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Intramolecular [4 + 2] cycloadditions of 1,3-enynes or arylalkynes with alkenes with highly reactive cationic phosphine Au(I) complexes.

Journal of the American Chemical Society

Nieto-Oberhuber C, López S, Echavarren AM.
PMID: 15853316
J Am Chem Soc. 2005 May 04;127(17):6178-9. doi: 10.1021/ja042257t.

New Au(I) complexes with bulky, biphenyl phosphines are the most reactive catalysts for the cyclizations of enynes. 1,6-Enynes with an aryl ring at the alkyne give 2,3,9,9a-tetrahydro-1H-cyclopenta[b]naphthalenes by a 5-exo-dig cyclization followed by a Nazarov-type ring expansion. 1,8-Dien-3-ynes also...

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Nieto-Oberhuber C, López S, Echavarren AM. Intramolecular [4 + 2] cycloadditions of 1,3-enynes or arylalkynes with alkenes with highly reactive cationic phosphine Au(I) complexes. J Am Chem Soc. 2005;127(17):6178-9doi: 10.1021/ja042257t.
Nieto-Oberhuber, C., López, S., & Echavarren, A. M. (2005). Intramolecular [4 + 2] cycloadditions of 1,3-enynes or arylalkynes with alkenes with highly reactive cationic phosphine Au(I) complexes. Journal of the American Chemical Society, 127(17), 6178-9. https://doi.org/10.1021/ja042257t
Nieto-Oberhuber, Cristina, et al. "Intramolecular [4 + 2] cycloadditions of 1,3-enynes or arylalkynes with alkenes with highly reactive cationic phosphine Au(I) complexes." Journal of the American Chemical Society vol. 127,17 (2005): 6178-9. doi: https://doi.org/10.1021/ja042257t
Nieto-Oberhuber C, López S, Echavarren AM. Intramolecular [4 + 2] cycloadditions of 1,3-enynes or arylalkynes with alkenes with highly reactive cationic phosphine Au(I) complexes. J Am Chem Soc. 2005 May 04;127(17):6178-9. doi: 10.1021/ja042257t. PMID: 15853316.
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Amphiphilic telechelic poly(N-isopropylacrylamide) in water: from micelles to gels.

The European physical journal. E, Soft matter

Kujawa P, Watanabe H, Tanaka F, Winnik FM.
PMID: 15880290
Eur Phys J E Soft Matter. 2005 Jun;17(2):129-37. doi: 10.1140/epje/i2004-10134-9. Epub 2005 May 06.

We report the first study of aqueous solutions (0.025 gL(-1) to 46 gL(-1)) of a telechelic poly(N-isopropylacrylamide) with octadecyl termini (C(18)-PNIPAM-C(18), M(w): 37000, 320 NIPAM units, M(w)/ M(n)=1.07) obtained by reversible addition-fragmentation chain transfer (RAFT) free radical polymerization of...

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Kujawa P, Watanabe H, Tanaka F, et al. Amphiphilic telechelic poly(N-isopropylacrylamide) in water: from micelles to gels. Eur Phys J E Soft Matter. 2005;17(2):129-37doi: 10.1140/epje/i2004-10134-9.
Kujawa, P., Watanabe, H., Tanaka, F., & Winnik, F. M. (2005). Amphiphilic telechelic poly(N-isopropylacrylamide) in water: from micelles to gels. The European physical journal. E, Soft matter, 17(2), 129-37. https://doi.org/10.1140/epje/i2004-10134-9
Kujawa, P, et al. "Amphiphilic telechelic poly(N-isopropylacrylamide) in water: from micelles to gels." The European physical journal. E, Soft matter vol. 17,2 (2005): 129-37. doi: https://doi.org/10.1140/epje/i2004-10134-9
Kujawa P, Watanabe H, Tanaka F, Winnik FM. Amphiphilic telechelic poly(N-isopropylacrylamide) in water: from micelles to gels. Eur Phys J E Soft Matter. 2005 Jun;17(2):129-37. doi: 10.1140/epje/i2004-10134-9. Epub 2005 May 06. PMID: 15880290.
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Influence of anionic sulfonate-containing co-ligands on the solid structures of silver complexes supported by 4,4'-bipyridine bridges.

Dalton transactions (Cambridge, England : 2003)

Wu H, Dong XW, Liu HY, Ma JF, Li SL, Yang J, Liu YY, Su ZM.
PMID: 18827940
Dalton Trans. 2008 Oct 21;(39):5331-41. doi: 10.1039/b806195e. Epub 2008 Aug 18.

In this paper, ten new silver compounds, namely [Ag(bipy)](L1).H2O (1), [Ag(bipy)](L2).2H2O (2), [Ag2(bipy)2(H2O)2](L3).H2O (3), [Ag(L4)(bipy)].H2O (4), [Ag(L5)(bipy)] (5), [Ag(L6)(bipy)].0.5CH3CN (6), [Ag3(L7)2(bipy)2].2(H2O) (7), [Ag2(L8)(bipy)1.5(H2O)].H2O (8), [Ag2(L9)(bipy)2(H2O)2] (9) and [Ag3(L10)(bipy)2][(bipy)(H2O)2].(H2O)3.5 (10) (where bipy = 4,4'-bipyridine, L1 = 6-amino-1-naphthalenesulfonate anion, L2 =...

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Wu H, Dong XW, Liu HY, et al. Influence of anionic sulfonate-containing co-ligands on the solid structures of silver complexes supported by 4,4'-bipyridine bridges. Dalton Trans. 2008;(39):5331-41doi: 10.1039/b806195e.
Wu, H., Dong, X. W., Liu, H. Y., Ma, J. F., Li, S. L., Yang, J., Liu, Y. Y., & Su, Z. M. (2008). Influence of anionic sulfonate-containing co-ligands on the solid structures of silver complexes supported by 4,4'-bipyridine bridges. Dalton transactions (Cambridge, England : 2003), (39), 5331-41. https://doi.org/10.1039/b806195e
Wu, Hua, et al. "Influence of anionic sulfonate-containing co-ligands on the solid structures of silver complexes supported by 4,4'-bipyridine bridges." Dalton transactions (Cambridge, England : 2003) vol. ,39 (2008): 5331-41. doi: https://doi.org/10.1039/b806195e
Wu H, Dong XW, Liu HY, Ma JF, Li SL, Yang J, Liu YY, Su ZM. Influence of anionic sulfonate-containing co-ligands on the solid structures of silver complexes supported by 4,4'-bipyridine bridges. Dalton Trans. 2008 Oct 21;(39):5331-41. doi: 10.1039/b806195e. Epub 2008 Aug 18. PMID: 18827940.
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Aromatic compounds in molecular phase of Baltic amber-synchronous luminescence analysis.

Talanta

Matuszewska A, Czaja M.
PMID: 18968585
Talanta. 2002 Apr 08;56(6):1049-59. doi: 10.1016/s0039-9140(01)00610-5.

Synchronous luminescence analysis was performed in order to identify aromatic compounds in solvent extracts of Baltic amber. The investigated extracts were obtained, for comparisons, as products of extraction by various techniques and solvents. Methylene chloride and ethanol were applied...

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Matuszewska A, Czaja M. Aromatic compounds in molecular phase of Baltic amber-synchronous luminescence analysis. Talanta. 2002;56(6):1049-59doi: 10.1016/s0039-9140(01)00610-5.
Matuszewska, A., & Czaja, M. (2002). Aromatic compounds in molecular phase of Baltic amber-synchronous luminescence analysis. Talanta, 56(6), 1049-59. https://doi.org/10.1016/s0039-9140(01)00610-5
Matuszewska, Aniela, and Czaja, Maria. "Aromatic compounds in molecular phase of Baltic amber-synchronous luminescence analysis." Talanta vol. 56,6 (2002): 1049-59. doi: https://doi.org/10.1016/s0039-9140(01)00610-5
Matuszewska A, Czaja M. Aromatic compounds in molecular phase of Baltic amber-synchronous luminescence analysis. Talanta. 2002 Apr 08;56(6):1049-59. doi: 10.1016/s0039-9140(01)00610-5. PMID: 18968585.
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Chemical fingerprinting of adhesive tapes by GCMS detection of petroleum hydrocarbon products.

Journal of forensic sciences

Aziz N, Greenwood PF, Grice K, John Watling R, van Bronswijk W.
PMID: 18631281
J Forensic Sci. 2008 Sep;53(5):1130-7. doi: 10.1111/j.1556-4029.2008.00798.x. Epub 2008 Jul 08.

Pressure-sensitive adhesive tapes often represent key evidence of crimes such as assault, rape or homicide; thus, the development of analytical techniques able to contribute to a detailed characterization of these materials is of forensic importance. The gas chromatography-mass spectrometry...

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Aziz N, Greenwood PF, Grice K, et al. Chemical fingerprinting of adhesive tapes by GCMS detection of petroleum hydrocarbon products. J Forensic Sci. 2008;53(5):1130-7doi: 10.1111/j.1556-4029.2008.00798.x.
Aziz, N., Greenwood, P. F., Grice, K., John Watling, R., & van Bronswijk, W. (2008). Chemical fingerprinting of adhesive tapes by GCMS detection of petroleum hydrocarbon products. Journal of forensic sciences, 53(5), 1130-7. https://doi.org/10.1111/j.1556-4029.2008.00798.x
Aziz, Nurhuda, et al. "Chemical fingerprinting of adhesive tapes by GCMS detection of petroleum hydrocarbon products." Journal of forensic sciences vol. 53,5 (2008): 1130-7. doi: https://doi.org/10.1111/j.1556-4029.2008.00798.x
Aziz N, Greenwood PF, Grice K, John Watling R, van Bronswijk W. Chemical fingerprinting of adhesive tapes by GCMS detection of petroleum hydrocarbon products. J Forensic Sci. 2008 Sep;53(5):1130-7. doi: 10.1111/j.1556-4029.2008.00798.x. Epub 2008 Jul 08. PMID: 18631281.
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Some aspects of room-temperature phosphorescence in liquid solutions.

Talanta

Donkerbroek JJ, Elzas JJ, Gooijer C, Frei RW, Velthorst NH.
PMID: 18962992
Talanta. 1981 Oct;28(10):717-23. doi: 10.1016/0039-9140(81)80112-9.

Experimental requirements for room-temperature phosphorescence measurements in liquids (RTPL) are discussed. Phosphorescence quantum yields and triplet lifetimes of some brominated naphthalenes and halogenated biphenyls at 77 K in 2-methyltetrahydrofuran and at room temperature in hexane are reported and compared....

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Donkerbroek JJ, Elzas JJ, Gooijer C, et al. Some aspects of room-temperature phosphorescence in liquid solutions. Talanta. 1981;28(10):717-23doi: 10.1016/0039-9140(81)80112-9.
Donkerbroek, J. J., Elzas, J. J., Gooijer, C., Frei, R. W., & Velthorst, N. H. (1981). Some aspects of room-temperature phosphorescence in liquid solutions. Talanta, 28(10), 717-23. https://doi.org/10.1016/0039-9140(81)80112-9
Donkerbroek, J J, et al. "Some aspects of room-temperature phosphorescence in liquid solutions." Talanta vol. 28,10 (1981): 717-23. doi: https://doi.org/10.1016/0039-9140(81)80112-9
Donkerbroek JJ, Elzas JJ, Gooijer C, Frei RW, Velthorst NH. Some aspects of room-temperature phosphorescence in liquid solutions. Talanta. 1981 Oct;28(10):717-23. doi: 10.1016/0039-9140(81)80112-9. PMID: 18962992.
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Determination of chromium(vi) in natural waters by the sorption of chromium-diphenylcarbazone with xad-2 resin.

Talanta

Osaki S, Osaki T, Takashima Y.
PMID: 18963443
Talanta. 1983 Sep;30(9):683-6. doi: 10.1016/0039-9140(83)80156-8.

The sorption of the chromium(III)-diphenylcarbazone complex (Cr-DPC) with XAD-2 has been investigated, for use in the separation of Cr(VI) from Cr(III) species in natural waters. Cr-DPC is formed from the reaction of Cr(VI) with diphenylcarbazide, but Cr(III) species give...

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Osaki S, Osaki T, Takashima Y. Determination of chromium(vi) in natural waters by the sorption of chromium-diphenylcarbazone with xad-2 resin. Talanta. 1983;30(9):683-6doi: 10.1016/0039-9140(83)80156-8.
Osaki, S., Osaki, T., & Takashima, Y. (1983). Determination of chromium(vi) in natural waters by the sorption of chromium-diphenylcarbazone with xad-2 resin. Talanta, 30(9), 683-6. https://doi.org/10.1016/0039-9140(83)80156-8
Osaki, S, et al. "Determination of chromium(vi) in natural waters by the sorption of chromium-diphenylcarbazone with xad-2 resin." Talanta vol. 30,9 (1983): 683-6. doi: https://doi.org/10.1016/0039-9140(83)80156-8
Osaki S, Osaki T, Takashima Y. Determination of chromium(vi) in natural waters by the sorption of chromium-diphenylcarbazone with xad-2 resin. Talanta. 1983 Sep;30(9):683-6. doi: 10.1016/0039-9140(83)80156-8. PMID: 18963443.
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Structures of 1-(arylseleninyl)naphthalenes: O, G, and Y dependences in 8-G-1-[p-YC6H4Se(O)]C10H6.

The Journal of organic chemistry

Hayashi S, Wada H, Ueno T, Nakanishi W.
PMID: 16839136
J Org Chem. 2006 Jul 21;71(15):5574-85. doi: 10.1021/jo060527f.

Structures of 8-G-1-[p-YC6H4Se(O)]C10H6 [1 (G = H), 2 (G = F), 3 (G = Cl), and 4 (G = Br): Y = H, OMe, OCH2Ph, t-Bu, Me, Cl, and NO2] and (1-C10H7)2SeO (5) are investigated by the X-ray crystallographic...

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Hayashi S, Wada H, Ueno T, et al. Structures of 1-(arylseleninyl)naphthalenes: O, G, and Y dependences in 8-G-1-[p-YC6H4Se(O)]C10H6. J Org Chem. 2006;71(15):5574-85doi: 10.1021/jo060527f.
Hayashi, S., Wada, H., Ueno, T., & Nakanishi, W. (2006). Structures of 1-(arylseleninyl)naphthalenes: O, G, and Y dependences in 8-G-1-[p-YC6H4Se(O)]C10H6. The Journal of organic chemistry, 71(15), 5574-85. https://doi.org/10.1021/jo060527f
Hayashi, Satoko, et al. "Structures of 1-(arylseleninyl)naphthalenes: O, G, and Y dependences in 8-G-1-[p-YC6H4Se(O)]C10H6." The Journal of organic chemistry vol. 71,15 (2006): 5574-85. doi: https://doi.org/10.1021/jo060527f
Hayashi S, Wada H, Ueno T, Nakanishi W. Structures of 1-(arylseleninyl)naphthalenes: O, G, and Y dependences in 8-G-1-[p-YC6H4Se(O)]C10H6. J Org Chem. 2006 Jul 21;71(15):5574-85. doi: 10.1021/jo060527f. PMID: 16839136.
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2-alpha-hydroxyalkyl- and 2,7-di(alpha-hydroxyalkyl)-1,8-bis(dimethylamino)naphthalenes: stabilization of nonconventional in/out conformers of "proton sponges" via N...H-O intramolecular hydrogen bonding. A remarkable kind of tandem nitrogen inversion.

The Journal of organic chemistry

Pozharskii AF, Degtyarev AV, Ryabtsova OV, Ozeryanskii VA, Kletskii ME, Starikova ZA, Sobczyk L, Filarowski A.
PMID: 17378612
J Org Chem. 2007 Apr 13;72(8):3006-19. doi: 10.1021/jo062667v. Epub 2007 Mar 23.

A regular set of 2-(alpha-hydroxymethyl)- and 2,7-di(alpha-hydroxymethyl)-1,8-bis(dimethylamino)naphthalenes has been prepared. Their X-ray, NMR, and IR studies have demonstrated that in tertiary mono-alcohols the orientation of free nitrogen electron pairs in crystals and solution corresponds to nonconventional in/out conformers stabilized...

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Pozharskii AF, Degtyarev AV, Ryabtsova OV, et al. 2-alpha-hydroxyalkyl- and 2,7-di(alpha-hydroxyalkyl)-1,8-bis(dimethylamino)naphthalenes: stabilization of nonconventional in/out conformers of "proton sponges" via N...H-O intramolecular hydrogen bonding. A remarkable kind of tandem nitrogen inversion. J Org Chem. 2007;72(8):3006-19doi: 10.1021/jo062667v.
Pozharskii, A. F., Degtyarev, A. V., Ryabtsova, O. V., Ozeryanskii, V. A., Kletskii, M. E., Starikova, Z. A., Sobczyk, L., & Filarowski, A. (2007). 2-alpha-hydroxyalkyl- and 2,7-di(alpha-hydroxyalkyl)-1,8-bis(dimethylamino)naphthalenes: stabilization of nonconventional in/out conformers of "proton sponges" via N...H-O intramolecular hydrogen bonding. A remarkable kind of tandem nitrogen inversion. The Journal of organic chemistry, 72(8), 3006-19. https://doi.org/10.1021/jo062667v
Pozharskii, Alexander F, et al. "2-alpha-hydroxyalkyl- and 2,7-di(alpha-hydroxyalkyl)-1,8-bis(dimethylamino)naphthalenes: stabilization of nonconventional in/out conformers of "proton sponges" via N...H-O intramolecular hydrogen bonding. A remarkable kind of tandem nitrogen inversion." The Journal of organic chemistry vol. 72,8 (2007): 3006-19. doi: https://doi.org/10.1021/jo062667v
Pozharskii AF, Degtyarev AV, Ryabtsova OV, Ozeryanskii VA, Kletskii ME, Starikova ZA, Sobczyk L, Filarowski A. 2-alpha-hydroxyalkyl- and 2,7-di(alpha-hydroxyalkyl)-1,8-bis(dimethylamino)naphthalenes: stabilization of nonconventional in/out conformers of "proton sponges" via N...H-O intramolecular hydrogen bonding. A remarkable kind of tandem nitrogen inversion. J Org Chem. 2007 Apr 13;72(8):3006-19. doi: 10.1021/jo062667v. Epub 2007 Mar 23. PMID: 17378612.
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Aromatic molecules in restricted geometries: photophysics of naphthalene included in a cyclodextrin functionalized layered solid.

The journal of physical chemistry. B

Mohanambe L, Vasudevan S.
PMID: 16853933
J Phys Chem B. 2005 Dec 01;109(47):22523-9. doi: 10.1021/jp053925f.

The galleries of an Mg-Al layered double hydroxide have been functionalized by intercalation of carboxymethyl beta-cyclodextrin cavities. The anchored cavities form a random array of identical-sized hydrophobic nanopockets arranged in a bilayer fashion in the interlamellar space of the...

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Mohanambe L, Vasudevan S. Aromatic molecules in restricted geometries: photophysics of naphthalene included in a cyclodextrin functionalized layered solid. J Phys Chem B. 2005;109(47):22523-9doi: 10.1021/jp053925f.
Mohanambe, L., & Vasudevan, S. (2005). Aromatic molecules in restricted geometries: photophysics of naphthalene included in a cyclodextrin functionalized layered solid. The journal of physical chemistry. B, 109(47), 22523-9. https://doi.org/10.1021/jp053925f
Mohanambe, L, and Vasudevan, S. "Aromatic molecules in restricted geometries: photophysics of naphthalene included in a cyclodextrin functionalized layered solid." The journal of physical chemistry. B vol. 109,47 (2005): 22523-9. doi: https://doi.org/10.1021/jp053925f
Mohanambe L, Vasudevan S. Aromatic molecules in restricted geometries: photophysics of naphthalene included in a cyclodextrin functionalized layered solid. J Phys Chem B. 2005 Dec 01;109(47):22523-9. doi: 10.1021/jp053925f. PMID: 16853933.
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Aromatic sulphonate ion-selective electrode membrane with crystal violet as ion-exchange site.

Talanta

Ishibashi N, Kohara H, Horinouchi K.
PMID: 18961356
Talanta. 1973 Sep;20(9):867-74. doi: 10.1016/0039-9140(73)80202-4.

Four triphenylmethane derivatives (cations) and a high molecular-weight quaternary ammonium ion were used as the ion-exchange site in the liquid membranes of electrodes responsive to aromatic sulphonate ions, such as benzenesulphonate and alpha-naphthalenesulphonate. The nitrobenzene or 1,2-dichloroethane membrane containing...

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Ishibashi N, Kohara H, Horinouchi K. Aromatic sulphonate ion-selective electrode membrane with crystal violet as ion-exchange site. Talanta. 1973;20(9):867-74doi: 10.1016/0039-9140(73)80202-4.
Ishibashi, N., Kohara, H., & Horinouchi, K. (1973). Aromatic sulphonate ion-selective electrode membrane with crystal violet as ion-exchange site. Talanta, 20(9), 867-74. https://doi.org/10.1016/0039-9140(73)80202-4
Ishibashi, N, et al. "Aromatic sulphonate ion-selective electrode membrane with crystal violet as ion-exchange site." Talanta vol. 20,9 (1973): 867-74. doi: https://doi.org/10.1016/0039-9140(73)80202-4
Ishibashi N, Kohara H, Horinouchi K. Aromatic sulphonate ion-selective electrode membrane with crystal violet as ion-exchange site. Talanta. 1973 Sep;20(9):867-74. doi: 10.1016/0039-9140(73)80202-4. PMID: 18961356.
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Use of an ipb-lux Fusion To Study Regulation of the Isopropylbenzene Catabolism Operon of Pseudomonas putida RE204 and To Detect Hydrophobic Pollutants in the Environment.

Applied and environmental microbiology

Selifonova OV, Eaton RW.
PMID: 16535269
Appl Environ Microbiol. 1996 Mar;62(3):778-83. doi: 10.1128/aem.62.3.778-783.1996.

A DNA segment involved in the regulation of the isopropylbenzene (cumene) catabolism operon (ipb) of plasmid pRE4 from Pseudomonas putida RE204 and the Vibrio fischeri luciferase genes, luxCDABE, were used to create an ipbRo/pA(prm1)-luxCDABE reporter fusion plasmid, pOS25. Escherichia...

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Selifonova OV, Eaton RW. Use of an ipb-lux Fusion To Study Regulation of the Isopropylbenzene Catabolism Operon of Pseudomonas putida RE204 and To Detect Hydrophobic Pollutants in the Environment. Appl Environ Microbiol. 1996;62(3):778-83doi: 10.1128/aem.62.3.778-783.1996.
Selifonova, O. V., & Eaton, R. W. (1996). Use of an ipb-lux Fusion To Study Regulation of the Isopropylbenzene Catabolism Operon of Pseudomonas putida RE204 and To Detect Hydrophobic Pollutants in the Environment. Applied and environmental microbiology, 62(3), 778-83. https://doi.org/10.1128/aem.62.3.778-783.1996
Selifonova, O V, and Eaton, R W. "Use of an ipb-lux Fusion To Study Regulation of the Isopropylbenzene Catabolism Operon of Pseudomonas putida RE204 and To Detect Hydrophobic Pollutants in the Environment." Applied and environmental microbiology vol. 62,3 (1996): 778-83. doi: https://doi.org/10.1128/aem.62.3.778-783.1996
Selifonova OV, Eaton RW. Use of an ipb-lux Fusion To Study Regulation of the Isopropylbenzene Catabolism Operon of Pseudomonas putida RE204 and To Detect Hydrophobic Pollutants in the Environment. Appl Environ Microbiol. 1996 Mar;62(3):778-83. doi: 10.1128/aem.62.3.778-783.1996. PMID: 16535269; PMCID: PMC1388794.
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