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Crystal Structure, Hirshfeld Surface Analysis and Computational Studies of Thiazolidin-4-one derivative: (Z)-5-(4-Chlorobenzylidene)-3-(2-ethoxyphenyl)-2-thioxothiazolidin-4-one.

Acta chimica Slovenica

Khelloul N, Toubal K, Benhalima N, Rahmani R, Chouaih A, Djafri A, Hamzaoui F.
PMID: 27640389
Acta Chim Slov. 2016;63(3):619-26. doi: 10.17344/acsi.2016.2362.

The title compound (Z)-5-(4-chlorobenzylidene)-3-(2-ethoxyphenyl)-2-thioxothiazolidin-4-one (CBBTZ) was characterized by X-ray single crystal diffraction, 1H NMR and 13C NMR spectra. Theoretical investigations were carried out using HF and DFT levels of theory at 6-31G(d,p) basis set. The X-ray structure is compared...

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Khelloul N, Toubal K, Benhalima N, et al. Crystal Structure, Hirshfeld Surface Analysis and Computational Studies of Thiazolidin-4-one derivative: (Z)-5-(4-Chlorobenzylidene)-3-(2-ethoxyphenyl)-2-thioxothiazolidin-4-one. Acta Chim Slov. 2016;63(3):619-26doi: 10.17344/acsi.2016.2362.
Khelloul, N., Toubal, K., Benhalima, N., Rahmani, R., Chouaih, A., Djafri, A., & Hamzaoui, F. (2016). Crystal Structure, Hirshfeld Surface Analysis and Computational Studies of Thiazolidin-4-one derivative: (Z)-5-(4-Chlorobenzylidene)-3-(2-ethoxyphenyl)-2-thioxothiazolidin-4-one. Acta chimica Slovenica, 63(3), 619-26. https://doi.org/10.17344/acsi.2016.2362
Khelloul, Nawel, et al. "Crystal Structure, Hirshfeld Surface Analysis and Computational Studies of Thiazolidin-4-one derivative: (Z)-5-(4-Chlorobenzylidene)-3-(2-ethoxyphenyl)-2-thioxothiazolidin-4-one." Acta chimica Slovenica vol. 63,3 (2016): 619-26. doi: https://doi.org/10.17344/acsi.2016.2362
Khelloul N, Toubal K, Benhalima N, Rahmani R, Chouaih A, Djafri A, Hamzaoui F. Crystal Structure, Hirshfeld Surface Analysis and Computational Studies of Thiazolidin-4-one derivative: (Z)-5-(4-Chlorobenzylidene)-3-(2-ethoxyphenyl)-2-thioxothiazolidin-4-one. Acta Chim Slov. 2016;63(3):619-26. doi: 10.17344/acsi.2016.2362. PMID: 27640389.
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Zwitterionic Cobalt Complexes with Bis(diphenylphosphino)(N-thioether)amine Assembling Ligands: Structural, EPR, Magnetic, and Computational Studies.

Inorganic chemistry

Fliedel C, Rosa V, Vileno B, Parizel N, Choua S, Gourlaouen C, Rosa P, Turek P, Braunstein P.
PMID: 27054464
Inorg Chem. 2016 May 02;55(9):4183-98. doi: 10.1021/acs.inorgchem.5b02889. Epub 2016 Apr 07.

The coordination of two heterofunctional P,P,S ligands of the N-functionalized DPPA-type bearing an alkylthioether or arylthioether N-substituent, (Ph2P)2N(CH2)3SMe (1) and (Ph2P)2N(p-C6H4)SMe (2), respectively, toward cobalt dichloride was investigated to examine the influence of the linker between the PNP nitrogen...

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Fliedel C, Rosa V, Vileno B, et al. Zwitterionic Cobalt Complexes with Bis(diphenylphosphino)(N-thioether)amine Assembling Ligands: Structural, EPR, Magnetic, and Computational Studies. Inorg Chem. 2016;55(9):4183-98doi: 10.1021/acs.inorgchem.5b02889.
Fliedel, C., Rosa, V., Vileno, B., Parizel, N., Choua, S., Gourlaouen, C., Rosa, P., Turek, P., & Braunstein, P. (2016). Zwitterionic Cobalt Complexes with Bis(diphenylphosphino)(N-thioether)amine Assembling Ligands: Structural, EPR, Magnetic, and Computational Studies. Inorganic chemistry, 55(9), 4183-98. https://doi.org/10.1021/acs.inorgchem.5b02889
Fliedel, Christophe, et al. "Zwitterionic Cobalt Complexes with Bis(diphenylphosphino)(N-thioether)amine Assembling Ligands: Structural, EPR, Magnetic, and Computational Studies." Inorganic chemistry vol. 55,9 (2016): 4183-98. doi: https://doi.org/10.1021/acs.inorgchem.5b02889
Fliedel C, Rosa V, Vileno B, Parizel N, Choua S, Gourlaouen C, Rosa P, Turek P, Braunstein P. Zwitterionic Cobalt Complexes with Bis(diphenylphosphino)(N-thioether)amine Assembling Ligands: Structural, EPR, Magnetic, and Computational Studies. Inorg Chem. 2016 May 02;55(9):4183-98. doi: 10.1021/acs.inorgchem.5b02889. Epub 2016 Apr 07. PMID: 27054464.
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The interscrotal approach to inguinoscrotal pathologies.

Arab journal of urology

Soualili Z, Achouri D, Haif A, Touabti S, Yahia SA, Benmahmoud M, Choutri H, Nedjar S, Mimoune M, Chouaib S.
PMID: 26413342
Arab J Urol. 2015 Sep;13(3):176-8. doi: 10.1016/j.aju.2015.05.002. Epub 2015 Jun 29.

OBJECTIVE: To determine the efficiency of the interscrotal approach to inguinoscrotal pathologies.PATIENTS AND METHODS: We report the use of the interscrotal approach in 21 boys, from September 2012 to November 2013, operated using an interscrotal access through a vertical...

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Soualili Z, Achouri D, Haif A, et al. The interscrotal approach to inguinoscrotal pathologies. Arab J Urol. 2015;13(3):176-8doi: 10.1016/j.aju.2015.05.002.
Soualili, Z., Achouri, D., Haif, A., Touabti, S., Yahia, S. A., Benmahmoud, M., Choutri, H., Nedjar, S., Mimoune, M., & Chouaib, S. (2015). The interscrotal approach to inguinoscrotal pathologies. Arab journal of urology, 13(3), 176-8. https://doi.org/10.1016/j.aju.2015.05.002
Soualili, Zineddine, et al. "The interscrotal approach to inguinoscrotal pathologies." Arab journal of urology vol. 13,3 (2015): 176-8. doi: https://doi.org/10.1016/j.aju.2015.05.002
Soualili Z, Achouri D, Haif A, Touabti S, Yahia SA, Benmahmoud M, Choutri H, Nedjar S, Mimoune M, Chouaib S. The interscrotal approach to inguinoscrotal pathologies. Arab J Urol. 2015 Sep;13(3):176-8. doi: 10.1016/j.aju.2015.05.002. Epub 2015 Jun 29. PMID: 26413342; PMCID: PMC4563009.
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Intrinsic and Tumor Microenvironment-Induced Metabolism Adaptations of T Cells and Impact on Their Differentiation and Function.

Frontiers in immunology

Kouidhi S, Noman MZ, Kieda C, Elgaaied AB, Chouaib S.
PMID: 27066006
Front Immunol. 2016 Mar 29;7:114. doi: 10.3389/fimmu.2016.00114. eCollection 2016.

It is well recognized that the immune system and metabolism are highly integrated. In this context, multilevel interactions between metabolic system and T lymphocyte signaling and fate exist. This review will discuss different potential cell metabolism pathways involved in...

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Kouidhi S, Noman MZ, Kieda C, et al. Intrinsic and Tumor Microenvironment-Induced Metabolism Adaptations of T Cells and Impact on Their Differentiation and Function. Front Immunol. 2016;7:114doi: 10.3389/fimmu.2016.00114.
Kouidhi, S., Noman, M. Z., Kieda, C., Elgaaied, A. B., & Chouaib, S. (2016). Intrinsic and Tumor Microenvironment-Induced Metabolism Adaptations of T Cells and Impact on Their Differentiation and Function. Frontiers in immunology, 7114. https://doi.org/10.3389/fimmu.2016.00114
Kouidhi, Soumaya, et al. "Intrinsic and Tumor Microenvironment-Induced Metabolism Adaptations of T Cells and Impact on Their Differentiation and Function." Frontiers in immunology vol. 7 (2016): 114. doi: https://doi.org/10.3389/fimmu.2016.00114
Kouidhi S, Noman MZ, Kieda C, Elgaaied AB, Chouaib S. Intrinsic and Tumor Microenvironment-Induced Metabolism Adaptations of T Cells and Impact on Their Differentiation and Function. Front Immunol. 2016 Mar 29;7:114. doi: 10.3389/fimmu.2016.00114. eCollection 2016. PMID: 27066006; PMCID: PMC4810024.
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Crystal structure of (2Z,5Z)-3-(4-meth-oxy-phen-yl)-2-[(4-meth-oxy-phenyl)-imino]-5-[(E)-3-(2-nitro-phen-yl)allyl-idene]-1,3-thia-zolidin-4-one.

Acta crystallographica. Section E, Crystallographic communications

Rahmani R, Djafri A, Daran JC, Djafri A, Chouaih A, Hamzaoui F.
PMID: 26958377
Acta Crystallogr E Crystallogr Commun. 2016 Jan 13;72:155-7. doi: 10.1107/S2056989016000207. eCollection 2016 Feb 01.

In the title compound, C26H21N3O5S, the thia-zole ring is nearly planar with a maximum deviation of 0.017 (2) Å, and is twisted with respect to the three benzene rings, making dihedral angles of 25.52 (12), 85.77 (12) and 81.85...

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Rahmani R, Djafri A, Daran JC, et al. Crystal structure of (2Z,5Z)-3-(4-meth-oxy-phen-yl)-2-[(4-meth-oxy-phenyl)-imino]-5-[(E)-3-(2-nitro-phen-yl)allyl-idene]-1,3-thia-zolidin-4-one. Acta Crystallogr E Crystallogr Commun. 2016;72:155-7doi: 10.1107/S2056989016000207.
Rahmani, R., Djafri, A., Daran, J. C., Djafri, A., Chouaih, A., & Hamzaoui, F. (2016). Crystal structure of (2Z,5Z)-3-(4-meth-oxy-phen-yl)-2-[(4-meth-oxy-phenyl)-imino]-5-[(E)-3-(2-nitro-phen-yl)allyl-idene]-1,3-thia-zolidin-4-one. Acta crystallographica. Section E, Crystallographic communications, 72155-7. https://doi.org/10.1107/S2056989016000207
Rahmani, Rachida, et al. "Crystal structure of (2Z,5Z)-3-(4-meth-oxy-phen-yl)-2-[(4-meth-oxy-phenyl)-imino]-5-[(E)-3-(2-nitro-phen-yl)allyl-idene]-1,3-thia-zolidin-4-one." Acta crystallographica. Section E, Crystallographic communications vol. 72 (2016): 155-7. doi: https://doi.org/10.1107/S2056989016000207
Rahmani R, Djafri A, Daran JC, Djafri A, Chouaih A, Hamzaoui F. Crystal structure of (2Z,5Z)-3-(4-meth-oxy-phen-yl)-2-[(4-meth-oxy-phenyl)-imino]-5-[(E)-3-(2-nitro-phen-yl)allyl-idene]-1,3-thia-zolidin-4-one. Acta Crystallogr E Crystallogr Commun. 2016 Jan 13;72:155-7. doi: 10.1107/S2056989016000207. eCollection 2016 Feb 01. PMID: 26958377; PMCID: PMC4770957.
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Nickel(II) meso-Hydroxyporphyrin Complexes Revisited: Palladium-Catalysed Synthesis, Electronic Structures of Derived Oxy Radicals, and Oxidative Coupling to a Dioxoporphodimethene Dyad.

Chemistry (Weinheim an der Bergstrasse, Germany)

Esdaile LJ, Rintoul L, Goh MS, Merahi K, Parizel N, Wellard RM, Choua S, Arnold DP.
PMID: 26833709
Chemistry. 2016 Mar 01;22(10):3430-3446. doi: 10.1002/chem.201504252. Epub 2016 Feb 02.

We report the synthesis and characterisation of new examples of meso-hydroxynickel(II) porphyrins with 5,15-diphenyl and 10-phenyl-5,15-diphenyl/diaryl substitution. The OH group was introduced by using carbonate or hydroxide as nucleophile by using palladium/phosphine catalysis. The NiPor-OHs exist in solution in...

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Esdaile LJ, Rintoul L, Goh MS, et al. Nickel(II) meso-Hydroxyporphyrin Complexes Revisited: Palladium-Catalysed Synthesis, Electronic Structures of Derived Oxy Radicals, and Oxidative Coupling to a Dioxoporphodimethene Dyad. Chemistry. 2016;22(10):3430-3446doi: 10.1002/chem.201504252.
Esdaile, L. J., Rintoul, L., Goh, M. S., Merahi, K., Parizel, N., Wellard, R. M., Choua, S., & Arnold, D. P. (2016). Nickel(II) meso-Hydroxyporphyrin Complexes Revisited: Palladium-Catalysed Synthesis, Electronic Structures of Derived Oxy Radicals, and Oxidative Coupling to a Dioxoporphodimethene Dyad. Chemistry (Weinheim an der Bergstrasse, Germany), 22(10), 3430-3446. https://doi.org/10.1002/chem.201504252
Esdaile, Louisa J, et al. "Nickel(II) meso-Hydroxyporphyrin Complexes Revisited: Palladium-Catalysed Synthesis, Electronic Structures of Derived Oxy Radicals, and Oxidative Coupling to a Dioxoporphodimethene Dyad." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 22,10 (2016): 3430-3446. doi: https://doi.org/10.1002/chem.201504252
Esdaile LJ, Rintoul L, Goh MS, Merahi K, Parizel N, Wellard RM, Choua S, Arnold DP. Nickel(II) meso-Hydroxyporphyrin Complexes Revisited: Palladium-Catalysed Synthesis, Electronic Structures of Derived Oxy Radicals, and Oxidative Coupling to a Dioxoporphodimethene Dyad. Chemistry. 2016 Mar 01;22(10):3430-3446. doi: 10.1002/chem.201504252. Epub 2016 Feb 02. PMID: 26833709.
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Ruthenium Carbon-Rich Complexes as Redox Switchable Metal Coupling Units.

Inorganic chemistry

Di Piazza E, Merhi A, Norel L, Choua S, Turek P, Rigaut S.
PMID: 26068041
Inorg Chem. 2015 Jul 06;54(13):6347-55. doi: 10.1021/acs.inorgchem.5b00667. Epub 2015 Jun 12.

With the help of EPR spectroscopy, we show that the diamagnetic [Ru(dppe)2(-C≡C-R)2] system sets up a magnetic coupling between two organic radicals R, i.e., two nitronyl nitroxide or two verdazyl units, which is stronger than that of related platinum...

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Di Piazza E, Merhi A, Norel L, et al. Ruthenium Carbon-Rich Complexes as Redox Switchable Metal Coupling Units. Inorg Chem. 2015;54(13):6347-55doi: 10.1021/acs.inorgchem.5b00667.
Di Piazza, E., Merhi, A., Norel, L., Choua, S., Turek, P., & Rigaut, S. (2015). Ruthenium Carbon-Rich Complexes as Redox Switchable Metal Coupling Units. Inorganic chemistry, 54(13), 6347-55. https://doi.org/10.1021/acs.inorgchem.5b00667
Di Piazza, Emmanuel, et al. "Ruthenium Carbon-Rich Complexes as Redox Switchable Metal Coupling Units." Inorganic chemistry vol. 54,13 (2015): 6347-55. doi: https://doi.org/10.1021/acs.inorgchem.5b00667
Di Piazza E, Merhi A, Norel L, Choua S, Turek P, Rigaut S. Ruthenium Carbon-Rich Complexes as Redox Switchable Metal Coupling Units. Inorg Chem. 2015 Jul 06;54(13):6347-55. doi: 10.1021/acs.inorgchem.5b00667. Epub 2015 Jun 12. PMID: 26068041.
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Electron transfer between two silyl-substituted phenylene rings: EPR/ENDOR spectra, DFT calculations, and crystal structure of the one-electron reduction compound of a di(m-silylphenylenedisiloxane).

Journal of the American Chemical Society

Dutan C, Choua S, Berclaz T, Geoffroy M, Mézailles N, Moores A, Ricard L, Le Floch P.
PMID: 12683819
J Am Chem Soc. 2003 Apr 16;125(15):4487-94. doi: 10.1021/ja0209060.

Reduction of a solution of octamethylcyclo-di(m-silylphenylenedisiloxane) 4 in THF on a potassium mirror leads to EPR/ENDOR spectra characterized by a large coupling (approximately 20 MHz) with two protons, similar to the spectra obtained after reduction of the m-disilylbenzene derivative...

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Dutan C, Choua S, Berclaz T, et al. Electron transfer between two silyl-substituted phenylene rings: EPR/ENDOR spectra, DFT calculations, and crystal structure of the one-electron reduction compound of a di(m-silylphenylenedisiloxane). J Am Chem Soc. 2003;125(15):4487-94doi: 10.1021/ja0209060.
Dutan, C., Choua, S., Berclaz, T., Geoffroy, M., Mézailles, N., Moores, A., Ricard, L., & Le Floch, P. (2003). Electron transfer between two silyl-substituted phenylene rings: EPR/ENDOR spectra, DFT calculations, and crystal structure of the one-electron reduction compound of a di(m-silylphenylenedisiloxane). Journal of the American Chemical Society, 125(15), 4487-94. https://doi.org/10.1021/ja0209060
Dutan, Cosmina, et al. "Electron transfer between two silyl-substituted phenylene rings: EPR/ENDOR spectra, DFT calculations, and crystal structure of the one-electron reduction compound of a di(m-silylphenylenedisiloxane)." Journal of the American Chemical Society vol. 125,15 (2003): 4487-94. doi: https://doi.org/10.1021/ja0209060
Dutan C, Choua S, Berclaz T, Geoffroy M, Mézailles N, Moores A, Ricard L, Le Floch P. Electron transfer between two silyl-substituted phenylene rings: EPR/ENDOR spectra, DFT calculations, and crystal structure of the one-electron reduction compound of a di(m-silylphenylenedisiloxane). J Am Chem Soc. 2003 Apr 16;125(15):4487-94. doi: 10.1021/ja0209060. PMID: 12683819.
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Menarcheal age - a tendency towards decline.

Journal of the College of Physicians and Surgeons--Pakistan : JCPSP

Hasan R, Adhi M, Shoaib S, Tauheed S.
PMID: 17999863
J Coll Physicians Surg Pak. 2007 Oct;17(10):642-3. doi: 10.2007/JCPSP.642643.

No abstract available.

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Hasan R, Adhi M, Shoaib S, et al. Menarcheal age - a tendency towards decline. J Coll Physicians Surg Pak. 2007;17(10):642-3doi: 10.2007/JCPSP.642643.
Hasan, R., Adhi, M., Shoaib, S., & Tauheed, S. (2007). Menarcheal age - a tendency towards decline. Journal of the College of Physicians and Surgeons--Pakistan : JCPSP, 17(10), 642-3. https://doi.org/10.2007/JCPSP.642643
Hasan, Rabia, et al. "Menarcheal age - a tendency towards decline." Journal of the College of Physicians and Surgeons--Pakistan : JCPSP vol. 17,10 (2007): 642-3. doi: https://doi.org/10.2007/JCPSP.642643
Hasan R, Adhi M, Shoaib S, Tauheed S. Menarcheal age - a tendency towards decline. J Coll Physicians Surg Pak. 2007 Oct;17(10):642-3. doi: 10.2007/JCPSP.642643. PMID: 17999863.
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Primary malignant melanoma of prostate.

Urology annals

Doublali M, Chouaib A, Khallouk A, Tazi MF, El Fassi MJ, Farih MH, Elfatmi H, Bendahou M, Benlemlih A, Lamarti O.
PMID: 20882159
Urol Ann. 2010 May;2(2):76-7. doi: 10.4103/0974-7796.65105.

Primary genitourinary melanoma accounts for less than one per cent of all cases of melanoma. Most cases attributed to the prostate actually originate from the prostatic urethra. Due to its infrequency, primary malignant melanoma of the genitourinary tract presents...

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Doublali M, Chouaib A, Khallouk A, et al. Primary malignant melanoma of prostate. Urol Ann. 2010;2(2):76-7doi: 10.4103/0974-7796.65105.
Doublali, M., Chouaib, A., Khallouk, A., Tazi, M. F., El Fassi, M. J., Farih, M. H., Elfatmi, H., Bendahou, M., Benlemlih, A., & Lamarti, O. (2010). Primary malignant melanoma of prostate. Urology annals, 2(2), 76-7. https://doi.org/10.4103/0974-7796.65105
Doublali, M, et al. "Primary malignant melanoma of prostate." Urology annals vol. 2,2 (2010): 76-7. doi: https://doi.org/10.4103/0974-7796.65105
Doublali M, Chouaib A, Khallouk A, Tazi MF, El Fassi MJ, Farih MH, Elfatmi H, Bendahou M, Benlemlih A, Lamarti O. Primary malignant melanoma of prostate. Urol Ann. 2010 May;2(2):76-7. doi: 10.4103/0974-7796.65105. PMID: 20882159; PMCID: PMC2943685.
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Diarylethene-containing carbon-rich ruthenium organometallics: tuning of electrochromism.

Inorganic chemistry

Liu Y, Ndiaye CM, Lagrost C, Costuas K, Choua S, Turek P, Norel L, Rigaut S.
PMID: 25033266
Inorg Chem. 2014 Aug 04;53(15):8172-88. doi: 10.1021/ic5013044. Epub 2014 Jul 17.

The association of a dithienylethene (DTE) system with ruthenium carbon-rich systems allows reaching sophisticated and efficient light- and electro-triggered multifunctional switches R-[Ru]-C≡C-DTE-C≡C-[Ru]-R, featuring multicolor electrochromism and electrochemical cyclization at remarkably low voltage. The spin density on the DTE ligand...

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Liu Y, Ndiaye CM, Lagrost C, et al. Diarylethene-containing carbon-rich ruthenium organometallics: tuning of electrochromism. Inorg Chem. 2014;53(15):8172-88doi: 10.1021/ic5013044.
Liu, Y., Ndiaye, C. M., Lagrost, C., Costuas, K., Choua, S., Turek, P., Norel, L., & Rigaut, S. (2014). Diarylethene-containing carbon-rich ruthenium organometallics: tuning of electrochromism. Inorganic chemistry, 53(15), 8172-88. https://doi.org/10.1021/ic5013044
Liu, Yifei, et al. "Diarylethene-containing carbon-rich ruthenium organometallics: tuning of electrochromism." Inorganic chemistry vol. 53,15 (2014): 8172-88. doi: https://doi.org/10.1021/ic5013044
Liu Y, Ndiaye CM, Lagrost C, Costuas K, Choua S, Turek P, Norel L, Rigaut S. Diarylethene-containing carbon-rich ruthenium organometallics: tuning of electrochromism. Inorg Chem. 2014 Aug 04;53(15):8172-88. doi: 10.1021/ic5013044. Epub 2014 Jul 17. PMID: 25033266.
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Mimicking PAMAM Dendrimers with Ampholytic, Hybrid Triazine Dendrimers: A Comparison of Dispersity and Stability.

Macromolecules

Lalwani S, Chouai A, Perez LM, Santiago V, Shaunak S, Simanek EE.
PMID: 20711424
Macromolecules. 2009 Aug 12;42(17):6723-3732. doi: 10.1021/ma9011818.

Two strategies are applied to mimic the ampholytic nature of the surfaces of half-generation PAMAM dendrimers and yet retain the very narrow dispersity inherent of triazine dendrimers. Both strategies start with a monodisperse, single-chemical entity, generation two triazine dendrimer...

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Lalwani S, Chouai A, Perez LM, et al. Mimicking PAMAM Dendrimers with Ampholytic, Hybrid Triazine Dendrimers: A Comparison of Dispersity and Stability. Macromolecules. 2009;42(17):6723-3732doi: 10.1021/ma9011818.
Lalwani, S., Chouai, A., Perez, L. M., Santiago, V., Shaunak, S., & Simanek, E. E. (2009). Mimicking PAMAM Dendrimers with Ampholytic, Hybrid Triazine Dendrimers: A Comparison of Dispersity and Stability. Macromolecules, 42(17), 6723-3732. https://doi.org/10.1021/ma9011818
Lalwani, Sanjiv, et al. "Mimicking PAMAM Dendrimers with Ampholytic, Hybrid Triazine Dendrimers: A Comparison of Dispersity and Stability." Macromolecules vol. 42,17 (2009): 6723-3732. doi: https://doi.org/10.1021/ma9011818
Lalwani S, Chouai A, Perez LM, Santiago V, Shaunak S, Simanek EE. Mimicking PAMAM Dendrimers with Ampholytic, Hybrid Triazine Dendrimers: A Comparison of Dispersity and Stability. Macromolecules. 2009 Aug 12;42(17):6723-3732. doi: 10.1021/ma9011818. PMID: 20711424; PMCID: PMC2920617.
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