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Vortexes tune the chirality of graphene oxide and its non-covalent hosts.

Chemical communications (Cambridge, England)

Di Mauro A, Randazzo R, Spanò SF, Compagnini G, Gaeta M, D'Urso L, Paolesse R, Pomarico G, Di Natale C, Villari V, Micali N, Fragalà ME, D'Urso A, Purrello R.
PMID: 27549164
Chem Commun (Camb). 2016 Nov 18;52(89):13094-13096. doi: 10.1039/c6cc05177d. Epub 2016 Aug 23.

Graphene oxide (GO) is one of the most appealing bidimensional materials able to interact non-covalently with achiral molecules and to act as chiral inducers. Vortexes can tune chirality and, consequently transfer a specific handedness to non-covalent host molecules, either...

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Di Mauro A, Randazzo R, Spanò SF, et al. Vortexes tune the chirality of graphene oxide and its non-covalent hosts. Chem Commun (Camb). 2016;52(89):13094-13096doi: 10.1039/c6cc05177d.
Di Mauro, A., Randazzo, R., Spanò, S. F., Compagnini, G., Gaeta, M., D'Urso, L., Paolesse, R., Pomarico, G., Di Natale, C., Villari, V., Micali, N., Fragalà, M. E., D'Urso, A., & Purrello, R. (2016). Vortexes tune the chirality of graphene oxide and its non-covalent hosts. Chemical communications (Cambridge, England), 52(89), 13094-13096. https://doi.org/10.1039/c6cc05177d
Di Mauro, A, et al. "Vortexes tune the chirality of graphene oxide and its non-covalent hosts." Chemical communications (Cambridge, England) vol. 52,89 (2016): 13094-13096. doi: https://doi.org/10.1039/c6cc05177d
Di Mauro A, Randazzo R, Spanò SF, Compagnini G, Gaeta M, D'Urso L, Paolesse R, Pomarico G, Di Natale C, Villari V, Micali N, Fragalà ME, D'Urso A, Purrello R. Vortexes tune the chirality of graphene oxide and its non-covalent hosts. Chem Commun (Camb). 2016 Nov 18;52(89):13094-13096. doi: 10.1039/c6cc05177d. Epub 2016 Aug 23. PMID: 27549164.
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Synthetic protocols for the nitration of corroles.

Journal of porphyrins and phthalocyanines

Pomarico G, Fronczek FR, Nardis S, Smith KM, Paolesse R.
PMID: 22287833
J Porphyr Phthalocyanines. 2011 Jul 15;15(9):1085-1092. doi: 10.1142/S1088424611004038.

The modification of peripheral positions of corroles by introduction of nitro groups is an important functionalization of this macrocycle. The nitro substituent strongly influences the corrole behavior leading to the preparation of macrocycles with different properties, which can be...

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Pomarico G, Fronczek FR, Nardis S, et al. Synthetic protocols for the nitration of corroles. J Porphyr Phthalocyanines. 2011;15(9):1085-1092doi: 10.1142/S1088424611004038.
Pomarico, G., Fronczek, F. R., Nardis, S., Smith, K. M., & Paolesse, R. (2011). Synthetic protocols for the nitration of corroles. Journal of porphyrins and phthalocyanines, 15(9), 1085-1092. https://doi.org/10.1142/S1088424611004038
Pomarico, Giuseppe, et al. "Synthetic protocols for the nitration of corroles." Journal of porphyrins and phthalocyanines vol. 15,9 (2011): 1085-1092. doi: https://doi.org/10.1142/S1088424611004038
Pomarico G, Fronczek FR, Nardis S, Smith KM, Paolesse R. Synthetic protocols for the nitration of corroles. J Porphyr Phthalocyanines. 2011 Jul 15;15(9):1085-1092. doi: 10.1142/S1088424611004038. PMID: 22287833; PMCID: PMC3266369.
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Scientific teaching targeting faculty from diverse institutions.

CBE life sciences education

Gregg CS, Ales JD, Pomarico SM, Wischusen EW, Siebenaller JF.
PMID: 24006387
CBE Life Sci Educ. 2013;12(3):383-93. doi: 10.1187/cbe.12-05-0061.

We offered four annual professional development workshops called STAR (for Scientific Teaching, Assessment, and Resources) modeled after the National Academies Summer Institute (SI) on Undergraduate Education in Biology. In contrast to the SI focus on training faculty from research...

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Gregg CS, Ales JD, Pomarico SM, et al. Scientific teaching targeting faculty from diverse institutions. CBE Life Sci Educ. 2013;12(3):383-93doi: 10.1187/cbe.12-05-0061.
Gregg, C. S., Ales, J. D., Pomarico, S. M., Wischusen, E. W., & Siebenaller, J. F. (2013). Scientific teaching targeting faculty from diverse institutions. CBE life sciences education, 12(3), 383-93. https://doi.org/10.1187/cbe.12-05-0061
Gregg, Christopher S, et al. "Scientific teaching targeting faculty from diverse institutions." CBE life sciences education vol. 12,3 (2013): 383-93. doi: https://doi.org/10.1187/cbe.12-05-0061
Gregg CS, Ales JD, Pomarico SM, Wischusen EW, Siebenaller JF. Scientific teaching targeting faculty from diverse institutions. CBE Life Sci Educ. 2013;12(3):383-93. doi: 10.1187/cbe.12-05-0061. PMID: 24006387; PMCID: PMC3763006.
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Silicon(IV) Corroles.

Chemistry (Weinheim an der Bergstrasse, Germany)

Pomarico G, Monti D, Bischetti M, Savoldelli A, Fronczek FR, Smith KM, Genovese D, Prodi L, Paolesse R.
PMID: 29637630
Chemistry. 2018 Jun 12;24(33):8438-8446. doi: 10.1002/chem.201801246. Epub 2018 May 17.

Silicon complexes of corrole were obtained for the first time by reaction of the free-base corrole with hexachlorodisilane. The peripheral substituents of corrole strongly influence the nature of the reaction products: β-octaalkyl corrole was mainly isolated as the μ-oxo...

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Pomarico G, Monti D, Bischetti M, et al. Silicon(IV) Corroles. Chemistry. 2018;24(33):8438-8446doi: 10.1002/chem.201801246.
Pomarico, G., Monti, D., Bischetti, M., Savoldelli, A., Fronczek, F. R., Smith, K. M., Genovese, D., Prodi, L., & Paolesse, R. (2018). Silicon(IV) Corroles. Chemistry (Weinheim an der Bergstrasse, Germany), 24(33), 8438-8446. https://doi.org/10.1002/chem.201801246
Pomarico, Giuseppe, et al. "Silicon(IV) Corroles." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 24,33 (2018): 8438-8446. doi: https://doi.org/10.1002/chem.201801246
Pomarico G, Monti D, Bischetti M, Savoldelli A, Fronczek FR, Smith KM, Genovese D, Prodi L, Paolesse R. Silicon(IV) Corroles. Chemistry. 2018 Jun 12;24(33):8438-8446. doi: 10.1002/chem.201801246. Epub 2018 May 17. PMID: 29637630.
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Photophysical Heavy-Atom Effect in Iodinated Metallocorroles: Spin-Orbit Coupling and Density of States.

The journal of physical chemistry. A

Pomarico E, Pospíšil P, Bouduban MEF, Vestfrid J, Gross Z, Záliš S, Chergui M, Vlček A.
PMID: 30141941
J Phys Chem A. 2018 Sep 20;122(37):7256-7266. doi: 10.1021/acs.jpca.8b05311. Epub 2018 Sep 06.

Excited-state dynamics and electronic structures of Al and Ga corrole complexes were studied as a function of the number of β-pyrrole iodine substituents. Using spectrally broad-band femtosecond-resolved fluorescence upconversion, we determined the kinetics of the Soret fluorescence decay, the...

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Pomarico E, Pospíšil P, Bouduban MEF, et al. Photophysical Heavy-Atom Effect in Iodinated Metallocorroles: Spin-Orbit Coupling and Density of States. J Phys Chem A. 2018;122(37):7256-7266doi: 10.1021/acs.jpca.8b05311.
Pomarico, E., Pospíšil, P., Bouduban, M. E. F., Vestfrid, J., Gross, Z., Záliš, S., Chergui, M., & Vlček, A. (2018). Photophysical Heavy-Atom Effect in Iodinated Metallocorroles: Spin-Orbit Coupling and Density of States. The journal of physical chemistry. A, 122(37), 7256-7266. https://doi.org/10.1021/acs.jpca.8b05311
Pomarico, Enrico, et al. "Photophysical Heavy-Atom Effect in Iodinated Metallocorroles: Spin-Orbit Coupling and Density of States." The journal of physical chemistry. A vol. 122,37 (2018): 7256-7266. doi: https://doi.org/10.1021/acs.jpca.8b05311
Pomarico E, Pospíšil P, Bouduban MEF, Vestfrid J, Gross Z, Záliš S, Chergui M, Vlček A. Photophysical Heavy-Atom Effect in Iodinated Metallocorroles: Spin-Orbit Coupling and Density of States. J Phys Chem A. 2018 Sep 20;122(37):7256-7266. doi: 10.1021/acs.jpca.8b05311. Epub 2018 Sep 06. PMID: 30141941.
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β-Arylethynyl substituted silver corrole complexes.

Dalton transactions (Cambridge, England : 2003)

Stefanelli M, Ricci A, Chiarini M, Lo Sterzo C, Berionni Berna B, Pomarico G, Sabuzi F, Galloni P, Fronczek FR, Smith KM, Wang L, Ou Z, Kadish KM, Paolesse R.
PMID: 31478049
Dalton Trans. 2019 Sep 17;48(36):13589-13598. doi: 10.1039/c9dt03166a.

Silver corrolates are attractive compounds from both practical and theoretical points of view. Indeed, they play a key role in peripheral functionalization reactions occurring at the macrocycle, enabling high-yield and regioselective group insertions useful to further elaborate the molecular...

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Stefanelli M, Ricci A, Chiarini M, et al. β-Arylethynyl substituted silver corrole complexes. Dalton Trans. 2019;48(36):13589-13598doi: 10.1039/c9dt03166a.
Stefanelli, M., Ricci, A., Chiarini, M., Lo Sterzo, C., Berionni Berna, B., Pomarico, G., Sabuzi, F., Galloni, P., Fronczek, F. R., Smith, K. M., Wang, L., Ou, Z., Kadish, K. M., & Paolesse, R. (2019). β-Arylethynyl substituted silver corrole complexes. Dalton transactions (Cambridge, England : 2003), 48(36), 13589-13598. https://doi.org/10.1039/c9dt03166a
Stefanelli, Manuela, et al. "β-Arylethynyl substituted silver corrole complexes." Dalton transactions (Cambridge, England : 2003) vol. 48,36 (2019): 13589-13598. doi: https://doi.org/10.1039/c9dt03166a
Stefanelli M, Ricci A, Chiarini M, Lo Sterzo C, Berionni Berna B, Pomarico G, Sabuzi F, Galloni P, Fronczek FR, Smith KM, Wang L, Ou Z, Kadish KM, Paolesse R. β-Arylethynyl substituted silver corrole complexes. Dalton Trans. 2019 Sep 17;48(36):13589-13598. doi: 10.1039/c9dt03166a. PMID: 31478049.
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Supramolecular Diblock Copolymers Featuring Well-defined Telechelic Building Blocks.

Angewandte Chemie (International ed. in English)

Elacqua E, Croom A, Manning KB, Pomarico SK, Lye D, Young L, Weck M.
PMID: 27860190
Angew Chem Int Ed Engl. 2016 Dec 19;55(51):15873-15878. doi: 10.1002/anie.201609103. Epub 2016 Nov 17.

We report supramolecular AB diblock copolymers comprised of well-defined telechelic building blocks. Helical motifs, formed via reversible addition-fragmentation chain-transfer (RAFT) or anionic polymerization, are assembled with coil-forming and sheet-featuring blocks obtained via atom-transfer radical polymerization (ATRP) or ring-opening metathesis...

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Elacqua E, Croom A, Manning KB, et al. Supramolecular Diblock Copolymers Featuring Well-defined Telechelic Building Blocks. Angew Chem Int Ed Engl. 2016;55(51):15873-15878doi: 10.1002/anie.201609103.
Elacqua, E., Croom, A., Manning, K. B., Pomarico, S. K., Lye, D., Young, L., & Weck, M. (2016). Supramolecular Diblock Copolymers Featuring Well-defined Telechelic Building Blocks. Angewandte Chemie (International ed. in English), 55(51), 15873-15878. https://doi.org/10.1002/anie.201609103
Elacqua, Elizabeth, et al. "Supramolecular Diblock Copolymers Featuring Well-defined Telechelic Building Blocks." Angewandte Chemie (International ed. in English) vol. 55,51 (2016): 15873-15878. doi: https://doi.org/10.1002/anie.201609103
Elacqua E, Croom A, Manning KB, Pomarico SK, Lye D, Young L, Weck M. Supramolecular Diblock Copolymers Featuring Well-defined Telechelic Building Blocks. Angew Chem Int Ed Engl. 2016 Dec 19;55(51):15873-15878. doi: 10.1002/anie.201609103. Epub 2016 Nov 17. PMID: 27860190.
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New example of hemiporphycene formation from the corrole ring expansion.

Inorganic chemistry

Fang Y, Mandoj F, Nardis S, Pomarico G, Stefanelli M, Cicero DO, Lentini S, Vecchi A, Cui Y, Zeng L, Kadish KM, Paolesse R.
PMID: 24979329
Inorg Chem. 2014 Jul 21;53(14):7404-15. doi: 10.1021/ic500757a. Epub 2014 Jun 30.

The reaction of 5,10,15-tris(4-tert-butylphenyl)corrole with 2,3-bis(bromomethyl)-5,6-dicyanopyrazine provides a new example of corrole ring expansion to a hemiporphycene derivative. The ring expansion is regioselective, with insertion of the pyrazine derivative at the 5-position of the corrole ring, affording the corresponding...

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Fang Y, Mandoj F, Nardis S, et al. New example of hemiporphycene formation from the corrole ring expansion. Inorg Chem. 2014;53(14):7404-15doi: 10.1021/ic500757a.
Fang, Y., Mandoj, F., Nardis, S., Pomarico, G., Stefanelli, M., Cicero, D. O., Lentini, S., Vecchi, A., Cui, Y., Zeng, L., Kadish, K. M., & Paolesse, R. (2014). New example of hemiporphycene formation from the corrole ring expansion. Inorganic chemistry, 53(14), 7404-15. https://doi.org/10.1021/ic500757a
Fang, Yuanyuan, et al. "New example of hemiporphycene formation from the corrole ring expansion." Inorganic chemistry vol. 53,14 (2014): 7404-15. doi: https://doi.org/10.1021/ic500757a
Fang Y, Mandoj F, Nardis S, Pomarico G, Stefanelli M, Cicero DO, Lentini S, Vecchi A, Cui Y, Zeng L, Kadish KM, Paolesse R. New example of hemiporphycene formation from the corrole ring expansion. Inorg Chem. 2014 Jul 21;53(14):7404-15. doi: 10.1021/ic500757a. Epub 2014 Jun 30. PMID: 24979329.
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Interfacial Electron Injection Probed by a Substrate-Specific Excitonic Signature.

Journal of the American Chemical Society

Baldini E, Palmieri T, Rossi T, Oppermann M, Pomarico E, Auböck G, Chergui M.
PMID: 28762734
J Am Chem Soc. 2017 Aug 23;139(33):11584-11589. doi: 10.1021/jacs.7b06322. Epub 2017 Aug 11.

Ultrafast interfacial electron transfer in sensitized solar cells has mostly been probed by visible-to-terahertz radiation, which is sensitive to the free carriers in the conduction band of the semiconductor substrate. Here, we demonstrate the use of deep-ultraviolet continuum pulses...

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Baldini E, Palmieri T, Rossi T, et al. Interfacial Electron Injection Probed by a Substrate-Specific Excitonic Signature. J Am Chem Soc. 2017;139(33):11584-11589doi: 10.1021/jacs.7b06322.
Baldini, E., Palmieri, T., Rossi, T., Oppermann, M., Pomarico, E., Auböck, G., & Chergui, M. (2017). Interfacial Electron Injection Probed by a Substrate-Specific Excitonic Signature. Journal of the American Chemical Society, 139(33), 11584-11589. https://doi.org/10.1021/jacs.7b06322
Baldini, Edoardo, et al. "Interfacial Electron Injection Probed by a Substrate-Specific Excitonic Signature." Journal of the American Chemical Society vol. 139,33 (2017): 11584-11589. doi: https://doi.org/10.1021/jacs.7b06322
Baldini E, Palmieri T, Rossi T, Oppermann M, Pomarico E, Auböck G, Chergui M. Interfacial Electron Injection Probed by a Substrate-Specific Excitonic Signature. J Am Chem Soc. 2017 Aug 23;139(33):11584-11589. doi: 10.1021/jacs.7b06322. Epub 2017 Aug 11. PMID: 28762734.
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Holographic imaging of electromagnetic fields via electron-light quantum interference.

Science advances

Madan I, Vanacore GM, Pomarico E, Berruto G, Lamb RJ, McGrouther D, Lummen TTA, Latychevskaia T, García de Abajo FJ, Carbone F.
PMID: 31058225
Sci Adv. 2019 May 03;5(5):eaav8358. doi: 10.1126/sciadv.aav8358. eCollection 2019 May.

Holography relies on the interference between a known reference and a signal of interest to reconstruct both the amplitude and the phase of that signal. With electrons, the extension of holography to the ultrafast time domain remains a challenge,...

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Madan I, Vanacore GM, Pomarico E, et al. Holographic imaging of electromagnetic fields via electron-light quantum interference. Sci Adv. 2019;5(5):eaav8358doi: 10.1126/sciadv.aav8358.
Madan, I., Vanacore, G. M., Pomarico, E., Berruto, G., Lamb, R. J., McGrouther, D., Lummen, T. T. A., Latychevskaia, T., García de Abajo, F. J., & Carbone, F. (2019). Holographic imaging of electromagnetic fields via electron-light quantum interference. Science advances, 5(5), eaav8358. https://doi.org/10.1126/sciadv.aav8358
Madan, I, et al. "Holographic imaging of electromagnetic fields via electron-light quantum interference." Science advances vol. 5,5 (2019): eaav8358. doi: https://doi.org/10.1126/sciadv.aav8358
Madan I, Vanacore GM, Pomarico E, Berruto G, Lamb RJ, McGrouther D, Lummen TTA, Latychevskaia T, García de Abajo FJ, Carbone F. Holographic imaging of electromagnetic fields via electron-light quantum interference. Sci Adv. 2019 May 03;5(5):eaav8358. doi: 10.1126/sciadv.aav8358. eCollection 2019 May. PMID: 31058225; PMCID: PMC6499551.
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Author Correction: Attosecond coherent control of free-electron wave functions using semi-infinite light fields.

Nature communications

Vanacore GM, Madan I, Berruto G, Wang K, Pomarico E, Lamb RJ, McGrouther D, Kaminer I, Barwick B, de Abajo FJG, Carbone F.
PMID: 30824703
Nat Commun. 2019 Mar 01;10(1):1069. doi: 10.1038/s41467-019-08996-3.

The authors became aware of a mistake in the original version of this Article. Specifically, an extra factor γ was incorrectly included in a number of mathematical equations and expressions. As a result of this, a number of changes...

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Vanacore GM, Madan I, Berruto G, et al. Author Correction: Attosecond coherent control of free-electron wave functions using semi-infinite light fields. Nat Commun. 2019;10(1):1069doi: 10.1038/s41467-019-08996-3.
Vanacore, G. M., Madan, I., Berruto, G., Wang, K., Pomarico, E., Lamb, R. J., McGrouther, D., Kaminer, I., Barwick, B., de Abajo, F. J. G., & Carbone, F. (2019). Author Correction: Attosecond coherent control of free-electron wave functions using semi-infinite light fields. Nature communications, 10(1), 1069. https://doi.org/10.1038/s41467-019-08996-3
Vanacore, G M, et al. "Author Correction: Attosecond coherent control of free-electron wave functions using semi-infinite light fields." Nature communications vol. 10,1 (2019): 1069. doi: https://doi.org/10.1038/s41467-019-08996-3
Vanacore GM, Madan I, Berruto G, Wang K, Pomarico E, Lamb RJ, McGrouther D, Kaminer I, Barwick B, de Abajo FJG, Carbone F. Author Correction: Attosecond coherent control of free-electron wave functions using semi-infinite light fields. Nat Commun. 2019 Mar 01;10(1):1069. doi: 10.1038/s41467-019-08996-3. PMID: 30824703; PMCID: PMC6397259.
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Interaction of independent single photons based on integrated nonlinear optics.

Nature communications

Guerreiro T, Pomarico E, Sanguinetti B, Sangouard N, Pelc JS, Langrock C, Fejer MM, Zbinden H, Thew RT, Gisin N.
PMID: 23945795
Nat Commun. 2013;4:2324. doi: 10.1038/ncomms3324.

The parametric interaction of light beams in nonlinear materials is usually thought to be too weak to be observed when the fields involved are at the single-photon level. However, such single-photon level nonlinearity is not only fundamentally fascinating but...

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Guerreiro T, Pomarico E, Sanguinetti B, et al. Interaction of independent single photons based on integrated nonlinear optics. Nat Commun. 2013;4:2324doi: 10.1038/ncomms3324.
Guerreiro, T., Pomarico, E., Sanguinetti, B., Sangouard, N., Pelc, J. S., Langrock, C., Fejer, M. M., Zbinden, H., Thew, R. T., & Gisin, N. (2013). Interaction of independent single photons based on integrated nonlinear optics. Nature communications, 42324. https://doi.org/10.1038/ncomms3324
Guerreiro, T, et al. "Interaction of independent single photons based on integrated nonlinear optics." Nature communications vol. 4 (2013): 2324. doi: https://doi.org/10.1038/ncomms3324
Guerreiro T, Pomarico E, Sanguinetti B, Sangouard N, Pelc JS, Langrock C, Fejer MM, Zbinden H, Thew RT, Gisin N. Interaction of independent single photons based on integrated nonlinear optics. Nat Commun. 2013;4:2324. doi: 10.1038/ncomms3324. PMID: 23945795.
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Showing 1 to 12 of 47 entries