Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 1 to 12 of 427 entries
Sorted by: Best Match Show Resources per page
The occurrence of similar inventions in areas widely apart

museums

Mason OT.
GSID: 0_cRzOSG2-cJ
OT Mason - Science, 1887 - science.org

SCIENCE. Page 1 534 SCIENCE. LETTERS TO THE EDITOR. ***The attentionof scientific men i8 called to the advantages ofthe correspondence columns of SciENc Efor placing promptly on …

Cite
Mason, O. T. (1887). The occurrence of similar inventions in areas widely apart. Science, (226), 534-535.
Mason, Otis T. "The occurrence of similar inventions in areas widely apart." Science 226 (1887): 534-535.
Copy Download .nbib Format: MLA
Stoichiometric and catalytic C-F bond activation by the trans-dihydride NHC complex [Ru(IEt2Me2)2(PPh3)2H2] (IEt2Me2 = 1,3-diethyl-4,5-dimethylimidazol-2-ylidene).

Dalton transactions (Cambridge, England : 2003)

Cybulski MK, Riddlestone IM, Mahon MF, Woodman TJ, Whittlesey MK.
PMID: 26185808
Dalton Trans. 2015 Dec 07;44(45):19597-605. doi: 10.1039/c5dt01996f.

The room temperature reaction of C6F6 or C6F5H with [Ru(IEt2Me2)2(PPh3)2H2] (; IEt2Me2 = 1,3-diethyl-4,5-dimethylimidazol-2-ylidene) generated a mixture of the trans-hydride fluoride complex [Ru(IEt2Me2)2(PPh3)2HF] () and the bis-carbene pentafluorophenyl species [Ru(IEt2Me2)2(PPh3)(C6F5)H] (). The formation of resulted from C-H activation of...

Cite
Cybulski MK, Riddlestone IM, Mahon MF, et al. Stoichiometric and catalytic C-F bond activation by the trans-dihydride NHC complex [Ru(IEt2Me2)2(PPh3)2H2] (IEt2Me2 = 1,3-diethyl-4,5-dimethylimidazol-2-ylidene). Dalton Trans. 2015;44(45):19597-605doi: 10.1039/c5dt01996f.
Cybulski, M. K., Riddlestone, I. M., Mahon, M. F., Woodman, T. J., & Whittlesey, M. K. (2015). Stoichiometric and catalytic C-F bond activation by the trans-dihydride NHC complex [Ru(IEt2Me2)2(PPh3)2H2] (IEt2Me2 = 1,3-diethyl-4,5-dimethylimidazol-2-ylidene). Dalton transactions (Cambridge, England : 2003), 44(45), 19597-605. https://doi.org/10.1039/c5dt01996f
Cybulski, Mateusz K, et al. "Stoichiometric and catalytic C-F bond activation by the trans-dihydride NHC complex [Ru(IEt2Me2)2(PPh3)2H2] (IEt2Me2 = 1,3-diethyl-4,5-dimethylimidazol-2-ylidene)." Dalton transactions (Cambridge, England : 2003) vol. 44,45 (2015): 19597-605. doi: https://doi.org/10.1039/c5dt01996f
Cybulski MK, Riddlestone IM, Mahon MF, Woodman TJ, Whittlesey MK. Stoichiometric and catalytic C-F bond activation by the trans-dihydride NHC complex [Ru(IEt2Me2)2(PPh3)2H2] (IEt2Me2 = 1,3-diethyl-4,5-dimethylimidazol-2-ylidene). Dalton Trans. 2015 Dec 07;44(45):19597-605. doi: 10.1039/c5dt01996f. PMID: 26185808.
Copy Download .nbib Format: NLM
Metal influence on the iso- and hetero-selectivity of complexes of bipyrrolidine derived salan ligands for the polymerisation of .

Chemical science

Jones MD, Brady L, McKeown P, Buchard A, Schäfer PM, Thomas LH, Mahon MF, Woodman TJ, Lowe JP.
PMID: 29142728
Chem Sci. 2015 Aug 01;6(8):5034-5039. doi: 10.1039/c5sc01819f. Epub 2015 Jun 17.

In this paper we have prepared a series of Ti(iv), Hf(iv) and Al(iii) complexes based on bipyrrolidine salan pro-ligands. The Hf(iv) complexes have all been characterised in the solid-state, the chiral ligands coordinate to Hf(iv) in an α-

Cite
Jones MD, Brady L, McKeown P, et al. Metal influence on the iso- and hetero-selectivity of complexes of bipyrrolidine derived salan ligands for the polymerisation of . Chem Sci. 2015;6(8):5034-5039doi: 10.1039/c5sc01819f.
Jones, M. D., Brady, L., McKeown, P., Buchard, A., Schäfer, P. M., Thomas, L. H., Mahon, M. F., Woodman, T. J., & Lowe, J. P. (2015). Metal influence on the iso- and hetero-selectivity of complexes of bipyrrolidine derived salan ligands for the polymerisation of . Chemical science, 6(8), 5034-5039. https://doi.org/10.1039/c5sc01819f
Jones, Matthew D, et al. "Metal influence on the iso- and hetero-selectivity of complexes of bipyrrolidine derived salan ligands for the polymerisation of ." Chemical science vol. 6,8 (2015): 5034-5039. doi: https://doi.org/10.1039/c5sc01819f
Jones MD, Brady L, McKeown P, Buchard A, Schäfer PM, Thomas LH, Mahon MF, Woodman TJ, Lowe JP. Metal influence on the iso- and hetero-selectivity of complexes of bipyrrolidine derived salan ligands for the polymerisation of . Chem Sci. 2015 Aug 01;6(8):5034-5039. doi: 10.1039/c5sc01819f. Epub 2015 Jun 17. PMID: 29142728; PMCID: PMC5664169.
Copy Download .nbib Format: NLM
Markovnikov versus anti-Markovnikov Hydrophosphination: Divergent Reactivity Using an Iron(II) β-Diketiminate Pre-Catalyst.

Chemistry (Weinheim an der Bergstrasse, Germany)

King AK, Gallagher KJ, Mahon MF, Webster RL.
PMID: 28544315
Chemistry. 2017 Jul 06;23(38):9039-9043. doi: 10.1002/chem.201702374. Epub 2017 Jun 19.

The ability to tune between different regioselectivities using a common pre-catalyst is an unusual yet highly desirable process. Here, we report the use of an iron(II) pre-catalyst that can be used to synthesize vinyl phosphines in a Markovnikov-selective manner...

Cite
King AK, Gallagher KJ, Mahon MF, et al. Markovnikov versus anti-Markovnikov Hydrophosphination: Divergent Reactivity Using an Iron(II) β-Diketiminate Pre-Catalyst. Chemistry. 2017;23(38):9039-9043doi: 10.1002/chem.201702374.
King, A. K., Gallagher, K. J., Mahon, M. F., & Webster, R. L. (2017). Markovnikov versus anti-Markovnikov Hydrophosphination: Divergent Reactivity Using an Iron(II) β-Diketiminate Pre-Catalyst. Chemistry (Weinheim an der Bergstrasse, Germany), 23(38), 9039-9043. https://doi.org/10.1002/chem.201702374
King, Andrew K, et al. "Markovnikov versus anti-Markovnikov Hydrophosphination: Divergent Reactivity Using an Iron(II) β-Diketiminate Pre-Catalyst." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 23,38 (2017): 9039-9043. doi: https://doi.org/10.1002/chem.201702374
King AK, Gallagher KJ, Mahon MF, Webster RL. Markovnikov versus anti-Markovnikov Hydrophosphination: Divergent Reactivity Using an Iron(II) β-Diketiminate Pre-Catalyst. Chemistry. 2017 Jul 06;23(38):9039-9043. doi: 10.1002/chem.201702374. Epub 2017 Jun 19. PMID: 28544315.
Copy Download .nbib Format: NLM
Accessing the single-electron manifold: magnesium-mediated hydrogen release from silanes.

Angewandte Chemie (International ed. in English)

Liptrot DJ, Hill MS, Mahon MF.
PMID: 24782354
Angew Chem Int Ed Engl. 2014 Jun 10;53(24):6224-7. doi: 10.1002/anie.201403208. Epub 2014 Apr 29.

Reactions of TEMPO (2,2,6,6-tetramethyl-1-piperidinyloxy) with magnesium hydride species initiate oxidative hydrogen release, which may be elaborated to a catalytic regime within a manifold constructed about sequential TEMPO-mediated redox and Mg-O/Si-H metathesis processes.

Cite
Liptrot DJ, Hill MS, Mahon MF. Accessing the single-electron manifold: magnesium-mediated hydrogen release from silanes. Angew Chem Int Ed Engl. 2014;53(24):6224-7doi: 10.1002/anie.201403208.
Liptrot, D. J., Hill, M. S., & Mahon, M. F. (2014). Accessing the single-electron manifold: magnesium-mediated hydrogen release from silanes. Angewandte Chemie (International ed. in English), 53(24), 6224-7. https://doi.org/10.1002/anie.201403208
Liptrot, David J, et al. "Accessing the single-electron manifold: magnesium-mediated hydrogen release from silanes." Angewandte Chemie (International ed. in English) vol. 53,24 (2014): 6224-7. doi: https://doi.org/10.1002/anie.201403208
Liptrot DJ, Hill MS, Mahon MF. Accessing the single-electron manifold: magnesium-mediated hydrogen release from silanes. Angew Chem Int Ed Engl. 2014 Jun 10;53(24):6224-7. doi: 10.1002/anie.201403208. Epub 2014 Apr 29. PMID: 24782354.
Copy Download .nbib Format: NLM
Metabotropic Glutamate Receptor 5 and Glutamate Involvement in Major Depressive Disorder: A Multimodal Imaging Study.

Biological psychiatry. Cognitive neuroscience and neuroimaging

Abdallah CG, Hannestad J, Mason GF, Holmes SE, DellaGioia N, Sanacora G, Jiang L, Matuskey D, Satodiya R, Gasparini F, Lin X, Javitch J, Planeta B, Nabulsi N, Carson RE, Esterlis I.
PMID: 28993818
Biol Psychiatry Cogn Neurosci Neuroimaging. 2017 Jul;2(5):449-456. doi: 10.1016/j.bpsc.2017.03.019. Epub 2017 Apr 06.

BACKGROUND: Preclinical and postmortem studies have implicated the metabotropic glutamate receptor 5 (mGluR5) in the pathophysiology of major depressive disorder (MDD). The goal of the present study was to determine the role of mGluR5 in a large group of...

Cite
Abdallah CG, Hannestad J, Mason GF, et al. Metabotropic Glutamate Receptor 5 and Glutamate Involvement in Major Depressive Disorder: A Multimodal Imaging Study. Biol Psychiatry Cogn Neurosci Neuroimaging. 2017;2(5):449-456doi: 10.1016/j.bpsc.2017.03.019.
Abdallah, C. G., Hannestad, J., Mason, G. F., Holmes, S. E., DellaGioia, N., Sanacora, G., Jiang, L., Matuskey, D., Satodiya, R., Gasparini, F., Lin, X., Javitch, J., Planeta, B., Nabulsi, N., Carson, R. E., & Esterlis, I. (2017). Metabotropic Glutamate Receptor 5 and Glutamate Involvement in Major Depressive Disorder: A Multimodal Imaging Study. Biological psychiatry. Cognitive neuroscience and neuroimaging, 2(5), 449-456. https://doi.org/10.1016/j.bpsc.2017.03.019
Abdallah, Chadi G, et al. "Metabotropic Glutamate Receptor 5 and Glutamate Involvement in Major Depressive Disorder: A Multimodal Imaging Study." Biological psychiatry. Cognitive neuroscience and neuroimaging vol. 2,5 (2017): 449-456. doi: https://doi.org/10.1016/j.bpsc.2017.03.019
Abdallah CG, Hannestad J, Mason GF, Holmes SE, DellaGioia N, Sanacora G, Jiang L, Matuskey D, Satodiya R, Gasparini F, Lin X, Javitch J, Planeta B, Nabulsi N, Carson RE, Esterlis I. Metabotropic Glutamate Receptor 5 and Glutamate Involvement in Major Depressive Disorder: A Multimodal Imaging Study. Biol Psychiatry Cogn Neurosci Neuroimaging. 2017 Jul;2(5):449-456. doi: 10.1016/j.bpsc.2017.03.019. Epub 2017 Apr 06. PMID: 28993818; PMCID: PMC5630181.
Copy Download .nbib Format: NLM
Growth Conditions Control the Elastic and Electrical Properties of ZnO Nanowires.

Nano letters

Wang X, Chen K, Zhang Y, Wan J, Warren OL, Oh J, Li J, Ma E, Shan Z.
PMID: 26510098
Nano Lett. 2015 Dec 09;15(12):7886-92. doi: 10.1021/acs.nanolett.5b02852. Epub 2015 Nov 05.

Great efforts have been made to synthesize ZnO nanowires (NWs) as building blocks for a broad range of applications because of their unique mechanical and mechanoelectrical properties. However, little attention has been paid to the correlation between the NWs...

Cite
Wang X, Chen K, Zhang Y, et al. Growth Conditions Control the Elastic and Electrical Properties of ZnO Nanowires. Nano Lett. 2015;15(12):7886-92doi: 10.1021/acs.nanolett.5b02852.
Wang, X., Chen, K., Zhang, Y., Wan, J., Warren, O. L., Oh, J., Li, J., Ma, E., & Shan, Z. (2015). Growth Conditions Control the Elastic and Electrical Properties of ZnO Nanowires. Nano letters, 15(12), 7886-92. https://doi.org/10.1021/acs.nanolett.5b02852
Wang, Xiaoguang, et al. "Growth Conditions Control the Elastic and Electrical Properties of ZnO Nanowires." Nano letters vol. 15,12 (2015): 7886-92. doi: https://doi.org/10.1021/acs.nanolett.5b02852
Wang X, Chen K, Zhang Y, Wan J, Warren OL, Oh J, Li J, Ma E, Shan Z. Growth Conditions Control the Elastic and Electrical Properties of ZnO Nanowires. Nano Lett. 2015 Dec 09;15(12):7886-92. doi: 10.1021/acs.nanolett.5b02852. Epub 2015 Nov 05. PMID: 26510098.
Copy Download .nbib Format: NLM
Iron catalysed Negishi cross-coupling using simple ethyl-monophosphines.

Dalton transactions (Cambridge, England : 2003)

Brown CA, Nile TA, Mahon MF, Webster RL.
PMID: 25730705
Dalton Trans. 2015 Jul 21;44(27):12189-95. doi: 10.1039/c5dt00112a. Epub 2015 Mar 02.

Monophosphines prepared by iron catalysed hydrophosphination have been used as pro-ligands in iron catalysed Negishi cross-coupling of alkyl bromides and diphenyl zinc reagents. The cross-coupling has been investigated with monophosphines with varying electronic properties and we find the simplest,...

Cite
Brown CA, Nile TA, Mahon MF, et al. Iron catalysed Negishi cross-coupling using simple ethyl-monophosphines. Dalton Trans. 2015;44(27):12189-95doi: 10.1039/c5dt00112a.
Brown, C. A., Nile, T. A., Mahon, M. F., & Webster, R. L. (2015). Iron catalysed Negishi cross-coupling using simple ethyl-monophosphines. Dalton transactions (Cambridge, England : 2003), 44(27), 12189-95. https://doi.org/10.1039/c5dt00112a
Brown, Caleb A, et al. "Iron catalysed Negishi cross-coupling using simple ethyl-monophosphines." Dalton transactions (Cambridge, England : 2003) vol. 44,27 (2015): 12189-95. doi: https://doi.org/10.1039/c5dt00112a
Brown CA, Nile TA, Mahon MF, Webster RL. Iron catalysed Negishi cross-coupling using simple ethyl-monophosphines. Dalton Trans. 2015 Jul 21;44(27):12189-95. doi: 10.1039/c5dt00112a. Epub 2015 Mar 02. PMID: 25730705.
Copy Download .nbib Format: NLM
Rhodium-Promoted Linear Tetramerization and Cyclization of 3,3-Dimethylbut-l-yne.

Angewandte Chemie (International ed. in English)

Burrows AD, Green M, Jeffery JC, Lynam JM, Mahon MF.
PMID: 10540415
Angew Chem Int Ed Engl. 1999 Oct 18;38(20):3043-3045. doi: 10.1002/(sici)1521-3773(19991018)38:20<3043::aid-anie3043>3.0.co;2-2.

With tetrahydrofuran as the solvent [Rh(thf)(2)(cod)](+) promotes the selective coupling of tBuC(2)H to form triene-yne 1; at high alkyne concentrations, however, an unusual C-H activation process intervenes, leading to the formation of complex 2, which contains two linked five-membered...

Cite
Burrows AD, Green M, Jeffery JC, et al. Rhodium-Promoted Linear Tetramerization and Cyclization of 3,3-Dimethylbut-l-yne. Angew Chem Int Ed Engl. 1999;38(20):3043-3045doi: 10.1002/(sici)1521-3773(19991018)38:20<3043::aid-anie3043>3.0.co;2-2.
Burrows, A. D., Green, M., Jeffery, J. C., Lynam, J. M., & Mahon, M. F. (1999). Rhodium-Promoted Linear Tetramerization and Cyclization of 3,3-Dimethylbut-l-yne. Angewandte Chemie (International ed. in English), 38(20), 3043-3045. https://doi.org/10.1002/(sici)1521-3773(19991018)38:20<3043::aid-anie3043>3.0.co;2-2
Burrows, et al. "Rhodium-Promoted Linear Tetramerization and Cyclization of 3,3-Dimethylbut-l-yne." Angewandte Chemie (International ed. in English) vol. 38,20 (1999): 3043-3045. doi: https://doi.org/10.1002/(sici)1521-3773(19991018)38:20<3043::aid-anie3043>3.0.co;2-2
Burrows AD, Green M, Jeffery JC, Lynam JM, Mahon MF. Rhodium-Promoted Linear Tetramerization and Cyclization of 3,3-Dimethylbut-l-yne. Angew Chem Int Ed Engl. 1999 Oct 18;38(20):3043-3045. doi: 10.1002/(sici)1521-3773(19991018)38:20<3043::aid-anie3043>3.0.co;2-2. PMID: 10540415.
Copy Download .nbib Format: NLM
Structures of Sb(OC(6)H(3)Me(2)-2,6)(3) and Sb(OEt)(5) x NH(3): the first authenticated monomeric Sb(OR)(n) (n = 3, 5).

Inorganic chemistry

Horley GA, Mahon MF, Molloy KC, Venter MM, Haycock PW, Myers CP.
PMID: 11896736
Inorg Chem. 2002 Mar 25;41(6):1652-7. doi: 10.1021/ic0106726.

The first monomeric antimony alkoxides, Sb(OC(6)H(3)Me(2))(3) (1) and Sb(OEt)(5) x NH(3) (2), have been crystallographically characterized. The former adopts a trigonal pyramidal geometry, while the latter is octahedral about antimony; hydrogen bonding between NH(3) and SbOEt groups in Sb(OEt)(5)...

Cite
Horley GA, Mahon MF, Molloy KC, et al. Structures of Sb(OC(6)H(3)Me(2)-2,6)(3) and Sb(OEt)(5) x NH(3): the first authenticated monomeric Sb(OR)(n) (n = 3, 5). Inorg Chem. 2002;41(6):1652-7doi: 10.1021/ic0106726.
Horley, G. A., Mahon, M. F., Molloy, K. C., Venter, M. M., Haycock, P. W., & Myers, C. P. (2002). Structures of Sb(OC(6)H(3)Me(2)-2,6)(3) and Sb(OEt)(5) x NH(3): the first authenticated monomeric Sb(OR)(n) (n = 3, 5). Inorganic chemistry, 41(6), 1652-7. https://doi.org/10.1021/ic0106726
Horley, Graeme A, et al. "Structures of Sb(OC(6)H(3)Me(2)-2,6)(3) and Sb(OEt)(5) x NH(3): the first authenticated monomeric Sb(OR)(n) (n = 3, 5)." Inorganic chemistry vol. 41,6 (2002): 1652-7. doi: https://doi.org/10.1021/ic0106726
Horley GA, Mahon MF, Molloy KC, Venter MM, Haycock PW, Myers CP. Structures of Sb(OC(6)H(3)Me(2)-2,6)(3) and Sb(OEt)(5) x NH(3): the first authenticated monomeric Sb(OR)(n) (n = 3, 5). Inorg Chem. 2002 Mar 25;41(6):1652-7. doi: 10.1021/ic0106726. PMID: 11896736.
Copy Download .nbib Format: NLM
Selective cleavage of P-N bonds and the conversion of rhodium N-pyrrolyl phosphine complexes into diphosphoxane-bridged dimers.

Inorganic chemistry

Burrows AD, Mahon MF, Palmer MT, Varrone M.
PMID: 11925157
Inorg Chem. 2002 Apr 08;41(7):1695-7. doi: 10.1021/ic0108989.

Rhodium(I) complexes trans-[RhCl(CO)(PR(2)[NC(4)H(3)C(O)Me-2])(2)] (R = Ph, NC(4)H(4)) react with water to give the diphosphoxane-bridged dimers [Rh(2)Cl(2)(CO)(2)(mu-PR(2)OPR(2))(2)] following cleavage of the P-N bonds to the 2-acetyl-N-pyrrolyl groups. The two dimers have been crystallographically characterized and show a number of structural...

Cite
Burrows AD, Mahon MF, Palmer MT, et al. Selective cleavage of P-N bonds and the conversion of rhodium N-pyrrolyl phosphine complexes into diphosphoxane-bridged dimers. Inorg Chem. 2002;41(7):1695-7doi: 10.1021/ic0108989.
Burrows, A. D., Mahon, M. F., Palmer, M. T., & Varrone, M. (2002). Selective cleavage of P-N bonds and the conversion of rhodium N-pyrrolyl phosphine complexes into diphosphoxane-bridged dimers. Inorganic chemistry, 41(7), 1695-7. https://doi.org/10.1021/ic0108989
Burrows, Andrew D, et al. "Selective cleavage of P-N bonds and the conversion of rhodium N-pyrrolyl phosphine complexes into diphosphoxane-bridged dimers." Inorganic chemistry vol. 41,7 (2002): 1695-7. doi: https://doi.org/10.1021/ic0108989
Burrows AD, Mahon MF, Palmer MT, Varrone M. Selective cleavage of P-N bonds and the conversion of rhodium N-pyrrolyl phosphine complexes into diphosphoxane-bridged dimers. Inorg Chem. 2002 Apr 08;41(7):1695-7. doi: 10.1021/ic0108989. PMID: 11925157.
Copy Download .nbib Format: NLM
[(iPr3P)6Rh6H12]2+: a high-hydride content octahedron that bridges the gap between late and early transition metal clusters.

Journal of the American Chemical Society

Ingleson MJ, Mahon MF, Raithby PR, Weller AS.
PMID: 15080675
J Am Chem Soc. 2004 Apr 21;126(15):4784-5. doi: 10.1021/ja049402n.

Treatment of [(iPr3P)2Rh(nbd)][Y] {nbd = norbornadiene, Y = B{3,5-(CF3)2C6H3}4- [B(ArF)4] or 1-H-closo-CB11Me11-} with H2 (ca. 4 atm) results in the isolation, in moderate yield, of the octahedral cluster complex [(iPr3P)6Rh6H12][Y]2 1. The cluster (for both anions) has been characterized...

Cite
Ingleson MJ, Mahon MF, Raithby PR, et al. [(iPr3P)6Rh6H12]2+: a high-hydride content octahedron that bridges the gap between late and early transition metal clusters. J Am Chem Soc. 2004;126(15):4784-5doi: 10.1021/ja049402n.
Ingleson, M. J., Mahon, M. F., Raithby, P. R., & Weller, A. S. (2004). [(iPr3P)6Rh6H12]2+: a high-hydride content octahedron that bridges the gap between late and early transition metal clusters. Journal of the American Chemical Society, 126(15), 4784-5. https://doi.org/10.1021/ja049402n
Ingleson, Michael J, et al. "[(iPr3P)6Rh6H12]2+: a high-hydride content octahedron that bridges the gap between late and early transition metal clusters." Journal of the American Chemical Society vol. 126,15 (2004): 4784-5. doi: https://doi.org/10.1021/ja049402n
Ingleson MJ, Mahon MF, Raithby PR, Weller AS. [(iPr3P)6Rh6H12]2+: a high-hydride content octahedron that bridges the gap between late and early transition metal clusters. J Am Chem Soc. 2004 Apr 21;126(15):4784-5. doi: 10.1021/ja049402n. PMID: 15080675.
Copy Download .nbib Format: NLM
Showing 1 to 12 of 427 entries