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Self-assembly synthesis, structure, topology, and magnetic properties of a mononuclear Fe(iii)-violurate derivative: a combined experimental and theoretical study.

Dalton transactions (Cambridge, England : 2003)

Banik R, Roy S, Dlháň Ľ, Titiš J, Boča R, Kirillov AM, Martin AD, Bauza A, Frontera A, Rodríguez-Diéguez A, Salas JM, Das S.
PMID: 27722577
Dalton Trans. 2016 Oct 18;45(41):16166-16172. doi: 10.1039/c6dt03139k.

A new iron(iii) complex [Fe(H

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Banik R, Roy S, Dlháň Ľ, et al. Self-assembly synthesis, structure, topology, and magnetic properties of a mononuclear Fe(iii)-violurate derivative: a combined experimental and theoretical study. Dalton Trans. 2016;45(41):16166-16172doi: 10.1039/c6dt03139k.
Banik, R., Roy, S., Dlháň, �. �., Titiš, J., Boča, R., Kirillov, A. M., Martin, A. D., Bauza, A., Frontera, A., Rodríguez-Diéguez, A., Salas, J. M., & Das, S. (2016). Self-assembly synthesis, structure, topology, and magnetic properties of a mononuclear Fe(iii)-violurate derivative: a combined experimental and theoretical study. Dalton transactions (Cambridge, England : 2003), 45(41), 16166-16172. https://doi.org/10.1039/c6dt03139k
Banik, Rupak, et al. "Self-assembly synthesis, structure, topology, and magnetic properties of a mononuclear Fe(iii)-violurate derivative: a combined experimental and theoretical study." Dalton transactions (Cambridge, England : 2003) vol. 45,41 (2016): 16166-16172. doi: https://doi.org/10.1039/c6dt03139k
Banik R, Roy S, Dlháň Ľ, Titiš J, Boča R, Kirillov AM, Martin AD, Bauza A, Frontera A, Rodríguez-Diéguez A, Salas JM, Das S. Self-assembly synthesis, structure, topology, and magnetic properties of a mononuclear Fe(iii)-violurate derivative: a combined experimental and theoretical study. Dalton Trans. 2016 Oct 18;45(41):16166-16172. doi: 10.1039/c6dt03139k. PMID: 27722577.
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Erratum to: Outcome of HIV-associated lymphoma in a resource-limited setting of Jos, Nigeria.

Infectious agents and cancer

Silas OA, Achenbach CJ, Hou L, Murphy RL, Egesie JO, Sagay SA, Agbaji OO, Agaba PA, Musa J, Manasseh AN, Jatau ED, Dauda AM, Akanbi MO, Mandong BM.
PMID: 28652861
Infect Agent Cancer. 2017 Jun 26;12:37. doi: 10.1186/s13027-017-0149-2. eCollection 2017.

[This corrects the article DOI: 10.1186/s13027-017-0144-7.].

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Silas OA, Achenbach CJ, Hou L, et al. Erratum to: Outcome of HIV-associated lymphoma in a resource-limited setting of Jos, Nigeria. Infect Agent Cancer. 2017;12:37doi: 10.1186/s13027-017-0149-2.
Silas, O. A., Achenbach, C. J., Hou, L., Murphy, R. L., Egesie, J. O., Sagay, S. A., Agbaji, O. O., Agaba, P. A., Musa, J., Manasseh, A. N., Jatau, E. D., Dauda, A. M., Akanbi, M. O., & Mandong, B. M. (2017). Erratum to: Outcome of HIV-associated lymphoma in a resource-limited setting of Jos, Nigeria. Infectious agents and cancer, 1237. https://doi.org/10.1186/s13027-017-0149-2
Silas, Olugbenga Akindele, et al. "Erratum to: Outcome of HIV-associated lymphoma in a resource-limited setting of Jos, Nigeria." Infectious agents and cancer vol. 12 (2017): 37. doi: https://doi.org/10.1186/s13027-017-0149-2
Silas OA, Achenbach CJ, Hou L, Murphy RL, Egesie JO, Sagay SA, Agbaji OO, Agaba PA, Musa J, Manasseh AN, Jatau ED, Dauda AM, Akanbi MO, Mandong BM. Erratum to: Outcome of HIV-associated lymphoma in a resource-limited setting of Jos, Nigeria. Infect Agent Cancer. 2017 Jun 26;12:37. doi: 10.1186/s13027-017-0149-2. eCollection 2017. PMID: 28652861; PMCID: PMC5483957.
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Hypersplenism in liver disease and SLE revisited: current evidence supports an active rather than passive process.

BMC hematology

Gemery JM, Forauer AR, Silas AM, Hoffer EK.
PMID: 26865982
BMC Hematol. 2016 Feb 09;16:3. doi: 10.1186/s12878-016-0042-z. eCollection 2016.

BACKGROUND: Active and passive theories have been advanced to explain splenomegaly and cytopenias in liver disease. Dameshek proposed active downregulation of hematopoiesis. Doan proposed passive trapping of blood components in a spleen enlarged by portal hypertension. Recent findings do...

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Gemery JM, Forauer AR, Silas AM, et al. Hypersplenism in liver disease and SLE revisited: current evidence supports an active rather than passive process. BMC Hematol. 2016;16:3doi: 10.1186/s12878-016-0042-z.
Gemery, J. M., Forauer, A. R., Silas, A. M., & Hoffer, E. K. (2016). Hypersplenism in liver disease and SLE revisited: current evidence supports an active rather than passive process. BMC hematology, 163. https://doi.org/10.1186/s12878-016-0042-z
Gemery, John M, et al. "Hypersplenism in liver disease and SLE revisited: current evidence supports an active rather than passive process." BMC hematology vol. 16 (2016): 3. doi: https://doi.org/10.1186/s12878-016-0042-z
Gemery JM, Forauer AR, Silas AM, Hoffer EK. Hypersplenism in liver disease and SLE revisited: current evidence supports an active rather than passive process. BMC Hematol. 2016 Feb 09;16:3. doi: 10.1186/s12878-016-0042-z. eCollection 2016. PMID: 26865982; PMCID: PMC4748462.
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Optical properties of Cu2ZnSnSe4 thin films and identification of secondary phases by spectroscopic ellipsometry.

Optics express

Demircioğlu Ö, Salas JF, Rey G, Weiss T, Mousel M, Redinger A, Siebentritt S, Parisi J, Gütay L.
PMID: 28380795
Opt Express. 2017 Mar 06;25(5):5327-5340. doi: 10.1364/OE.25.005327.

We apply spectroscopic ellipsometry (SE) to identify secondary phases in Cu2ZnSnSe4 (CZTSe) absorbers and to investigate the optical properties of CZTSe. A detailed optical model is used to extract the optical parameters, such as refractive index and extinction coefficient...

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Demircioğlu Ö, Salas JF, Rey G, et al. Optical properties of Cu2ZnSnSe4 thin films and identification of secondary phases by spectroscopic ellipsometry. Opt Express. 2017;25(5):5327-5340doi: 10.1364/OE.25.005327.
Demircioğlu, �. �., Salas, J. F., Rey, G., Weiss, T., Mousel, M., Redinger, A., Siebentritt, S., Parisi, J., & Gütay, L. (2017). Optical properties of Cu2ZnSnSe4 thin films and identification of secondary phases by spectroscopic ellipsometry. Optics express, 25(5), 5327-5340. https://doi.org/10.1364/OE.25.005327
Demircioğlu, Özden, et al. "Optical properties of Cu2ZnSnSe4 thin films and identification of secondary phases by spectroscopic ellipsometry." Optics express vol. 25,5 (2017): 5327-5340. doi: https://doi.org/10.1364/OE.25.005327
Demircioğlu Ö, Salas JF, Rey G, Weiss T, Mousel M, Redinger A, Siebentritt S, Parisi J, Gütay L. Optical properties of Cu2ZnSnSe4 thin films and identification of secondary phases by spectroscopic ellipsometry. Opt Express. 2017 Mar 06;25(5):5327-5340. doi: 10.1364/OE.25.005327. PMID: 28380795.
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Complexes of Oxygenated trans-Azoalkanes and Tetracyanoethylene. The Interaction of pi Oxygen Dipoles with an Electron Poor Alkene.

The Journal of organic chemistry

Greer ML, Blackstock SC.
PMID: 11667749
J Org Chem. 1996 Nov 01;61(22):7895-7903. doi: 10.1021/jo960998+.

The N-oxide and N,N'-dioxide (1ao and 1ado) of trans-1,1'-azonorbornane (1) associate with TCNE in solution and in the solid state. The solution complexes are characterized by charge-transfer optical absorptions at lambda(m) 364 and 540 nm in CH(2)Cl(2) for 1ao/TCNE...

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Greer ML, Blackstock SC. Complexes of Oxygenated trans-Azoalkanes and Tetracyanoethylene. The Interaction of pi Oxygen Dipoles with an Electron Poor Alkene. J Org Chem. 1996;61(22):7895-7903doi: 10.1021/jo960998+.
Greer, M. L., & Blackstock, S. C. (1996). Complexes of Oxygenated trans-Azoalkanes and Tetracyanoethylene. The Interaction of pi Oxygen Dipoles with an Electron Poor Alkene. The Journal of organic chemistry, 61(22), 7895-7903. https://doi.org/10.1021/jo960998+
Greer, Melinda L., and Blackstock, Silas C.. "Complexes of Oxygenated trans-Azoalkanes and Tetracyanoethylene. The Interaction of pi Oxygen Dipoles with an Electron Poor Alkene." The Journal of organic chemistry vol. 61,22 (1996): 7895-7903. doi: https://doi.org/10.1021/jo960998+
Greer ML, Blackstock SC. Complexes of Oxygenated trans-Azoalkanes and Tetracyanoethylene. The Interaction of pi Oxygen Dipoles with an Electron Poor Alkene. J Org Chem. 1996 Nov 01;61(22):7895-7903. doi: 10.1021/jo960998+. PMID: 11667749.
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The Novel Hybrid Antitumor Compound Premithramycinone H Provides Indirect Evidence for a Tricyclic Intermediate of the Biosynthesis of the Aureolic Acid Antibiotic Mithramycin.

Angewandte Chemie (International ed. in English)

Lombó F, Künzel E, Prado L, Braña AF, Bindseil KU, Frevert J, Bearden D, Méndez C, Salas JA, Rohr J.
PMID: 10760873
Angew Chem Int Ed Engl. 2000 Feb;39(4):796-799. doi: 10.1002/(sici)1521-3773(20000218)39:4<796::aid-anie796>3.0.co;2-n.

No abstract available.

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Lombó F, Künzel E, Prado L, et al. The Novel Hybrid Antitumor Compound Premithramycinone H Provides Indirect Evidence for a Tricyclic Intermediate of the Biosynthesis of the Aureolic Acid Antibiotic Mithramycin. Angew Chem Int Ed Engl. 2000;39(4):796-799doi: 10.1002/(sici)1521-3773(20000218)39:4<796::aid-anie796>3.0.co;2-n.
Lombó, F., Künzel, E., Prado, L., Braña, A. F., Bindseil, K. U., Frevert, J., Bearden, D., Méndez, C., Salas, J. A., & Rohr, J. (2000). The Novel Hybrid Antitumor Compound Premithramycinone H Provides Indirect Evidence for a Tricyclic Intermediate of the Biosynthesis of the Aureolic Acid Antibiotic Mithramycin. Angewandte Chemie (International ed. in English), 39(4), 796-799. https://doi.org/10.1002/(sici)1521-3773(20000218)39:4<796::aid-anie796>3.0.co;2-n
Lombó, et al. "The Novel Hybrid Antitumor Compound Premithramycinone H Provides Indirect Evidence for a Tricyclic Intermediate of the Biosynthesis of the Aureolic Acid Antibiotic Mithramycin." Angewandte Chemie (International ed. in English) vol. 39,4 (2000): 796-799. doi: https://doi.org/10.1002/(sici)1521-3773(20000218)39:4<796::aid-anie796>3.0.co;2-n
Lombó F, Künzel E, Prado L, Braña AF, Bindseil KU, Frevert J, Bearden D, Méndez C, Salas JA, Rohr J. The Novel Hybrid Antitumor Compound Premithramycinone H Provides Indirect Evidence for a Tricyclic Intermediate of the Biosynthesis of the Aureolic Acid Antibiotic Mithramycin. Angew Chem Int Ed Engl. 2000 Feb;39(4):796-799. doi: 10.1002/(sici)1521-3773(20000218)39:4<796::aid-anie796>3.0.co;2-n. PMID: 10760873.
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Congenital ureteral valves: two new cases and a review of the literature.

Journal of pediatric urology

Rossi E, Salas JR, Aucatoma FC, Muñoz MO, Fochs LM.
PMID: 18947772
J Pediatr Urol. 2007 Oct;3(5):344-9. doi: 10.1016/j.jpurol.2007.02.002. Epub 2007 Apr 18.

Ureteral valves are a rare clinical finding. Frequently they are associated with other urological anomalies such as complete or incomplete renal duplication, ectopic ureter, vesicoureteral reflux and horseshoe kidney. Hydronephrosis is the most common clinical sign. We report two...

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Rossi E, Salas JR, Aucatoma FC, et al. Congenital ureteral valves: two new cases and a review of the literature. J Pediatr Urol. 2007;3(5):344-9doi: 10.1016/j.jpurol.2007.02.002.
Rossi, E., Salas, J. R., Aucatoma, F. C., Muñoz, M. O., & Fochs, L. M. (2007). Congenital ureteral valves: two new cases and a review of the literature. Journal of pediatric urology, 3(5), 344-9. https://doi.org/10.1016/j.jpurol.2007.02.002
Rossi, Enrica, et al. "Congenital ureteral valves: two new cases and a review of the literature." Journal of pediatric urology vol. 3,5 (2007): 344-9. doi: https://doi.org/10.1016/j.jpurol.2007.02.002
Rossi E, Salas JR, Aucatoma FC, Muñoz MO, Fochs LM. Congenital ureteral valves: two new cases and a review of the literature. J Pediatr Urol. 2007 Oct;3(5):344-9. doi: 10.1016/j.jpurol.2007.02.002. Epub 2007 Apr 18. PMID: 18947772.
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Activity of Pt(II) and Ru(III) Triazolopyrimidine Complexes Against Parasites of the Genus Leishmania, Trypanosomas and Phytomonas.

Metal-based drugs

Salas JM, Quirós M, Abul Haj M, Magán R, Marín C, Sáchez-Moreno M, Faure R.
PMID: 18475985
Met Based Drugs. 2001;8(3):119-24. doi: 10.1155/MBD.2001.119.

The synthesis and characterization of two Pt(II) Complexes with the isomeric ligands 4,5-dihydro-5-oxo- [1,2,4]triazolo-[ 1,5-a]pyrimidine (5HtpO) and 4,7-dihydro-7-oxo-[ 1,2,4]-triazolo-[ 1,5-a]pyrimidine (7HtpO) are described, as well as a Ru(III) complex with 7HtpO. The crystal structure of cis-[PtCl(2)(7HtpO)(2)].2H(2)O has been solved...

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Salas JM, Quirós M, Abul Haj M, et al. Activity of Pt(II) and Ru(III) Triazolopyrimidine Complexes Against Parasites of the Genus Leishmania, Trypanosomas and Phytomonas. Met Based Drugs. 2001;8(3):119-24doi: 10.1155/MBD.2001.119.
Salas, J. M., Quirós, M., Abul Haj, M., Magán, R., Marín, C., Sáchez-Moreno, M., & Faure, R. (2001). Activity of Pt(II) and Ru(III) Triazolopyrimidine Complexes Against Parasites of the Genus Leishmania, Trypanosomas and Phytomonas. Metal-based drugs, 8(3), 119-24. https://doi.org/10.1155/MBD.2001.119
Salas, J M, et al. "Activity of Pt(II) and Ru(III) Triazolopyrimidine Complexes Against Parasites of the Genus Leishmania, Trypanosomas and Phytomonas." Metal-based drugs vol. 8,3 (2001): 119-24. doi: https://doi.org/10.1155/MBD.2001.119
Salas JM, Quirós M, Abul Haj M, Magán R, Marín C, Sáchez-Moreno M, Faure R. Activity of Pt(II) and Ru(III) Triazolopyrimidine Complexes Against Parasites of the Genus Leishmania, Trypanosomas and Phytomonas. Met Based Drugs. 2001;8(3):119-24. doi: 10.1155/MBD.2001.119. PMID: 18475985; PMCID: PMC2365262.
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Coordination frameworks containing the pyrimidin-4-olate ligand. Synthesis, thermal, magnetic, and ab initio XRPD structural characterization of nickel and zinc derivatives.

Inorganic chemistry

Barea E, Navarro JA, Salas JM, Masciocchi N, Galli S, Sironi A.
PMID: 14731009
Inorg Chem. 2004 Jan 26;43(2):473-81. doi: 10.1021/ic0351287.

Extended coordination frameworks containing the pyrimidin-4-olate ligand (4-pymo) and Zn(II) and Ni(II) metal ions have been obtained by solid state reactions and have been fully characterized by spectroscopic, thermal, and magnetic measurements and by ab initio XRPD. The reaction...

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Barea E, Navarro JA, Salas JM, et al. Coordination frameworks containing the pyrimidin-4-olate ligand. Synthesis, thermal, magnetic, and ab initio XRPD structural characterization of nickel and zinc derivatives. Inorg Chem. 2004;43(2):473-81doi: 10.1021/ic0351287.
Barea, E., Navarro, J. A., Salas, J. M., Masciocchi, N., Galli, S., & Sironi, A. (2004). Coordination frameworks containing the pyrimidin-4-olate ligand. Synthesis, thermal, magnetic, and ab initio XRPD structural characterization of nickel and zinc derivatives. Inorganic chemistry, 43(2), 473-81. https://doi.org/10.1021/ic0351287
Barea, Elisa, et al. "Coordination frameworks containing the pyrimidin-4-olate ligand. Synthesis, thermal, magnetic, and ab initio XRPD structural characterization of nickel and zinc derivatives." Inorganic chemistry vol. 43,2 (2004): 473-81. doi: https://doi.org/10.1021/ic0351287
Barea E, Navarro JA, Salas JM, Masciocchi N, Galli S, Sironi A. Coordination frameworks containing the pyrimidin-4-olate ligand. Synthesis, thermal, magnetic, and ab initio XRPD structural characterization of nickel and zinc derivatives. Inorg Chem. 2004 Jan 26;43(2):473-81. doi: 10.1021/ic0351287. PMID: 14731009.
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Synthesis, Structure and Antitumour Properties of a New 1,2-Propylenediaminetetraacetate-Ruthenium(III) Compound.

Metal-based drugs

Vilaplana R, Romero MA, Quirós M, Salas JM, González-Vílchez F.
PMID: 18472768
Met Based Drugs. 1995;2(4):211-9. doi: 10.1155/MBD.1995.211.

A novel complex formed by ruthenium (III) and the sequestering ligand 1,2-propylenediaminetetraacetic acid (PDTA) has been synthetized and characterized. The structure of the monomeric compound, studied by X-ray diffraction , shows an almost symmetric octahedral geometry around the metal...

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Vilaplana R, Romero MA, Quirós M, et al. Synthesis, Structure and Antitumour Properties of a New 1,2-Propylenediaminetetraacetate-Ruthenium(III) Compound. Met Based Drugs. 1995;2(4):211-9doi: 10.1155/MBD.1995.211.
Vilaplana, R., Romero, M. A., Quirós, M., Salas, J. M., & González-Vílchez, F. (1995). Synthesis, Structure and Antitumour Properties of a New 1,2-Propylenediaminetetraacetate-Ruthenium(III) Compound. Metal-based drugs, 2(4), 211-9. https://doi.org/10.1155/MBD.1995.211
Vilaplana, R, et al. "Synthesis, Structure and Antitumour Properties of a New 1,2-Propylenediaminetetraacetate-Ruthenium(III) Compound." Metal-based drugs vol. 2,4 (1995): 211-9. doi: https://doi.org/10.1155/MBD.1995.211
Vilaplana R, Romero MA, Quirós M, Salas JM, González-Vílchez F. Synthesis, Structure and Antitumour Properties of a New 1,2-Propylenediaminetetraacetate-Ruthenium(III) Compound. Met Based Drugs. 1995;2(4):211-9. doi: 10.1155/MBD.1995.211. PMID: 18472768; PMCID: PMC2364974.
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4,7-Phenanthrolinium perchlorate-5-methyl-1,2,4-triazolo[1,5-a]pyrimidin-7(4H)-one-water (1/1/2).

Acta crystallographica. Section E, Structure reports online

Caballero AB, Quirós M, Salas JM.
PMID: 21579873
Acta Crystallogr Sect E Struct Rep Online. 2010 Jan 27;66:o459-60. doi: 10.1107/S1600536810002564.

The asymmetric unit of the title compound, C(12)H(9)N(2) (+)·ClO(4) (-)·C(6)H(6)N(4)O·2H(2)O, contains a monoprotonated 4,7-phenanthrolinium (47phen) cation, a perchlorate anion balancing its charge, a neutral mol-ecule of 5-methyl-1,2,4-triazolo[1,5-a]pyrimidin-7(4H)-one (HmtpO) and two inter-stitial water mol-ecules. In the crystal structure, the acidic...

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Caballero AB, Quirós M, Salas JM. 4,7-Phenanthrolinium perchlorate-5-methyl-1,2,4-triazolo[1,5-a]pyrimidin-7(4H)-one-water (1/1/2). Acta Crystallogr Sect E Struct Rep Online. 2010;66:o459-60doi: 10.1107/S1600536810002564.
Caballero, A. B., Quirós, M., & Salas, J. M. (2010). 4,7-Phenanthrolinium perchlorate-5-methyl-1,2,4-triazolo[1,5-a]pyrimidin-7(4H)-one-water (1/1/2). Acta crystallographica. Section E, Structure reports online, 66o459-60. https://doi.org/10.1107/S1600536810002564
Caballero, Ana B, et al. "4,7-Phenanthrolinium perchlorate-5-methyl-1,2,4-triazolo[1,5-a]pyrimidin-7(4H)-one-water (1/1/2)." Acta crystallographica. Section E, Structure reports online vol. 66 (2010): o459-60. doi: https://doi.org/10.1107/S1600536810002564
Caballero AB, Quirós M, Salas JM. 4,7-Phenanthrolinium perchlorate-5-methyl-1,2,4-triazolo[1,5-a]pyrimidin-7(4H)-one-water (1/1/2). Acta Crystallogr Sect E Struct Rep Online. 2010 Jan 27;66:o459-60. doi: 10.1107/S1600536810002564. PMID: 21579873; PMCID: PMC2979915.
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Energy transfer mechanisms in a dipole chain: From energy equipartition to the formation of breathers.

Physical review. E

Zampetaki A, Salas JP, Schmelcher P.
PMID: 30253512
Phys Rev E. 2018 Aug;98(2):022202. doi: 10.1103/PhysRevE.98.022202.

We study the energy transfer in a classical dipole chain of N interacting rigid rotating dipoles. The underlying high-dimensional potential energy landscape is analyzed in particular by determining the equilibrium points and their stability in the common plane of...

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Zampetaki A, Salas JP, Schmelcher P. Energy transfer mechanisms in a dipole chain: From energy equipartition to the formation of breathers. Phys Rev E. 2018;98(2):022202doi: 10.1103/PhysRevE.98.022202.
Zampetaki, A., Salas, J. P., & Schmelcher, P. (2018). Energy transfer mechanisms in a dipole chain: From energy equipartition to the formation of breathers. Physical review. E, 98(2), 022202. https://doi.org/10.1103/PhysRevE.98.022202
Zampetaki, Alexandra, et al. "Energy transfer mechanisms in a dipole chain: From energy equipartition to the formation of breathers." Physical review. E vol. 98,2 (2018): 022202. doi: https://doi.org/10.1103/PhysRevE.98.022202
Zampetaki A, Salas JP, Schmelcher P. Energy transfer mechanisms in a dipole chain: From energy equipartition to the formation of breathers. Phys Rev E. 2018 Aug;98(2):022202. doi: 10.1103/PhysRevE.98.022202. PMID: 30253512.
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