Gallucci, Judith

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  • Gallucci, Judith (4)
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Author's Bibliography

Supplementary data for article: Chen, S.; Ruan, Y.; Brown, J. D.; Gallucci, J.; Maslak, V.; Hadad, C. M.; Bađić, J. D. Assembly of Amphiphilic Baskets into Stimuli-Responsive Vesicles. Developing a Strategy for the Detection of Organophosphorus Chemical Nerve Agents. Journal of the American Chemical Society 2013, 135 (40), 14964–14967. https://doi.org/10.1021/ja408585j

Chen, Shigui; Ruan, Yian; Brown, Jason D.; Gallucci, Judith; Maslak, Veselin; Hadad, Christopher M.; Bađić, Jovica D.

(Amer Chemical Soc, Washington, 2013)

TY  - DATA
AU  - Chen, Shigui
AU  - Ruan, Yian
AU  - Brown, Jason D.
AU  - Gallucci, Judith
AU  - Maslak, Veselin
AU  - Hadad, Christopher M.
AU  - Bađić, Jovica D.
PY  - 2013
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3469
PB  - Amer Chemical Soc, Washington
T2  - Journal of the American Chemical Society
T1  - Supplementary data for article: Chen, S.; Ruan, Y.; Brown, J. D.; Gallucci, J.; Maslak, V.; Hadad, C. M.; Bađić, J. D. Assembly of Amphiphilic Baskets into Stimuli-Responsive Vesicles. Developing a Strategy for the Detection of Organophosphorus Chemical Nerve Agents. Journal of the American Chemical Society 2013, 135 (40), 14964–14967. https://doi.org/10.1021/ja408585j
UR  - https://hdl.handle.net/21.15107/rcub_cherry_3469
ER  - 
@misc{
author = "Chen, Shigui and Ruan, Yian and Brown, Jason D. and Gallucci, Judith and Maslak, Veselin and Hadad, Christopher M. and Bađić, Jovica D.",
year = "2013",
publisher = "Amer Chemical Soc, Washington",
journal = "Journal of the American Chemical Society",
title = "Supplementary data for article: Chen, S.; Ruan, Y.; Brown, J. D.; Gallucci, J.; Maslak, V.; Hadad, C. M.; Bađić, J. D. Assembly of Amphiphilic Baskets into Stimuli-Responsive Vesicles. Developing a Strategy for the Detection of Organophosphorus Chemical Nerve Agents. Journal of the American Chemical Society 2013, 135 (40), 14964–14967. https://doi.org/10.1021/ja408585j",
url = "https://hdl.handle.net/21.15107/rcub_cherry_3469"
}
Chen, S., Ruan, Y., Brown, J. D., Gallucci, J., Maslak, V., Hadad, C. M.,& Bađić, J. D.. (2013). Supplementary data for article: Chen, S.; Ruan, Y.; Brown, J. D.; Gallucci, J.; Maslak, V.; Hadad, C. M.; Bađić, J. D. Assembly of Amphiphilic Baskets into Stimuli-Responsive Vesicles. Developing a Strategy for the Detection of Organophosphorus Chemical Nerve Agents. Journal of the American Chemical Society 2013, 135 (40), 14964–14967. https://doi.org/10.1021/ja408585j. in Journal of the American Chemical Society
Amer Chemical Soc, Washington..
https://hdl.handle.net/21.15107/rcub_cherry_3469
Chen S, Ruan Y, Brown JD, Gallucci J, Maslak V, Hadad CM, Bađić JD. Supplementary data for article: Chen, S.; Ruan, Y.; Brown, J. D.; Gallucci, J.; Maslak, V.; Hadad, C. M.; Bađić, J. D. Assembly of Amphiphilic Baskets into Stimuli-Responsive Vesicles. Developing a Strategy for the Detection of Organophosphorus Chemical Nerve Agents. Journal of the American Chemical Society 2013, 135 (40), 14964–14967. https://doi.org/10.1021/ja408585j. in Journal of the American Chemical Society. 2013;.
https://hdl.handle.net/21.15107/rcub_cherry_3469 .
Chen, Shigui, Ruan, Yian, Brown, Jason D., Gallucci, Judith, Maslak, Veselin, Hadad, Christopher M., Bađić, Jovica D., "Supplementary data for article: Chen, S.; Ruan, Y.; Brown, J. D.; Gallucci, J.; Maslak, V.; Hadad, C. M.; Bađić, J. D. Assembly of Amphiphilic Baskets into Stimuli-Responsive Vesicles. Developing a Strategy for the Detection of Organophosphorus Chemical Nerve Agents. Journal of the American Chemical Society 2013, 135 (40), 14964–14967. https://doi.org/10.1021/ja408585j" in Journal of the American Chemical Society (2013),
https://hdl.handle.net/21.15107/rcub_cherry_3469 .

Assembly of Amphiphilic Baskets into Stimuli-Responsive Vesicles. Developing a Strategy for the Detection of Organophosphorus Chemical Nerve Agents

Chen, Shigui; Ruan, Yian; Brown, Jason D.; Gallucci, Judith; Maslak, Veselin; Hadad, Christopher M.; Bađić, Jovica D.

(Amer Chemical Soc, Washington, 2013)

TY  - JOUR
AU  - Chen, Shigui
AU  - Ruan, Yian
AU  - Brown, Jason D.
AU  - Gallucci, Judith
AU  - Maslak, Veselin
AU  - Hadad, Christopher M.
AU  - Bađić, Jovica D.
PY  - 2013
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1427
AB  - We designed basket 1 to comprise a C-3-symmetric hydrophobic cage (477 angstrom(3)) at its southern edge and three polar ammonium caps at the northern edge. This amphiphilic molecule was observed to assemble into large unilamellar vesicles (350 nm, TEM) in water and thereby entrap dimethyl phenylphosphonate (184 angstrom(3)) in its cavity (K-app = (1.97 +/- 0.02) X 10(3) M-1). The entrapment of the organophosphonate, akin to soman in size (186 angstrom(3)), triggers the transformation of the vesicular material into nanoparticles (100 nm,of type 1 in their bilayer membrane, are unique assemblies and important for obtaining novel sensing devices.
PB  - Amer Chemical Soc, Washington
T2  - Journal of the American Chemical Society
T1  - Assembly of Amphiphilic Baskets into Stimuli-Responsive Vesicles. Developing a Strategy for the Detection of Organophosphorus Chemical Nerve Agents
VL  - 135
IS  - 40
SP  - 14964
EP  - 14967
DO  - 10.1021/ja408585j
ER  - 
@article{
author = "Chen, Shigui and Ruan, Yian and Brown, Jason D. and Gallucci, Judith and Maslak, Veselin and Hadad, Christopher M. and Bađić, Jovica D.",
year = "2013",
abstract = "We designed basket 1 to comprise a C-3-symmetric hydrophobic cage (477 angstrom(3)) at its southern edge and three polar ammonium caps at the northern edge. This amphiphilic molecule was observed to assemble into large unilamellar vesicles (350 nm, TEM) in water and thereby entrap dimethyl phenylphosphonate (184 angstrom(3)) in its cavity (K-app = (1.97 +/- 0.02) X 10(3) M-1). The entrapment of the organophosphonate, akin to soman in size (186 angstrom(3)), triggers the transformation of the vesicular material into nanoparticles (100 nm,of type 1 in their bilayer membrane, are unique assemblies and important for obtaining novel sensing devices.",
publisher = "Amer Chemical Soc, Washington",
journal = "Journal of the American Chemical Society",
title = "Assembly of Amphiphilic Baskets into Stimuli-Responsive Vesicles. Developing a Strategy for the Detection of Organophosphorus Chemical Nerve Agents",
volume = "135",
number = "40",
pages = "14964-14967",
doi = "10.1021/ja408585j"
}
Chen, S., Ruan, Y., Brown, J. D., Gallucci, J., Maslak, V., Hadad, C. M.,& Bađić, J. D.. (2013). Assembly of Amphiphilic Baskets into Stimuli-Responsive Vesicles. Developing a Strategy for the Detection of Organophosphorus Chemical Nerve Agents. in Journal of the American Chemical Society
Amer Chemical Soc, Washington., 135(40), 14964-14967.
https://doi.org/10.1021/ja408585j
Chen S, Ruan Y, Brown JD, Gallucci J, Maslak V, Hadad CM, Bađić JD. Assembly of Amphiphilic Baskets into Stimuli-Responsive Vesicles. Developing a Strategy for the Detection of Organophosphorus Chemical Nerve Agents. in Journal of the American Chemical Society. 2013;135(40):14964-14967.
doi:10.1021/ja408585j .
Chen, Shigui, Ruan, Yian, Brown, Jason D., Gallucci, Judith, Maslak, Veselin, Hadad, Christopher M., Bađić, Jovica D., "Assembly of Amphiphilic Baskets into Stimuli-Responsive Vesicles. Developing a Strategy for the Detection of Organophosphorus Chemical Nerve Agents" in Journal of the American Chemical Society, 135, no. 40 (2013):14964-14967,
https://doi.org/10.1021/ja408585j . .
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Supramolecular catalysis at work: Diastereoselective synthesis of a molecular bowl with dynamic inner space

Yan, Zhiqing; McCracken, Troy; Xia, Shijing; Maslak, Veselin; Gallucci, Judith; Hadad, Christopher M.; Bađić, Jovica D.

(Amer Chemical Soc, Washington, 2008)

TY  - JOUR
AU  - Yan, Zhiqing
AU  - McCracken, Troy
AU  - Xia, Shijing
AU  - Maslak, Veselin
AU  - Gallucci, Judith
AU  - Hadad, Christopher M.
AU  - Bađić, Jovica D.
PY  - 2008
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/899
AB  - [GRAPHICS] The supramolecular assistance to Pd(0)/Cu(I)-catalyzed cyclotrimerization of stannylated norbornene 7 has been investigated to give molecular bowl 1(syn) in a stereoselective fashion. Following a divergent strategy, racemic norbornene 7 was synthesized in satisfactory yield. Self-coupling, promoted by Pd(0)/Cu(I) catalysis acting in synergy with CsF, yielded molecular bowl 1(syn) in a moderate 30% yield. The reaction diastereoselectivity is affected by the concentration of Cu(I) and Cs+: increasing quantities of the cations enhanced the synlanti ratio of the isolated cyclotrimer from statistical (1:3) to a more desirable (4.5:1) ratio, in favor of the molecular bowl 1(syn) H-1 NMR spectroscopic studies suggested the coordinating affinity of 1(syn) toward transition metals Cu(I), Ag(I), and Au(I), to account for the observed templation effect. In particular, the tridentate 1(syn) has been shown to bind to one Ag(I) cation in the assembly process that is driven with enthalpy (Delta H-0 = - 19 +/- 2 kcal/mol, Delta S-0 = -45 eu). The complete coordination was not cooperative, and was hypothesized to be impeded with the adverse entropy. Accordingly, density functional theory (BP86) calculations of 1(syn) and its mono-, bis-, and tris-Ag(I) complexes suggested that the coordination of one to three silver cations is highly exothermic. The calculations also revealed that the bowl constriction is necessary for the aromatic arms to become preorganized and bind to a silver cation(s) (Delta E approximate to 8 kcal/mol). Ultimately, Ag(I) has been shown to assist the diastereoselective formation of lending support to the notion, of template-directed synthesis.
PB  - Amer Chemical Soc, Washington
T2  - Journal of Organic Chemistry
T1  - Supramolecular catalysis at work: Diastereoselective synthesis of a molecular bowl with dynamic inner space
VL  - 73
IS  - 2
SP  - 355
EP  - 363
DO  - 10.1021/jo701538g
ER  - 
@article{
author = "Yan, Zhiqing and McCracken, Troy and Xia, Shijing and Maslak, Veselin and Gallucci, Judith and Hadad, Christopher M. and Bađić, Jovica D.",
year = "2008",
abstract = "[GRAPHICS] The supramolecular assistance to Pd(0)/Cu(I)-catalyzed cyclotrimerization of stannylated norbornene 7 has been investigated to give molecular bowl 1(syn) in a stereoselective fashion. Following a divergent strategy, racemic norbornene 7 was synthesized in satisfactory yield. Self-coupling, promoted by Pd(0)/Cu(I) catalysis acting in synergy with CsF, yielded molecular bowl 1(syn) in a moderate 30% yield. The reaction diastereoselectivity is affected by the concentration of Cu(I) and Cs+: increasing quantities of the cations enhanced the synlanti ratio of the isolated cyclotrimer from statistical (1:3) to a more desirable (4.5:1) ratio, in favor of the molecular bowl 1(syn) H-1 NMR spectroscopic studies suggested the coordinating affinity of 1(syn) toward transition metals Cu(I), Ag(I), and Au(I), to account for the observed templation effect. In particular, the tridentate 1(syn) has been shown to bind to one Ag(I) cation in the assembly process that is driven with enthalpy (Delta H-0 = - 19 +/- 2 kcal/mol, Delta S-0 = -45 eu). The complete coordination was not cooperative, and was hypothesized to be impeded with the adverse entropy. Accordingly, density functional theory (BP86) calculations of 1(syn) and its mono-, bis-, and tris-Ag(I) complexes suggested that the coordination of one to three silver cations is highly exothermic. The calculations also revealed that the bowl constriction is necessary for the aromatic arms to become preorganized and bind to a silver cation(s) (Delta E approximate to 8 kcal/mol). Ultimately, Ag(I) has been shown to assist the diastereoselective formation of lending support to the notion, of template-directed synthesis.",
publisher = "Amer Chemical Soc, Washington",
journal = "Journal of Organic Chemistry",
title = "Supramolecular catalysis at work: Diastereoselective synthesis of a molecular bowl with dynamic inner space",
volume = "73",
number = "2",
pages = "355-363",
doi = "10.1021/jo701538g"
}
Yan, Z., McCracken, T., Xia, S., Maslak, V., Gallucci, J., Hadad, C. M.,& Bađić, J. D.. (2008). Supramolecular catalysis at work: Diastereoselective synthesis of a molecular bowl with dynamic inner space. in Journal of Organic Chemistry
Amer Chemical Soc, Washington., 73(2), 355-363.
https://doi.org/10.1021/jo701538g
Yan Z, McCracken T, Xia S, Maslak V, Gallucci J, Hadad CM, Bađić JD. Supramolecular catalysis at work: Diastereoselective synthesis of a molecular bowl with dynamic inner space. in Journal of Organic Chemistry. 2008;73(2):355-363.
doi:10.1021/jo701538g .
Yan, Zhiqing, McCracken, Troy, Xia, Shijing, Maslak, Veselin, Gallucci, Judith, Hadad, Christopher M., Bađić, Jovica D., "Supramolecular catalysis at work: Diastereoselective synthesis of a molecular bowl with dynamic inner space" in Journal of Organic Chemistry, 73, no. 2 (2008):355-363,
https://doi.org/10.1021/jo701538g . .
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Silver(I) mediated folding of a molecular basket

Yan, Zhiqing; Xia, Shijing; Gardlik, Matthew; Seo, Wanji; Maslak, Veselin; Gallucci, Judith; Hadad, Christopher M.; Bađić, Jovica D.

(Amer Chemical Soc, Washington, 2007)

TY  - JOUR
AU  - Yan, Zhiqing
AU  - Xia, Shijing
AU  - Gardlik, Matthew
AU  - Seo, Wanji
AU  - Maslak, Veselin
AU  - Gallucci, Judith
AU  - Hadad, Christopher M.
AU  - Bađić, Jovica D.
PY  - 2007
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/835
AB  - We have investigated Ag(I) mediated folding of a tridentate compound, containing three pyridine flaps tethered to a semirigid scaffold, into a molecular basket, using both experimental and theoretical methods. The basket formation has been shown to be highly favorable in organic media (Delta G degrees = -7.2 kcal/mol), with the assembly process allowing for another ligand to bind preferentially on the outer side.
PB  - Amer Chemical Soc, Washington
T2  - Organic Letters
T1  - Silver(I) mediated folding of a molecular basket
VL  - 9
IS  - 12
SP  - 2301
EP  - 2304
DO  - 10.1021/ol0705595
ER  - 
@article{
author = "Yan, Zhiqing and Xia, Shijing and Gardlik, Matthew and Seo, Wanji and Maslak, Veselin and Gallucci, Judith and Hadad, Christopher M. and Bađić, Jovica D.",
year = "2007",
abstract = "We have investigated Ag(I) mediated folding of a tridentate compound, containing three pyridine flaps tethered to a semirigid scaffold, into a molecular basket, using both experimental and theoretical methods. The basket formation has been shown to be highly favorable in organic media (Delta G degrees = -7.2 kcal/mol), with the assembly process allowing for another ligand to bind preferentially on the outer side.",
publisher = "Amer Chemical Soc, Washington",
journal = "Organic Letters",
title = "Silver(I) mediated folding of a molecular basket",
volume = "9",
number = "12",
pages = "2301-2304",
doi = "10.1021/ol0705595"
}
Yan, Z., Xia, S., Gardlik, M., Seo, W., Maslak, V., Gallucci, J., Hadad, C. M.,& Bađić, J. D.. (2007). Silver(I) mediated folding of a molecular basket. in Organic Letters
Amer Chemical Soc, Washington., 9(12), 2301-2304.
https://doi.org/10.1021/ol0705595
Yan Z, Xia S, Gardlik M, Seo W, Maslak V, Gallucci J, Hadad CM, Bađić JD. Silver(I) mediated folding of a molecular basket. in Organic Letters. 2007;9(12):2301-2304.
doi:10.1021/ol0705595 .
Yan, Zhiqing, Xia, Shijing, Gardlik, Matthew, Seo, Wanji, Maslak, Veselin, Gallucci, Judith, Hadad, Christopher M., Bađić, Jovica D., "Silver(I) mediated folding of a molecular basket" in Organic Letters, 9, no. 12 (2007):2301-2304,
https://doi.org/10.1021/ol0705595 . .
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