LIVIVO - Search results -

Search results

Result 1 - 10 of total 17

Search options

Article ; Online: Solvent-Free Aerobic Oxidative Cleavage of Methyl Oleate to Biobased Aldehydes over Mechanochemically Synthesized Supported AgAu Nanoparticles.

da Silva, Rafael T P / Silva, Dagoberto O / de Oliveira, Paulo F M / Bellabarba, Ronan / Johnston, Peter / Smit, Joost / Holt, Jarle / Betham, Michael / Rossi, Liane M

ChemPlusChem

2023 Volume 88, Issue 10, Page(s) e202300268

Abstract: The performance of mechanochemically synthesized supported bimetallic AgAu nanoalloy catalysts was evaluated in the oxidative cleavage of methyl oleate, a commonly available unsaturated bio-derived raw material. An extensive screening of supports ( ... ...

Abstract	The performance of mechanochemically synthesized supported bimetallic AgAu nanoalloy catalysts was evaluated in the oxidative cleavage of methyl oleate, a commonly available unsaturated bio-derived raw material. An extensive screening of supports (SiO
Language	English
Publishing date	2023-08-16
Publishing country	Germany
Document type	Journal Article
ISSN	2192-6506
ISSN (online)	2192-6506
DOI	10.1002/cplu.202300268
Database	MEDical Literature Analysis and Retrieval System OnLINE

Full text online

Accessible to users with ZB MED library card

Order via subito

This service is chargeable due to the Delivery terms set by subito. Orders including an article and supplementary material will be classified as separate orders. In these cases, fees will be demanded for each order.

Inter-library loan at ZB MED

Your chosen title can be delivered directly to ZB MED Cologne location if you are registered as a user at ZB MED Cologne.

Details ▾
- Full text online
- Order with fees

Article ; Online: Size dependent reduction-oxidation-reduction behaviour of cobalt oxide nanocrystals.

Sadasivan, Sajanikumari / Bellabarba, Ronan M / Tooze, Robert P

Nanoscale

2013 Volume 5, Issue 22, Page(s) 11139–11146

Abstract: Morphologically similar cobalt oxide nanoparticles (Co3O4) of four different sizes (3 nm, 6 nm, 11 nm and 29 nm) with narrow size distribution were prepared by subtle variation of synthesis conditions. These nanoparticles were used as model materials to ... ...

Abstract	Morphologically similar cobalt oxide nanoparticles (Co3O4) of four different sizes (3 nm, 6 nm, 11 nm and 29 nm) with narrow size distribution were prepared by subtle variation of synthesis conditions. These nanoparticles were used as model materials to understand the structural and morphological changes that occur to cobalt oxide during sequential reduction, oxidation and further re-reduction process as a function of the initial size of cobalt oxide. On reduction, spherical cobalt nanoparticles were obtained independent of the original size of cobalt oxide. In contrast, subsequent oxidation of the metal particles led to solid spheres, hollow spheres or core-shell structures depending on the size of the initial metal particle. Further re-reduction of the oxidized structures was also observed to be size dependent. The hollow oxide shells formed by the large particles (29 nm) fragmented into smaller particles on reduction, while the hollow shells of the medium sized particles (11 nm) did not re-disperse on further reduction. Similarly, no re-dispersion was observed in the case of the small particles (6 nm). This model study provides useful insights into the size dependent behavior of metal/metal oxide particles during oxidation/reduction. This has important implications in petrochemical industry where cobalt is used as a catalyst in the Fischer-Tropsch process.
Language	English
Publishing date	2013-11-21
Publishing country	England
Document type	Journal Article
ZDB-ID	2515664-0
ISSN	2040-3372 ; 2040-3364
ISSN (online)	2040-3372
ISSN	2040-3364
DOI	10.1039/c3nr02877a
Database	MEDical Literature Analysis and Retrieval System OnLINE

Order via subito

Article: Scalable strategies for the synthesis of well-defined copper metal and oxide nanocrystals

Lignier, Pascal / Bellabarba, Ronan / Tooze, Robert P

Chemical Society reviews. 2012 Feb. 13, v. 41, no. 5

2012

Abstract: This tutorial review highlights the most promising methods for the preparation of well-defined copper metal and oxide nanocrystals. These methodologies could be applied to other metals. We present the main synthetic strategies and associated mechanisms ... ...

Abstract	This tutorial review highlights the most promising methods for the preparation of well-defined copper metal and oxide nanocrystals. These methodologies could be applied to other metals. We present the main synthetic strategies and associated mechanisms to control monodispersity, size, morphology and structure of metal and oxide nanomaterials which can adopt spherical, polyhedral, cubic, rod, wire, plate shapes and possibly hollow structures. We also consider the scale-up of the production of these nanocrystals, which is crucial for a wide range of potential applications such as catalysis, photovoltaics, electronics, optics and electrocatalysis.
Keywords	catalytic activity ; copper ; copper nanoparticles ; electrochemistry ; electronics ; nanocrystals ; optics ; solar energy
Language	English
Dates of publication	2012-0213
Size	p. 1708-1720.
Publishing place	The Royal Society of Chemistry
Document type	Article
ZDB-ID	1472875-8
ISSN	1460-4744 ; 0306-0012
ISSN (online)	1460-4744
ISSN	0306-0012
DOI	10.1039/c1cs15223h
Database	NAL-Catalogue (AGRICOLA)

Order via subito

Article ; Online: Scalable strategies for the synthesis of well-defined copper metal and oxide nanocrystals.

Lignier, Pascal / Bellabarba, Ronan / Tooze, Robert P

Chemical Society reviews

2012 Volume 41, Issue 5, Page(s) 1708–1720

Abstract	This tutorial review highlights the most promising methods for the preparation of well-defined copper metal and oxide nanocrystals. These methodologies could be applied to other metals. We present the main synthetic strategies and associated mechanisms to control monodispersity, size, morphology and structure of metal and oxide nanomaterials which can adopt spherical, polyhedral, cubic, rod, wire, plate shapes and possibly hollow structures. We also consider the scale-up of the production of these nanocrystals, which is crucial for a wide range of potential applications such as catalysis, photovoltaics, electronics, optics and electrocatalysis.
Language	English
Publishing date	2012-03-07
Publishing country	England
Document type	Journal Article
ZDB-ID	1472875-8
ISSN	1460-4744 ; 0306-0012
ISSN (online)	1460-4744
ISSN	0306-0012
DOI	10.1039/c1cs15223h
Database	MEDical Literature Analysis and Retrieval System OnLINE

Order via subito

Article ; Online: One-step synthesis and shape-control of CuPd nanowire networks.

Yu, Fengjiao / Zhou, Wuzong / Bellabarba, Ronan M / Tooze, Robert P

Nanoscale

2014 Volume 6, Issue 2, Page(s) 1093–1098

Abstract: An effective one-step method has been developed to synthesize CuPd bimetallic nanowire networks. Investigation of the growth process revealed that the nanowires were formed by attachment of spherical particles and strongly influenced by interactions ... ...

Abstract	An effective one-step method has been developed to synthesize CuPd bimetallic nanowire networks. Investigation of the growth process revealed that the nanowires were formed by attachment of spherical particles and strongly influenced by interactions between surface ligands and metals. The morphology of CuPd nanoparticles is tuned via changing the molecular weight of polyvinylpyrrolidone (PVP) and solvents. The versatility of this method was further demonstrated by preparation of AgPd nanowires. An electrochemical study of CuPd nanowire networks shows morphology dependent activity in oxygen reduction reaction (ORR), which is comparable to that of platinum.
Language	English
Publishing date	2014-01-21
Publishing country	England
Document type	Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID	2515664-0
ISSN	2040-3372 ; 2040-3364
ISSN (online)	2040-3372
ISSN	2040-3364
DOI	10.1039/c3nr04223e
Database	MEDical Literature Analysis and Retrieval System OnLINE

Order via subito

Article ; Online: Activation of carbon dioxide and carbon disulfide by a scandium N-heterocyclic carbene complex.

Arnold, Polly L / Marr, Isobel A / Zlatogorsky, Sergey / Bellabarba, Ronan / Tooze, Robert P

Dalton transactions (Cambridge, England : 2003)

2014 Volume 43, Issue 1, Page(s) 34–37

Abstract: A Sc NHC complex readily activates three equivalents of CO2 showing 'Frustrated Lewis Pair' type reactivity with each metal-carbene bond, but whilst CS2 is also activated by the labile carbenes, no metal involvement is observed. ...

Abstract	A Sc NHC complex readily activates three equivalents of CO2 showing 'Frustrated Lewis Pair' type reactivity with each metal-carbene bond, but whilst CS2 is also activated by the labile carbenes, no metal involvement is observed.
Language	English
Publishing date	2014-01-07
Publishing country	England
Document type	Journal Article
ZDB-ID	1472887-4
ISSN	1477-9234 ; 1364-5447 ; 0300-9246 ; 1477-9226
ISSN (online)	1477-9234 ; 1364-5447
ISSN	0300-9246 ; 1477-9226
DOI	10.1039/c3dt52762j
Database	MEDical Literature Analysis and Retrieval System OnLINE

Order via subito

Article ; Online: Carbon-silicon and carbon-carbon bond formation by elimination reactions at metal N-heterocyclic carbene complexes.

Arnold, Polly L / Turner, Zoë R / Bellabarba, Ronan / Tooze, Robert P

Journal of the American Chemical Society

2011 Volume 133, Issue 30, Page(s) 11744–11756

Abstract: Two functional groups can be delivered at once to organo-rare earth complexes, (L)MR(2) and (L)(2)MR (M = Sc, Y; L = ({1-C(NDippCH(2)CH(2)N)}CH(2)CMe(2)O), Dipp = 2,6-(i)Pr(2)-C(6)H(3); R = CH(2)SiMe(3), CH(2)CMe(3)), via the addition of E-X across the ... ...

Abstract	Two functional groups can be delivered at once to organo-rare earth complexes, (L)MR(2) and (L)(2)MR (M = Sc, Y; L = ({1-C(NDippCH(2)CH(2)N)}CH(2)CMe(2)O), Dipp = 2,6-(i)Pr(2)-C(6)H(3); R = CH(2)SiMe(3), CH(2)CMe(3)), via the addition of E-X across the metal-carbene bond to form a zwitterionic imidazolinium-metal complex, (L(E))MR(2)X, where L(E) = {1-EC(NDippCH(2)CH(2)N)}CH(2)CMe(2)O, E is a p-block functional group such as SiR(3), PR(2), or SnR(3), and X is a halide. The "ate" complex (L(Li))ScR(3) is readily accessible and is best described as a Li carbene adduct, ({1-Li(THF)C(NDippCH(2)CH(2)N)}CH(2)CMe(2)O)Sc(CH(2)SiMe(3))(3), since structural characterization shows the alkoxide ligand bridging the two metals and the carbene Li-bound with the shortest yet recorded Li-C bond distance. This can be converted via lithium halide-eliminating salt metathesis reactions to alkylated or silylated imidazolinium derivatives, (L(E))ScR(3) (E = SiMe(3) or CPh(3)). All the E-functionalized imidazolinium complexes spontaneously eliminate functionalized hydrocarbyl compounds upon warming to room temperature or slightly above, forming new organic products ER, i.e., forming C-Si, C-P, and C-Sn bonds, and re-forming the inorganic metal carbene (L)MR(X) or (L)(2)MX complex, respectively. Warming the tris(alkyl) complexes (L(E))MR(3) forms organic products arising from C-C or C-Si bond formation, which appears to proceed via the same elimination route. Treatment of (L)(2)Sc(CH(2)SiMe(3)) with iodopentafluorobenzene results in the "reverse sense" addition, which upon thermolysis forms the metal aryl complex (L)(2)Sc(C(6)F(5)) and releases the iodoalkane Me(3)SiCH(2)I, again facilitated by the reversible functionalization of the N-heterocyclic carbene group in these tethered systems.
MeSH term(s)	Carbon/chemistry ; Crystallography, X-Ray ; Heterocyclic Compounds/chemistry ; Methane/analogs & derivatives ; Methane/chemistry ; Models, Molecular ; Molecular Conformation ; Organometallic Compounds/chemical synthesis ; Organometallic Compounds/chemistry ; Scandium/chemistry ; Silicon/chemistry ; Stereoisomerism ; Yttrium/chemistry
Chemical Substances	Heterocyclic Compounds ; Organometallic Compounds ; carbene (2465-56-7) ; Yttrium (58784XQC3Y) ; Carbon (7440-44-0) ; Methane (OP0UW79H66) ; Scandium (YUJ4U1EW7R) ; Silicon (Z4152N8IUI)
Language	English
Publishing date	2011-08-03
Publishing country	United States
Document type	Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID	3155-0
ISSN	1520-5126 ; 0002-7863
ISSN (online)	1520-5126
ISSN	0002-7863
DOI	10.1021/ja204209t
Database	MEDical Literature Analysis and Retrieval System OnLINE

In stock of ZB MED Bonn / Germany

Z 4' 55/32: Show issues
Z 7.3: Show issues

Order via subito

Inter-library loan at ZB MED

Your chosen title can be delivered directly to ZB MED Cologne location if you are registered as a user at ZB MED Cologne.

Details ▾
- See ZB MED holdings
- Order with fees

Article ; Online: Addition-elimination reactions across the M-C bond of metal N-heterocyclic carbenes.

Turner, Zoë R / Bellabarba, Ronan / Tooze, Robert P / Arnold, Polly L

Journal of the American Chemical Society

2010 Volume 132, Issue 12, Page(s) 4050–4051

Abstract: Silyl, phosphinyl, stannyl, and boryl reagents can be added across the neutral metal-carbon dative bond in d(0) f-block metal N-heterocyclic carbene complexes in a reversible manner, allowing additional functional groups to be incorporated into redox- ... ...

Abstract	Silyl, phosphinyl, stannyl, and boryl reagents can be added across the neutral metal-carbon dative bond in d(0) f-block metal N-heterocyclic carbene complexes in a reversible manner, allowing additional functional groups to be incorporated into redox-inactive organo-f-block compounds.
Language	English
Publishing date	2010-03-31
Publishing country	United States
Document type	Journal Article
ZDB-ID	3155-0
ISSN	1520-5126 ; 0002-7863
ISSN (online)	1520-5126
ISSN	0002-7863
DOI	10.1021/ja910673q
Database	MEDical Literature Analysis and Retrieval System OnLINE

In stock of ZB MED Bonn / Germany

Z 4' 55/32: Show issues
Z 7.3: Show issues

Order via subito

Inter-library loan at ZB MED

Your chosen title can be delivered directly to ZB MED Cologne location if you are registered as a user at ZB MED Cologne.

Details ▾
- See ZB MED holdings
- Order with fees

Article ; Online: Homo- and heteroleptic alkoxycarbene f-element complexes and their reactivity towards acidic N-H and C-H bonds.

Arnold, Polly L / Cadenbach, Thomas / Marr, Isobel H / Fyfe, Andrew A / Bell, Nicola L / Bellabarba, Ronan / Tooze, Robert P / Love, Jason B

Dalton transactions (Cambridge, England : 2003)

2014 Volume 43, Issue 38, Page(s) 14346–14358

Abstract: The reactivity of a series of organometallic rare earth and actinide complexes with hemilabile NHC-ligands towards substrates with acidic C-H and N-H bonds is described. The synthesis, characterisation and X-ray structures of the new heteroleptic mono- ... ...

Abstract	The reactivity of a series of organometallic rare earth and actinide complexes with hemilabile NHC-ligands towards substrates with acidic C-H and N-H bonds is described. The synthesis, characterisation and X-ray structures of the new heteroleptic mono- and bis(NHC) cyclopentadienyl complexes LnCp2(L) 1 (Ln = Sc, Y, Ce; L = alkoxy-tethered carbene [OCMe2CH2(1-C{NCHCHN(i)Pr})]), LnCp(L)2 (Ln = Y) , and the homoleptic tetrakis(NHC) complex Th(L)4 4 are described. The reactivity of these complexes, and of the homoleptic complexes Ln(L)3 (Ln = Sc 3, Ce), with E-H substrates is described, where EH = pyrrole C4H4NH, indole C8H6NH, diphenylacetone Ph2CC(O)Me, terminal alkynes RC≡CH (R = Me3Si, Ph), and cyclopentadiene C5H6. Complex 1-Y heterolytically cleaves and adds pyrrole and indole N-H across the metal carbene bond, whereas 1-Ce does not, although 3 and 4 form H-bonded adducts. Complexes 1-Y and 1-Sc form adducts with CpH without cleaving the acidic C-H bond, 1-Ce cleaves the Cp-H bond, but 2 reacts to form the very rare H(+)-[C5H5](-)-H(+) motif. Complex 1-Ce cleaves alkyne C-H bonds but the products rearrange upon formation, while complex 1-Y cleaves the C-H bond in diphenylacetone forming a product which rearranges to the Y-O bonded enolate product.
Language	English
Publishing date	2014-10-14
Publishing country	England
Document type	Journal Article
ZDB-ID	1472887-4
ISSN	1477-9234 ; 1364-5447 ; 0300-9246 ; 1477-9226
ISSN (online)	1477-9234 ; 1364-5447
ISSN	0300-9246 ; 1477-9226
DOI	10.1039/c4dt01442a
Database	MEDical Literature Analysis and Retrieval System OnLINE

Order via subito

Article ; Online: Covalency in Ce(IV) and U(IV) halide and N-heterocyclic carbene bonds.

Arnold, Polly L / Turner, Zoë R / Kaltsoyannis, Nikolas / Pelekanaki, Panagiota / Bellabarba, Ronan M / Tooze, Robert P

Chemistry (Weinheim an der Bergstrasse, Germany)

2010 Volume 16, Issue 31, Page(s) 9623–9629

Abstract: Oxidative halogenation with trityl chloride provides convenient access to Ce(IV) and U(IV) chloroamides [M(N{SiMe(3)}(2))(3)Cl] and their N-heterocyclic carbene derivatives, [M(L)(N{SiMe(3)}(2))(2)Cl] (L = OCMe(2)CH(2)(CNCH(2)CH(2)NDipp) Dipp = 2,6-iPr(2) ...

Abstract	Oxidative halogenation with trityl chloride provides convenient access to Ce(IV) and U(IV) chloroamides [M(N{SiMe(3)}(2))(3)Cl] and their N-heterocyclic carbene derivatives, [M(L)(N{SiMe(3)}(2))(2)Cl] (L = OCMe(2)CH(2)(CNCH(2)CH(2)NDipp) Dipp = 2,6-iPr(2)C(6)H(3)). Computational analysis of the bonding in these and a fluoro analogue, [U(L)(N{SiMe(3)}(2))(2)F], provides new information on the covalency in this relative rare oxidation state for molecular cerium complexes. Computational studies reveal increased Mayer bond orders in the actinide carbene bond compared with the lanthanide carbene bond, and natural and atoms-in-molecules analyses suggest greater overall ionicity in the cerium complexes than in the uranium analogues.
Language	English
Publishing date	2010-08-16
Publishing country	Germany
Document type	Journal Article
ZDB-ID	1478547-x
ISSN	1521-3765 ; 0947-6539
ISSN (online)	1521-3765
ISSN	0947-6539
DOI	10.1002/chem.201001471
Database	MEDical Literature Analysis and Retrieval System OnLINE

Full text online

Accessible to users with ZB MED library card

Order via subito

Details ▾
- Full text online
- Order with fees

To top

Your last searches

Full text online

More links

Kategorien

Order via subito

Inter-library loan at ZB MED

More links

Kategorien

Order via subito

More links

Kategorien

Order via subito

More links

Kategorien

Order via subito

More links

Kategorien

Order via subito

More links

Kategorien

Order via subito

More links

Kategorien

In stock of ZB MED Bonn / Germany

Order via subito

Inter-library loan at ZB MED

More links

Kategorien

In stock of ZB MED Bonn / Germany

Order via subito

Inter-library loan at ZB MED

More links

Kategorien

Order via subito

Full text online

More links

Kategorien

Order via subito