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Showing 1 to 12 of 18 entries
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Beryllium Chelation by Dicarboxylic Acids in Aqueous Solution.

Inorganic chemistry

Schmidt M, Bauer A, Schmidbaur H.
PMID: 11669821
Inorg Chem. 1997 May 07;36(10):2040-2043. doi: 10.1021/ic961410k.

Maleic and phthalic acids are found to react with Be(OH)(2), generated in situ from BeSO(4)(aq) and Ba(OH)(2)(aq), in aqueous solution at pH 3.0 or 4.4, respectively (25 degrees C), to give solutions containing the complexes (H(2)O)(2)Be[(OOCCH)(2)] (1) and (H(2)O)(2)Be[(OOC)(2)C(6)H(4)]...

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Schmidt M, Bauer A, Schmidbaur H. Beryllium Chelation by Dicarboxylic Acids in Aqueous Solution. Inorg Chem. 1997;36(10):2040-2043doi: 10.1021/ic961410k.
Schmidt, M., Bauer, A., & Schmidbaur, H. (1997). Beryllium Chelation by Dicarboxylic Acids in Aqueous Solution. Inorganic chemistry, 36(10), 2040-2043. https://doi.org/10.1021/ic961410k
Schmidt, Michael, et al. "Beryllium Chelation by Dicarboxylic Acids in Aqueous Solution." Inorganic chemistry vol. 36,10 (1997): 2040-2043. doi: https://doi.org/10.1021/ic961410k
Schmidt M, Bauer A, Schmidbaur H. Beryllium Chelation by Dicarboxylic Acids in Aqueous Solution. Inorg Chem. 1997 May 07;36(10):2040-2043. doi: 10.1021/ic961410k. PMID: 11669821.
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Heterogeneous chemistry of organic acids on soot surfaces.

The journal of physical chemistry. A

Levitt NP, Zhang R, Xue H, Chen J.
PMID: 17497835
J Phys Chem A. 2007 Jun 07;111(22):4804-14. doi: 10.1021/jp0700480. Epub 2007 May 12.

We have investigated the heterogeneous interaction between a number of carboxylic acids and soot generated from different fuel sources and formation mechanisms. A low-pressure fast flow reactor in conjunction with ion drift-chemical ionization mass spectrometry detection was employed to...

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Levitt NP, Zhang R, Xue H, et al. Heterogeneous chemistry of organic acids on soot surfaces. J Phys Chem A. 2007;111(22):4804-14doi: 10.1021/jp0700480.
Levitt, N. P., Zhang, R., Xue, H., & Chen, J. (2007). Heterogeneous chemistry of organic acids on soot surfaces. The journal of physical chemistry. A, 111(22), 4804-14. https://doi.org/10.1021/jp0700480
Levitt, Nicholas P, et al. "Heterogeneous chemistry of organic acids on soot surfaces." The journal of physical chemistry. A vol. 111,22 (2007): 4804-14. doi: https://doi.org/10.1021/jp0700480
Levitt NP, Zhang R, Xue H, Chen J. Heterogeneous chemistry of organic acids on soot surfaces. J Phys Chem A. 2007 Jun 07;111(22):4804-14. doi: 10.1021/jp0700480. Epub 2007 May 12. PMID: 17497835.
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Degradation of phthalic acids by denitrifying, mixed cultures of bacteria.

Applied and environmental microbiology

Aftring RP, Chalker BE, Taylor BF.
PMID: 16345769
Appl Environ Microbiol. 1981 May;41(5):1177-83. doi: 10.1128/aem.41.5.1177-1183.1981.

Mixed cultures of bacteria, enriched from aquatic sediments, grew anaerobically on all three isomers of phthalic acid. Each culture grew anaerobically on only one isomer and also grew aerobically on the same isomer. Pure cultures were isolated from the...

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Aftring RP, Chalker BE, Taylor BF. Degradation of phthalic acids by denitrifying, mixed cultures of bacteria. Appl Environ Microbiol. 1981;41(5):1177-83doi: 10.1128/aem.41.5.1177-1183.1981.
Aftring, R. P., Chalker, B. E., & Taylor, B. F. (1981). Degradation of phthalic acids by denitrifying, mixed cultures of bacteria. Applied and environmental microbiology, 41(5), 1177-83. https://doi.org/10.1128/aem.41.5.1177-1183.1981
Aftring, R P, et al. "Degradation of phthalic acids by denitrifying, mixed cultures of bacteria." Applied and environmental microbiology vol. 41,5 (1981): 1177-83. doi: https://doi.org/10.1128/aem.41.5.1177-1183.1981
Aftring RP, Chalker BE, Taylor BF. Degradation of phthalic acids by denitrifying, mixed cultures of bacteria. Appl Environ Microbiol. 1981 May;41(5):1177-83. doi: 10.1128/aem.41.5.1177-1183.1981. PMID: 16345769; PMCID: PMC243886.
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Synthesis of Multisubstituted 1-Naphthoic Acids via Ru-Catalyzed C-H Activation and Double-Alkyne Annulation under Air.

The Journal of organic chemistry

Chen H, Ouyang L, Liu J, Shi WJ, Chen G, Zheng L.
PMID: 31190536
J Org Chem. 2019 Oct 18;84(20):12755-12763. doi: 10.1021/acs.joc.9b00926. Epub 2019 Jun 25.

An efficient [2 + 2 + 2] benzannulation of phthalic acids/anhydrides with two alkynes was developed for synthesis of multisubstituted 1-naphthoic acids via Ru-catalyzed C-H activation. The reaction preceded well using atmospheric oxygen as the sole oxidant with high...

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Chen H, Ouyang L, Liu J, et al. Synthesis of Multisubstituted 1-Naphthoic Acids via Ru-Catalyzed C-H Activation and Double-Alkyne Annulation under Air. J Org Chem. 2019;84(20):12755-12763doi: 10.1021/acs.joc.9b00926.
Chen, H., Ouyang, L., Liu, J., Shi, W. J., Chen, G., & Zheng, L. (2019). Synthesis of Multisubstituted 1-Naphthoic Acids via Ru-Catalyzed C-H Activation and Double-Alkyne Annulation under Air. The Journal of organic chemistry, 84(20), 12755-12763. https://doi.org/10.1021/acs.joc.9b00926
Chen, Honghao, et al. "Synthesis of Multisubstituted 1-Naphthoic Acids via Ru-Catalyzed C-H Activation and Double-Alkyne Annulation under Air." The Journal of organic chemistry vol. 84,20 (2019): 12755-12763. doi: https://doi.org/10.1021/acs.joc.9b00926
Chen H, Ouyang L, Liu J, Shi WJ, Chen G, Zheng L. Synthesis of Multisubstituted 1-Naphthoic Acids via Ru-Catalyzed C-H Activation and Double-Alkyne Annulation under Air. J Org Chem. 2019 Oct 18;84(20):12755-12763. doi: 10.1021/acs.joc.9b00926. Epub 2019 Jun 25. PMID: 31190536.
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Selective Host-Guest Co-crystallization of Pyridine-Functionalized Tetraphenylethylenes with Phthalic Acids and Multicolor Emission of the Co-crystals.

Chemistry (Weinheim an der Bergstrasse, Germany)

Feng HT, Xiong JB, Luo J, Feng WF, Yang D, Zheng YS.
PMID: 27739616
Chemistry. 2017 Jan 12;23(3):644-651. doi: 10.1002/chem.201604133. Epub 2016 Dec 05.

Tetraphenylethylene (TPE) and its derivatives are the most typical and most widely studied organic compounds showing aggregation-induced emission (AIE). Due to their propeller-like structures, V-like clefts exist between the aryl rings, which make them promising host compounds. However, such...

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Feng HT, Xiong JB, Luo J, et al. Selective Host-Guest Co-crystallization of Pyridine-Functionalized Tetraphenylethylenes with Phthalic Acids and Multicolor Emission of the Co-crystals. Chemistry. 2016;23(3):644-651doi: 10.1002/chem.201604133.
Feng, H. T., Xiong, J. B., Luo, J., Feng, W. F., Yang, D., & Zheng, Y. S. (2017). Selective Host-Guest Co-crystallization of Pyridine-Functionalized Tetraphenylethylenes with Phthalic Acids and Multicolor Emission of the Co-crystals. Chemistry (Weinheim an der Bergstrasse, Germany), 23(3), 644-651. https://doi.org/10.1002/chem.201604133
Feng, Hai-Tao, et al. "Selective Host-Guest Co-crystallization of Pyridine-Functionalized Tetraphenylethylenes with Phthalic Acids and Multicolor Emission of the Co-crystals." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 23,3 (2017): 644-651. doi: https://doi.org/10.1002/chem.201604133
Feng HT, Xiong JB, Luo J, Feng WF, Yang D, Zheng YS. Selective Host-Guest Co-crystallization of Pyridine-Functionalized Tetraphenylethylenes with Phthalic Acids and Multicolor Emission of the Co-crystals. Chemistry. 2017 Jan 12;23(3):644-651. doi: 10.1002/chem.201604133. Epub 2016 Dec 05. PMID: 27739616.
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Separation of o-, m- and p-phthalic acids by high-field asymmetric waveform ion mobility spectrometry (FAIMS) using mixed carrier gases.

Journal of mass spectrometry : JMS

Barnett DA, Purves RW, Ells B, Guevremont R.
PMID: 10972997
J Mass Spectrom. 2000 Aug;35(8):976-80. doi: 10.1002/1096-9888(200008)35:8<976::AID-JMS25>3.0.CO;2-Q.

Baseline separation of the three isomers of phthalic acid was achieved in a mixed gas system containing a 95 : 5 mixture of N(2) and CO(2), even though the acids could not be distinguished by high-field asymmetric waveform ion...

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Barnett DA, Purves RW, Ells B, et al. Separation of o-, m- and p-phthalic acids by high-field asymmetric waveform ion mobility spectrometry (FAIMS) using mixed carrier gases. J Mass Spectrom. 2000;35(8):976-80doi: 10.1002/1096-9888(200008)35:8<976::AID-JMS25>3.0.CO;2-Q.
Barnett, D. A., Purves, R. W., Ells, B., & Guevremont, R. (2000). Separation of o-, m- and p-phthalic acids by high-field asymmetric waveform ion mobility spectrometry (FAIMS) using mixed carrier gases. Journal of mass spectrometry : JMS, 35(8), 976-80. https://doi.org/10.1002/1096-9888(200008)35:8<976::AID-JMS25>3.0.CO;2-Q
Barnett, et al. "Separation of o-, m- and p-phthalic acids by high-field asymmetric waveform ion mobility spectrometry (FAIMS) using mixed carrier gases." Journal of mass spectrometry : JMS vol. 35,8 (2000): 976-80. doi: https://doi.org/10.1002/1096-9888(200008)35:8<976::AID-JMS25>3.0.CO;2-Q
Barnett DA, Purves RW, Ells B, Guevremont R. Separation of o-, m- and p-phthalic acids by high-field asymmetric waveform ion mobility spectrometry (FAIMS) using mixed carrier gases. J Mass Spectrom. 2000 Aug;35(8):976-80. doi: 10.1002/1096-9888(200008)35:8<976::AID-JMS25>3.0.CO;2-Q. PMID: 10972997.
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Bacterial Decarboxylation of o-Phthalic Acids.

Applied and environmental microbiology

Taylor BF, Ribbons DW.
PMID: 16346440
Appl Environ Microbiol. 1983 Dec;46(6):1276-81. doi: 10.1128/aem.46.6.1276-1281.1983.

The decarboxylation of phthalic acids was studied with Bacillus sp. strain FO, a marine mixed culture ON-7, and Pseudomonas testosteroni. The mixed culture ON-7, when grown anaerobically on phthalate but incubated aerobically with chloramphenicol, quantitatively converted phthalic acid to...

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Taylor BF, Ribbons DW. Bacterial Decarboxylation of o-Phthalic Acids. Appl Environ Microbiol. 1983;46(6):1276-81doi: 10.1128/aem.46.6.1276-1281.1983.
Taylor, B. F., & Ribbons, D. W. (1983). Bacterial Decarboxylation of o-Phthalic Acids. Applied and environmental microbiology, 46(6), 1276-81. https://doi.org/10.1128/aem.46.6.1276-1281.1983
Taylor, B F, and Ribbons, D W. "Bacterial Decarboxylation of o-Phthalic Acids." Applied and environmental microbiology vol. 46,6 (1983): 1276-81. doi: https://doi.org/10.1128/aem.46.6.1276-1281.1983
Taylor BF, Ribbons DW. Bacterial Decarboxylation of o-Phthalic Acids. Appl Environ Microbiol. 1983 Dec;46(6):1276-81. doi: 10.1128/aem.46.6.1276-1281.1983. PMID: 16346440; PMCID: PMC239563.
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Organic Acid specificity for Acid-induced ATP synthesis by isolated chloroplasts.

Plant physiology

Uribe EG, Jagendorf AT.
PMID: 16656559
Plant Physiol. 1967 May;42(5):706-11. doi: 10.1104/pp.42.5.706.

A study has been made of the structural requirements for organic acids that increase the yield of ATP formed by spinach chloroplasts in the dark due to an acid-base transition. Dicarboxylic acids of 4 and 5 carbon atoms with...

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Uribe EG, Jagendorf AT. Organic Acid specificity for Acid-induced ATP synthesis by isolated chloroplasts. Plant Physiol. 1967;42(5):706-11doi: 10.1104/pp.42.5.706.
Uribe, E. G., & Jagendorf, A. T. (1967). Organic Acid specificity for Acid-induced ATP synthesis by isolated chloroplasts. Plant physiology, 42(5), 706-11. https://doi.org/10.1104/pp.42.5.706
Uribe, E G, and Jagendorf, A T. "Organic Acid specificity for Acid-induced ATP synthesis by isolated chloroplasts." Plant physiology vol. 42,5 (1967): 706-11. doi: https://doi.org/10.1104/pp.42.5.706
Uribe EG, Jagendorf AT. Organic Acid specificity for Acid-induced ATP synthesis by isolated chloroplasts. Plant Physiol. 1967 May;42(5):706-11. doi: 10.1104/pp.42.5.706. PMID: 16656559; PMCID: PMC1086606.
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Strontium-coordination polymers based on tetrafluorophthalic and phthalic acids: mechanochemical synthesis, ab initio structures determination, and spectroscopic characterization.

Dalton transactions (Cambridge, England : 2003)

Al-Terkawi AA, Scholz G, Emmerling F, Kemnitz E.
PMID: 28906520
Dalton Trans. 2017 Sep 26;46(37):12574-12587. doi: 10.1039/c7dt02564e.

Two strontium-based dicarboxylate systems [Sr(oBDC-F

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Al-Terkawi AA, Scholz G, Emmerling F, et al. Strontium-coordination polymers based on tetrafluorophthalic and phthalic acids: mechanochemical synthesis, ab initio structures determination, and spectroscopic characterization. Dalton Trans. 2017;46(37):12574-12587doi: 10.1039/c7dt02564e.
Al-Terkawi, A. A., Scholz, G., Emmerling, F., & Kemnitz, E. (2017). Strontium-coordination polymers based on tetrafluorophthalic and phthalic acids: mechanochemical synthesis, ab initio structures determination, and spectroscopic characterization. Dalton transactions (Cambridge, England : 2003), 46(37), 12574-12587. https://doi.org/10.1039/c7dt02564e
Al-Terkawi, Abdal-Azim, et al. "Strontium-coordination polymers based on tetrafluorophthalic and phthalic acids: mechanochemical synthesis, ab initio structures determination, and spectroscopic characterization." Dalton transactions (Cambridge, England : 2003) vol. 46,37 (2017): 12574-12587. doi: https://doi.org/10.1039/c7dt02564e
Al-Terkawi AA, Scholz G, Emmerling F, Kemnitz E. Strontium-coordination polymers based on tetrafluorophthalic and phthalic acids: mechanochemical synthesis, ab initio structures determination, and spectroscopic characterization. Dalton Trans. 2017 Sep 26;46(37):12574-12587. doi: 10.1039/c7dt02564e. PMID: 28906520.
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Solvent effects on the dissociation reactions of tartaric, maleic and phthalic acids; comparative study and analysis of thermodynamic functions.

Talanta

Zaghloul AA, El-Naggar GA, El-Shazly SA, Amira MF.
PMID: 18966994
Talanta. 1997 Dec 12;45(1):189-201. doi: 10.1016/s0039-9140(97)00119-7.

The first and second dissociation constants of tartaric, maleic and phthalic acids have been determined using EMF method in water-ethanol mixed solvents, over a wide range of solvent composition (0-60 wt% ethanol) at six different temperatures (ranging from 30...

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Zaghloul AA, El-Naggar GA, El-Shazly SA, et al. Solvent effects on the dissociation reactions of tartaric, maleic and phthalic acids; comparative study and analysis of thermodynamic functions. Talanta. 1997;45(1):189-201doi: 10.1016/s0039-9140(97)00119-7.
Zaghloul, A. A., El-Naggar, G. A., El-Shazly, S. A., & Amira, M. F. (1997). Solvent effects on the dissociation reactions of tartaric, maleic and phthalic acids; comparative study and analysis of thermodynamic functions. Talanta, 45(1), 189-201. https://doi.org/10.1016/s0039-9140(97)00119-7
Zaghloul, A A, et al. "Solvent effects on the dissociation reactions of tartaric, maleic and phthalic acids; comparative study and analysis of thermodynamic functions." Talanta vol. 45,1 (1997): 189-201. doi: https://doi.org/10.1016/s0039-9140(97)00119-7
Zaghloul AA, El-Naggar GA, El-Shazly SA, Amira MF. Solvent effects on the dissociation reactions of tartaric, maleic and phthalic acids; comparative study and analysis of thermodynamic functions. Talanta. 1997 Dec 12;45(1):189-201. doi: 10.1016/s0039-9140(97)00119-7. PMID: 18966994.
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Binary and ternary complexes of inosine.

Talanta

Khalil MM, Radalla AM.
PMID: 18967127
Talanta. 1998 May;46(1):53-61. doi: 10.1016/s0039-9140(97)00255-5.

Formation of binary and ternary complexes of Cu(II) and Ni(II) metal ions with inosine as a primary ligand and some biologically important aliphatic and aromatic carboxylic acids (succinic, oxalic, malic, maleic, malonic, tartaric, 5-sulfosalicylic, salicylic and phthalic acids) as...

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Khalil MM, Radalla AM. Binary and ternary complexes of inosine. Talanta. 1998;46(1):53-61doi: 10.1016/s0039-9140(97)00255-5.
Khalil, M. M., & Radalla, A. M. (1998). Binary and ternary complexes of inosine. Talanta, 46(1), 53-61. https://doi.org/10.1016/s0039-9140(97)00255-5
Khalil, M M, and Radalla, A M. "Binary and ternary complexes of inosine." Talanta vol. 46,1 (1998): 53-61. doi: https://doi.org/10.1016/s0039-9140(97)00255-5
Khalil MM, Radalla AM. Binary and ternary complexes of inosine. Talanta. 1998 May;46(1):53-61. doi: 10.1016/s0039-9140(97)00255-5. PMID: 18967127.
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Methacrylate-based diol monolithic stationary phase for the separation of polar and non-polar compounds in capillary liquid chromatography.

Analytical sciences : the international journal of the Japan Society for Analytical Chemistry

Linda R, Lim LW, Takeuchi T.
PMID: 23749129
Anal Sci. 2013;29(6):631-5. doi: 10.2116/analsci.29.631.

A monolithic capillary column prepared with glycidyl methacrylate (GMA) and poly(ethylene glycol) dimethacrylate (PEGDMA) was investigated and used in capillary liquid chromatography. The polymer monolith was synthesized in the presence of methanol and decanol as the biporogenic solvents by...

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Linda R, Lim LW, Takeuchi T. Methacrylate-based diol monolithic stationary phase for the separation of polar and non-polar compounds in capillary liquid chromatography. Anal Sci. 2013;29(6):631-5doi: 10.2116/analsci.29.631.
Linda, R., Lim, L. W., & Takeuchi, T. (2013). Methacrylate-based diol monolithic stationary phase for the separation of polar and non-polar compounds in capillary liquid chromatography. Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 29(6), 631-5. https://doi.org/10.2116/analsci.29.631
Linda, Roza, et al. "Methacrylate-based diol monolithic stationary phase for the separation of polar and non-polar compounds in capillary liquid chromatography." Analytical sciences : the international journal of the Japan Society for Analytical Chemistry vol. 29,6 (2013): 631-5. doi: https://doi.org/10.2116/analsci.29.631
Linda R, Lim LW, Takeuchi T. Methacrylate-based diol monolithic stationary phase for the separation of polar and non-polar compounds in capillary liquid chromatography. Anal Sci. 2013;29(6):631-5. doi: 10.2116/analsci.29.631. PMID: 23749129.
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Showing 1 to 12 of 18 entries