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43
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67849113379
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See the Experimental Section and the Supporting Information for further details
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See the Experimental Section and the Supporting Information for further details.
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44
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33947088034
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49
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84869554041
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amide linkage, see:
-
amide linkage, see:
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50
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0037575035
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2], U-N = 2.29(1) Å: Cramer, R. E.; Engelhardt, U.; Higa, K. T.; Gilje, J. W. Organometallics 1987, 6, 41-45.
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51
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84869557716
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2. U-N = 2.267(6) Å: Straub. T.; Frank. W.; Reiss, G. J.: Eisen, M. S J. Chem. Soc., Dalton Trans, 1996, 2541-2546.
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2. U-N = 2.267(6) Å: Straub. T.; Frank. W.; Reiss, G. J.: Eisen, M. S J. Chem. Soc., Dalton Trans, 1996, 2541-2546.
-
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52
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0345016345
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2, U-N = 2.278(4), 2.207(4) 2.212(4) Å: Stubbert, B. D.; Stern, C. L.: Marks, T. J. Organometallics 2003, 22, 4836-4838.
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11344284526
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55
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84869583360
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amide linkage, see:
-
amide linkage, see:
-
-
-
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56
-
-
33845560995
-
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ave = 2.32(2) Å: Turner. H. W.; Andersen, R. A.; Zalkin. A.: Templeton, D. H. Inorg. Chem, 1979,18, 1221-1224.
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ave = 2.32(2) Å: Turner. H. W.; Andersen, R. A.; Zalkin. A.: Templeton, D. H. Inorg. Chem, 1979,18, 1221-1224.
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-
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57
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33845283427
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ave = 2.46(1) Å: Sternal, R. S.; Sabat, M.; Marks, T. J. J. Am. Chem. Soc, 1987, 109, 7920-7921.
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ave = 2.46(1) Å: Sternal, R. S.; Sabat, M.; Marks, T. J. J. Am. Chem. Soc, 1987, 109, 7920-7921.
-
-
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58
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0008701405
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ave = 2.34(1) Å: Gilbert. T. M.; Ryan, R. R.: Sattelberger, A. P. Organometallics 1988, 7, 2514-2518.
-
ave = 2.34(1) Å: Gilbert. T. M.; Ryan, R. R.: Sattelberger, A. P. Organometallics 1988, 7, 2514-2518.
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60
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33748224052
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63
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84869561800
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44 The additional possibilities provided by f-orbital interactions in bent-metallocene uranium(IV) bis(pyrazolate) and bis(acyl) complexes were noted by Tatsumi and Nakamura; see:
-
44 The additional possibilities provided by f-orbital interactions in bent-metallocene uranium(IV) bis(pyrazolate) and bis(acyl) complexes were noted by Tatsumi and Nakamura; see:
-
-
-
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64
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0000220429
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(a) Tatsumi, K.; Nakamura, A.; Hofmann, P.; Hoffmann, R.; Moloy. K. G.; Marks, T. J. J. Am. Chem. Soc, 1986, 108, 4467-4476.
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66
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84869583351
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-
ave ≈ 0°) that allows for a better aim separation, thereby facilitating the description of the bonding scheme. However, we also show that the twist between the hydrazonato ligands observed in isomers M-IIa and M-IIc (M = Th, U, Zr) does not affect the overall metal-ligand interactions in these complexes.
-
ave ≈ 0°) that allows for a better aim separation, thereby facilitating the description of the bonding scheme. However, we also show that the twist between the hydrazonato ligands observed in isomers M-IIa and M-IIc (M = Th, U, Zr) does not affect the overall metal-ligand interactions in these complexes.
-
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67
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84962433687
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Yang. P.; Warnke, I.: Martin, R. L.: Hav. P. J. Oreanometallics 2008, 27, 1384-1392.
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67849091646
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Glendening, E. D.; Badenhoop, F. K.; Reed, A. E.; Carpenter, J. E.; Bohmann, J. A.; Morales, C. M.; Weinhold, F. NBO.5.0; Theoretical Chemistry Institute, Univeristy of Wisconsin: Madison, WI, 2001.
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Glendening, E. D.; Badenhoop, F. K.; Reed, A. E.; Carpenter, J. E.; Bohmann, J. A.; Morales, C. M.; Weinhold, F. NBO.5.0; Theoretical Chemistry Institute, Univeristy of Wisconsin: Madison, WI, 2001.
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-
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69
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84869561801
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2 σ bonds (with 84.7% d character)
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2 σ bonds (with 84.7% d character)
-
-
-
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70
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22444445896
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Clark, A. E.; Martin, R. L.; Hay, P. J.; Green, J. C; Jantunen, K. C; Kiplinger, J. L. J. Phys. Chem. A 2005, 109, 5481-5491.
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71
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84869583353
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In the experimental systems, the π(an-N) orbitals are found to be slightly below the π(An-c5Me5) MOs. This small difference with the model compounds An-IIb is due to the presence of the phenyl rings in the real systems that stabilize die nitrogen π lone pairs
-
5) MOs. This small difference with the model compounds An-IIb is due to the presence of the phenyl rings in the real systems that stabilize die nitrogen π lone pairs.
-
-
-
-
72
-
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67849111079
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-
We have limited our investigation to the a isomers, as the same profiles could be reasonably admitted for isomers b and c. This has been verified previously in the case of Zr see ref 43
-
We have limited our investigation to the a isomers, as the same profiles could be reasonably admitted for isomers b and c. This has been verified previously in the case of Zr (see ref 43)
-
-
-
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74
-
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84869557713
-
-
2 toward diazoalkanes can be attributed to the Zr-P bonds, which are weaker and more polarizable than Zr-C bonds.
-
2 toward diazoalkanes can be attributed to the Zr-P bonds, which are weaker and more polarizable than Zr-C bonds.
-
-
-
-
76
-
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67849087930
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-
See the Supporting Information for further details
-
See the Supporting Information for further details.
-
-
-
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77
-
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84869561794
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5 ligand. Attempts to further optimize diis saddle point were unsuccessful.
-
5 ligand. Attempts to further optimize diis saddle point were unsuccessful.
-
-
-
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78
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67849113377
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The higher reactivity of uranium compared with thorium has previously been observed: see refs 61 and 62 for examples
-
The higher reactivity of uranium compared with thorium has previously been observed: see refs 61 and 62 for examples.
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-
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79
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33845556470
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