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Stability of the Parent Anion of the Potential Radiosensitizer 8-Bromoadenine Formed by Low-Energy (<3 eV) Electron Attachment.

The journal of physical chemistry. B

Schürmann R, Tanzer K, Dąbkowska I, Denifl S, Bald I.
PMID: 28525718
J Phys Chem B. 2017 Jun 15;121(23):5730-5734. doi: 10.1021/acs.jpcb.7b02130. Epub 2017 Jun 02.

8-Bromoadenine (

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Schürmann R, Tanzer K, Dąbkowska I, et al. Stability of the Parent Anion of the Potential Radiosensitizer 8-Bromoadenine Formed by Low-Energy (<3 eV) Electron Attachment. J Phys Chem B. 2017;121(23):5730-5734doi: 10.1021/acs.jpcb.7b02130.
Schürmann, R., Tanzer, K., Dąbkowska, I., Denifl, S., & Bald, I. (2017). Stability of the Parent Anion of the Potential Radiosensitizer 8-Bromoadenine Formed by Low-Energy (<3 eV) Electron Attachment. The journal of physical chemistry. B, 121(23), 5730-5734. https://doi.org/10.1021/acs.jpcb.7b02130
Schürmann, Robin, et al. "Stability of the Parent Anion of the Potential Radiosensitizer 8-Bromoadenine Formed by Low-Energy (<3 eV) Electron Attachment." The journal of physical chemistry. B vol. 121,23 (2017): 5730-5734. doi: https://doi.org/10.1021/acs.jpcb.7b02130
Schürmann R, Tanzer K, Dąbkowska I, Denifl S, Bald I. Stability of the Parent Anion of the Potential Radiosensitizer 8-Bromoadenine Formed by Low-Energy (<3 eV) Electron Attachment. J Phys Chem B. 2017 Jun 15;121(23):5730-5734. doi: 10.1021/acs.jpcb.7b02130. Epub 2017 Jun 02. PMID: 28525718.
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Some relevant points on sperm DNA fragmentation tests.

Translational andrology and urology

Muratori M, Baldi E.
PMID: 29082178
Transl Androl Urol. 2017 Sep;6:S560-S563. doi: 10.21037/tau.2017.03.47.

No abstract available.

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Muratori M, Baldi E. Some relevant points on sperm DNA fragmentation tests. Transl Androl Urol. 2017;6:S560-S563doi: 10.21037/tau.2017.03.47.
Muratori, M., & Baldi, E. (2017). Some relevant points on sperm DNA fragmentation tests. Translational andrology and urology, 6S560-S563. https://doi.org/10.21037/tau.2017.03.47
Muratori, Monica, and Baldi, Elisabetta. "Some relevant points on sperm DNA fragmentation tests." Translational andrology and urology vol. 6 (2017): S560-S563. doi: https://doi.org/10.21037/tau.2017.03.47
Muratori M, Baldi E. Some relevant points on sperm DNA fragmentation tests. Transl Androl Urol. 2017 Sep;6:S560-S563. doi: 10.21037/tau.2017.03.47. PMID: 29082178; PMCID: PMC5643625.
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Low-valent iron: an Fe(I) ate compound as a building block for a linear trinuclear Fe cluster.

Chemical communications (Cambridge, England)

Lichtenberg C, Viciu L, Vogt M, Rodríguez-Lugo RE, Adelhardt M, Sutter J, Khusniyarov MM, Meyer K, de Bruin B, Bill E, Grützmacher H.
PMID: 26221636
Chem Commun (Camb). 2015 Sep 21;51(73):13890-3. doi: 10.1039/c5cc04908c.

A low-valent trinuclear iron complex with an unusual linear Fe(I)-Fe(II)-Fe(I) unit is presented. It is accessed in a rational approach using a salt metathesis reaction between a new anionic Fe(I) containing heterocycle and FeCl2. Its electronic structure was studied...

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Lichtenberg C, Viciu L, Vogt M, et al. Low-valent iron: an Fe(I) ate compound as a building block for a linear trinuclear Fe cluster. Chem Commun (Camb). 2015;51(73):13890-3doi: 10.1039/c5cc04908c.
Lichtenberg, C., Viciu, L., Vogt, M., Rodríguez-Lugo, R. E., Adelhardt, M., Sutter, J., Khusniyarov, M. M., Meyer, K., de Bruin, B., Bill, E., & Grützmacher, H. (2015). Low-valent iron: an Fe(I) ate compound as a building block for a linear trinuclear Fe cluster. Chemical communications (Cambridge, England), 51(73), 13890-3. https://doi.org/10.1039/c5cc04908c
Lichtenberg, C, et al. "Low-valent iron: an Fe(I) ate compound as a building block for a linear trinuclear Fe cluster." Chemical communications (Cambridge, England) vol. 51,73 (2015): 13890-3. doi: https://doi.org/10.1039/c5cc04908c
Lichtenberg C, Viciu L, Vogt M, Rodríguez-Lugo RE, Adelhardt M, Sutter J, Khusniyarov MM, Meyer K, de Bruin B, Bill E, Grützmacher H. Low-valent iron: an Fe(I) ate compound as a building block for a linear trinuclear Fe cluster. Chem Commun (Camb). 2015 Sep 21;51(73):13890-3. doi: 10.1039/c5cc04908c. PMID: 26221636.
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Fast piezoelectric valve offering controlled gas injection in magnetically confined fusion plasmas for diagnostic and fuelling purposes.

The Review of scientific instruments

Griener M, Schmitz O, Bald K, Bösser D, Cavedon M, De Marné P, Eich T, Fuchert G, Herrmann A, Kappatou A, Lunt T, Rohde V, Schweer B, Sochor M, Stroth U, Terra A, Wolfrum E.
PMID: 28372367
Rev Sci Instrum. 2017 Mar;88(3):033509. doi: 10.1063/1.4978629.

In magnetically confined fusion plasmas controlled gas injection is crucial for plasma fuelling as well as for various diagnostic applications such as active spectroscopy. We present a new, versatile system for the injection of collimated thermal gas beams into...

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Griener M, Schmitz O, Bald K, et al. Fast piezoelectric valve offering controlled gas injection in magnetically confined fusion plasmas for diagnostic and fuelling purposes. Rev Sci Instrum. 2017;88(3):033509doi: 10.1063/1.4978629.
Griener, M., Schmitz, O., Bald, K., Bösser, D., Cavedon, M., De Marné, P., Eich, T., Fuchert, G., Herrmann, A., Kappatou, A., Lunt, T., Rohde, V., Schweer, B., Sochor, M., Stroth, U., Terra, A., Wolfrum, E. (2017). Fast piezoelectric valve offering controlled gas injection in magnetically confined fusion plasmas for diagnostic and fuelling purposes. The Review of scientific instruments, 88(3), 033509. https://doi.org/10.1063/1.4978629
Griener, M, et al. "Fast piezoelectric valve offering controlled gas injection in magnetically confined fusion plasmas for diagnostic and fuelling purposes." The Review of scientific instruments vol. 88,3 (2017): 033509. doi: https://doi.org/10.1063/1.4978629
Griener M, Schmitz O, Bald K, Bösser D, Cavedon M, De Marné P, Eich T, Fuchert G, Herrmann A, Kappatou A, Lunt T, Rohde V, Schweer B, Sochor M, Stroth U, Terra A, Wolfrum E. Fast piezoelectric valve offering controlled gas injection in magnetically confined fusion plasmas for diagnostic and fuelling purposes. Rev Sci Instrum. 2017 Mar;88(3):033509. doi: 10.1063/1.4978629. PMID: 28372367.
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Dickkopf-3 Contributes to the Regulation of Anti-Tumor Immune Responses by Mesenchymal Stem Cells.

Frontiers in immunology

Lu KH, Tounsi A, Shridhar N, Küblbeck G, Klevenz A, Prokosch S, Bald T, Tüting T, Arnold B.
PMID: 26734010
Front Immunol. 2015 Dec 24;6:645. doi: 10.3389/fimmu.2015.00645. eCollection 2015.

Mesenchymal stem cells (MSCs) are known to limit immune responses in vivo by multiple soluble factors. Dickkopf-3 (DKK3), a secreted glycoprotein, has recently been identified as a novel immune modulator. Since DKK3 has been reported to be produced by...

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Lu KH, Tounsi A, Shridhar N, et al. Dickkopf-3 Contributes to the Regulation of Anti-Tumor Immune Responses by Mesenchymal Stem Cells. Front Immunol. 2015;6:645doi: 10.3389/fimmu.2015.00645.
Lu, K. H., Tounsi, A., Shridhar, N., Küblbeck, G., Klevenz, A., Prokosch, S., Bald, T., Tüting, T., & Arnold, B. (2015). Dickkopf-3 Contributes to the Regulation of Anti-Tumor Immune Responses by Mesenchymal Stem Cells. Frontiers in immunology, 6645. https://doi.org/10.3389/fimmu.2015.00645
Lu, Kun-Hui, et al. "Dickkopf-3 Contributes to the Regulation of Anti-Tumor Immune Responses by Mesenchymal Stem Cells." Frontiers in immunology vol. 6 (2015): 645. doi: https://doi.org/10.3389/fimmu.2015.00645
Lu KH, Tounsi A, Shridhar N, Küblbeck G, Klevenz A, Prokosch S, Bald T, Tüting T, Arnold B. Dickkopf-3 Contributes to the Regulation of Anti-Tumor Immune Responses by Mesenchymal Stem Cells. Front Immunol. 2015 Dec 24;6:645. doi: 10.3389/fimmu.2015.00645. eCollection 2015. PMID: 26734010; PMCID: PMC4689786.
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A cubic Fe4Mo4 oxo framework and its reversible four-electron redox chemistry.

Inorganic chemistry

Falkenhagen JP, Braun B, Bill E, Sattler D, Limberg C.
PMID: 24981960
Inorg Chem. 2014 Jul 21;53(14):7294-308. doi: 10.1021/ic500584a. Epub 2014 Jul 01.

The potential of iron molybdates as catalysts in the Formox process stimulates research on aggregated but molecular iron-molybdenum oxo compounds. In this context, [(Me3TACN)Fe](OTf)2 was reacted with (nBu4N)2[MoO4], which led to an oxo cluster, [[(Me3TACN)Fe][μ-(MoO4-κ(3)O,O',O″)]]4 (1, Fe4Mo4) with a...

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Falkenhagen JP, Braun B, Bill E, et al. A cubic Fe4Mo4 oxo framework and its reversible four-electron redox chemistry. Inorg Chem. 2014;53(14):7294-308doi: 10.1021/ic500584a.
Falkenhagen, J. P., Braun, B., Bill, E., Sattler, D., & Limberg, C. (2014). A cubic Fe4Mo4 oxo framework and its reversible four-electron redox chemistry. Inorganic chemistry, 53(14), 7294-308. https://doi.org/10.1021/ic500584a
Falkenhagen, Jan P, et al. "A cubic Fe4Mo4 oxo framework and its reversible four-electron redox chemistry." Inorganic chemistry vol. 53,14 (2014): 7294-308. doi: https://doi.org/10.1021/ic500584a
Falkenhagen JP, Braun B, Bill E, Sattler D, Limberg C. A cubic Fe4Mo4 oxo framework and its reversible four-electron redox chemistry. Inorg Chem. 2014 Jul 21;53(14):7294-308. doi: 10.1021/ic500584a. Epub 2014 Jul 01. PMID: 24981960.
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Exchange Coupling in an Isostructural Series of Face-Sharing Bioctahedral Complexes [LM(II)(&mgr;-X)(3)M(II)L]BPh(4) (M = Mn, Fe, Co, Ni, Zn; X = Cl, Br; L = 1,4,7-Trimethyl-1,4,7-triazacyclononane).

Inorganic chemistry

Bossek U, Nühlen D, Bill E, Glaser T, Krebs C, Weyhermüller T, Wieghardt K, Lengen M, Trautwein AX.
PMID: 11669919
Inorg Chem. 1997 Jun 18;36(13):2834-2843. doi: 10.1021/ic970119h.

The reaction of the divalent metal halides ZnCl(2), ZnBr(2), MnCl(2).4CH(3)CN, MnBr(2), FeCl(2).4CH(3)CN, CoCl(2).4CH(3)CN, CoBr(2), NiCl(2).6H(2)O, and NiBr(2), respectively, with the macrocycle 1,4,7-trimethyl-1,4,7-triazacyclononane (L) (1:1) in anhydrous acetonitrile, acetone, chloroform, or ethanol affords upon additon of NaBPh(4) the isomorphous series...

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Bossek U, Nühlen D, Bill E, et al. Exchange Coupling in an Isostructural Series of Face-Sharing Bioctahedral Complexes [LM(II)(&mgr;-X)(3)M(II)L]BPh(4) (M = Mn, Fe, Co, Ni, Zn; X = Cl, Br; L = 1,4,7-Trimethyl-1,4,7-triazacyclononane). Inorg Chem. 1997;36(13):2834-2843doi: 10.1021/ic970119h.
Bossek, U., Nühlen, D., Bill, E., Glaser, T., Krebs, C., Weyhermüller, T., Wieghardt, K., Lengen, M., & Trautwein, A. X. (1997). Exchange Coupling in an Isostructural Series of Face-Sharing Bioctahedral Complexes [LM(II)(&mgr;-X)(3)M(II)L]BPh(4) (M = Mn, Fe, Co, Ni, Zn; X = Cl, Br; L = 1,4,7-Trimethyl-1,4,7-triazacyclononane). Inorganic chemistry, 36(13), 2834-2843. https://doi.org/10.1021/ic970119h
Bossek, Ursula, et al. "Exchange Coupling in an Isostructural Series of Face-Sharing Bioctahedral Complexes [LM(II)(&mgr;-X)(3)M(II)L]BPh(4) (M = Mn, Fe, Co, Ni, Zn; X = Cl, Br; L = 1,4,7-Trimethyl-1,4,7-triazacyclononane)." Inorganic chemistry vol. 36,13 (1997): 2834-2843. doi: https://doi.org/10.1021/ic970119h
Bossek U, Nühlen D, Bill E, Glaser T, Krebs C, Weyhermüller T, Wieghardt K, Lengen M, Trautwein AX. Exchange Coupling in an Isostructural Series of Face-Sharing Bioctahedral Complexes [LM(II)(&mgr;-X)(3)M(II)L]BPh(4) (M = Mn, Fe, Co, Ni, Zn; X = Cl, Br; L = 1,4,7-Trimethyl-1,4,7-triazacyclononane). Inorg Chem. 1997 Jun 18;36(13):2834-2843. doi: 10.1021/ic970119h. PMID: 11669919.
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Compound I and Compound II Analogues from Porpholactones.

Inorganic chemistry

Jayaraj K, Gold A, Austin RN, Ball LM, Terner J, Mandon D, Weiss R, Fischer J, DeCian A, Bill E, Müther M, Schünemann V, Trautwein AX.
PMID: 11670121
Inorg Chem. 1997 Sep 24;36(20):4555-4566. doi: 10.1021/ic970597s.

The tetraaza macrocycles 2-oxa-3-oxotetramesitylporphine (|H(2) 1|) and 2-oxa-3-oxotetrakis(2,6-dichlorophenyl)porphine (|H(2) 2|) and the corresponding iron complexes (|Fe(III)(X) 1| and |Fe(III)(X) 2|; X= Cl(-), OH(-), or SO(3)CF(3)(-)) have been synthesized. These macrocycles are derived from porphyrins by transformation of one pyrrole...

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Jayaraj K, Gold A, Austin RN, et al. Compound I and Compound II Analogues from Porpholactones. Inorg Chem. 1997;36(20):4555-4566doi: 10.1021/ic970597s.
Jayaraj, K., Gold, A., Austin, R. N., Ball, L. M., Terner, J., Mandon, D., Weiss, R., Fischer, J., DeCian, A., Bill, E., Müther, M., Schünemann, V., & Trautwein, A. X. (1997). Compound I and Compound II Analogues from Porpholactones. Inorganic chemistry, 36(20), 4555-4566. https://doi.org/10.1021/ic970597s
Jayaraj, K., et al. "Compound I and Compound II Analogues from Porpholactones." Inorganic chemistry vol. 36,20 (1997): 4555-4566. doi: https://doi.org/10.1021/ic970597s
Jayaraj K, Gold A, Austin RN, Ball LM, Terner J, Mandon D, Weiss R, Fischer J, DeCian A, Bill E, Müther M, Schünemann V, Trautwein AX. Compound I and Compound II Analogues from Porpholactones. Inorg Chem. 1997 Sep 24;36(20):4555-4566. doi: 10.1021/ic970597s. PMID: 11670121.
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Molecular and electronic structures of iron(II)/(III) complexes containing N,S-coordinated, closed-shell o-aminothiophenolato(1-) and o-iminothiophenolato(2-) ligands.

Inorganic chemistry

Ghosh P, Begum A, Bill E, Weyhermüller T, Wieghardt K.
PMID: 12739961
Inorg Chem. 2003 May 19;42(10):3208-15. doi: 10.1021/ic020617c.

The coordination chemistry of the ligands o-aminothiophenol, H(abt), 4,6-di-tert-butyl-2-aminothiophenol, H[L(AP)], and 1,2-ethanediamine-N,N'-bis(2-benzenethiol), H(4)('N(2)S(2')), with FeCl(2) under strictly anaerobic and increasingly aerobic conditions has been systematically investigated. Using strictly anaerobic conditions, the neutral, air-sensitive, yellow complexes (mu-S,S)[Fe(II)(abt)(2)](2) (1), (mu-S,S)[Fe(II)(L(AP))(2)](2).8CH(3)OH (2),...

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Ghosh P, Begum A, Bill E, et al. Molecular and electronic structures of iron(II)/(III) complexes containing N,S-coordinated, closed-shell o-aminothiophenolato(1-) and o-iminothiophenolato(2-) ligands. Inorg Chem. 2003;42(10):3208-15doi: 10.1021/ic020617c.
Ghosh, P., Begum, A., Bill, E., Weyhermüller, T., & Wieghardt, K. (2003). Molecular and electronic structures of iron(II)/(III) complexes containing N,S-coordinated, closed-shell o-aminothiophenolato(1-) and o-iminothiophenolato(2-) ligands. Inorganic chemistry, 42(10), 3208-15. https://doi.org/10.1021/ic020617c
Ghosh, Prasanta, et al. "Molecular and electronic structures of iron(II)/(III) complexes containing N,S-coordinated, closed-shell o-aminothiophenolato(1-) and o-iminothiophenolato(2-) ligands." Inorganic chemistry vol. 42,10 (2003): 3208-15. doi: https://doi.org/10.1021/ic020617c
Ghosh P, Begum A, Bill E, Weyhermüller T, Wieghardt K. Molecular and electronic structures of iron(II)/(III) complexes containing N,S-coordinated, closed-shell o-aminothiophenolato(1-) and o-iminothiophenolato(2-) ligands. Inorg Chem. 2003 May 19;42(10):3208-15. doi: 10.1021/ic020617c. PMID: 12739961.
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Long-range exchange interactions and integer-spin S(t) = 2 EPR spectra of a Cr(III)Zn(II)Cr(III) species with multiplet mixing.

Inorganic chemistry

Burdinski D, Bill E, Birkelbach F, Wieghardt K, Chaudhuri P.
PMID: 11300812
Inorg Chem. 2001 Mar 12;40(6):1160-6. doi: 10.1021/ic000870h.

Synthesis, structural, and spectroscopic characterization of the linear cationic complex [LCr(III)(mu-[dmg)(3)Zn(II))Cr(III)L](2+) (1) in which L = 1,4,7-trimethyl-1,4,7-triazacyclononane and dmg is the dimethylglyoximato anion are reported. The Cr...Cr distance of 1 is 7 A. SQUID magnetic susceptibility measurements reveal the...

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Burdinski D, Bill E, Birkelbach F, et al. Long-range exchange interactions and integer-spin S(t) = 2 EPR spectra of a Cr(III)Zn(II)Cr(III) species with multiplet mixing. Inorg Chem. 2001;40(6):1160-6doi: 10.1021/ic000870h.
Burdinski, D., Bill, E., Birkelbach, F., Wieghardt, K., & Chaudhuri, P. (2001). Long-range exchange interactions and integer-spin S(t) = 2 EPR spectra of a Cr(III)Zn(II)Cr(III) species with multiplet mixing. Inorganic chemistry, 40(6), 1160-6. https://doi.org/10.1021/ic000870h
Burdinski, D, et al. "Long-range exchange interactions and integer-spin S(t) = 2 EPR spectra of a Cr(III)Zn(II)Cr(III) species with multiplet mixing." Inorganic chemistry vol. 40,6 (2001): 1160-6. doi: https://doi.org/10.1021/ic000870h
Burdinski D, Bill E, Birkelbach F, Wieghardt K, Chaudhuri P. Long-range exchange interactions and integer-spin S(t) = 2 EPR spectra of a Cr(III)Zn(II)Cr(III) species with multiplet mixing. Inorg Chem. 2001 Mar 12;40(6):1160-6. doi: 10.1021/ic000870h. PMID: 11300812.
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Influence of Meso Substituents on Electronic States of (Oxoferryl)porphyrin pi-Cation Radicals.

Inorganic chemistry

Jayaraj K, Terner J, Gold A, Roberts DA, Austin RN, Mandon D, Weiss R, Bill E, Müther M, Trautwein AX.
PMID: 11666384
Inorg Chem. 1996 Mar 13;35(6):1632-1640. doi: 10.1021/ic951058v.

A series of (oxoferryl)porphyrin pi-cation radicals generated from porphyrins substituted at the meso positions with highly electron-withdrawing aryl groups has been characterized: tetrakis-5,10,15,20-(2,6-dichlorophenyl)-, 5-(2-chloro-6-nitrophenyl)-10,15,20-tris(2,6-dichlorophenyl)-, and 5-(2,6-dinitrophenyl)-10,15,20-tris(2,6-dichlorophenyl)porphyrins (porphyrins 1-3, respectively). The physical-chemical properties of the oxidized complexes of 1-3 are...

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Jayaraj K, Terner J, Gold A, et al. Influence of Meso Substituents on Electronic States of (Oxoferryl)porphyrin pi-Cation Radicals. Inorg Chem. 1996;35(6):1632-1640doi: 10.1021/ic951058v.
Jayaraj, K., Terner, J., Gold, A., Roberts, D. A., Austin, R. N., Mandon, D., Weiss, R., Bill, E., Müther, M., & Trautwein, A. X. (1996). Influence of Meso Substituents on Electronic States of (Oxoferryl)porphyrin pi-Cation Radicals. Inorganic chemistry, 35(6), 1632-1640. https://doi.org/10.1021/ic951058v
Jayaraj, K., et al. "Influence of Meso Substituents on Electronic States of (Oxoferryl)porphyrin pi-Cation Radicals." Inorganic chemistry vol. 35,6 (1996): 1632-1640. doi: https://doi.org/10.1021/ic951058v
Jayaraj K, Terner J, Gold A, Roberts DA, Austin RN, Mandon D, Weiss R, Bill E, Müther M, Trautwein AX. Influence of Meso Substituents on Electronic States of (Oxoferryl)porphyrin pi-Cation Radicals. Inorg Chem. 1996 Mar 13;35(6):1632-1640. doi: 10.1021/ic951058v. PMID: 11666384.
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Analytical utility of 2-halopyridinium salts-II Acidimetric determination of thiol groups.

Talanta

Bald E.
PMID: 18962663
Talanta. 1980 Mar;27(3):281-2. doi: 10.1016/0039-9140(80)80057-9.

2-Chloro-1-methylpyridinium iodide reacts rapidly and quantitatively with thiol groups in the presence of excess of triethylamine to give the 2-alkyl(aryl)thio-1-methylpyridinium iodide and an equimolar amount of hydrogen chloride which is trapped by the triethylamine. The excess of triethylamine is...

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Bald E. Analytical utility of 2-halopyridinium salts-II Acidimetric determination of thiol groups. Talanta. 1980;27(3):281-2doi: 10.1016/0039-9140(80)80057-9.
Bald, E. (1980). Analytical utility of 2-halopyridinium salts-II Acidimetric determination of thiol groups. Talanta, 27(3), 281-2. https://doi.org/10.1016/0039-9140(80)80057-9
Bald, E. "Analytical utility of 2-halopyridinium salts-II Acidimetric determination of thiol groups." Talanta vol. 27,3 (1980): 281-2. doi: https://doi.org/10.1016/0039-9140(80)80057-9
Bald E. Analytical utility of 2-halopyridinium salts-II Acidimetric determination of thiol groups. Talanta. 1980 Mar;27(3):281-2. doi: 10.1016/0039-9140(80)80057-9. PMID: 18962663.
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