278
Ran X, Yang L, Qu Q, Li S, Chen Y, Zuo L, Li L (2017) Synthesis of well-dispersive 2.0 nm Pd-Pt
bimetallic nanoclusters supported on β-cyclodextrin functionalized graphene with excellent
electrocatalytic activity. RSC Adv 7:1947–1955. https://doi.org/10.1039/c6ra24893d
Sadjadi S (2018) Palladium nanoparticles immobilized on cyclodextrin-decorated halloysite nanotubes: efficient heterogeneous catalyst for promoting copper- and ligand-free Sonogashira
reaction in water-ethanol mixture. Appl Organomet Chem 32:4211. https://doi.org/10.1002/
aoc.4211
Sadjadi S, Malmir M, Heravi MM (2017) A green approach to the synthesis of Ag doped nano
magnetic γ-Fe 2 O 3 @SiO 2 -CD core-shell hollow spheres as an efficient and heterogeneous catalyst for ultrasonic-assisted A3 and KA2 coupling reactions. RSC Adv 7:36807–36818. https://
doi.org/10.1039/C7RA04635A
Sadjadi S, Heravi MM, Malmir M (2018a) Pd@HNTs-CDNS-g-C 3 N 4 : a novel heterogeneous catalyst for promoting ligand and copper-free Sonogashira and Heck coupling reactions, benefits
from halloysite and cyclodextrin chemistry and g-C 3 N 4 contribution to sup. Carbohydr Polym
186:25–34. https://doi.org/10.1016/j.carbpol.2018.01.023
Sadjadi S, Heravi MM, Raja M (2018b) Combination of carbon nanotube and cyclodextrin
nanosponge chemistry to develop a heterogeneous Pd-based catalyst for ligand and copper free C-C coupling reactions. Carbohydr Polym 185:48–55. https://doi.org/10.1016/j.
carbpol.2018.01.020
Sagir H, Rahila RP, Singh PK, Siddiqui LR (2016) ZnO nanoparticle–β-cyclodextrin: a recyclable
heterogeneous catalyst for the synthesis of 3-aryl-4H-benzo[1,4]thiazin-2-amine in water. New
J Chem 40:6819–6824. https://doi.org/10.1039/C5NJ03273C
Senra JD, Malta LFB, da Costa MEHM, MIchel RC, Aguiar LCS, Simas ABC, Antunes OAC
(2009) Hydroxypropyl-α-cyclodextrin-capped palladium nanoparticles: active scaffolds for efficient carbon-carbon bond forming cross-couplings in water. Adv Synth Catal 351:2411–2422.
https://doi.org/10.1002/adsc.200900348
Senra JD, Viana GM, Malta LFB, Simas ABC, Aguiar LCS (2016) Selectivity studies towards
the synthesis of novel biaryl ureas by (hetero)nanocatalysis: size control and support effects.
ChemCatChem 8:192–199. https://doi.org/10.1002/cctc.201500889
Shen J, Li N, Ye M (2013) Supramolecular photocatalyst of RGO-cyclodextrin-TiO 2 . J Alloys
Compd 580:239–244. https://doi.org/10.1016/j.jallcom.2013.05.090
Shiraishi Y, Hayashi M, Toshima N (2007) Preparation and catalysis of poly(β-cyclodextrin)stabilized palladium nanoparticles. Kobunshi Ronbunshu 64:74–76
Strimbu L, Liu J, Kaifer AE (2003) Cyclodextrin-capped palladium nanoparticles as catalysts for
the Suzuki reaction. Langmuir 19:483–485. https://doi.org/10.1021/la026550n
Tang J, Shi Z, Berry RM, Tam KC (2015) Mussel-inspired green metallization of silver nanoparticles on cellulose nanocrystals and their enhanced catalytic reduction of 4-nitrophenol in the
presence of β-cyclodextrin. Ind Eng Chem Res 54:3299–3308. https://doi.org/10.1021/acs.
iecr.5b00177
Taylor P, Shiraishi Y, Hashimura M, Nakao M, Ishizu T, Kazita M, Miyamoto Y, Toshima N
(2010) Syntheses of poly (cyclodextrin)-stabilised metal nanoparticles and their quenching
abilities of active oxygen species. Supramol Chem 23:37–41. https://doi.org/10.1080/1061027
8.2010.521831
Thanh Chau NT, Menuel S, Colombel-Rouen S, Guerrero M, Monflier E, Philippot K, DenicourtNowicki A, Roucoux A (2016) Active hydrogenation Rh nanocatalysts protected by new selfassembled supramolecular complexes of cyclodextrins and surfactants in water. RSC Adv
6:108125–108131. https://doi.org/10.1039/C6RA21851B
Vasconcelos DA, Kubota T, Santos DC, Araujo MV, Teixeira Z, Gimenez IF (2016) Preparation
of Au n quantum clusters with catalytic activity in β-cyclodextrin polyurethane nanosponges.
Carbohydr Polym 136:54–62. https://doi.org/10.1016/j.carbpol.2015.09.010
Wang J, Gao P, Ye L, Feng Z (2010) Solvent and thermoresponsive polyrotaxanes with cyclodextrin
dispersed/aggregated structures on a pluronic F127 backbone. J Phys Chem B 114:5342–5349.
https://doi.org/10.1021/jp101068b
S. Noël et al.
Ran X, Yang L, Qu Q, Li S, Chen Y, Zuo L, Li L (2017) Synthesis of well-dispersive 2.0 nm Pd-Pt
bimetallic nanoclusters supported on β-cyclodextrin functionalized graphene with excellent
electrocatalytic activity. RSC Adv 7:1947–1955. https://doi.org/10.1039/c6ra24893d
Sadjadi S (2018) Palladium nanoparticles immobilized on cyclodextrin-decorated halloysite nanotubes: efficient heterogeneous catalyst for promoting copper- and ligand-free Sonogashira
reaction in water-ethanol mixture. Appl Organomet Chem 32:4211. https://doi.org/10.1002/
aoc.4211
Sadjadi S, Malmir M, Heravi MM (2017) A green approach to the synthesis of Ag doped nano
magnetic γ-Fe 2 O 3 @SiO 2 -CD core-shell hollow spheres as an efficient and heterogeneous catalyst for ultrasonic-assisted A3 and KA2 coupling reactions. RSC Adv 7:36807–36818. https://
doi.org/10.1039/C7RA04635A
Sadjadi S, Heravi MM, Malmir M (2018a) Pd@HNTs-CDNS-g-C 3 N 4 : a novel heterogeneous catalyst for promoting ligand and copper-free Sonogashira and Heck coupling reactions, benefits
from halloysite and cyclodextrin chemistry and g-C 3 N 4 contribution to sup. Carbohydr Polym
186:25–34. https://doi.org/10.1016/j.carbpol.2018.01.023
Sadjadi S, Heravi MM, Raja M (2018b) Combination of carbon nanotube and cyclodextrin
nanosponge chemistry to develop a heterogeneous Pd-based catalyst for ligand and copper free C-C coupling reactions. Carbohydr Polym 185:48–55. https://doi.org/10.1016/j.
carbpol.2018.01.020
Sagir H, Rahila RP, Singh PK, Siddiqui LR (2016) ZnO nanoparticle–β-cyclodextrin: a recyclable
heterogeneous catalyst for the synthesis of 3-aryl-4H-benzo[1,4]thiazin-2-amine in water. New
J Chem 40:6819–6824. https://doi.org/10.1039/C5NJ03273C
Senra JD, Malta LFB, da Costa MEHM, MIchel RC, Aguiar LCS, Simas ABC, Antunes OAC
(2009) Hydroxypropyl-α-cyclodextrin-capped palladium nanoparticles: active scaffolds for efficient carbon-carbon bond forming cross-couplings in water. Adv Synth Catal 351:2411–2422.
https://doi.org/10.1002/adsc.200900348
Senra JD, Viana GM, Malta LFB, Simas ABC, Aguiar LCS (2016) Selectivity studies towards
the synthesis of novel biaryl ureas by (hetero)nanocatalysis: size control and support effects.
ChemCatChem 8:192–199. https://doi.org/10.1002/cctc.201500889
Shen J, Li N, Ye M (2013) Supramolecular photocatalyst of RGO-cyclodextrin-TiO 2 . J Alloys
Compd 580:239–244. https://doi.org/10.1016/j.jallcom.2013.05.090
Shiraishi Y, Hayashi M, Toshima N (2007) Preparation and catalysis of poly(β-cyclodextrin)stabilized palladium nanoparticles. Kobunshi Ronbunshu 64:74–76
Strimbu L, Liu J, Kaifer AE (2003) Cyclodextrin-capped palladium nanoparticles as catalysts for
the Suzuki reaction. Langmuir 19:483–485. https://doi.org/10.1021/la026550n
Tang J, Shi Z, Berry RM, Tam KC (2015) Mussel-inspired green metallization of silver nanoparticles on cellulose nanocrystals and their enhanced catalytic reduction of 4-nitrophenol in the
presence of β-cyclodextrin. Ind Eng Chem Res 54:3299–3308. https://doi.org/10.1021/acs.
iecr.5b00177
Taylor P, Shiraishi Y, Hashimura M, Nakao M, Ishizu T, Kazita M, Miyamoto Y, Toshima N
(2010) Syntheses of poly (cyclodextrin)-stabilised metal nanoparticles and their quenching
abilities of active oxygen species. Supramol Chem 23:37–41. https://doi.org/10.1080/1061027
8.2010.521831
Thanh Chau NT, Menuel S, Colombel-Rouen S, Guerrero M, Monflier E, Philippot K, DenicourtNowicki A, Roucoux A (2016) Active hydrogenation Rh nanocatalysts protected by new selfassembled supramolecular complexes of cyclodextrins and surfactants in water. RSC Adv
6:108125–108131. https://doi.org/10.1039/C6RA21851B
Vasconcelos DA, Kubota T, Santos DC, Araujo MV, Teixeira Z, Gimenez IF (2016) Preparation
of Au n quantum clusters with catalytic activity in β-cyclodextrin polyurethane nanosponges.
Carbohydr Polym 136:54–62. https://doi.org/10.1016/j.carbpol.2015.09.010
Wang J, Gao P, Ye L, Feng Z (2010) Solvent and thermoresponsive polyrotaxanes with cyclodextrin
dispersed/aggregated structures on a pluronic F127 backbone. J Phys Chem B 114:5342–5349.
https://doi.org/10.1021/jp101068b
S. Noël et al.