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Dive into the research topics where Suzy Surblé is active.

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Featured researches published by Suzy Surblé.


Chemical Communications | 2007

Synthesis and catalytic properties of MIL-100(Fe), an iron(III) carboxylate with large pores

Patricia Horcajada; Suzy Surblé; Christian Serre; Do-Young Hong; You-Kyong Seo; Jong-San Chang; Jean-Marc Greneche; I. Margiolaki; Gérard Férey

The large-pore iron(III) carboxylate MIL-100(Fe) with a zeotype architecture has been isolated under hydrothermal conditions, its structure solved from synchrotron X-ray powder diffraction data, while Friedel-Crafts benzylation catalytic tests indicate a high activity and selectivity for MIL-100(Fe).


Science | 2007

Role of Solvent-Host Interactions That Lead to Very Large Swelling of Hybrid Frameworks

Christian Serre; Caroline Mellot-Draznieks; Suzy Surblé; N. Audebrand; Yaroslav Filinchuk; Gérard Férey

An unusually large expansion upon solvent adsorption occurs without apparent bond breaking in the network of a series of isoreticular chromium(III) or iron(III) diarboxylates labeled MIL-88A to D [dicarbox = fumarate (88A); terephthalate (1,4-BDC) (88B); 2,6-naphthalenedicarboxylate (2,6-NDC) (88C); and 4-4′-biphenyldicarboxylate (4-4′-BPDC) (88D)]. This reversible “breathing” motion was analyzed in terms of cell dimensions (extent of breathing), movements within the framework (mechanism of transformation), and the interactions between the guests and the skeleton. In situ techniques show that these flexible solids are highly selective absorbents and that this selectivity is strongly dependent on the nature of the organic linker.


Chemical Communications | 2006

A new isoreticular class of metal-organic-frameworks with the MIL-88 topology

Suzy Surblé; Christian Serre; Caroline Mellot-Draznieks; Franck Millange; Gérard Férey

We report here a new family of isoreticular MOFs, comprising three larger analogues of the nanoporous metallocarboxylate MIL-88; these solids were synthesized using a controlled SBU approach and the three crystal structures were solved using an original simulation-assisted structure determination method in direct space.


Journal of Toxicology and Environmental Health | 2012

Comparative uptake and impact of TiO₂ nanoparticles in wheat and rapeseed.

Camille Larue; Giulia Veronesi; Anne-Marie Flank; Suzy Surblé; Nathalie Herlin-Boime; Marie Carrière

Up to 2 million tons per year of titanium dioxide (TiO2) nanoparticles (NP) are produced worldwide. This extensive production is postulated to result in release into the environment with subsequent contamination of soils and plants; however, few studies have examined TiO2-NP uptake and impact on plants. In this study, wheat and rapeseed plantlets were exposed to 14 nm or 25 nm anatase TiO2-NP in hydroponics conditions, either through root or leaf exposure. Microparticle-induced x-ray emission (μPIXE) coupled with Rutherford backscattering spectroscopy (RBS) was used to quantify absorbed titanium (Ti). Micro x-ray fluorescence (μXRF) based on synchrotron radiation was used to evaluate Ti distribution in roots and leaves. Our results show that both TiO2-NP are accumulated in these plantlets upon root exposure and that Ti content is higher in rapeseed than wheat. Ti distribution in root cross sections depended on NP agglomeration state. NP are also accumulated in plantlets upon leaf exposure. Finally, it was found that TiO2-NP exposure induced increased root elongation but did not affect germination, evapotranspiration, and plant biomass. Taken together, these results confirm that TiO2-NP may be accumulated in plant crops but may only moderately impact plant development.


Chemical Communications | 2006

An EXAFS study of the formation of a nanoporous metal-organic framework: evidence for the retention of secondary building units during synthesis.

Suzy Surblé; Franck Millange; Christian Serre; Gérard Férey; Richard I. Walton

EXAFS data measured from amorphous intermediates and crystallisation solutions provides the first evidence that trimeric iron oxide secondary building units remain intact during crystallisation of the metal-organic framework MIL-89 from starting materials to products.


Nature plants | 2016

Mother-plant-mediated pumping of zinc into the developing seed

Lene Irene Olsen; Thomas H. Hansen; Camille Larue; Jeppe Thulin Østerberg; Robert D. Hoffmann; Johannes Liesche; Ute Krämer; Suzy Surblé; Stéphanie Cadarsi; Vallerie Samson; Daniel Grolimund; Søren Husted; Michael G. Palmgren

Insufficient intake of zinc and iron from a cereal-based diet is one of the causes of ‘hidden hunger’ (micronutrient deficiency), which affects some two billion people1,2. Identifying a limiting factor in the molecular mechanism of zinc loading into seeds is an important step towards determining the genetic basis for variation of grain micronutrient content and developing breeding strategies to improve this trait3. Nutrients are translocated to developing seeds at a rate that is regulated by transport processes in source leaves, in the phloem vascular pathway, and at seed sinks. Nutrients are released from a symplasmic maternal seed domain into the seed apoplasm surrounding the endosperm and embryo by poorly understood membrane transport processes4–6. Plants are unique among eukaryotes in having specific P1B-ATPase pumps for the cellular export of zinc7. In Arabidopsis, we show that two zinc transporting P1B-ATPases actively export zinc from the mother plant to the filial tissues. Mutant plants that lack both zinc pumps accumulate zinc in the seed coat and consequently have vastly reduced amounts of zinc inside the seed. Blockage of zinc transport was observed at both high and low external zinc supplies. The phenotype was determined by the mother plant and is thus due to a lack of zinc pump activity in the seed coat and not in the filial tissues. The finding that P1B-ATPases are one of the limiting factors controlling the amount of zinc inside a seed is an important step towards combating nutritional zinc deficiency worldwide.


Molecular Simulation | 2015

Computational exploration of the gas adsorption on the iron tetracarboxylate metal-organic framework MIL-102

D. Damasceno Borges; M. Prakash; N.A. Ramsahye; Philip Llewellyn; Suzy Surblé; Patricia Horcajada; Christian Serre; Guillaume Maurin

Density functional theory calculations have been combined with forcefield-based grand canonical Monte Carlo simulations to explore the adsorption of CO2, N2, CH4 and H2 on the small one-dimensional channel MIL-102, a naphthalene tetracarboxylate-based metal-organic framework (MOF) built up from a connection of trimers of trivalent iron. A detailed analysis is provided on the preferential arrangement of the confined adsorbates as well as the energetics of the host/guest interactions. The co-adsorption properties of this solid for the elimination of CO2 from hydrogen, natural and flue gases are then revealed. The so-predicted performances are further compared with those reported so far for a diverse series of MOFs.


Science | 2005

A Chromium Terephthalate-Based Solid with Unusually Large Pore Volumes and Surface Area

Gérard Férey; Caroline Mellot-Draznieks; Christian Serre; Franck Millange; Julien Dutour; Suzy Surblé; I. Margiolaki


Angewandte Chemie | 2006

Hydrogen Storage in the Giant-Pore Metal–Organic Frameworks MIL-100 and MIL-101†

M. Latroche; Suzy Surblé; Christian Serre; Caroline Mellot-Draznieks; Philip Llewellyn; Jin-Ho Lee; Jong-San Chang; Sung Hwa Jhung; Gérard Férey


Angewandte Chemie | 2004

A hybrid solid with giant pores prepared by a combination of targeted chemistry, simulation, and powder diffraction.

Gérard Férey; Christian Serre; Caroline Mellot-Draznieks; Franck Millange; Suzy Surblé; Julien Dutour; I. Margiolaki

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Christian Serre

Centre national de la recherche scientifique

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Gérard Férey

Centre national de la recherche scientifique

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Franck Millange

Centre national de la recherche scientifique

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David Simeone

Université Paris-Saclay

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H. Khodja

Université Paris-Saclay

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F. Pellé

Centre national de la recherche scientifique

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Mickael Dollé

Centre national de la recherche scientifique

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