Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 1 to 12 of 81 entries
Sorted by: Best Match Show Resources per page
Effective separation of the actinides Am(III) and Cm(III) by electronic modulation of bis-(1,2,4-triazin-3-yl)phenanthrolines.

Chemical communications (Cambridge, England)

Afsar A, Harwood LM, Hudson MJ, Westwood J, Geist A.
PMID: 25727341
Chem Commun (Camb). 2015 Apr 07;51(27):5860-3. doi: 10.1039/c5cc00567a. Epub 2015 Mar 02.

It has been shown that modification of the phenanthroline backbone of CyMe4-BTPhen leads to subtle electronic modulation, permitting differential ligation of Am(III) and Cm(III) resulting in separation factors up to 7.

Cite
Afsar A, Harwood LM, Hudson MJ, et al. Effective separation of the actinides Am(III) and Cm(III) by electronic modulation of bis-(1,2,4-triazin-3-yl)phenanthrolines. Chem Commun (Camb). 2015;51(27):5860-3doi: 10.1039/c5cc00567a.
Afsar, A., Harwood, L. M., Hudson, M. J., Westwood, J., & Geist, A. (2015). Effective separation of the actinides Am(III) and Cm(III) by electronic modulation of bis-(1,2,4-triazin-3-yl)phenanthrolines. Chemical communications (Cambridge, England), 51(27), 5860-3. https://doi.org/10.1039/c5cc00567a
Afsar, Ashfaq, et al. "Effective separation of the actinides Am(III) and Cm(III) by electronic modulation of bis-(1,2,4-triazin-3-yl)phenanthrolines." Chemical communications (Cambridge, England) vol. 51,27 (2015): 5860-3. doi: https://doi.org/10.1039/c5cc00567a
Afsar A, Harwood LM, Hudson MJ, Westwood J, Geist A. Effective separation of the actinides Am(III) and Cm(III) by electronic modulation of bis-(1,2,4-triazin-3-yl)phenanthrolines. Chem Commun (Camb). 2015 Apr 07;51(27):5860-3. doi: 10.1039/c5cc00567a. Epub 2015 Mar 02. PMID: 25727341.
Copy Download .nbib Format: NLM
HOF·CH3CN: probably the best oxygen transfer agent organic chemistry has to offer.

Accounts of chemical research

Rozen S.
PMID: 24871453
Acc Chem Res. 2014 Aug 19;47(8):2378-89. doi: 10.1021/ar500107b. Epub 2014 May 28.

The complex HOF·CH3CN is readily obtained by bubbling dilute fluorine into aqueous acetonitrile solution. It does not have to be purified or isolated, and its solution can react as is, after the concentration has been establish by any iodometric...

Cite
Rozen S. HOF·CH3CN: probably the best oxygen transfer agent organic chemistry has to offer. Acc Chem Res. 2014;47(8):2378-89doi: 10.1021/ar500107b.
Rozen, S. (2014). HOF·CH3CN: probably the best oxygen transfer agent organic chemistry has to offer. Accounts of chemical research, 47(8), 2378-89. https://doi.org/10.1021/ar500107b
Rozen, Shlomo. "HOF·CH3CN: probably the best oxygen transfer agent organic chemistry has to offer." Accounts of chemical research vol. 47,8 (2014): 2378-89. doi: https://doi.org/10.1021/ar500107b
Rozen S. HOF·CH3CN: probably the best oxygen transfer agent organic chemistry has to offer. Acc Chem Res. 2014 Aug 19;47(8):2378-89. doi: 10.1021/ar500107b. Epub 2014 May 28. PMID: 24871453.
Copy Download .nbib Format: NLM
π-Conjugated [2]Catenanes Based on Oligothiophenes and Phenanthrolines: Efficient Synthesis and Electronic Properties.

Chemistry (Weinheim an der Bergstrasse, Germany)

Götz G, Zhu X, Mishra A, Segura JL, Mena-Osteritz E, Bäuerle P.
PMID: 25820180
Chemistry. 2015 May 04;21(19):7193-210. doi: 10.1002/chem.201406039. Epub 2015 Mar 25.

Novel π-conjugated topologies based on oligothiophenes and phenanthroline have been assembled by combining their outstanding electronic and structural benefits with the specific properties of the topological structure. Macrocycles and catenanes are prepared by using an optimized protocol of transition...

Cite
Götz G, Zhu X, Mishra A, et al. π-Conjugated [2]Catenanes Based on Oligothiophenes and Phenanthrolines: Efficient Synthesis and Electronic Properties. Chemistry. 2015;21(19):7193-210doi: 10.1002/chem.201406039.
Götz, G., Zhu, X., Mishra, A., Segura, J. L., Mena-Osteritz, E., & Bäuerle, P. (2015). π-Conjugated [2]Catenanes Based on Oligothiophenes and Phenanthrolines: Efficient Synthesis and Electronic Properties. Chemistry (Weinheim an der Bergstrasse, Germany), 21(19), 7193-210. https://doi.org/10.1002/chem.201406039
Götz, Günther, et al. "π-Conjugated [2]Catenanes Based on Oligothiophenes and Phenanthrolines: Efficient Synthesis and Electronic Properties." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 21,19 (2015): 7193-210. doi: https://doi.org/10.1002/chem.201406039
Götz G, Zhu X, Mishra A, Segura JL, Mena-Osteritz E, Bäuerle P. π-Conjugated [2]Catenanes Based on Oligothiophenes and Phenanthrolines: Efficient Synthesis and Electronic Properties. Chemistry. 2015 May 04;21(19):7193-210. doi: 10.1002/chem.201406039. Epub 2015 Mar 25. PMID: 25820180.
Copy Download .nbib Format: NLM
Torands Revisited: Metal Sequestration and Self-Assembly of Cyclo-2,9-tris-1,10-phenanthroline Hexaaza Macrocycles.

Chemistry (Weinheim an der Bergstrasse, Germany)

Schwab MG, Takase M, Mavrinsky A, Pisula W, Feng X, Gámez JA, Thiel W, Mali KS, de Feyter S, Müllen K.
PMID: 25867924
Chemistry. 2015 Jun 01;21(23):8426-34. doi: 10.1002/chem.201406602. Epub 2015 Apr 13.

A series of novel toroidal cyclo-2,9-tris-1,10-phenanthroline macrocycles with an unusual hexaaza cavity are reported. Nickel-mediated Yamamoto aryl-aryl coupling was found to be a versatile tool for the cyclotrimerization of functionalized 1,10-phenathroline precursors. Due to the now improved processability, both...

Cite
Schwab MG, Takase M, Mavrinsky A, et al. Torands Revisited: Metal Sequestration and Self-Assembly of Cyclo-2,9-tris-1,10-phenanthroline Hexaaza Macrocycles. Chemistry. 2015;21(23):8426-34doi: 10.1002/chem.201406602.
Schwab, M. G., Takase, M., Mavrinsky, A., Pisula, W., Feng, X., Gámez, J. A., Thiel, W., Mali, K. S., de Feyter, S., & Müllen, K. (2015). Torands Revisited: Metal Sequestration and Self-Assembly of Cyclo-2,9-tris-1,10-phenanthroline Hexaaza Macrocycles. Chemistry (Weinheim an der Bergstrasse, Germany), 21(23), 8426-34. https://doi.org/10.1002/chem.201406602
Schwab, Matthias Georg, et al. "Torands Revisited: Metal Sequestration and Self-Assembly of Cyclo-2,9-tris-1,10-phenanthroline Hexaaza Macrocycles." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 21,23 (2015): 8426-34. doi: https://doi.org/10.1002/chem.201406602
Schwab MG, Takase M, Mavrinsky A, Pisula W, Feng X, Gámez JA, Thiel W, Mali KS, de Feyter S, Müllen K. Torands Revisited: Metal Sequestration and Self-Assembly of Cyclo-2,9-tris-1,10-phenanthroline Hexaaza Macrocycles. Chemistry. 2015 Jun 01;21(23):8426-34. doi: 10.1002/chem.201406602. Epub 2015 Apr 13. PMID: 25867924.
Copy Download .nbib Format: NLM
Steric Crowding and Redox Reactivity in Platinum(II) and Platinum(IV) Complexes Containing Substituted 1,10-Phenanthrolines.

Inorganic chemistry

Fanizzi FP, Natile G, Lanfranchi M, Tiripicchio A, Laschi F, Zanello P.
PMID: 11666514
Inorg Chem. 1996 May 22;35(11):3173-3182. doi: 10.1021/ic960125y.

The effect of the phenanthroline substituents on the structure and reactivity of platinum(II) and platinum(IV) complexes has been investigated. The X-ray crystal structures of the compounds [PtI(2)(4,7-Ph(2)phen)].CHCl(3) (1dz.CHCl(3)), [PtI(4)(4,7-Ph(2)phen)].CHCl(3) (2dz.CHCl(3)), [PtI(2)(2,9-Me(2)-4,7-Ph(2)phen)] (1fz), and [PtI(4)(2,9-Me(2)-4,7-Ph(2)phen)].I(2) (2fz.I(2)) have shown that complexes...

Cite
Fanizzi FP, Natile G, Lanfranchi M, et al. Steric Crowding and Redox Reactivity in Platinum(II) and Platinum(IV) Complexes Containing Substituted 1,10-Phenanthrolines. Inorg Chem. 1996;35(11):3173-3182doi: 10.1021/ic960125y.
Fanizzi, F. P., Natile, G., Lanfranchi, M., Tiripicchio, A., Laschi, F., & Zanello, P. (1996). Steric Crowding and Redox Reactivity in Platinum(II) and Platinum(IV) Complexes Containing Substituted 1,10-Phenanthrolines. Inorganic chemistry, 35(11), 3173-3182. https://doi.org/10.1021/ic960125y
Fanizzi, Francesco P., et al. "Steric Crowding and Redox Reactivity in Platinum(II) and Platinum(IV) Complexes Containing Substituted 1,10-Phenanthrolines." Inorganic chemistry vol. 35,11 (1996): 3173-3182. doi: https://doi.org/10.1021/ic960125y
Fanizzi FP, Natile G, Lanfranchi M, Tiripicchio A, Laschi F, Zanello P. Steric Crowding and Redox Reactivity in Platinum(II) and Platinum(IV) Complexes Containing Substituted 1,10-Phenanthrolines. Inorg Chem. 1996 May 22;35(11):3173-3182. doi: 10.1021/ic960125y. PMID: 11666514.
Copy Download .nbib Format: NLM
Diastereoselective Formation and Photophysical Behavior of a Chiral Copper(I) Phenanthroline Complex.

Inorganic chemistry

Riesgo EC, Credi A, De Cola L, Thummel RP.
PMID: 11670368
Inorg Chem. 1998 May 04;37(9):2145-2149. doi: 10.1021/ic971267a.

The Friedländer condensation of (1R,5S)-(+)- and (1S,5R)-(-)-nopinone with 8-aminoquinoline-7-carbaldehyde leads to the corresponding enantiomerically pure (2,3-b)-pineno-1,10-phenanthrolines. Coordination of these ligands with Cu(I) affords non-interconvertable chiral complexes which show equal and opposite Cotton effects in their CD spectra as well...

Cite
Riesgo EC, Credi A, De Cola L, et al. Diastereoselective Formation and Photophysical Behavior of a Chiral Copper(I) Phenanthroline Complex. Inorg Chem. 1998;37(9):2145-2149doi: 10.1021/ic971267a.
Riesgo, E. C., Credi, A., De Cola, L., & Thummel, R. P. (1998). Diastereoselective Formation and Photophysical Behavior of a Chiral Copper(I) Phenanthroline Complex. Inorganic chemistry, 37(9), 2145-2149. https://doi.org/10.1021/ic971267a
Riesgo, Elvira C., et al. "Diastereoselective Formation and Photophysical Behavior of a Chiral Copper(I) Phenanthroline Complex." Inorganic chemistry vol. 37,9 (1998): 2145-2149. doi: https://doi.org/10.1021/ic971267a
Riesgo EC, Credi A, De Cola L, Thummel RP. Diastereoselective Formation and Photophysical Behavior of a Chiral Copper(I) Phenanthroline Complex. Inorg Chem. 1998 May 04;37(9):2145-2149. doi: 10.1021/ic971267a. PMID: 11670368.
Copy Download .nbib Format: NLM
Cooperative Substituent Effects on the Excited States of Copper Phenanthrolines.

Inorganic chemistry

Cunningham CT, Cunningham KL, Michalec JF, McMillin DR.
PMID: 11671147
Inorg Chem. 1999 Oct 04;38(20):4388-4392. doi: 10.1021/ic9906611.

Copper phenanthrolines are attractive as potential photosensitizers because of the ready availability of the metal, but efficient nonradiative decay including a solvent-induced quenching phenomenon ordinarily limits their utility. However, the present studies show that the addition of methyl substituents...

Cite
Cunningham CT, Cunningham KL, Michalec JF, et al. Cooperative Substituent Effects on the Excited States of Copper Phenanthrolines. Inorg Chem. 1999;38(20):4388-4392doi: 10.1021/ic9906611.
Cunningham, C. T., Cunningham, K. L., Michalec, J. F., & McMillin, D. R. (1999). Cooperative Substituent Effects on the Excited States of Copper Phenanthrolines. Inorganic chemistry, 38(20), 4388-4392. https://doi.org/10.1021/ic9906611
Cunningham, Corey T., et al. "Cooperative Substituent Effects on the Excited States of Copper Phenanthrolines." Inorganic chemistry vol. 38,20 (1999): 4388-4392. doi: https://doi.org/10.1021/ic9906611
Cunningham CT, Cunningham KL, Michalec JF, McMillin DR. Cooperative Substituent Effects on the Excited States of Copper Phenanthrolines. Inorg Chem. 1999 Oct 04;38(20):4388-4392. doi: 10.1021/ic9906611. PMID: 11671147.
Copy Download .nbib Format: NLM
Ruthenium(II) Complexes of 2-Aryl-1,10-phenanthrolines: Synthesis, Structure, and Photophysical Properties.

Inorganic chemistry

Wu F, Riesgo E, Pavalova A, Kipp RA, Schmehl RH, Thummel RP.
PMID: 11671292
Inorg Chem. 1999 Nov 29;38(24):5620-5628. doi: 10.1021/ic990706y.

The synthesis, characterization, and photochemical investigation of a series of Ru(II) complexes having 2-phenyl- and 2,9-diphenyl substituted phenanthroline ligands are reported. Structural characterization of some of the complexes revealed that the phenyl substituents of the phenanthroline ligand are oriented...

Cite
Wu F, Riesgo E, Pavalova A, et al. Ruthenium(II) Complexes of 2-Aryl-1,10-phenanthrolines: Synthesis, Structure, and Photophysical Properties. Inorg Chem. 1999;38(24):5620-5628doi: 10.1021/ic990706y.
Wu, F., Riesgo, E., Pavalova, A., Kipp, R. A., Schmehl, R. H., & Thummel, R. P. (1999). Ruthenium(II) Complexes of 2-Aryl-1,10-phenanthrolines: Synthesis, Structure, and Photophysical Properties. Inorganic chemistry, 38(24), 5620-5628. https://doi.org/10.1021/ic990706y
Wu, Feiyue, et al. "Ruthenium(II) Complexes of 2-Aryl-1,10-phenanthrolines: Synthesis, Structure, and Photophysical Properties." Inorganic chemistry vol. 38,24 (1999): 5620-5628. doi: https://doi.org/10.1021/ic990706y
Wu F, Riesgo E, Pavalova A, Kipp RA, Schmehl RH, Thummel RP. Ruthenium(II) Complexes of 2-Aryl-1,10-phenanthrolines: Synthesis, Structure, and Photophysical Properties. Inorg Chem. 1999 Nov 29;38(24):5620-5628. doi: 10.1021/ic990706y. PMID: 11671292.
Copy Download .nbib Format: NLM
Cyclometallated iridium(III) complexes with substituted 1,10-phenanthrolines: a new class of highly active organometallic second order NLO-phores with excellent transparency with respect to second harmonic emission.

Chemical communications (Cambridge, England)

Dragonetti C, Righetto S, Roberto D, Ugo R, Valore A, Fantacci S, Sgamellotti A, De Angelis F.
PMID: 17925947
Chem Commun (Camb). 2007 Oct 28;(40):4116-8. doi: 10.1039/b708073e. Epub 2007 Aug 02.

[Ir(ppy)(2)(5-R-1,10-phen)][PF(6)] (ppy = cyclometallated 2-phenylpyridine, phen = phenanthroline, R = H, Me, NMe(2), NO(2)) and [Ir(ppy)(2)(4-R',7-R'-1,10-phen)][PF(6)] (R' = Me, Ph) complexes are characterized by one of the highest second order NLO response (measured by the EFISH technique) reported for...

Cite
Dragonetti C, Righetto S, Roberto D, et al. Cyclometallated iridium(III) complexes with substituted 1,10-phenanthrolines: a new class of highly active organometallic second order NLO-phores with excellent transparency with respect to second harmonic emission. Chem Commun (Camb). 2007;(40):4116-8doi: 10.1039/b708073e.
Dragonetti, C., Righetto, S., Roberto, D., Ugo, R., Valore, A., Fantacci, S., Sgamellotti, A., & De Angelis, F. (2007). Cyclometallated iridium(III) complexes with substituted 1,10-phenanthrolines: a new class of highly active organometallic second order NLO-phores with excellent transparency with respect to second harmonic emission. Chemical communications (Cambridge, England), (40), 4116-8. https://doi.org/10.1039/b708073e
Dragonetti, Claudia, et al. "Cyclometallated iridium(III) complexes with substituted 1,10-phenanthrolines: a new class of highly active organometallic second order NLO-phores with excellent transparency with respect to second harmonic emission." Chemical communications (Cambridge, England) vol. ,40 (2007): 4116-8. doi: https://doi.org/10.1039/b708073e
Dragonetti C, Righetto S, Roberto D, Ugo R, Valore A, Fantacci S, Sgamellotti A, De Angelis F. Cyclometallated iridium(III) complexes with substituted 1,10-phenanthrolines: a new class of highly active organometallic second order NLO-phores with excellent transparency with respect to second harmonic emission. Chem Commun (Camb). 2007 Oct 28;(40):4116-8. doi: 10.1039/b708073e. Epub 2007 Aug 02. PMID: 17925947.
Copy Download .nbib Format: NLM
Synthesis and Biological Activity of Manganese (II) Complexes of Phthalic and Isophthalic Acid: X-Ray Crystal Structures of [Mn(ph)(Phen)(2)(H(2)O)]. 4H(2)O, [Mn(Phen)(2)(H(2)O)(2)](2)(Isoph)(2)(Phen). 12H(2)O and {[Mn(Isoph)(bipy)](4). 2.75biby}(n)(phH(2) = Phthalic Acid; isoph = Isophthalic Acid; phen = 1,10-Phenanthroline; bipy = 2,2-Bipyridine).

Metal-based drugs

Devereux M, McCann M, Leon V, Geraghty M, McKee V, Wikaira J.
PMID: 18475957
Met Based Drugs. 2000;7(5):275-88. doi: 10.1155/MBD.2000.275.

Manganese(II) acetate reacts with phthalic acid (phH(2)) to give [Mn(ph)].0.5H(2)O (1). Reaction of 1 with 1,10-phenanthroline produces [Mn(ph)(phen)].2H(2)O (2) and [Mn(ph)(phen)(2)(H(2)O)].4H(2)O (3). Reaction of isophthalic acid (isophH(2)) with manganese(II) acetate results in the formation of [Mn(isoph)].2H(2)O (4). The addition...

Cite
Devereux M, McCann M, Leon V, et al. Synthesis and Biological Activity of Manganese (II) Complexes of Phthalic and Isophthalic Acid: X-Ray Crystal Structures of [Mn(ph)(Phen)(2)(H(2)O)]. 4H(2)O, [Mn(Phen)(2)(H(2)O)(2)](2)(Isoph)(2)(Phen). 12H(2)O and {[Mn(Isoph)(bipy)](4). 2.75biby}(n)(phH(2) = Phthalic Acid; isoph = Isophthalic Acid; phen = 1,10-Phenanthroline; bipy = 2,2-Bipyridine). Met Based Drugs. 2000;7(5):275-88doi: 10.1155/MBD.2000.275.
Devereux, M., McCann, M., Leon, V., Geraghty, M., McKee, V., & Wikaira, J. (2000). Synthesis and Biological Activity of Manganese (II) Complexes of Phthalic and Isophthalic Acid: X-Ray Crystal Structures of [Mn(ph)(Phen)(2)(H(2)O)]. 4H(2)O, [Mn(Phen)(2)(H(2)O)(2)](2)(Isoph)(2)(Phen). 12H(2)O and {[Mn(Isoph)(bipy)](4). 2.75biby}(n)(phH(2) = Phthalic Acid; isoph = Isophthalic Acid; phen = 1,10-Phenanthroline; bipy = 2,2-Bipyridine). Metal-based drugs, 7(5), 275-88. https://doi.org/10.1155/MBD.2000.275
Devereux, M, et al. "Synthesis and Biological Activity of Manganese (II) Complexes of Phthalic and Isophthalic Acid: X-Ray Crystal Structures of [Mn(ph)(Phen)(2)(H(2)O)]. 4H(2)O, [Mn(Phen)(2)(H(2)O)(2)](2)(Isoph)(2)(Phen). 12H(2)O and {[Mn(Isoph)(bipy)](4). 2.75biby}(n)(phH(2) = Phthalic Acid; isoph = Isophthalic Acid; phen = 1,10-Phenanthroline; bipy = 2,2-Bipyridine)." Metal-based drugs vol. 7,5 (2000): 275-88. doi: https://doi.org/10.1155/MBD.2000.275
Devereux M, McCann M, Leon V, Geraghty M, McKee V, Wikaira J. Synthesis and Biological Activity of Manganese (II) Complexes of Phthalic and Isophthalic Acid: X-Ray Crystal Structures of [Mn(ph)(Phen)(2)(H(2)O)]. 4H(2)O, [Mn(Phen)(2)(H(2)O)(2)](2)(Isoph)(2)(Phen). 12H(2)O and {[Mn(Isoph)(bipy)](4). 2.75biby}(n)(phH(2) = Phthalic Acid; isoph = Isophthalic Acid; phen = 1,10-Phenanthroline; bipy = 2,2-Bipyridine). Met Based Drugs. 2000;7(5):275-88. doi: 10.1155/MBD.2000.275. PMID: 18475957; PMCID: PMC2365232.
Copy Download .nbib Format: NLM
Evaluation of the donor ability of phenanthrolines in iridium complexes by means of synchrotron radiation photoemission spectroscopy and DFT calculations.

Dalton transactions (Cambridge, England : 2003)

Crotti C, Farnetti E, Filipuzzi S, Stener M, Zangrando E, Moras P.
PMID: 17160183
Dalton Trans. 2007 Jan 07;(1):133-42. doi: 10.1039/b613837c. Epub 2006 Nov 08.

Synchrotron radiation XPS measurements of Ir 4f, N 1s and I 4d core levels for the compounds Ir(cod)(N-N)X (cod=1,5-cyclooctadiene; N-N=1,10-phenanthroline and substituted derivatives; X=Cl, I) are reported. The compounds Ir(cod)(3,4,7,8-Me4phen)X (3,4,7,8-Me4phen=3,4,7,8-tetramethyl-1,10-phenanthroline) were structurally characterized by single crystal X-ray analyses....

Cite
Crotti C, Farnetti E, Filipuzzi S, et al. Evaluation of the donor ability of phenanthrolines in iridium complexes by means of synchrotron radiation photoemission spectroscopy and DFT calculations. Dalton Trans. 2006;(1):133-42doi: 10.1039/b613837c.
Crotti, C., Farnetti, E., Filipuzzi, S., Stener, M., Zangrando, E., & Moras, P. (2007). Evaluation of the donor ability of phenanthrolines in iridium complexes by means of synchrotron radiation photoemission spectroscopy and DFT calculations. Dalton transactions (Cambridge, England : 2003), (1), 133-42. https://doi.org/10.1039/b613837c
Crotti, Corrado, et al. "Evaluation of the donor ability of phenanthrolines in iridium complexes by means of synchrotron radiation photoemission spectroscopy and DFT calculations." Dalton transactions (Cambridge, England : 2003) vol. ,1 (2007): 133-42. doi: https://doi.org/10.1039/b613837c
Crotti C, Farnetti E, Filipuzzi S, Stener M, Zangrando E, Moras P. Evaluation of the donor ability of phenanthrolines in iridium complexes by means of synchrotron radiation photoemission spectroscopy and DFT calculations. Dalton Trans. 2007 Jan 07;(1):133-42. doi: 10.1039/b613837c. Epub 2006 Nov 08. PMID: 17160183.
Copy Download .nbib Format: NLM
Chromium(III) complexes bearing 2-benzazole-1,10-phenanthrolines: synthesis, molecular structures and ethylene oligomerization and polymerization.

Dalton transactions (Cambridge, England : 2003)

Zhang M, Wang K, Sun WH.
PMID: 19655069
Dalton Trans. 2009 Aug 28;(32):6354-63. doi: 10.1039/b902361e. Epub 2009 Jun 24.

The 2-benzazole-1,10-phenanthrolines and their chromium(III) complexes were synthesized and characterized by elemental and spectroscopic analyses as well as by single-crystal X-ray crystallography. X-Ray crystallographic analyses of C6 and C8 reveal an octahedral geometry around both chromium centers. The electronic...

Cite
Zhang M, Wang K, Sun WH. Chromium(III) complexes bearing 2-benzazole-1,10-phenanthrolines: synthesis, molecular structures and ethylene oligomerization and polymerization. Dalton Trans. 2009;(32):6354-63doi: 10.1039/b902361e.
Zhang, M., Wang, K., & Sun, W. H. (2009). Chromium(III) complexes bearing 2-benzazole-1,10-phenanthrolines: synthesis, molecular structures and ethylene oligomerization and polymerization. Dalton transactions (Cambridge, England : 2003), (32), 6354-63. https://doi.org/10.1039/b902361e
Zhang, Min, et al. "Chromium(III) complexes bearing 2-benzazole-1,10-phenanthrolines: synthesis, molecular structures and ethylene oligomerization and polymerization." Dalton transactions (Cambridge, England : 2003) vol. ,32 (2009): 6354-63. doi: https://doi.org/10.1039/b902361e
Zhang M, Wang K, Sun WH. Chromium(III) complexes bearing 2-benzazole-1,10-phenanthrolines: synthesis, molecular structures and ethylene oligomerization and polymerization. Dalton Trans. 2009 Aug 28;(32):6354-63. doi: 10.1039/b902361e. Epub 2009 Jun 24. PMID: 19655069.
Copy Download .nbib Format: NLM
Showing 1 to 12 of 81 entries