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A take-home physics experiment kit for on-campus and off-campus students

science campus

Turner J, Parisi A.
GSID: Q_ypQb9F5rwJ
J Turner, A Parisi - Teaching Science, 2008 - search.informit.org

A take-home experiment kit has been developed to reinforce the concepts in a first year physics course that both on and off campus students from a variety of educational backgrounds can successfully use. The kit is inexpensive and is...

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Turner, J., & Parisi, A. (2008). A take-home physics experiment kit for on-campus and off-campus students. Teaching Science, 54(2), 20-23.
Turner, Joanna, and Alfio Parisi. "A take-home physics experiment kit for on-campus and off-campus students." Teaching Science 54.2 (2008): 20-23.
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On the Angular Dependence of the Vicinal Fluorine-Fluorine Coupling Constant in 1,2-Difluoroethane:  Deviation from a Karplus-like Shape.

Journal of chemical theory and computation

Provasi PF, Sauer SP.
PMID: 26633061
J Chem Theory Comput. 2006 Jul;2(4):1019-27. doi: 10.1021/ct6000973.

The angular dependence of the vicinal fluorine-fluorine coupling constant, (3)JFF, for 1,2-difluoroethane has been investigated with several polarization propagator methods. (3)JFF and its four Ramsey contributions were calculated using the random phase approximation (RPA), its multiconfigurational generalization, and both...

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Provasi PF, Sauer SP. On the Angular Dependence of the Vicinal Fluorine-Fluorine Coupling Constant in 1,2-Difluoroethane:  Deviation from a Karplus-like Shape. J Chem Theory Comput. 2006;2(4):1019-27doi: 10.1021/ct6000973.
Provasi, P. F., & Sauer, S. P. (2006). On the Angular Dependence of the Vicinal Fluorine-Fluorine Coupling Constant in 1,2-Difluoroethane:  Deviation from a Karplus-like Shape. Journal of chemical theory and computation, 2(4), 1019-27. https://doi.org/10.1021/ct6000973
Provasi, Patricio F, and Sauer, Stephan P A. "On the Angular Dependence of the Vicinal Fluorine-Fluorine Coupling Constant in 1,2-Difluoroethane:  Deviation from a Karplus-like Shape." Journal of chemical theory and computation vol. 2,4 (2006): 1019-27. doi: https://doi.org/10.1021/ct6000973
Provasi PF, Sauer SP. On the Angular Dependence of the Vicinal Fluorine-Fluorine Coupling Constant in 1,2-Difluoroethane:  Deviation from a Karplus-like Shape. J Chem Theory Comput. 2006 Jul;2(4):1019-27. doi: 10.1021/ct6000973. PMID: 26633061.
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Starch-Based Layer by Layer Assembly: Efficient and Sustainable Approach to Cotton Fire Protection.

ACS applied materials & interfaces

Carosio F, Fontaine G, Alongi J, Bourbigot S.
PMID: 25978652
ACS Appl Mater Interfaces. 2015 Jun 10;7(22):12158-67. doi: 10.1021/acsami.5b02507. Epub 2015 May 26.

Starch has been employed via layer by layer assembly for building an efficient and sustainable biobased coatings capable of protecting cotton from fire. In order to obtain a better understanding of the coating to substrate relationship, the coating efficiency...

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Carosio F, Fontaine G, Alongi J, et al. Starch-Based Layer by Layer Assembly: Efficient and Sustainable Approach to Cotton Fire Protection. ACS Appl Mater Interfaces. 2015;7(22):12158-67doi: 10.1021/acsami.5b02507.
Carosio, F., Fontaine, G., Alongi, J., & Bourbigot, S. (2015). Starch-Based Layer by Layer Assembly: Efficient and Sustainable Approach to Cotton Fire Protection. ACS applied materials & interfaces, 7(22), 12158-67. https://doi.org/10.1021/acsami.5b02507
Carosio, F, et al. "Starch-Based Layer by Layer Assembly: Efficient and Sustainable Approach to Cotton Fire Protection." ACS applied materials & interfaces vol. 7,22 (2015): 12158-67. doi: https://doi.org/10.1021/acsami.5b02507
Carosio F, Fontaine G, Alongi J, Bourbigot S. Starch-Based Layer by Layer Assembly: Efficient and Sustainable Approach to Cotton Fire Protection. ACS Appl Mater Interfaces. 2015 Jun 10;7(22):12158-67. doi: 10.1021/acsami.5b02507. Epub 2015 May 26. PMID: 25978652.
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Synthesis, electronic properties and WOLED devices of planar phosphorus-containing polycyclic aromatic hydrocarbons.

Chemistry (Weinheim an der Bergstrasse, Germany)

Riobé F, Szűcs R, Bouit PA, Tondelier D, Geffroy B, Aparicio F, Buendía J, Sánchez L, Réau R, Nyulászi L, Hissler M.
PMID: 25760307
Chemistry. 2015 Apr 20;21(17):6547-56. doi: 10.1002/chem.201500203. Epub 2015 Mar 11.

We describe the synthesis and the physical properties of polyaromatic hydrocarbons (PAHs) containing a phosphorus atom at the edge. In particular, the impact of the successive addition of aromatic rings on the electronic properties was investigated by experimental (UV/Vis...

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Riobé F, Szűcs R, Bouit PA, et al. Synthesis, electronic properties and WOLED devices of planar phosphorus-containing polycyclic aromatic hydrocarbons. Chemistry. 2015;21(17):6547-56doi: 10.1002/chem.201500203.
Riobé, F., Szűcs, R., Bouit, P. A., Tondelier, D., Geffroy, B., Aparicio, F., Buendía, J., Sánchez, L., Réau, R., Nyulászi, L., & Hissler, M. (2015). Synthesis, electronic properties and WOLED devices of planar phosphorus-containing polycyclic aromatic hydrocarbons. Chemistry (Weinheim an der Bergstrasse, Germany), 21(17), 6547-56. https://doi.org/10.1002/chem.201500203
Riobé, François, et al. "Synthesis, electronic properties and WOLED devices of planar phosphorus-containing polycyclic aromatic hydrocarbons." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 21,17 (2015): 6547-56. doi: https://doi.org/10.1002/chem.201500203
Riobé F, Szűcs R, Bouit PA, Tondelier D, Geffroy B, Aparicio F, Buendía J, Sánchez L, Réau R, Nyulászi L, Hissler M. Synthesis, electronic properties and WOLED devices of planar phosphorus-containing polycyclic aromatic hydrocarbons. Chemistry. 2015 Apr 20;21(17):6547-56. doi: 10.1002/chem.201500203. Epub 2015 Mar 11. PMID: 25760307.
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Saffman-Taylor problem on a sphere.

Physical review. E, Statistical, nonlinear, and soft matter physics

Parisio F, Moraes F, Miranda JA, Widom M.
PMID: 11308768
Phys Rev E Stat Nonlin Soft Matter Phys. 2001 Mar;63(3):036307. doi: 10.1103/PhysRevE.63.036307. Epub 2001 Feb 27.

The Saffman-Taylor problem addresses the morphological instability of an interface separating two immiscible, viscous fluids when they move in a narrow gap between two flat parallel plates (Hele-Shaw cell). In this work, we extend the classic Saffman-Taylor situation, by...

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Parisio F, Moraes F, Miranda JA, et al. Saffman-Taylor problem on a sphere. Phys Rev E Stat Nonlin Soft Matter Phys. 2001;63(3):036307doi: 10.1103/PhysRevE.63.036307.
Parisio, F., Moraes, F., Miranda, J. A., & Widom, M. (2001). Saffman-Taylor problem on a sphere. Physical review. E, Statistical, nonlinear, and soft matter physics, 63(3), 036307. https://doi.org/10.1103/PhysRevE.63.036307
Parisio, F, et al. "Saffman-Taylor problem on a sphere." Physical review. E, Statistical, nonlinear, and soft matter physics vol. 63,3 (2001): 036307. doi: https://doi.org/10.1103/PhysRevE.63.036307
Parisio F, Moraes F, Miranda JA, Widom M. Saffman-Taylor problem on a sphere. Phys Rev E Stat Nonlin Soft Matter Phys. 2001 Mar;63(3):036307. doi: 10.1103/PhysRevE.63.036307. Epub 2001 Feb 27. PMID: 11308768.
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Synthesis, Optical Resolution and Complexation Properties of Inherently Chiral Monoalkylated p-tert-Butyl-(1,2)-calix[4]crown Ethers.

The Journal of organic chemistry

Arnaud-Neu F, Caccamese S, Fuangswasdi S, Pappalardo S, Parisi MF, Petringa A, Principato G.
PMID: 11671909
J Org Chem. 1997 Nov 14;62(23):8041-8048. doi: 10.1021/jo970934e.

Reaction of mono-O-alkylated calix[4]arenes 2 with tri- to pentaethylene glycol ditosylates and K(2)CO(3) affords asymmetrical (1,2)-calix[4]crown ether derivatives 3 as the main product, along with minor amounts of calix[4]arene dimers 4 and mixed syn-distal di-O-alkylated calix[4]arenes 5. A reaction...

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Arnaud-Neu F, Caccamese S, Fuangswasdi S, et al. Synthesis, Optical Resolution and Complexation Properties of Inherently Chiral Monoalkylated p-tert-Butyl-(1,2)-calix[4]crown Ethers. J Org Chem. 1997;62(23):8041-8048doi: 10.1021/jo970934e.
Arnaud-Neu, F., Caccamese, S., Fuangswasdi, S., Pappalardo, S., Parisi, M. F., Petringa, A., & Principato, G. (1997). Synthesis, Optical Resolution and Complexation Properties of Inherently Chiral Monoalkylated p-tert-Butyl-(1,2)-calix[4]crown Ethers. The Journal of organic chemistry, 62(23), 8041-8048. https://doi.org/10.1021/jo970934e
Arnaud-Neu, Francoise, et al. "Synthesis, Optical Resolution and Complexation Properties of Inherently Chiral Monoalkylated p-tert-Butyl-(1,2)-calix[4]crown Ethers." The Journal of organic chemistry vol. 62,23 (1997): 8041-8048. doi: https://doi.org/10.1021/jo970934e
Arnaud-Neu F, Caccamese S, Fuangswasdi S, Pappalardo S, Parisi MF, Petringa A, Principato G. Synthesis, Optical Resolution and Complexation Properties of Inherently Chiral Monoalkylated p-tert-Butyl-(1,2)-calix[4]crown Ethers. J Org Chem. 1997 Nov 14;62(23):8041-8048. doi: 10.1021/jo970934e. PMID: 11671909.
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Shape recognition of alkylammonium ions by 1,3-bridged calix[5]arene crown-6 ethers: endo- vs exo-cavity complexation.

The Journal of organic chemistry

De Salvo G, Gattuso G, Notti A, Parisi MF, Pappalardo S.
PMID: 11856007
J Org Chem. 2002 Feb 08;67(3):684-92. doi: 10.1021/jo015982k.

A series of tri-O-substituted 1,3-bridged calix[5]arene crown-6 ethers bearing alkyl, arylalkyl, alkoxyalkyl, and alkoxycarbonylmethyl residues at the lower rim and either (t)()Bu or H substituents at the upper rim have been synthesized. (1)H NMR studies have shown that p-tert-butylcalix[5]crowns,...

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De Salvo G, Gattuso G, Notti A, et al. Shape recognition of alkylammonium ions by 1,3-bridged calix[5]arene crown-6 ethers: endo- vs exo-cavity complexation. J Org Chem. 2002;67(3):684-92doi: 10.1021/jo015982k.
De Salvo, G., Gattuso, G., Notti, A., Parisi, M. F., & Pappalardo, S. (2002). Shape recognition of alkylammonium ions by 1,3-bridged calix[5]arene crown-6 ethers: endo- vs exo-cavity complexation. The Journal of organic chemistry, 67(3), 684-92. https://doi.org/10.1021/jo015982k
De Salvo, Gabriella, et al. "Shape recognition of alkylammonium ions by 1,3-bridged calix[5]arene crown-6 ethers: endo- vs exo-cavity complexation." The Journal of organic chemistry vol. 67,3 (2002): 684-92. doi: https://doi.org/10.1021/jo015982k
De Salvo G, Gattuso G, Notti A, Parisi MF, Pappalardo S. Shape recognition of alkylammonium ions by 1,3-bridged calix[5]arene crown-6 ethers: endo- vs exo-cavity complexation. J Org Chem. 2002 Feb 08;67(3):684-92. doi: 10.1021/jo015982k. PMID: 11856007.
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Stereochemical dependence of NMR geminal spin-spin coupling constants.

Magnetic resonance in chemistry : MRC

Contreras RH, Provasi PF, dos Santos FP, Tormena CF.
PMID: 18991325
Magn Reson Chem. 2009 Feb;47(2):113-20. doi: 10.1002/mrc.2359.

In this work it was sought to explore the versatility of geminal spin-spin coupling constants, (2)J(XY) SSCCs, as probes for stereochemical studies. A set of compounds, where their experimental (2)J(XY) SSCCs through the X-C-Y molecular fragment are predicted to...

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Contreras RH, Provasi PF, dos Santos FP, et al. Stereochemical dependence of NMR geminal spin-spin coupling constants. Magn Reson Chem. 2009;47(2):113-20doi: 10.1002/mrc.2359.
Contreras, R. H., Provasi, P. F., dos Santos, F. P., & Tormena, C. F. (2009). Stereochemical dependence of NMR geminal spin-spin coupling constants. Magnetic resonance in chemistry : MRC, 47(2), 113-20. https://doi.org/10.1002/mrc.2359
Contreras, Rubén H, et al. "Stereochemical dependence of NMR geminal spin-spin coupling constants." Magnetic resonance in chemistry : MRC vol. 47,2 (2009): 113-20. doi: https://doi.org/10.1002/mrc.2359
Contreras RH, Provasi PF, dos Santos FP, Tormena CF. Stereochemical dependence of NMR geminal spin-spin coupling constants. Magn Reson Chem. 2009 Feb;47(2):113-20. doi: 10.1002/mrc.2359. PMID: 18991325.
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The anomalous deuterium isotope effect in the NMR spectrum of methane: an analysis in localized molecular orbitals.

Chemphyschem : a European journal of chemical physics and physical chemistry

Sauer SP, Provasi PF.
PMID: 18461588
Chemphyschem. 2008 Jun 23;9(9):1259-61. doi: 10.1002/cphc.200800119.

No abstract available.

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Sauer SP, Provasi PF. The anomalous deuterium isotope effect in the NMR spectrum of methane: an analysis in localized molecular orbitals. Chemphyschem. 2008;9(9):1259-61doi: 10.1002/cphc.200800119.
Sauer, S. P., & Provasi, P. F. (2008). The anomalous deuterium isotope effect in the NMR spectrum of methane: an analysis in localized molecular orbitals. Chemphyschem : a European journal of chemical physics and physical chemistry, 9(9), 1259-61. https://doi.org/10.1002/cphc.200800119
Sauer, Stephan P A, and Provasi, Patricio F. "The anomalous deuterium isotope effect in the NMR spectrum of methane: an analysis in localized molecular orbitals." Chemphyschem : a European journal of chemical physics and physical chemistry vol. 9,9 (2008): 1259-61. doi: https://doi.org/10.1002/cphc.200800119
Sauer SP, Provasi PF. The anomalous deuterium isotope effect in the NMR spectrum of methane: an analysis in localized molecular orbitals. Chemphyschem. 2008 Jun 23;9(9):1259-61. doi: 10.1002/cphc.200800119. PMID: 18461588.
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Induction of chirality in porphyrin-(bis)calixarene assemblies: a mixed covalent-non-covalent vs a fully non-covalent approach.

Chemical communications (Cambridge, England)

D'Urso A, Nicotra PF, Centonze G, Fragalà ME, Gattuso G, Notti A, Pappalardo A, Pappalardo S, Parisi MF, Purrello R.
PMID: 22430063
Chem Commun (Camb). 2012 Apr 28;48(34):4046-8. doi: 10.1039/c2cc30366c. Epub 2012 Mar 20.

CD and UV-vis measurements were carried out to demonstrate chirality induction-promoted by chiral covalently linked groups and non-covalently bound Δ- and Λ-[Ru(phen)(3)](2+) enantiomers-in metallo-porphyrin-calixarene and metallo-porphyrin-bis-calixarene non-covalent assemblies, respectively.

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D'Urso A, Nicotra PF, Centonze G, et al. Induction of chirality in porphyrin-(bis)calixarene assemblies: a mixed covalent-non-covalent vs a fully non-covalent approach. Chem Commun (Camb). 2012;48(34):4046-8doi: 10.1039/c2cc30366c.
D'Urso, A., Nicotra, P. F., Centonze, G., Fragalà, M. E., Gattuso, G., Notti, A., Pappalardo, A., Pappalardo, S., Parisi, M. F., & Purrello, R. (2012). Induction of chirality in porphyrin-(bis)calixarene assemblies: a mixed covalent-non-covalent vs a fully non-covalent approach. Chemical communications (Cambridge, England), 48(34), 4046-8. https://doi.org/10.1039/c2cc30366c
D'Urso, Alessandro, et al. "Induction of chirality in porphyrin-(bis)calixarene assemblies: a mixed covalent-non-covalent vs a fully non-covalent approach." Chemical communications (Cambridge, England) vol. 48,34 (2012): 4046-8. doi: https://doi.org/10.1039/c2cc30366c
D'Urso A, Nicotra PF, Centonze G, Fragalà ME, Gattuso G, Notti A, Pappalardo A, Pappalardo S, Parisi MF, Purrello R. Induction of chirality in porphyrin-(bis)calixarene assemblies: a mixed covalent-non-covalent vs a fully non-covalent approach. Chem Commun (Camb). 2012 Apr 28;48(34):4046-8. doi: 10.1039/c2cc30366c. Epub 2012 Mar 20. PMID: 22430063.
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Expression of drug targets in primary and matched metastatic renal cell carcinoma tumors.

BMC clinical pathology

Aziz SA, Sznol JA, Adeniran A, Parisi F, Kluger Y, Camp RL, Kluger HM.
PMID: 23374878
BMC Clin Pathol. 2013 Feb 01;13:3. doi: 10.1186/1472-6890-13-3.

BACKGROUND: Targeted therapies in renal cell carcinoma can have different effects on primary and metastatic tumors. To pave the way for predictive biomarker development, we assessed differences in expression of targets of currently approved drugs in matched primary and...

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Aziz SA, Sznol JA, Adeniran A, et al. Expression of drug targets in primary and matched metastatic renal cell carcinoma tumors. BMC Clin Pathol. 2013;13:3doi: 10.1186/1472-6890-13-3.
Aziz, S. A., Sznol, J. A., Adeniran, A., Parisi, F., Kluger, Y., Camp, R. L., & Kluger, H. M. (2013). Expression of drug targets in primary and matched metastatic renal cell carcinoma tumors. BMC clinical pathology, 133. https://doi.org/10.1186/1472-6890-13-3
Aziz, Saadia A, et al. "Expression of drug targets in primary and matched metastatic renal cell carcinoma tumors." BMC clinical pathology vol. 13 (2013): 3. doi: https://doi.org/10.1186/1472-6890-13-3
Aziz SA, Sznol JA, Adeniran A, Parisi F, Kluger Y, Camp RL, Kluger HM. Expression of drug targets in primary and matched metastatic renal cell carcinoma tumors. BMC Clin Pathol. 2013 Feb 01;13:3. doi: 10.1186/1472-6890-13-3. PMID: 23374878; PMCID: PMC3575219.
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Supramolecular polymerization of C3-symmetric organogelators: cooperativity, solvent, and gelation relationship.

Chemistry (Weinheim an der Bergstrasse, Germany)

Aparicio F, García F, Sánchez L.
PMID: 23345173
Chemistry. 2013 Feb 25;19(9):3239-48. doi: 10.1002/chem.201202584. Epub 2013 Jan 23.

A systematic study of the influence of solvent and the size of C(3)-symmetric discotics on their supramolecular polymerization mechanism is presented. The cooperativity of the self-assembly of the reported compounds is directly related to their gelation ability. The two...

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Aparicio F, García F, Sánchez L. Supramolecular polymerization of C3-symmetric organogelators: cooperativity, solvent, and gelation relationship. Chemistry. 2013;19(9):3239-48doi: 10.1002/chem.201202584.
Aparicio, F., García, F., & Sánchez, L. (2013). Supramolecular polymerization of C3-symmetric organogelators: cooperativity, solvent, and gelation relationship. Chemistry (Weinheim an der Bergstrasse, Germany), 19(9), 3239-48. https://doi.org/10.1002/chem.201202584
Aparicio, Fátima, et al. "Supramolecular polymerization of C3-symmetric organogelators: cooperativity, solvent, and gelation relationship." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 19,9 (2013): 3239-48. doi: https://doi.org/10.1002/chem.201202584
Aparicio F, García F, Sánchez L. Supramolecular polymerization of C3-symmetric organogelators: cooperativity, solvent, and gelation relationship. Chemistry. 2013 Feb 25;19(9):3239-48. doi: 10.1002/chem.201202584. Epub 2013 Jan 23. PMID: 23345173.
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Showing 1 to 12 of 292 entries