francisco M, van den Bruinhorst A, Kroon MC (2013) Low-transition-temperature mixtures
(LTTMs): a new generation of designer solvents. Angew Chem Int Ed Engl 52:3074–3085.
https://doi.org/10.1002/anie.201207548
Gannimani R, Ramesh M, Mtambo S, Pillay K, Soliman ME, Govender P (2016) γ-Cyclodextrin
capped silver nanoparticles for molecular recognition and enhancement of antibacterial activity of chloramphenicol. J Inorg Biochem 157:15–24. https://doi.org/10.1016/j.
jinorgbio.2016.01.008
Girish YR, Sharath Kumar KS, Thimmaiah KN, Rangappa KS, Shashikanth S (2015) ZrO 2 -βcyclodextrin catalyzed synthesis of 2,4,5-trisubstituted imidazoles and 1,2-disubstituted benzimidazoles under solvent free conditions and evaluation of their antibacterial study. RSC Adv
5:75533–75546. https://doi.org/10.1039/C5RA13891D
Gopalan AI, Lee K-P, Manesh KM, Santhosh P, Kim JH (2006) Gold nanoparticles dispersed into
poly(aminothiophenol) as a novel electrocatalyst – fabrication of modified electrode and evaluation of electrocatalytic activities for dioxygen reduction. J Mol Catal A Chem 256:335–345.
https://doi.org/10.1016/j.molcata.2006.05.027
Guerrero M, Coppel Y, Chau NTT, Rucoux A, Denicourt-Nowicki A, Monflier E, Bricout H,
Lecante P, Philippot K (2013) Efficient ruthenium nanocatalysts in liquid-liquid biphasic
hydrogenation catalysis: towards a supramolecular control through a sulfonated diphosphinecyclodextrin smart combination. ChemCatChem 5:3802–3811. https://doi.org/10.1002/
cctc.201300467
Guerrero M, Chau NTT, Roucoux A, Nowicki-Denicourt A, Monflier E, Bricout H, Philippot K
(2014) Organometallic synthesis of water-soluble ruthenium nanoparticles in the presence of
sulfonated diphosphines and cyclodextrins. Mater Res Soc Symp Proc 1675:219–225. https://
doi.org/10.1557/opl.2014.888
Haldar KK, Kundu S, Patra A (2014) Core-size-dependent catalytic properties of bimetallic Au/Ag
core-shell nanoparticles. ACS Appl Mater Interfaces 6:21946–21953. https://doi.org/10.1021/
am507391d
Haw C, Chiu W, Khanis NH, Rahman SA, Khiew P, Radiman S, Abd-Shukor R, Abdul Hamid
MA (2016) Tin stearate organometallic precursor prepared SnO 2 quantum dots nanopowder
for aqueous- and non-aqueous medium photocatalytic hydrogen gas evolution. J Energy Chem
25:691–701. https://doi.org/10.1016/j.jechem.2016.04.006
Herbois R, Noël S, Léger B, Bai L, Roucoux A, Monflier E, Ponchel A (2012) Cyclodextrins as
growth controlling agents for enhancing the catalytic activity of PVP-stabilized Ru(0) nanoparticles. Chem Commun 48:3451–3453. https://doi.org/10.1039/c2cc17355g
Herbois R, Noël S, Léger B, Tilloy S, Menuel S, Addad A, Martel B, Ponchel A, Monflier E
(2015) Ruthenium-containing β-cyclodextrin polymer globules for the catalytic hydrogenation
of biomass-derived furanic compounds. Green Chem 17:2444–2454. https://doi.org/10.1039/
c5gc00005j
Hirano K, Takano S, Tsukuda T (2019) Asymmetric aerobic oxidation of secondary alcohols
catalyzed by poly(N-vinyl-2-pyrrolidone)-stabilized gold clusters modified with cyclodextrin
derivatives. Chem Commun 55:15033–15036. https://doi.org/10.1039/C9CC06770A
Huang T, Meng F, Qi L (2009) Facile synthesis and one-dimensional assembly of cyclodextrincapped gold nanoparticles and their applications in catalysis and surface-enhanced Raman
scattering. J Phys Chem C 113:13636–13642. https://doi.org/10.1021/jp903405y
5 Metal Nanoparticles and Cyclodextrins for Catalytic Applications