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[Hypertension and work environment].

Archives des maladies professionnelles de medecine du travail et de securite sociale

Cosset JC.
PMID: 5362960
Arch Mal Prof. 1969 Mar;30(3):155-7.

No abstract available.

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Cosset JC. Hypertension et milieu de travail. [Hypertension and work environment]. Arch Mal Prof. 1969;30(3):155-7
Cosset, J. C. (1969). Hypertension et milieu de travail. [Hypertension and work environment]. Archives des maladies professionnelles de medecine du travail et de securite sociale, 30(3), 155-7.
Cosset, J C. "Hypertension et milieu de travail." [Hypertension and work environment]. Archives des maladies professionnelles de medecine du travail et de securite sociale vol. 30,3 (1969): 155-7.
Cosset JC. Hypertension et milieu de travail. [Hypertension and work environment]. Arch Mal Prof. 1969 Mar;30(3):155-7. French. PMID: 5362960.
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Reactive surface organometallic complexes observed using dynamic nuclear polarization surface enhanced NMR spectroscopy.

Chemical science

Pump E, Viger-Gravel J, Abou-Hamad E, Samantaray MK, Hamzaoui B, Gurinov A, Anjum DH, Gajan D, Lesage A, Bendjeriou-Sedjerari A, Emsley L, Basset JM.
PMID: 28451174
Chem Sci. 2017 Jan 01;8(1):284-290. doi: 10.1039/c6sc02379g. Epub 2016 Aug 15.

Dynamic Nuclear Polarization Surface Enhanced NMR Spectroscopy (DNP SENS) is an emerging technique that allows access to high-sensitivity NMR spectra from surfaces. However, DNP SENS usually requires the use of radicals as an exogenous source of polarization, which has...

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Pump E, Viger-Gravel J, Abou-Hamad E, et al. Reactive surface organometallic complexes observed using dynamic nuclear polarization surface enhanced NMR spectroscopy. Chem Sci. 2016;8(1):284-290doi: 10.1039/c6sc02379g.
Pump, E., Viger-Gravel, J., Abou-Hamad, E., Samantaray, M. K., Hamzaoui, B., Gurinov, A., Anjum, D. H., Gajan, D., Lesage, A., Bendjeriou-Sedjerari, A., Emsley, L., & Basset, J. M. (2017). Reactive surface organometallic complexes observed using dynamic nuclear polarization surface enhanced NMR spectroscopy. Chemical science, 8(1), 284-290. https://doi.org/10.1039/c6sc02379g
Pump, Eva, et al. "Reactive surface organometallic complexes observed using dynamic nuclear polarization surface enhanced NMR spectroscopy." Chemical science vol. 8,1 (2017): 284-290. doi: https://doi.org/10.1039/c6sc02379g
Pump E, Viger-Gravel J, Abou-Hamad E, Samantaray MK, Hamzaoui B, Gurinov A, Anjum DH, Gajan D, Lesage A, Bendjeriou-Sedjerari A, Emsley L, Basset JM. Reactive surface organometallic complexes observed using dynamic nuclear polarization surface enhanced NMR spectroscopy. Chem Sci. 2017 Jan 01;8(1):284-290. doi: 10.1039/c6sc02379g. Epub 2016 Aug 15. PMID: 28451174; PMCID: PMC5365068.
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Structured Ni catalysts on porous anodic alumina membranes for methane dry reforming: NiAl2O4 formation and characterization.

Chemical communications (Cambridge, England)

Zhou L, Guo Y, Basset JM, Kameyama H.
PMID: 26121050
Chem Commun (Camb). 2015 Aug 04;51(60):12044-7. doi: 10.1039/c5cc03173g.

This communication presents the successful design of a structured catalyst based on porous anodic alumina membranes for methane dry reforming. The catalyst with a strong Ni-NiAl2O4 interaction shows both excellent activity and stability.

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Zhou L, Guo Y, Basset JM, et al. Structured Ni catalysts on porous anodic alumina membranes for methane dry reforming: NiAl2O4 formation and characterization. Chem Commun (Camb). 2015;51(60):12044-7doi: 10.1039/c5cc03173g.
Zhou, L., Guo, Y., Basset, J. M., & Kameyama, H. (2015). Structured Ni catalysts on porous anodic alumina membranes for methane dry reforming: NiAl2O4 formation and characterization. Chemical communications (Cambridge, England), 51(60), 12044-7. https://doi.org/10.1039/c5cc03173g
Zhou, L, et al. "Structured Ni catalysts on porous anodic alumina membranes for methane dry reforming: NiAl2O4 formation and characterization." Chemical communications (Cambridge, England) vol. 51,60 (2015): 12044-7. doi: https://doi.org/10.1039/c5cc03173g
Zhou L, Guo Y, Basset JM, Kameyama H. Structured Ni catalysts on porous anodic alumina membranes for methane dry reforming: NiAl2O4 formation and characterization. Chem Commun (Camb). 2015 Aug 04;51(60):12044-7. doi: 10.1039/c5cc03173g. PMID: 26121050.
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Synthesis, characterization, and reactivity of furan- and thiophene-functionalized bis(N-heterocyclic carbene) complexes of iron(II).

Inorganic chemistry

Rieb J, Raba A, Haslinger S, Kaspar M, Pöthig A, Cokoja M, Basset JM, Kühn FE.
PMID: 25188636
Inorg Chem. 2014 Sep 15;53(18):9598-606. doi: 10.1021/ic500959m. Epub 2014 Sep 04.

The synthesis of iron(II) complexes bearing new heteroatom-functionalized methylene-bridged bis(N-heterocyclic carbene) ligands is reported. All complexes are characterized by single-crystal X-ray diffraction (SC-XRD), nuclear magnetic resonance (NMR) spectroscopy, and elemental analysis. Tetrakis(acetonitrile)-cis-[bis(o-imidazol-2-ylidenefuran)methane]iron(II) hexafluorophosphate (2a) and tetrakis(acetonitrile)-cis-[bis(o-imidazol-2-ylidenethiophene)methane]iron(II) hexafluorophosphate (2b) were...

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Rieb J, Raba A, Haslinger S, et al. Synthesis, characterization, and reactivity of furan- and thiophene-functionalized bis(N-heterocyclic carbene) complexes of iron(II). Inorg Chem. 2014;53(18):9598-606doi: 10.1021/ic500959m.
Rieb, J., Raba, A., Haslinger, S., Kaspar, M., Pöthig, A., Cokoja, M., Basset, J. M., & Kühn, F. E. (2014). Synthesis, characterization, and reactivity of furan- and thiophene-functionalized bis(N-heterocyclic carbene) complexes of iron(II). Inorganic chemistry, 53(18), 9598-606. https://doi.org/10.1021/ic500959m
Rieb, Julia, et al. "Synthesis, characterization, and reactivity of furan- and thiophene-functionalized bis(N-heterocyclic carbene) complexes of iron(II)." Inorganic chemistry vol. 53,18 (2014): 9598-606. doi: https://doi.org/10.1021/ic500959m
Rieb J, Raba A, Haslinger S, Kaspar M, Pöthig A, Cokoja M, Basset JM, Kühn FE. Synthesis, characterization, and reactivity of furan- and thiophene-functionalized bis(N-heterocyclic carbene) complexes of iron(II). Inorg Chem. 2014 Sep 15;53(18):9598-606. doi: 10.1021/ic500959m. Epub 2014 Sep 04. PMID: 25188636.
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Well-defined single-site monohydride silica-supported zirconium from azazirconacyclopropane.

Chemistry (Weinheim an der Bergstrasse, Germany)

Hamzaoui B, El Eter M, Abou-Hamad E, Chen Y, Pelletier JD, Basset JM.
PMID: 25585538
Chemistry. 2015 Mar 09;21(11):4294-9. doi: 10.1002/chem.201405788. Epub 2015 Jan 13.

The silica-supported azazirconacyclopropane ≡SiOZr(HNMe2)(η(2)-NMeCH2)(NMe2) (1) leads exclusively under hydrogenolysis conditions (H2, 150 °C) to the single-site monopodal monohydride silica-supported zirconium species ≡SiOZr(HNMe2)(NMe2)2H (2). Reactivity studies by contacting compound 2 with ethylene, hydrogen/ethylene, propene, or hydrogen/propene, at a temperature of...

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Hamzaoui B, El Eter M, Abou-Hamad E, et al. Well-defined single-site monohydride silica-supported zirconium from azazirconacyclopropane. Chemistry. 2015;21(11):4294-9doi: 10.1002/chem.201405788.
Hamzaoui, B., El Eter, M., Abou-Hamad, E., Chen, Y., Pelletier, J. D., & Basset, J. M. (2015). Well-defined single-site monohydride silica-supported zirconium from azazirconacyclopropane. Chemistry (Weinheim an der Bergstrasse, Germany), 21(11), 4294-9. https://doi.org/10.1002/chem.201405788
Hamzaoui, Bilel, et al. "Well-defined single-site monohydride silica-supported zirconium from azazirconacyclopropane." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 21,11 (2015): 4294-9. doi: https://doi.org/10.1002/chem.201405788
Hamzaoui B, El Eter M, Abou-Hamad E, Chen Y, Pelletier JD, Basset JM. Well-defined single-site monohydride silica-supported zirconium from azazirconacyclopropane. Chemistry. 2015 Mar 09;21(11):4294-9. doi: 10.1002/chem.201405788. Epub 2015 Jan 13. PMID: 25585538.
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Tungsten(VI) Carbyne/Bis(carbene) Tautomerization Enabled by N-Donor SBA15 Surface Ligands: A Solid-State NMR and DFT Study.

Angewandte Chemie (International ed. in English)

Bendjeriou-Sedjerari A, Sofack-Kreutzer J, Minenkov Y, Abou-Hamad E, Hamzaoui B, Werghi B, Anjum DH, Cavallo L, Huang KW, Basset JM.
PMID: 27514022
Angew Chem Int Ed Engl. 2016 Sep 05;55(37):11162-6. doi: 10.1002/anie.201605934. Epub 2016 Aug 11.

Designing supported well-defined bis(carbene) complexes remains a key challenge in heterogeneous catalysis. The reaction of W(≡CtBu)(CH2 tBu)3 with amine-modified mesoporous SBA15 silica, which has vicinal silanol/silylamine pairs [(≡SiOH)(≡SiNH2 )], leads to [(≡SiNH2 -)(≡SiO-)W(≡CHtBu)(CH2 tBu)2 ] and [(≡SiNH2 -)(≡SiO-)W(=CHtBu)2 (CH2...

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Bendjeriou-Sedjerari A, Sofack-Kreutzer J, Minenkov Y, et al. Tungsten(VI) Carbyne/Bis(carbene) Tautomerization Enabled by N-Donor SBA15 Surface Ligands: A Solid-State NMR and DFT Study. Angew Chem Int Ed Engl. 2016;55(37):11162-6doi: 10.1002/anie.201605934.
Bendjeriou-Sedjerari, A., Sofack-Kreutzer, J., Minenkov, Y., Abou-Hamad, E., Hamzaoui, B., Werghi, B., Anjum, D. H., Cavallo, L., Huang, K. W., & Basset, J. M. (2016). Tungsten(VI) Carbyne/Bis(carbene) Tautomerization Enabled by N-Donor SBA15 Surface Ligands: A Solid-State NMR and DFT Study. Angewandte Chemie (International ed. in English), 55(37), 11162-6. https://doi.org/10.1002/anie.201605934
Bendjeriou-Sedjerari, Anissa, et al. "Tungsten(VI) Carbyne/Bis(carbene) Tautomerization Enabled by N-Donor SBA15 Surface Ligands: A Solid-State NMR and DFT Study." Angewandte Chemie (International ed. in English) vol. 55,37 (2016): 11162-6. doi: https://doi.org/10.1002/anie.201605934
Bendjeriou-Sedjerari A, Sofack-Kreutzer J, Minenkov Y, Abou-Hamad E, Hamzaoui B, Werghi B, Anjum DH, Cavallo L, Huang KW, Basset JM. Tungsten(VI) Carbyne/Bis(carbene) Tautomerization Enabled by N-Donor SBA15 Surface Ligands: A Solid-State NMR and DFT Study. Angew Chem Int Ed Engl. 2016 Sep 05;55(37):11162-6. doi: 10.1002/anie.201605934. Epub 2016 Aug 11. PMID: 27514022.
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Intervention Engagement Moderates the Dose-Response Relationships in a Dietary Intervention.

Dose-response : a publication of International Hormesis Society

Lippke S, Corbet JM, Lange D, Parschau L, Schwarzer R.
PMID: 27069440
Dose Response. 2016 Mar 16;14(1):1559325816637515. doi: 10.1177/1559325816637515. eCollection 2016.

Behavioral interventions could lead to changes in behavior through changes in a mediator. This dose-response relationship might only hold true for those participants who are actively engaged in interventions. This Internet study investigated the role of engagement in a...

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Lippke S, Corbet JM, Lange D, et al. Intervention Engagement Moderates the Dose-Response Relationships in a Dietary Intervention. Dose Response. 2016;14(1):1559325816637515doi: 10.1177/1559325816637515.
Lippke, S., Corbet, J. M., Lange, D., Parschau, L., & Schwarzer, R. (2016). Intervention Engagement Moderates the Dose-Response Relationships in a Dietary Intervention. Dose-response : a publication of International Hormesis Society, 14(1), 1559325816637515. https://doi.org/10.1177/1559325816637515
Lippke, Sonia, et al. "Intervention Engagement Moderates the Dose-Response Relationships in a Dietary Intervention." Dose-response : a publication of International Hormesis Society vol. 14,1 (2016): 1559325816637515. doi: https://doi.org/10.1177/1559325816637515
Lippke S, Corbet JM, Lange D, Parschau L, Schwarzer R. Intervention Engagement Moderates the Dose-Response Relationships in a Dietary Intervention. Dose Response. 2016 Mar 16;14(1):1559325816637515. doi: 10.1177/1559325816637515. eCollection 2016. PMID: 27069440; PMCID: PMC4811006.
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A New Class of Atomically Precise, Hydride-Rich Silver Nanoclusters Co-Protected by Phosphines.

Journal of the American Chemical Society

Bootharaju MS, Dey R, Gevers LE, Hedhili MN, Basset JM, Bakr OM.
PMID: 27718553
J Am Chem Soc. 2016 Oct 26;138(42):13770-13773. doi: 10.1021/jacs.6b05482. Epub 2016 Oct 18.

Thiols and phosphines are the most widely used organic ligands to attain atomically precise metal nanoclusters (NCs). Here, we used simple hydrides (e.g., H

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Bootharaju MS, Dey R, Gevers LE, et al. A New Class of Atomically Precise, Hydride-Rich Silver Nanoclusters Co-Protected by Phosphines. J Am Chem Soc. 2016;138(42):13770-13773doi: 10.1021/jacs.6b05482.
Bootharaju, M. S., Dey, R., Gevers, L. E., Hedhili, M. N., Basset, J. M., & Bakr, O. M. (2016). A New Class of Atomically Precise, Hydride-Rich Silver Nanoclusters Co-Protected by Phosphines. Journal of the American Chemical Society, 138(42), 13770-13773. https://doi.org/10.1021/jacs.6b05482
Bootharaju, Megalamane S, et al. "A New Class of Atomically Precise, Hydride-Rich Silver Nanoclusters Co-Protected by Phosphines." Journal of the American Chemical Society vol. 138,42 (2016): 13770-13773. doi: https://doi.org/10.1021/jacs.6b05482
Bootharaju MS, Dey R, Gevers LE, Hedhili MN, Basset JM, Bakr OM. A New Class of Atomically Precise, Hydride-Rich Silver Nanoclusters Co-Protected by Phosphines. J Am Chem Soc. 2016 Oct 26;138(42):13770-13773. doi: 10.1021/jacs.6b05482. Epub 2016 Oct 18. PMID: 27718553.
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Changes in muscle activation during gait of children with duchenne muscular dystrophy.

Computer methods in biomechanics and biomedical engineering

Ropars J, Lemeur M, Vuillerot C, Tiffreau V, Peudenier S, Cuisset JM, Pereon Y, Leboeuf F, Delporte L, Delpierre Y, Gross R, Brochard S.
PMID: 26467719
Comput Methods Biomech Biomed Engin. 2015;18:2042-3. doi: 10.1080/10255842.2015.1069615. Epub 2015 Sep 01.

No abstract available.

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Ropars J, Lemeur M, Vuillerot C, et al. Changes in muscle activation during gait of children with duchenne muscular dystrophy. Comput Methods Biomech Biomed Engin. 2015;18:2042-3doi: 10.1080/10255842.2015.1069615.
Ropars, J., Lemeur, M., Vuillerot, C., Tiffreau, V., Peudenier, S., Cuisset, J. M., Pereon, Y., Leboeuf, F., Delporte, L., Delpierre, Y., Gross, R., & Brochard, S. (2015). Changes in muscle activation during gait of children with duchenne muscular dystrophy. Computer methods in biomechanics and biomedical engineering, 182042-3. https://doi.org/10.1080/10255842.2015.1069615
Ropars, J, et al. "Changes in muscle activation during gait of children with duchenne muscular dystrophy." Computer methods in biomechanics and biomedical engineering vol. 18 (2015): 2042-3. doi: https://doi.org/10.1080/10255842.2015.1069615
Ropars J, Lemeur M, Vuillerot C, Tiffreau V, Peudenier S, Cuisset JM, Pereon Y, Leboeuf F, Delporte L, Delpierre Y, Gross R, Brochard S. Changes in muscle activation during gait of children with duchenne muscular dystrophy. Comput Methods Biomech Biomed Engin. 2015;18:2042-3. doi: 10.1080/10255842.2015.1069615. Epub 2015 Sep 01. PMID: 26467719.
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Cooperative Effect of Monopodal Silica-Supported Niobium Complex Pairs Enhancing Catalytic Cyclic Carbonate Production.

Journal of the American Chemical Society

D'Elia V, Dong H, Rossini AJ, Widdifield CM, Vummaleti SV, Minenkov Y, Poater A, Abou-Hamad E, Pelletier JD, Cavallo L, Emsley L, Basset JM.
PMID: 25950495
J Am Chem Soc. 2015 Jun 24;137(24):7728-39. doi: 10.1021/jacs.5b02872. Epub 2015 Jun 15.

Recent discoveries highlighted the activity and the intriguing mechanistic features of NbCl5 as a molecular catalyst for the cycloaddition of CO2 and epoxides under ambient conditions. This has inspired the preparation of novel silica-supported Nb species by reacting a...

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D'Elia V, Dong H, Rossini AJ, et al. Cooperative Effect of Monopodal Silica-Supported Niobium Complex Pairs Enhancing Catalytic Cyclic Carbonate Production. J Am Chem Soc. 2015;137(24):7728-39doi: 10.1021/jacs.5b02872.
D'Elia, V., Dong, H., Rossini, A. J., Widdifield, C. M., Vummaleti, S. V., Minenkov, Y., Poater, A., Abou-Hamad, E., Pelletier, J. D., Cavallo, L., Emsley, L., & Basset, J. M. (2015). Cooperative Effect of Monopodal Silica-Supported Niobium Complex Pairs Enhancing Catalytic Cyclic Carbonate Production. Journal of the American Chemical Society, 137(24), 7728-39. https://doi.org/10.1021/jacs.5b02872
D'Elia, Valerio, et al. "Cooperative Effect of Monopodal Silica-Supported Niobium Complex Pairs Enhancing Catalytic Cyclic Carbonate Production." Journal of the American Chemical Society vol. 137,24 (2015): 7728-39. doi: https://doi.org/10.1021/jacs.5b02872
D'Elia V, Dong H, Rossini AJ, Widdifield CM, Vummaleti SV, Minenkov Y, Poater A, Abou-Hamad E, Pelletier JD, Cavallo L, Emsley L, Basset JM. Cooperative Effect of Monopodal Silica-Supported Niobium Complex Pairs Enhancing Catalytic Cyclic Carbonate Production. J Am Chem Soc. 2015 Jun 24;137(24):7728-39. doi: 10.1021/jacs.5b02872. Epub 2015 Jun 15. PMID: 25950495.
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CO2 activation through silylimido and silylamido zirconium hydrides supported on N-donor chelating SBA15 surface ligands.

Chemical communications (Cambridge, England)

Pasha FA, Bendjeriou-Sedjerari A, Abou-Hamad E, Huang KW, Basset JM.
PMID: 26750777
Chem Commun (Camb). 2016 Feb 11;52(12):2577-80. doi: 10.1039/c5cc08821f. Epub 2016 Jan 11.

Density functional theory calculations and 2D 1H-13C HETCOR solid state NMR spectroscopy prove that CO2 can be used to probe, by its own reactivity, different types of N-donor surface ligands on SBA15-supported Zr(IV) hydrides: [≡(Si-O-)(≡Si-N=)[Zr]H] and [≡(Si-NH-)(≡Si-X-)[Zr]H2] (X=O or...

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Pasha FA, Bendjeriou-Sedjerari A, Abou-Hamad E, et al. CO2 activation through silylimido and silylamido zirconium hydrides supported on N-donor chelating SBA15 surface ligands. Chem Commun (Camb). 2016;52(12):2577-80doi: 10.1039/c5cc08821f.
Pasha, F. A., Bendjeriou-Sedjerari, A., Abou-Hamad, E., Huang, K. W., & Basset, J. M. (2016). CO2 activation through silylimido and silylamido zirconium hydrides supported on N-donor chelating SBA15 surface ligands. Chemical communications (Cambridge, England), 52(12), 2577-80. https://doi.org/10.1039/c5cc08821f
Pasha, Farhan Ahmad, et al. "CO2 activation through silylimido and silylamido zirconium hydrides supported on N-donor chelating SBA15 surface ligands." Chemical communications (Cambridge, England) vol. 52,12 (2016): 2577-80. doi: https://doi.org/10.1039/c5cc08821f
Pasha FA, Bendjeriou-Sedjerari A, Abou-Hamad E, Huang KW, Basset JM. CO2 activation through silylimido and silylamido zirconium hydrides supported on N-donor chelating SBA15 surface ligands. Chem Commun (Camb). 2016 Feb 11;52(12):2577-80. doi: 10.1039/c5cc08821f. Epub 2016 Jan 11. PMID: 26750777.
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Homogeneous and heterogeneous catalysis: bridging the gap through surface organometallic chemistry.

Angewandte Chemie (International ed. in English)

Copéret C, Chabanas M, Petroff Saint-Arroman R, Basset JM.
PMID: 12532344
Angew Chem Int Ed Engl. 2003 Jan 13;42(2):156-81. doi: 10.1002/anie.200390072.

Surface organometallic chemistry is an area of heterogeneous catalysis which has recently emerged as a result of a comparative analysis of homogeneous and heterogeneous catalysis. The chemical industry has often favored heterogeneous catalysis, but the development of better catalysts...

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Copéret C, Chabanas M, Petroff Saint-Arroman R, et al. Homogeneous and heterogeneous catalysis: bridging the gap through surface organometallic chemistry. Angew Chem Int Ed Engl. 2003;42(2):156-81doi: 10.1002/anie.200390072.
Copéret, C., Chabanas, M., Petroff Saint-Arroman, R., & Basset, J. M. (2003). Homogeneous and heterogeneous catalysis: bridging the gap through surface organometallic chemistry. Angewandte Chemie (International ed. in English), 42(2), 156-81. https://doi.org/10.1002/anie.200390072
Copéret, Christophe, et al. "Homogeneous and heterogeneous catalysis: bridging the gap through surface organometallic chemistry." Angewandte Chemie (International ed. in English) vol. 42,2 (2003): 156-81. doi: https://doi.org/10.1002/anie.200390072
Copéret C, Chabanas M, Petroff Saint-Arroman R, Basset JM. Homogeneous and heterogeneous catalysis: bridging the gap through surface organometallic chemistry. Angew Chem Int Ed Engl. 2003 Jan 13;42(2):156-81. doi: 10.1002/anie.200390072. PMID: 12532344.
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