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Facile preparation of oriented nanoporous silica films from solvent-free liquid-crystalline mixtures.

Chemical communications (Cambridge, England)

Mizoshita N, Tani T, Inagaki S.
PMID: 23023655
Chem Commun (Camb). 2012 Nov 11;48(87):10772-4. doi: 10.1039/c2cc36306b.

Mixtures of an amphiphilic perylene bisimide derivative and tetramethoxysilane in the absence of solvents have been found to exhibit stable columnar liquid-crystalline phases which transform into macroscopically oriented nanoporous silica films as a result of simple mechanical shearing.

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Mizoshita N, Tani T, Inagaki S. Facile preparation of oriented nanoporous silica films from solvent-free liquid-crystalline mixtures. Chem Commun (Camb). 2012;48(87):10772-4doi: 10.1039/c2cc36306b.
Mizoshita, N., Tani, T., & Inagaki, S. (2012). Facile preparation of oriented nanoporous silica films from solvent-free liquid-crystalline mixtures. Chemical communications (Cambridge, England), 48(87), 10772-4. https://doi.org/10.1039/c2cc36306b
Mizoshita, Norihiro, et al. "Facile preparation of oriented nanoporous silica films from solvent-free liquid-crystalline mixtures." Chemical communications (Cambridge, England) vol. 48,87 (2012): 10772-4. doi: https://doi.org/10.1039/c2cc36306b
Mizoshita N, Tani T, Inagaki S. Facile preparation of oriented nanoporous silica films from solvent-free liquid-crystalline mixtures. Chem Commun (Camb). 2012 Nov 11;48(87):10772-4. doi: 10.1039/c2cc36306b. PMID: 23023655.
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Thiazole as a weak electron-donor unit to lower the frontier orbital energy levels of donor-acceptor alternating conjugated materials.

Chemical communications (Cambridge, England)

Zaborova E, Chávez P, Bechara R, Lévêque P, Heiser T, Méry S, Leclerc N.
PMID: 24036612
Chem Commun (Camb). 2013 Nov 04;49(85):9938-40. doi: 10.1039/c3cc45481a.

We demonstrate that the substitution of the thiophene by the thiazole heterocyclic compound as a weak electron-donor unit, in donor-acceptor alternating conjugated materials, allows a simultaneous downshift of both HOMO and LUMO levels while keeping the energy bandgap almost...

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Zaborova E, Chávez P, Bechara R, et al. Thiazole as a weak electron-donor unit to lower the frontier orbital energy levels of donor-acceptor alternating conjugated materials. Chem Commun (Camb). 2013;49(85):9938-40doi: 10.1039/c3cc45481a.
Zaborova, E., Chávez, P., Bechara, R., Lévêque, P., Heiser, T., Méry, S., & Leclerc, N. (2013). Thiazole as a weak electron-donor unit to lower the frontier orbital energy levels of donor-acceptor alternating conjugated materials. Chemical communications (Cambridge, England), 49(85), 9938-40. https://doi.org/10.1039/c3cc45481a
Zaborova, Elena, et al. "Thiazole as a weak electron-donor unit to lower the frontier orbital energy levels of donor-acceptor alternating conjugated materials." Chemical communications (Cambridge, England) vol. 49,85 (2013): 9938-40. doi: https://doi.org/10.1039/c3cc45481a
Zaborova E, Chávez P, Bechara R, Lévêque P, Heiser T, Méry S, Leclerc N. Thiazole as a weak electron-donor unit to lower the frontier orbital energy levels of donor-acceptor alternating conjugated materials. Chem Commun (Camb). 2013 Nov 04;49(85):9938-40. doi: 10.1039/c3cc45481a. PMID: 24036612.
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Unprecedented stacking of MV2+ dications and MV˙+ radical cations in the mixed-valence viologen salt (MV)2(BF4)3 (MV = methylviologen).

Chemical communications (Cambridge, England)

Leblanc N, Mercier N, Toma O, Kassiba AH, Zorina L, Auban-Senzier P, Pasquier C.
PMID: 24067860
Chem Commun (Camb). 2013 Nov 11;49(87):10272-4. doi: 10.1039/c3cc45690k.

Using a slow liquid-gas diffusion method, the mixed-valence viologen salt (MV)2(BF4)3 (1) and the radical cation salt (MV)(BF4) (2) are crystallized. Both structures contain regular stacks of MV˙(+) radical cations (2) or alternating MV˙(+) and MV(2+) entities (1). A...

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Leblanc N, Mercier N, Toma O, et al. Unprecedented stacking of MV2+ dications and MV˙+ radical cations in the mixed-valence viologen salt (MV)2(BF4)3 (MV = methylviologen). Chem Commun (Camb). 2013;49(87):10272-4doi: 10.1039/c3cc45690k.
Leblanc, N., Mercier, N., Toma, O., Kassiba, A. H., Zorina, L., Auban-Senzier, P., & Pasquier, C. (2013). Unprecedented stacking of MV2+ dications and MV˙+ radical cations in the mixed-valence viologen salt (MV)2(BF4)3 (MV = methylviologen). Chemical communications (Cambridge, England), 49(87), 10272-4. https://doi.org/10.1039/c3cc45690k
Leblanc, Nicolas, et al. "Unprecedented stacking of MV2+ dications and MV˙+ radical cations in the mixed-valence viologen salt (MV)2(BF4)3 (MV = methylviologen)." Chemical communications (Cambridge, England) vol. 49,87 (2013): 10272-4. doi: https://doi.org/10.1039/c3cc45690k
Leblanc N, Mercier N, Toma O, Kassiba AH, Zorina L, Auban-Senzier P, Pasquier C. Unprecedented stacking of MV2+ dications and MV˙+ radical cations in the mixed-valence viologen salt (MV)2(BF4)3 (MV = methylviologen). Chem Commun (Camb). 2013 Nov 11;49(87):10272-4. doi: 10.1039/c3cc45690k. PMID: 24067860.
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First practical cross-alkylation of primary alcohols with a new and recyclable impregnated iridium on magnetite catalyst.

Chemical communications (Cambridge, England)

Cano R, Yus M, Ramón DJ.
PMID: 22732869
Chem Commun (Camb). 2012 Aug 07;48(61):7628-30. doi: 10.1039/c2cc33101b. Epub 2012 Jun 26.

A new impregnated iridium on magnetite catalyst has been prepared, characterized, used and recycled, up to ten times with practically the same activity, for the first practical cross-alkylation of primary alcohols. The catalyst showed a wide reaction scope, is...

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Cano R, Yus M, Ramón DJ. First practical cross-alkylation of primary alcohols with a new and recyclable impregnated iridium on magnetite catalyst. Chem Commun (Camb). 2012;48(61):7628-30doi: 10.1039/c2cc33101b.
Cano, R., Yus, M., & Ramón, D. J. (2012). First practical cross-alkylation of primary alcohols with a new and recyclable impregnated iridium on magnetite catalyst. Chemical communications (Cambridge, England), 48(61), 7628-30. https://doi.org/10.1039/c2cc33101b
Cano, Rafael, et al. "First practical cross-alkylation of primary alcohols with a new and recyclable impregnated iridium on magnetite catalyst." Chemical communications (Cambridge, England) vol. 48,61 (2012): 7628-30. doi: https://doi.org/10.1039/c2cc33101b
Cano R, Yus M, Ramón DJ. First practical cross-alkylation of primary alcohols with a new and recyclable impregnated iridium on magnetite catalyst. Chem Commun (Camb). 2012 Aug 07;48(61):7628-30. doi: 10.1039/c2cc33101b. Epub 2012 Jun 26. PMID: 22732869.
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Ionic-passivated FeS2 photocapacitors for energy conversion and storage.

Chemical communications (Cambridge, England)

Gong M, Kirkeminde A, Kumar N, Zhao H, Ren S.
PMID: 23995298
Chem Commun (Camb). 2013 Oct 18;49(81):9260-2. doi: 10.1039/c3cc45088k.

A solid-state photocapacitor is prepared, utilizing iron pyrite (FeS2) as both the photoactive material and blocking electrode, which exhibits a high performance near-infrared (NIR) photodetectivity of 1.6 × 10(11) Jones, an energy density of 1.13 × 10(4) J g(-1)...

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Gong M, Kirkeminde A, Kumar N, et al. Ionic-passivated FeS2 photocapacitors for energy conversion and storage. Chem Commun (Camb). 2013;49(81):9260-2doi: 10.1039/c3cc45088k.
Gong, M., Kirkeminde, A., Kumar, N., Zhao, H., & Ren, S. (2013). Ionic-passivated FeS2 photocapacitors for energy conversion and storage. Chemical communications (Cambridge, England), 49(81), 9260-2. https://doi.org/10.1039/c3cc45088k
Gong, Maogang, et al. "Ionic-passivated FeS2 photocapacitors for energy conversion and storage." Chemical communications (Cambridge, England) vol. 49,81 (2013): 9260-2. doi: https://doi.org/10.1039/c3cc45088k
Gong M, Kirkeminde A, Kumar N, Zhao H, Ren S. Ionic-passivated FeS2 photocapacitors for energy conversion and storage. Chem Commun (Camb). 2013 Oct 18;49(81):9260-2. doi: 10.1039/c3cc45088k. PMID: 23995298.
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Electronic communication through molecular bridges.

Chemical communications (Cambridge, England)

Herrmann C, Elmisz J.
PMID: 23995380
Chem Commun (Camb). 2013 Nov 18;49(89):10456-8. doi: 10.1039/c3cc45125a.

A concept that plays an important role in chemistry in general and in molecular spintronics in particular is electronic communication through molecular bridges. An improved understanding of this concept may help to transfer knowledge between different areas of chemistry...

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Herrmann C, Elmisz J. Electronic communication through molecular bridges. Chem Commun (Camb). 2013;49(89):10456-8doi: 10.1039/c3cc45125a.
Herrmann, C., & Elmisz, J. (2013). Electronic communication through molecular bridges. Chemical communications (Cambridge, England), 49(89), 10456-8. https://doi.org/10.1039/c3cc45125a
Herrmann, Carmen, and Elmisz, Jan. "Electronic communication through molecular bridges." Chemical communications (Cambridge, England) vol. 49,89 (2013): 10456-8. doi: https://doi.org/10.1039/c3cc45125a
Herrmann C, Elmisz J. Electronic communication through molecular bridges. Chem Commun (Camb). 2013 Nov 18;49(89):10456-8. doi: 10.1039/c3cc45125a. PMID: 23995380.
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J-aggregation induced low bandgap anthracene-based conjugated molecule for solution-processed solar cells.

Chemical communications (Cambridge, England)

Shin J, Kang NS, Kim KH, Lee TW, Jin JI, Kim M, Lee K, Ju BK, Hong JM, Choi DH.
PMID: 22801585
Chem Commun (Camb). 2012 Sep 04;48(68):8490-2. doi: 10.1039/c2cc34109c. Epub 2012 Jul 17.

A new anthracene-based X-shaped conjugated molecule, HBTATHT, was synthesized. Thin film transistors based on unannealed HBTATHT showed a carrier mobility of 0.15 cm(2) V(-1) s(-1) (I(on/off) = 7.9 × 10(6)). Further, a solution processed solar cell made of HBTATHT...

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Shin J, Kang NS, Kim KH, et al. J-aggregation induced low bandgap anthracene-based conjugated molecule for solution-processed solar cells. Chem Commun (Camb). 2012;48(68):8490-2doi: 10.1039/c2cc34109c.
Shin, J., Kang, N. S., Kim, K. H., Lee, T. W., Jin, J. I., Kim, M., Lee, K., Ju, B. K., Hong, J. M., & Choi, D. H. (2012). J-aggregation induced low bandgap anthracene-based conjugated molecule for solution-processed solar cells. Chemical communications (Cambridge, England), 48(68), 8490-2. https://doi.org/10.1039/c2cc34109c
Shin, Jicheol, et al. "J-aggregation induced low bandgap anthracene-based conjugated molecule for solution-processed solar cells." Chemical communications (Cambridge, England) vol. 48,68 (2012): 8490-2. doi: https://doi.org/10.1039/c2cc34109c
Shin J, Kang NS, Kim KH, Lee TW, Jin JI, Kim M, Lee K, Ju BK, Hong JM, Choi DH. J-aggregation induced low bandgap anthracene-based conjugated molecule for solution-processed solar cells. Chem Commun (Camb). 2012 Sep 04;48(68):8490-2. doi: 10.1039/c2cc34109c. Epub 2012 Jul 17. PMID: 22801585.
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Iridium phosphors with peripheral triphenylamine encapsulation: highly efficient solution-processed red electrophosphorescence.

Chemical communications (Cambridge, England)

Zhu M, Li Y, Hu S, Li C, Yang C, Wu H, Qin J, Cao Y.
PMID: 22306807
Chem Commun (Camb). 2012 Mar 11;48(21):2695-7. doi: 10.1039/c2cc17515k. Epub 2012 Feb 03.

The peripheral triphenylamine-encapsulated red-emitting iridium(III) complexes have been designed and synthesized. External quantum efficiency over 15% has been realized in single-layer polymer light-emitting diodes, which is the highest ever reported for solution-processed red phosphorescence.

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Zhu M, Li Y, Hu S, et al. Iridium phosphors with peripheral triphenylamine encapsulation: highly efficient solution-processed red electrophosphorescence. Chem Commun (Camb). 2012;48(21):2695-7doi: 10.1039/c2cc17515k.
Zhu, M., Li, Y., Hu, S., Li, C., Yang, C., Wu, H., Qin, J., & Cao, Y. (2012). Iridium phosphors with peripheral triphenylamine encapsulation: highly efficient solution-processed red electrophosphorescence. Chemical communications (Cambridge, England), 48(21), 2695-7. https://doi.org/10.1039/c2cc17515k
Zhu, Minrong, et al. "Iridium phosphors with peripheral triphenylamine encapsulation: highly efficient solution-processed red electrophosphorescence." Chemical communications (Cambridge, England) vol. 48,21 (2012): 2695-7. doi: https://doi.org/10.1039/c2cc17515k
Zhu M, Li Y, Hu S, Li C, Yang C, Wu H, Qin J, Cao Y. Iridium phosphors with peripheral triphenylamine encapsulation: highly efficient solution-processed red electrophosphorescence. Chem Commun (Camb). 2012 Mar 11;48(21):2695-7. doi: 10.1039/c2cc17515k. Epub 2012 Feb 03. PMID: 22306807.
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Ordered mesoporous materials as solid supports for rhodium-diphosphine catalysts with remarkable hydroformylation activity.

Chemical communications (Cambridge, England)

Marras F, Wang J, Coppens MO, Reek JN.
PMID: 20697633
Chem Commun (Camb). 2010 Sep 21;46(35):6587-9. doi: 10.1039/c0cc00924e. Epub 2010 Aug 09.

A rhodium-diphosphine complex based on Xantphos-type ligands was anchored on mesoporous silica SBA-15, and the material showed remarkably high catalytic activity in the hydroformylation of 1-octene, even exceeding its homogeneous analogue under certain conditions.

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Marras F, Wang J, Coppens MO, et al. Ordered mesoporous materials as solid supports for rhodium-diphosphine catalysts with remarkable hydroformylation activity. Chem Commun (Camb). 2010;46(35):6587-9doi: 10.1039/c0cc00924e.
Marras, F., Wang, J., Coppens, M. O., & Reek, J. N. (2010). Ordered mesoporous materials as solid supports for rhodium-diphosphine catalysts with remarkable hydroformylation activity. Chemical communications (Cambridge, England), 46(35), 6587-9. https://doi.org/10.1039/c0cc00924e
Marras, Fabrizio, et al. "Ordered mesoporous materials as solid supports for rhodium-diphosphine catalysts with remarkable hydroformylation activity." Chemical communications (Cambridge, England) vol. 46,35 (2010): 6587-9. doi: https://doi.org/10.1039/c0cc00924e
Marras F, Wang J, Coppens MO, Reek JN. Ordered mesoporous materials as solid supports for rhodium-diphosphine catalysts with remarkable hydroformylation activity. Chem Commun (Camb). 2010 Sep 21;46(35):6587-9. doi: 10.1039/c0cc00924e. Epub 2010 Aug 09. PMID: 20697633.
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Controlled synthesis of nanocrystalline Li2MnSiO4 particles for high capacity cathode application in lithium-ion batteries.

Chemical communications (Cambridge, England)

Kempaiah DM, Rangappa D, Honma I.
PMID: 22307175
Chem Commun (Camb). 2012 Mar 11;48(21):2698-700. doi: 10.1039/c2cc17234h. Epub 2012 Feb 03.

Monodispersed Li(2)MnSiO(4) nanoparticles are synthesized via a supercritical solvothermal method at 300 °C for 5 min reaction time. The as-synthesized nanoparticles are free from impurities and have 15-20 nm diameter. After coating with conductive polymer, a discharge capacity of...

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Kempaiah DM, Rangappa D, Honma I. Controlled synthesis of nanocrystalline Li2MnSiO4 particles for high capacity cathode application in lithium-ion batteries. Chem Commun (Camb). 2012;48(21):2698-700doi: 10.1039/c2cc17234h.
Kempaiah, D. M., Rangappa, D., & Honma, I. (2012). Controlled synthesis of nanocrystalline Li2MnSiO4 particles for high capacity cathode application in lithium-ion batteries. Chemical communications (Cambridge, England), 48(21), 2698-700. https://doi.org/10.1039/c2cc17234h
Kempaiah, Devaraju M, et al. "Controlled synthesis of nanocrystalline Li2MnSiO4 particles for high capacity cathode application in lithium-ion batteries." Chemical communications (Cambridge, England) vol. 48,21 (2012): 2698-700. doi: https://doi.org/10.1039/c2cc17234h
Kempaiah DM, Rangappa D, Honma I. Controlled synthesis of nanocrystalline Li2MnSiO4 particles for high capacity cathode application in lithium-ion batteries. Chem Commun (Camb). 2012 Mar 11;48(21):2698-700. doi: 10.1039/c2cc17234h. Epub 2012 Feb 03. PMID: 22307175.
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Incorporation of active metal sites in MOFs via in situ generated ligand deficient metal-linker complexes.

Chemical communications (Cambridge, England)

Barman S, Furukawa H, Blacque O, Venkatesan K, Yaghi OM, Jin GX, Berke H.
PMID: 21983899
Chem Commun (Camb). 2011 Nov 21;47(43):11882-4. doi: 10.1039/c1cc14387e. Epub 2011 Oct 10.

Two novel 3D MOFs, namely MOF-647A and MOF-648 (previously unknown trinodal 4-connected net), comprised of Cu ions and pyrazole-3,5-dicarboxylate were synthesized and characterized. A strategy for incorporating open metal sites in MOFs was investigated by utilizing an in situ...

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Barman S, Furukawa H, Blacque O, et al. Incorporation of active metal sites in MOFs via in situ generated ligand deficient metal-linker complexes. Chem Commun (Camb). 2011;47(43):11882-4doi: 10.1039/c1cc14387e.
Barman, S., Furukawa, H., Blacque, O., Venkatesan, K., Yaghi, O. M., Jin, G. X., & Berke, H. (2011). Incorporation of active metal sites in MOFs via in situ generated ligand deficient metal-linker complexes. Chemical communications (Cambridge, England), 47(43), 11882-4. https://doi.org/10.1039/c1cc14387e
Barman, Samir, et al. "Incorporation of active metal sites in MOFs via in situ generated ligand deficient metal-linker complexes." Chemical communications (Cambridge, England) vol. 47,43 (2011): 11882-4. doi: https://doi.org/10.1039/c1cc14387e
Barman S, Furukawa H, Blacque O, Venkatesan K, Yaghi OM, Jin GX, Berke H. Incorporation of active metal sites in MOFs via in situ generated ligand deficient metal-linker complexes. Chem Commun (Camb). 2011 Nov 21;47(43):11882-4. doi: 10.1039/c1cc14387e. Epub 2011 Oct 10. PMID: 21983899.
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Activation of [(99(m))TcO4](-) by phosphonium cations.

Chemical communications (Cambridge, England)

Braband H, Benz M, Tooyama Y, Alberto R.
PMID: 24622855
Chem Commun (Camb). 2014 Apr 21;50(31):4126-9. doi: 10.1039/c4cc00718b.

Phosphonium salts in solution or bound to solid phase supports interact with the robust [(99(m))TcO4](-) anion in neutral water. This activated form of [(99(m))TcO4](-) represents a source for complexes with the fac-{(99m)Tc(VII)O3}(+) core, which can be synthesized in high...

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Braband H, Benz M, Tooyama Y, et al. Activation of [(99(m))TcO4](-) by phosphonium cations. Chem Commun (Camb). 2014;50(31):4126-9doi: 10.1039/c4cc00718b.
Braband, H., Benz, M., Tooyama, Y., & Alberto, R. (2014). Activation of [(99(m))TcO4](-) by phosphonium cations. Chemical communications (Cambridge, England), 50(31), 4126-9. https://doi.org/10.1039/c4cc00718b
Braband, Henrik, et al. "Activation of [(99(m))TcO4](-) by phosphonium cations." Chemical communications (Cambridge, England) vol. 50,31 (2014): 4126-9. doi: https://doi.org/10.1039/c4cc00718b
Braband H, Benz M, Tooyama Y, Alberto R. Activation of [(99(m))TcO4](-) by phosphonium cations. Chem Commun (Camb). 2014 Apr 21;50(31):4126-9. doi: 10.1039/c4cc00718b. PMID: 24622855.
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Showing 1 to 12 of 30881 entries