Crystalline γ-cyclodextrin metal organic framework nano-containers for encapsulation of benzaldehyde and their host–guest interactions

[1]  A. Bacchi,et al.  Dispensing Essential Oil Components through Cocrystallization: Sustainable and Smart Materials for Food Preservation and Agricultural Applications , 2022, ACS Sustainable Chemistry & Engineering.

[2]  Kirtiraj K. Gaikwad,et al.  Metal–organic frameworks for active food packaging. A review , 2022, Environmental Chemistry Letters.

[3]  Amr Zaitoon,et al.  Triggered and controlled release of active gaseous/volatile compounds for active packaging applications of agri-food products: A review. , 2021, Comprehensive reviews in food science and food safety.

[4]  Jayanthi Ranjan,et al.  Encapsulation of a Volatile Biomolecule (Hexanal) in Cyclodextrin Metal–Organic Frameworks for Slow Release and Its Effect on Preservation of Mangoes , 2021, ACS Food Science & Technology.

[5]  R. Auras,et al.  Encapsulation of hexanal in bio-based cyclodextrin metal organic framework for extended release , 2021, Journal of Inclusion Phenomena and Macrocyclic Chemistry.

[6]  L. Lim,et al.  Activated release of hexanal and salicylaldehyde from imidazolidine precursors encapsulated in electrospun ethylcellulose-poly(ethylene oxide) fibers , 2021, SN Applied Sciences.

[7]  Songnan Li,et al.  Encapsulation of menthol into cyclodextrin metal-organic frameworks: Preparation, structure characterization and evaluation of complexing capacity. , 2020, Food chemistry.

[8]  Xiong Fu,et al.  Metal-Organic Framework Based on α-cyclodextrin Gives High Ethylene Gas Adsorption Capacity and Storage Stability. , 2020, ACS applied materials & interfaces.

[9]  Peter G. Boyd,et al.  Understanding the diversity of the metal-organic framework ecosystem , 2020, Nature Communications.

[10]  M. Tenkanen,et al.  Active food packaging through controlled in situ production and release of hexanal , 2019, Food chemistry: X.

[11]  Zhuxian Zhou,et al.  Biocompatible Cyclodextrin-Based Metal–Organic Frameworks for Long-Term Sustained Release of Fragrances , 2019, Industrial & Engineering Chemistry Research.

[12]  M. Buntinx,et al.  Inclusion of ethanol in a nano-porous, bio-based metal organic framework , 2019, Journal of Inclusion Phenomena and Macrocyclic Chemistry.

[13]  K. O’Shea,et al.  Enhanced host–guest complexation of short chain perfluoroalkyl substances with positively charged β-cyclodextrin derivatives , 2019, Journal of Inclusion Phenomena and Macrocyclic Chemistry.

[14]  N. Oulahal,et al.  Antibacterial Properties of Polyphenols: Characterization and QSAR (Quantitative Structure–Activity Relationship) Models , 2019, Front. Microbiol..

[15]  R. LoPachin,et al.  Mechanisms of soft and hard electrophile toxicities. , 2019, Toxicology.

[16]  Vikramjeet Singh,et al.  Drug nanoclusters formed in confined nano-cages of CD-MOF: dramatic enhancement of solubility and bioavailability of azilsartan , 2018, Acta pharmaceutica Sinica. B.

[17]  L. Lim,et al.  Activated release of bioactive aldehydes from their precursors embedded in electrospun poly(lactic acid) nonwovens , 2018, RSC advances.

[18]  K. Yam,et al.  Innovative application of metal-organic frameworks for encapsulation and controlled release of allyl isothiocyanate. , 2017, Food chemistry.

[19]  Mohamad G. Abiad,et al.  Synthesis of nanoporous carbohydrate metal-organic framework and encapsulation of acetaldehyde , 2016 .

[20]  A. Isaev.  Intermolecular charge transfer as evidence for unusual O–H⋯C(sp3) hydrogen bond , 2016 .

[21]  P. Ballester,et al.  Stabilization of reactive species by supramolecular encapsulation. , 2016, Chemical Society reviews.

[22]  R. LoPachin,et al.  Reactions of electrophiles with nucleophilic thiolate sites: relevance to pathophysiological mechanisms and remediation , 2016, Free radical research.

[23]  K. Yam,et al.  The moisture-triggered controlled release of a natural food preservative from a microporous metal-organic framework. , 2016, Chemical communications.

[24]  T. Lectka,et al.  Search for a strong, virtually "no-shift" hydrogen bond: a cage molecule with an exceptional OH⋅⋅⋅F interaction. , 2014, Angewandte Chemie.

[25]  R. LoPachin,et al.  Molecular Mechanisms of Aldehyde Toxicity: A Chemical Perspective , 2014, Chemical research in toxicology.

[26]  Marcus D. Hanwell,et al.  Avogadro: an advanced semantic chemical editor, visualization, and analysis platform , 2012, Journal of Cheminformatics.

[27]  Hui Zhang,et al.  FT-IR spectroscopy and DFT calculation study on the solvent effects of benzaldehyde in organic solvents. , 2012, Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy.

[28]  Fujio Izumi,et al.  VESTA 3 for three-dimensional visualization of crystal, volumetric and morphology data , 2011 .

[29]  P. Zimniak.  Relationship of electrophilic stress to aging. , 2011, Free radical biology & medicine.

[30]  Hongbing Ji,et al.  Selective inclusion and separation of cinnamaldehyde and benzaldehyde by insoluble β-cyclodextrin polymer , 2011 .

[31]  J. Schwöbel,et al.  Measurement and estimation of electrophilic reactivity for predictive toxicology. , 2011, Chemical reviews.

[32]  Ronald A. Smaldone,et al.  Metal-organic frameworks from edible natural products. , 2010, Angewandte Chemie.

[33]  David S. Goodsell,et al.  AutoDock4 and AutoDockTools4: Automated docking with selective receptor flexibility , 2009, J. Comput. Chem..

[34]  Arthur J. Olson,et al.  AutoDock Vina: Improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading , 2009, J. Comput. Chem..

[35]  E. Farmer,et al.  Reactive electrophile species. , 2007, Current opinion in plant biology.

[36]  John Frederick Beck,et al.  How resonance assists hydrogen bonding interactions: An energy decomposition analysis , 2007, J. Comput. Chem..

[37]  R. Sinisterra,et al.  Inclusion of Benzaldehyde Semicarbazone into β-Cyclodextrin Produces a Very Effective Anticonvulsant Formulation , 2003 .

[38]  Q. Guo,et al.  PM3 studies on the complexation of α-cyclodextrin with benzaldehyde and acetophenone , 2000 .

[39]  Guoxi Xi,et al.  Mechanism and Kinetics of Thermal Dissociation of Inclusion Complex of Benzaldehyde with β-Cyclodextrin , 1998 .

[40]  G. A. Jeffrey,et al.  An Introduction to Hydrogen Bonding , 1997 .

[41]  M. Gorman.  The evidence from infrared spectroscopy for hydrogen bonding: A case history of the correlation and interpretation of data , 1957 .

[42]  Tian Ding,et al.  Cyclodextrin-metal-organic frameworks (CD-MOFs): main aspects and perspectives in food applications , 2021 .

[43]  Gabriela Bitencourt-Ferreira,et al.  Molecular Docking Simulations with ArgusLab. , 2019, Methods in molecular biology.

[44]  R. Parthasarathi,et al.  Characterization of Hydrogen Bonding: From van der Waals Interactions to Covalency , 2006 .