Theoretical insights into the separation of Am(III) over Eu(III) with PhenBHPPA

Dalton Transactions

Volumn 44, Issue 38, 2015, Pages 16737-16745

  Wu, Han ^a,b   Wu, Qun Yan ^a   Wang, Cong Zhi ^a   Lan, Jian Hui ^a   Liu, Zhi Rong ^b   Chai, Zhi Fang ^a,c   Shi, Wei Qun ^a  

^a INSTITUTE OF HIGH ENERGY PHYSICS   (China)

^b EAST CHINA UNIVERSITY OF TECHNOLOGY   (China)

^c MEDICAL COLLEGE OF SOOCHOW UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ACTINIDES; AMERICIUM; CHEMICAL BONDS; COMPLEXATION; DENSITY FUNCTIONAL THEORY; ELECTRONIC STRUCTURE; EXTRACTION; LIGANDS; NUCLEAR FUEL REPROCESSING; QUANTUM THEORY; RADIOACTIVE WASTES; SEPARATION; THERMOANALYSIS;

1 ,10-PHENANTHROLINE; INTERACTION MECHANISMS; LIQUID-LIQUID EXTRACTION; QUANTUM THEORY OF ATOMS IN MOLECULES; SPENT NUCLEAR FUEL REPROCESSING; THEORETICAL CALCULATIONS; THERMO DYNAMIC ANALYSIS; THERMODYNAMIC BEHAVIORS;

EUROPIUM;

1,10-PHENANTHROLINE; ACTINIDE; AMERICIUM; AMIDE; COORDINATION COMPOUND; EUROPIUM; LANTHANIDE; PHENANTHROLINE DERIVATIVE; PICOLINAMIDE; PICOLINIC ACID DERIVATIVE;

CHEMICAL STRUCTURE; CHEMISTRY; ISOLATION AND PURIFICATION; LIQUID LIQUID EXTRACTION; QUANTUM THEORY; THERMODYNAMICS;

ACTINOID SERIES ELEMENTS; AMERICIUM; AMIDES; COORDINATION COMPLEXES; EUROPIUM; LANTHANOID SERIES ELEMENTS; LIQUID-LIQUID EXTRACTION; MODELS, MOLECULAR; MOLECULAR STRUCTURE; PHENANTHROLINES; PICOLINIC ACIDS; QUANTUM THEORY; THERMODYNAMICS;

EID: 84942284189     PISSN: 14779226     EISSN: 14779234     Source Type: Journal    
DOI: 10.1039/c5dt02528a     Document Type: Article

References (60)

1. H. Yapici G. Genç N. Demir Ann. Nucl. Energy 2008 35 1264 1273
2. A. Herrera-Martínez Y. Kadi G. Parks Ann. Nucl. Energy 2007 34 550 563
3. X. Wang J. Li S. Dai T. Hayat A. Alsaedi X. Wang Chem. Eng. J. 2015 273 588 594
4. X. Cao D. Heidelberg J. Ciupka M. Dolg Inorg. Chem. 2010 49 10307 10315
5. P. J. Panak A. Geist Chem. Rev. 2013 113 1199 1236
6. H. H. Dam D. N. Reinhoudt W. Verboom Chem. Soc. Rev. 2007 36 367 377
7. A. Bhattacharyya T. K. Ghanty P. K. Mohapatra V. K. Manchanda Inorg. Chem. 2011 50 3913 3921
8. R. D. Hancock Chem. Soc. Rev. 2013 42 1500 1524
9. N. Boubals M. G. Drew C. Hill M. J. Hudson P. B. Iveson C. Madic M. L. Russell T. G. Youngs J. Chem. Soc., Dalton Trans. 2002 55 62
10. M. G. Drew P. B. Iveson M. J. Hudson J. O. Liljenzin L. Spjuth P.-Y. Cordier Å. Enarsson C. Hill C. Madic J. Chem. Soc., Dalton Trans. 2000 821 830
11. M. A. Denecke A. Rossberg P. J. Panak M. Weigl B. Schimmelpfennig A. Geist Inorg. Chem. 2005 44 8418 8425
12. P. Paul B. Tyagi A. K. Bilakhiya M. M. Bhadbhade E. Suresh G. Ramachandraiah Inorg. Chem. 1998 37 5733 5742
13. M. Miguirditchian D. Guillaneux D. Guillaumont P. Moisy C. Madic M. P. Jensen K. L. Nash Inorg. Chem. 2005 44 1404 1412
14. M. Weigl A. Geist U. Müllich K. Gompper Solvent Extr. Ion Exch. 2006 24 845 860
15. N. L. Banik B. Schimmelpfennig C. M. Marquardt B. Brendebach A. Geist M. A. Denecke Dalton Trans. 2010 39 5117 5122
16. M. R. Foreman M. J. Hudson M. G. Drew C. Hill C. Madic Dalton Trans. 2006 1645 1653
17. M. Steppert I. Císařová T. Fanghänel A. Geist P. Lindqvist-Reis P. Panak P. Štěpnička S. Trumm C. Walther Inorg. Chem. 2011 51 591 600
18. Z. Kolarik U. Müllich F. Gassner Solvent Extr. Ion Exch. 1999 17 23 32
19. M. J. Hudson C. E. Boucher D. Braekers J. F. Desreux M. G. Drew M. R. S. J. Foreman L. M. Harwood C. Hill C. Madic F. Marken New J. Chem. 2006 30 1171 1183
20. S. Trumm A. Geist P. J. Panak T. Fanghänel Solvent Extr. Ion Exch. 2011 29 213 229
21. C. Ekberg E. Aneheim A. Fermvik M. Foreman E. Löfström-Engdahl T. Retegan I. Spendlikova J. Chem. Eng. Data 2010 55 5133 5137
22. D. Manna T. K. Ghanty Phys. Chem. Chem. Phys. 2012 14 11060 11069
23. J. Bisson C. Berthon L. Berthon N. Boubals D. Dubreuil M. C. Charbonnel Procedia Chem. 2012 7 13 19
24. T. Kobayashi T. Yaita S. Suzuki H. Shiwaku Y. Okamoto K. Akutsu Y. Nakano Y. Fujii Sep. Sci. Technol. 2010 45 2431 2436
25. F. W. Lewis L. M. Harwood M. J. Hudson M. G. Drew J. F. Desreux G. Vidick N. Bouslimani G. Modolo A. Wilden M. Sypula T. H. Vu J. P. Simonin J. Am. Chem. Soc. 2011 133 13093 13102
26. C. L. Xiao C. Z. Wang L. Y. Yuan B. Li H. He S. Wang Y. L. Zhao Z. F. Chai W. Q. Shi Inorg. Chem. 2014 53 1712 1720
27. R. D. Hancock D. L. Melton J. M. Harrington F. C. McDonald R. T. Gephart L. L. Boone S. B. Jones N. E. Dean J. R. Whitehead G. M. Cockrell Coord. Chem. Rev. 2007 251 1678 1689
28. R. D. Hancock A. E. Martell Chem. Rev. 1989 89 1875 1914
29. J. Bisson J. Dehaudt M. C. Charbonnel D. Guillaneux M. Miguirditchian C. Marie N. Boubals G. Dutech M. Pipelier V. Blot D. Dubreuil Chem.-Eur. J. 2014 20 7819 7829
30. C. L. Xiao Q. Y. Wu C. Z. Wang Y. L. Zhao Z. F. Chai W. Q. Shi Inorg. Chem. 2014 53 10846 10853
31. C. Z. Wang J. H. Lan Q. Y. Wu Y. L. Zhao X. K. Wang Z. F. Chai W. Q. Shi Dalton Trans. 2014 43 8713 8720
32. J. H. Lan W. Q. Shi L. Y. Yuan Y. L. Zhao J. Li Z. F. Chai Inorg. Chem. 2011 50 9230 9237
33. A. Prestianni L. Joubert A. Chagnes G. Cote C. Adamo Phys. Chem. Chem. Phys. 2011 13 19371 19377
34. Q. Y. Wu C. Z. Wang J. H. Lan C. L. Xiao X. K. Wang Y. L. Zhao Z. F. Chai W. Q. Shi Inorg. Chem. 2014 53 9607 9614
35. P. Hohenberg W. Kohn Phys. Rev. 1964 136 B864
36. W. Kohn L. J. Sham Phys. Rev. 1965 140 A1133
37. M. Frisch, G. Trucks, H. B. Schlegel, G. Scuseria, M. Robb, J. Cheeseman, G. Scalmani, V. Barone, B. Mennucci and G. Petersson, Gaussian 09, Revision A.1, Gaussian, Inc., Wallingford, CT, 2009, vol. 200
38. C. Lee W. Yang R. G. Parr Phys. Rev. B: Condens. Matter 1988 37 785
39. A. D. Becke J. Chem. Phys. 1993 98 5648 5652
40. X. Cao M. Dolg J. Mol. Struct. (THEOCHEM) 2004 673 203 209
41. X. Cao M. Dolg J. Mol. Struct. (THEOCHEM) 2002 581 139 147
42. A. Klamt G. Schüürmann J. Chem. Soc., Perkin Trans. 1993 799 805
43. C. W. Abney S. Liu W. Lin J. Phys. Chem. A 2013 117 11558 11565
44. L. E. Roy N. J. Bridges L. R. Martin Dalton Trans. 2013 42 2636 2642
45. B. Niepotter R. Herbst-Irmer D. Kratzert P. P. Samuel K. C. Mondal H. W. Roesky P. Jerabek G. Frenking D. Stalke Angew. Chem., Int. Ed. 2014 53 2766 2770
46. T. Lu F. Chen J. Comput. Chem. 2012 33 580 592
47. P. Thakur J. L. Conca G. R. Choppin J. Solution Chem. 2012 41 599 615
48. R. J. Silva G. Bidoglio M. H. Rand P. B. Robouch H. Wanner I. Puigdomenech Chymist Com 1979 35 1 12
49. T. Kimura Y. Kato H. Takeishi G. R. Choppin J. Alloys Compd. 1998 271 719 722
50. C. Marie M. Miguirditchian D. Guillaumont A. Tosseng C. Berthon P. Guilbaud M. Duvail J. Bisson D. Guillaneux M. Pipelier D. Dubreuil Inorg. Chem. 2011 50 6557 6566
51. J. Narbutt A. Wodynski M. Pecul Dalton Trans. 2015 44 2657 2666
52. B. Ribár A. Kapor G. Argay A. Kálmán Acta Crystallogr., Sect. C: Cryst. Struct. Commun. 1986 42 1450 1452
53. C. Ekberg I. Dubois A. Fermvik T. Retegan G. Skarnemark M. G. B. W Solvent Extr. Ion Exch. 2007 25 603 617
54. R. Gerkin W. Reppart Acta Crystallogr., Sect. C: Cryst. Struct. Commun. 1984 40 781 786
55. F. David R. Revel B. Fourest S. Hubert J. Le Du C. Den Auwer C. Madic L. Morss V. Mikhalko V. Vokhmin Proc. Actinide XAS 1998 98 2 4
56. L. Petit L. Joubert P. Maldivi C. Adamo J. Am. Chem. Soc. 2006 128 2190 2191
57. P. L. Arnold Z. R. Turner N. Kaltsoyannis P. Pelekanaki R. M. Bellabarba R. P. Tooze Chem.-Eur. J. 2010 16 9623 9629
58. D. Guillaumont J. Mol. Struct. (THEOCHEM) 2006 771 105 110
59. P. Maldivi L. Petit C. Adamo V. Vetere C. R. Chim. 2007 10 888 896
60. J. Narbutt W. P. Oziminski Dalton Trans. 2012 41 14416 14424