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Combined theoretical and experimental study of the valence, Rydberg, and ionic states of chlorobenzene.

The Journal of chemical physics

Palmer MH, Ridley T, Vrønning Hoffmann S, Jones NC, Coreno M, de Simone M, Grazioli C, Zhang T, Biczysko M, Baiardi A, Peterson KA.
PMID: 27036443
J Chem Phys. 2016 Mar 28;144(12):124302. doi: 10.1063/1.4944078.

New photoelectron (PE) and ultra violet (UV) and vacuum UV (VUV) spectra have been obtained for chlorobenzene by synchrotron study with higher sensitivity and resolution than previous work and are subjected to detailed analysis. In addition, we report on...

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Palmer MH, Ridley T, Vrønning Hoffmann S, et al. Combined theoretical and experimental study of the valence, Rydberg, and ionic states of chlorobenzene. J Chem Phys. 2016;144(12):124302doi: 10.1063/1.4944078.
Palmer, M. H., Ridley, T., Vrønning Hoffmann, S., Jones, N. C., Coreno, M., de Simone, M., Grazioli, C., Zhang, T., Biczysko, M., Baiardi, A., & Peterson, K. A. (2016). Combined theoretical and experimental study of the valence, Rydberg, and ionic states of chlorobenzene. The Journal of chemical physics, 144(12), 124302. https://doi.org/10.1063/1.4944078
Palmer, Michael H, et al. "Combined theoretical and experimental study of the valence, Rydberg, and ionic states of chlorobenzene." The Journal of chemical physics vol. 144,12 (2016): 124302. doi: https://doi.org/10.1063/1.4944078
Palmer MH, Ridley T, Vrønning Hoffmann S, Jones NC, Coreno M, de Simone M, Grazioli C, Zhang T, Biczysko M, Baiardi A, Peterson KA. Combined theoretical and experimental study of the valence, Rydberg, and ionic states of chlorobenzene. J Chem Phys. 2016 Mar 28;144(12):124302. doi: 10.1063/1.4944078. PMID: 27036443.
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One-Pot Synthesis of Pyrrolo[3,2,1-kl]phenothiazines through Copper-Catalyzed Tandem Coupling/Double Cyclization Reaction.

The Journal of organic chemistry

Tang J, Xu B, Mao X, Yang H, Wang X, Lv X.
PMID: 26430717
J Org Chem. 2015 Nov 06;80(21):11108-14. doi: 10.1021/acs.joc.5b01745. Epub 2015 Oct 09.

A novel and efficient synthesis of pyrrolo[3,2,1-kl]phenothiazines has been developed through a Cu(I)-catalyzed tandem C-S coupling/double cyclization process. Using 2-alkynyl-6-iodoanilines and o-bromobenzenethiols as the starting materials, a wide range of pyrrolo[3,2,1-kl]phenothiazine derivatives were facilely and efficiently generated in one...

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Tang J, Xu B, Mao X, et al. One-Pot Synthesis of Pyrrolo[3,2,1-kl]phenothiazines through Copper-Catalyzed Tandem Coupling/Double Cyclization Reaction. J Org Chem. 2015;80(21):11108-14doi: 10.1021/acs.joc.5b01745.
Tang, J., Xu, B., Mao, X., Yang, H., Wang, X., & Lv, X. (2015). One-Pot Synthesis of Pyrrolo[3,2,1-kl]phenothiazines through Copper-Catalyzed Tandem Coupling/Double Cyclization Reaction. The Journal of organic chemistry, 80(21), 11108-14. https://doi.org/10.1021/acs.joc.5b01745
Tang, Jiaming, et al. "One-Pot Synthesis of Pyrrolo[3,2,1-kl]phenothiazines through Copper-Catalyzed Tandem Coupling/Double Cyclization Reaction." The Journal of organic chemistry vol. 80,21 (2015): 11108-14. doi: https://doi.org/10.1021/acs.joc.5b01745
Tang J, Xu B, Mao X, Yang H, Wang X, Lv X. One-Pot Synthesis of Pyrrolo[3,2,1-kl]phenothiazines through Copper-Catalyzed Tandem Coupling/Double Cyclization Reaction. J Org Chem. 2015 Nov 06;80(21):11108-14. doi: 10.1021/acs.joc.5b01745. Epub 2015 Oct 09. PMID: 26430717.
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Rapid electrochemical reduction of Ni(II) generates reactive monolayers for conjugated polymer brushes in one step.

Langmuir : the ACS journal of surfaces and colloids

Roy A, Gao J, Bilbrey JA, Huddleston NE, Locklin J.
PMID: 25115133
Langmuir. 2014 Sep 02;30(34):10465-70. doi: 10.1021/la502050n. Epub 2014 Aug 20.

This article reports the development of a robust, one-step electrochemical technique to generate surface-bound conjugated polymers. The electrochemical reduction of arene diazonium salts at the surface of a gold electrode is used to generate tethered bromobenzene monolayers quickly. The...

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Roy A, Gao J, Bilbrey JA, et al. Rapid electrochemical reduction of Ni(II) generates reactive monolayers for conjugated polymer brushes in one step. Langmuir. 2014;30(34):10465-70doi: 10.1021/la502050n.
Roy, A., Gao, J., Bilbrey, J. A., Huddleston, N. E., & Locklin, J. (2014). Rapid electrochemical reduction of Ni(II) generates reactive monolayers for conjugated polymer brushes in one step. Langmuir : the ACS journal of surfaces and colloids, 30(34), 10465-70. https://doi.org/10.1021/la502050n
Roy, Anandi, et al. "Rapid electrochemical reduction of Ni(II) generates reactive monolayers for conjugated polymer brushes in one step." Langmuir : the ACS journal of surfaces and colloids vol. 30,34 (2014): 10465-70. doi: https://doi.org/10.1021/la502050n
Roy A, Gao J, Bilbrey JA, Huddleston NE, Locklin J. Rapid electrochemical reduction of Ni(II) generates reactive monolayers for conjugated polymer brushes in one step. Langmuir. 2014 Sep 02;30(34):10465-70. doi: 10.1021/la502050n. Epub 2014 Aug 20. PMID: 25115133.
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Solid-phase microextraction with a graphene-composite-coated fiber coupled with GC for the determination of some halogenated aromatic hydrocarbons in water samples.

Journal of separation science

Zhang G, Li Z, Zang X, Wang C, Wang Z.
PMID: 24318069
J Sep Sci. 2014 Feb;37(4):440-6. doi: 10.1002/jssc.201301183. Epub 2014 Jan 06.

In this work, a graphene composite was coated onto etched stainless-steel wire through a sol-gel technique and it was used as a solid-phase microextraction (SPME) fiber. The prepared fiber was characterized by SEM, which revealed that the fiber had...

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Zhang G, Li Z, Zang X, et al. Solid-phase microextraction with a graphene-composite-coated fiber coupled with GC for the determination of some halogenated aromatic hydrocarbons in water samples. J Sep Sci. 2014;37(4):440-6doi: 10.1002/jssc.201301183.
Zhang, G., Li, Z., Zang, X., Wang, C., & Wang, Z. (2014). Solid-phase microextraction with a graphene-composite-coated fiber coupled with GC for the determination of some halogenated aromatic hydrocarbons in water samples. Journal of separation science, 37(4), 440-6. https://doi.org/10.1002/jssc.201301183
Zhang, Guijiang, et al. "Solid-phase microextraction with a graphene-composite-coated fiber coupled with GC for the determination of some halogenated aromatic hydrocarbons in water samples." Journal of separation science vol. 37,4 (2014): 440-6. doi: https://doi.org/10.1002/jssc.201301183
Zhang G, Li Z, Zang X, Wang C, Wang Z. Solid-phase microextraction with a graphene-composite-coated fiber coupled with GC for the determination of some halogenated aromatic hydrocarbons in water samples. J Sep Sci. 2014 Feb;37(4):440-6. doi: 10.1002/jssc.201301183. Epub 2014 Jan 06. PMID: 24318069.
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Resonance-enhanced multiphoton ionization (REMPI) spectroscopy of bromobenzene and its perdeuterated isotopologue: Assignment of the vibrations of the S(0), S(1), and D(0)(+) states of bromobenzene and the S(0) and D(0)(+) states of iodobenzene.

The Journal of chemical physics

Andrejeva A, Tuttle WD, Harris JP, Wright TG.
PMID: 26723684
J Chem Phys. 2015 Dec 28;143(24):244320. doi: 10.1063/1.4938501.

We report vibrationally resolved spectra of the S1←S0 transition of bromobenzene using resonance-enhanced multiphoton ionization spectroscopy. We study bromobenzene-h5 as well as its perdeuterated isotopologue, bromobenzene-d5. The form of the vibrational modes between the isotopologues and also between the...

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Andrejeva A, Tuttle WD, Harris JP, et al. Resonance-enhanced multiphoton ionization (REMPI) spectroscopy of bromobenzene and its perdeuterated isotopologue: Assignment of the vibrations of the S(0), S(1), and D(0)(+) states of bromobenzene and the S(0) and D(0)(+) states of iodobenzene. J Chem Phys. 2015;143(24):244320doi: 10.1063/1.4938501.
Andrejeva, A., Tuttle, W. D., Harris, J. P., & Wright, T. G. (2015). Resonance-enhanced multiphoton ionization (REMPI) spectroscopy of bromobenzene and its perdeuterated isotopologue: Assignment of the vibrations of the S(0), S(1), and D(0)(+) states of bromobenzene and the S(0) and D(0)(+) states of iodobenzene. The Journal of chemical physics, 143(24), 244320. https://doi.org/10.1063/1.4938501
Andrejeva, Anna, et al. "Resonance-enhanced multiphoton ionization (REMPI) spectroscopy of bromobenzene and its perdeuterated isotopologue: Assignment of the vibrations of the S(0), S(1), and D(0)(+) states of bromobenzene and the S(0) and D(0)(+) states of iodobenzene." The Journal of chemical physics vol. 143,24 (2015): 244320. doi: https://doi.org/10.1063/1.4938501
Andrejeva A, Tuttle WD, Harris JP, Wright TG. Resonance-enhanced multiphoton ionization (REMPI) spectroscopy of bromobenzene and its perdeuterated isotopologue: Assignment of the vibrations of the S(0), S(1), and D(0)(+) states of bromobenzene and the S(0) and D(0)(+) states of iodobenzene. J Chem Phys. 2015 Dec 28;143(24):244320. doi: 10.1063/1.4938501. PMID: 26723684.
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Aggregation and Alkylation of the Cesium Enolate of 2-p-Biphenylylcyclohexanone(1).

The Journal of organic chemistry

Streitwieser A, Wang DZ, Stratakis M.
PMID: 11674562
J Org Chem. 1999 Jun 25;64(13):4860-4864. doi: 10.1021/jo990251u.

The cesium enolate of 2-biphenylylcyclohexanone (CsBPCH), generated by deprotonation of 2-biphenylylcyclohexanone with diphenylmethylcesium, is shown to be a mixture of monomer and dimer in THF, with a dimerization constant of 1.9 x 10(3) M(-)(1). The ion pair acidity corresponds...

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Streitwieser A, Wang DZ, Stratakis M. Aggregation and Alkylation of the Cesium Enolate of 2-p-Biphenylylcyclohexanone(1). J Org Chem. 1999;64(13):4860-4864doi: 10.1021/jo990251u.
Streitwieser, A., Wang, D. Z., & Stratakis, M. (1999). Aggregation and Alkylation of the Cesium Enolate of 2-p-Biphenylylcyclohexanone(1). The Journal of organic chemistry, 64(13), 4860-4864. https://doi.org/10.1021/jo990251u
Streitwieser, Andrew, et al. "Aggregation and Alkylation of the Cesium Enolate of 2-p-Biphenylylcyclohexanone(1)." The Journal of organic chemistry vol. 64,13 (1999): 4860-4864. doi: https://doi.org/10.1021/jo990251u
Streitwieser A, Wang DZ, Stratakis M. Aggregation and Alkylation of the Cesium Enolate of 2-p-Biphenylylcyclohexanone(1). J Org Chem. 1999 Jun 25;64(13):4860-4864. doi: 10.1021/jo990251u. PMID: 11674562.
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Dimethylformamide as a carbon monoxide source in fast palladium-catalyzed aminocarbonylations of aryl bromides.

The Journal of organic chemistry

Wan Y, Alterman M, Larhed M, Hallberg A.
PMID: 12182668
J Org Chem. 2002 Aug 23;67(17):6232-5. doi: 10.1021/jo025965a.

Dimethylformamide (DMF) acts as an efficient source of carbon monoxide and dimethylamine in the palladium-catalyzed aminocarbonylation (Heck carbonylation) of p-tolyl bromide to provide the dimethylamide. Addition of amines to the reaction mixture in excess delivers the corresponding aryl amides...

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Wan Y, Alterman M, Larhed M, et al. Dimethylformamide as a carbon monoxide source in fast palladium-catalyzed aminocarbonylations of aryl bromides. J Org Chem. 2002;67(17):6232-5doi: 10.1021/jo025965a.
Wan, Y., Alterman, M., Larhed, M., & Hallberg, A. (2002). Dimethylformamide as a carbon monoxide source in fast palladium-catalyzed aminocarbonylations of aryl bromides. The Journal of organic chemistry, 67(17), 6232-5. https://doi.org/10.1021/jo025965a
Wan, Yiqian, et al. "Dimethylformamide as a carbon monoxide source in fast palladium-catalyzed aminocarbonylations of aryl bromides." The Journal of organic chemistry vol. 67,17 (2002): 6232-5. doi: https://doi.org/10.1021/jo025965a
Wan Y, Alterman M, Larhed M, Hallberg A. Dimethylformamide as a carbon monoxide source in fast palladium-catalyzed aminocarbonylations of aryl bromides. J Org Chem. 2002 Aug 23;67(17):6232-5. doi: 10.1021/jo025965a. PMID: 12182668.
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Cationic hafnium silyl complexes and their enhanced reactivity in sigma-bond metathesis processes with Si-H and C-H bonds.

Journal of the American Chemical Society

Sadow AD, Tilley TD.
PMID: 12889977
J Am Chem Soc. 2003 Aug 06;125(31):9462-75. doi: 10.1021/ja030024g.

Reaction of the mixed-ring silyl methyl complex CpCp*Hf[Si(SiMe3)3]Me (4) with B(C6F5)3 in bromobenzene-d5 yielded the zwitterionic hafnium silyl complex [CpCpHfSi(SiMe3)3][MeB(C6F5)3] (7), which is stable for at least 12 h in solution. Addition of PhSiH3 to 7 rapidly produced HSi(SiMe3)3,...

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Sadow AD, Tilley TD. Cationic hafnium silyl complexes and their enhanced reactivity in sigma-bond metathesis processes with Si-H and C-H bonds. J Am Chem Soc. 2003;125(31):9462-75doi: 10.1021/ja030024g.
Sadow, A. D., & Tilley, T. D. (2003). Cationic hafnium silyl complexes and their enhanced reactivity in sigma-bond metathesis processes with Si-H and C-H bonds. Journal of the American Chemical Society, 125(31), 9462-75. https://doi.org/10.1021/ja030024g
Sadow, Aaron D, and Tilley, T Don. "Cationic hafnium silyl complexes and their enhanced reactivity in sigma-bond metathesis processes with Si-H and C-H bonds." Journal of the American Chemical Society vol. 125,31 (2003): 9462-75. doi: https://doi.org/10.1021/ja030024g
Sadow AD, Tilley TD. Cationic hafnium silyl complexes and their enhanced reactivity in sigma-bond metathesis processes with Si-H and C-H bonds. J Am Chem Soc. 2003 Aug 06;125(31):9462-75. doi: 10.1021/ja030024g. PMID: 12889977.
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Specific rate constants k(E) of the dissociation of the halobenzene ions: analysis by statistical unimolecular rate theories.

The journal of physical chemistry. A

Stevens W, Sztáray B, Shuman N, Baer T, Troe J.
PMID: 19099449
J Phys Chem A. 2009 Jan 22;113(3):573-82. doi: 10.1021/jp807930k.

Specific rate constants k(E) of the dissociation of the halobenzene ions C6H5X+ --> C6H5+ + X* (X* = Cl, Br, and I) were measured over a range of 10(3)-10(7) s-1 by threshold photoelectron-photoion coincidence (TPEPICO) spectroscopy. The experimental data...

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Stevens W, Sztáray B, Shuman N, et al. Specific rate constants k(E) of the dissociation of the halobenzene ions: analysis by statistical unimolecular rate theories. J Phys Chem A. 2009;113(3):573-82doi: 10.1021/jp807930k.
Stevens, W., Sztáray, B., Shuman, N., Baer, T., & Troe, J. (2009). Specific rate constants k(E) of the dissociation of the halobenzene ions: analysis by statistical unimolecular rate theories. The journal of physical chemistry. A, 113(3), 573-82. https://doi.org/10.1021/jp807930k
Stevens, William, et al. "Specific rate constants k(E) of the dissociation of the halobenzene ions: analysis by statistical unimolecular rate theories." The journal of physical chemistry. A vol. 113,3 (2009): 573-82. doi: https://doi.org/10.1021/jp807930k
Stevens W, Sztáray B, Shuman N, Baer T, Troe J. Specific rate constants k(E) of the dissociation of the halobenzene ions: analysis by statistical unimolecular rate theories. J Phys Chem A. 2009 Jan 22;113(3):573-82. doi: 10.1021/jp807930k. PMID: 19099449.
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Photodissociation of bromobenzene, dibromobenzene, and 1,3,5-tribromobenzene.

The Journal of chemical physics

Liu YJ, Persson P, Karlsson HO, Lunell S, Kadi M, Karlsson D, Davidsson J.
PMID: 15267540
J Chem Phys. 2004 Apr 08;120(14):6502-9. doi: 10.1063/1.1667460.

Quantum chemical calculations have been performed on the ground state and several low-lying excited states of bromobenzene, ortho-, meta-, and para-dibromobenzene, and 1,3,5-tribromobenzene using high-level ab initio and hybrid density-functional methods. Experimental observations of ultrafast predissociation in these molecules...

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Liu YJ, Persson P, Karlsson HO, et al. Photodissociation of bromobenzene, dibromobenzene, and 1,3,5-tribromobenzene. J Chem Phys. 2004;120(14):6502-9doi: 10.1063/1.1667460.
Liu, Y. J., Persson, P., Karlsson, H. O., Lunell, S., Kadi, M., Karlsson, D., & Davidsson, J. (2004). Photodissociation of bromobenzene, dibromobenzene, and 1,3,5-tribromobenzene. The Journal of chemical physics, 120(14), 6502-9. https://doi.org/10.1063/1.1667460
Liu, Ya-Jun, et al. "Photodissociation of bromobenzene, dibromobenzene, and 1,3,5-tribromobenzene." The Journal of chemical physics vol. 120,14 (2004): 6502-9. doi: https://doi.org/10.1063/1.1667460
Liu YJ, Persson P, Karlsson HO, Lunell S, Kadi M, Karlsson D, Davidsson J. Photodissociation of bromobenzene, dibromobenzene, and 1,3,5-tribromobenzene. J Chem Phys. 2004 Apr 08;120(14):6502-9. doi: 10.1063/1.1667460. PMID: 15267540.
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Synthesis and characterisation of benzyl phosphino-thioether and -thiolato Pd(II) complexes and their applications in Suzuki coupling reactions.

Dalton transactions (Cambridge, England : 2003)

Dervisi A, Koursarou D, Ooi LL, Horton PN, Hursthouse MB.
PMID: 17146536
Dalton Trans. 2006 Dec 28;(48):5717-24. doi: 10.1039/b609607g. Epub 2006 Oct 18.

The synthesis of the benzyl phosphinothioether derivatives Ph(2)PCH(2)CH(Et)SR and their corresponding palladium complexes are reported, where R = CH(2)Ph, R = CH(2)-3,5-Me-C(6)H(3) and R = 1-CH(2)C(10)H(7)(5). Crystallographic data obtained for the complexes Pd(3)Cl(2) and Pd(4)Cl(2) show intra- and inter-molecular...

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Dervisi A, Koursarou D, Ooi LL, et al. Synthesis and characterisation of benzyl phosphino-thioether and -thiolato Pd(II) complexes and their applications in Suzuki coupling reactions. Dalton Trans. 2006;(48):5717-24doi: 10.1039/b609607g.
Dervisi, A., Koursarou, D., Ooi, L. L., Horton, P. N., & Hursthouse, M. B. (2006). Synthesis and characterisation of benzyl phosphino-thioether and -thiolato Pd(II) complexes and their applications in Suzuki coupling reactions. Dalton transactions (Cambridge, England : 2003), (48), 5717-24. https://doi.org/10.1039/b609607g
Dervisi, Athanasia, et al. "Synthesis and characterisation of benzyl phosphino-thioether and -thiolato Pd(II) complexes and their applications in Suzuki coupling reactions." Dalton transactions (Cambridge, England : 2003) vol. ,48 (2006): 5717-24. doi: https://doi.org/10.1039/b609607g
Dervisi A, Koursarou D, Ooi LL, Horton PN, Hursthouse MB. Synthesis and characterisation of benzyl phosphino-thioether and -thiolato Pd(II) complexes and their applications in Suzuki coupling reactions. Dalton Trans. 2006 Dec 28;(48):5717-24. doi: 10.1039/b609607g. Epub 2006 Oct 18. PMID: 17146536.
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Relative rates of bromine-magnesium exchange reactions in substituted bromobenzene derivatives.

Angewandte Chemie (International ed. in English)

Shi L, Chu Y, Knochel P, Mayr H.
PMID: 18038441
Angew Chem Int Ed Engl. 2008;47(1):202-4. doi: 10.1002/anie.200704100.

No abstract available.

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Shi L, Chu Y, Knochel P, et al. Relative rates of bromine-magnesium exchange reactions in substituted bromobenzene derivatives. Angew Chem Int Ed Engl. 2008;47(1):202-4doi: 10.1002/anie.200704100.
Shi, L., Chu, Y., Knochel, P., & Mayr, H. (2008). Relative rates of bromine-magnesium exchange reactions in substituted bromobenzene derivatives. Angewandte Chemie (International ed. in English), 47(1), 202-4. https://doi.org/10.1002/anie.200704100
Shi, Lei, et al. "Relative rates of bromine-magnesium exchange reactions in substituted bromobenzene derivatives." Angewandte Chemie (International ed. in English) vol. 47,1 (2008): 202-4. doi: https://doi.org/10.1002/anie.200704100
Shi L, Chu Y, Knochel P, Mayr H. Relative rates of bromine-magnesium exchange reactions in substituted bromobenzene derivatives. Angew Chem Int Ed Engl. 2008;47(1):202-4. doi: 10.1002/anie.200704100. PMID: 18038441.
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Showing 1 to 12 of 217 entries