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1
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0001518798
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and references cited therein
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Denti, G.1
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4
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Denti, G.; Campagna, S.; Sabatino, L.; Lerroni, S.; Ciano, M.; Balzani, V. Inorg. Chem. 1990, 29, 4750.
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5
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0040257744
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6
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0037119317
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(b) Schubert, U. S.; Eschbaumer, C. Angew. Chem., Int. Ed. 2002, 41, 2892.
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Schubert, U.S.1
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7
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3042544088
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(c) Polson, M. I. J.; Hanan, G. S.; Nicholas, J. T.; Hasenknopf, B.; Thouvenot R. Chem. Commun. 2004, 1314.
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Polson, M.I.J.1
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Hasenknopf, B.4
Thouvenot, R.5
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8
-
-
34247102632
-
-
(d) Weldon, S.; Hammarstrom, L.; Mukhtar, E.; Hage, R.; Gunneweg, E.; Haasnoot, J. G.; Reedijk, J.; Browne, W. R.; Guckian, A. L.; Vos, J. G. Inorg. Chem. 2004, 43, 4411.
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Weldon, S.1
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Gunneweg, E.5
Haasnoot, J.G.6
Reedijk, J.7
Browne, W.R.8
Guckian, A.L.9
Vos, J.G.10
-
9
-
-
34247095490
-
-
Catalytic olefin isomerization on Ru: Osawa, M.; Hoshino, M.; Wakatsuki, Y. Angew. Chem., Int. Ed. 2001, 40, 3472.
-
(a) Catalytic olefin isomerization on Ru: Osawa, M.; Hoshino, M.; Wakatsuki, Y. Angew. Chem., Int. Ed. 2001, 40, 3472.
-
-
-
-
10
-
-
0001762202
-
-
Stoichiometric oxidative addition on Pt: Yam, V. W.-W.; Lee, V. W.-M.; Cheung, K.-K. Organometallics 1997, 16, 2833.
-
(b) Stoichiometric oxidative addition on Pt: Yam, V. W.-W.; Lee, V. W.-M.; Cheung, K.-K. Organometallics 1997, 16, 2833.
-
-
-
-
11
-
-
33646158232
-
-
Catalytic photoreduction on Pt: Ozawa, H.; Haga, M.; Sakai, K. J. Am. Chem. Soc. 2006, 128, 4926.
-
(c) Catalytic photoreduction on Pt: Ozawa, H.; Haga, M.; Sakai, K. J. Am. Chem. Soc. 2006, 128, 4926.
-
-
-
-
12
-
-
33751390844
-
-
Catalytic photoreduction on Ni: Kimura, E.; Bu, X.; Shionoya, M.; Wada, S.; Maruyama, S. Inorg. Chem. 1992, 31, 4542.
-
(d) Catalytic photoreduction on Ni: Kimura, E.; Bu, X.; Shionoya, M.; Wada, S.; Maruyama, S. Inorg. Chem. 1992, 31, 4542.
-
-
-
-
13
-
-
33749005697
-
Catalytic hydrogen production on Pd
-
(e) Rau, S.; Schäfer, D.; Gleich, D.; Anderson, E.; Rudolph, M.; Friedrich, M.; Görls, H.; Henry, W.; Vos, J. G. Catalytic hydrogen production on Pd. Angew. Chem. Int. Ed. 2006, 45, 6215.
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Angew. Chem. Int. Ed
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Rau, S.1
Schäfer, D.2
Gleich, D.3
Anderson, E.4
Rudolph, M.5
Friedrich, M.6
Görls, H.7
Henry, W.8
Vos, J.G.9
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16
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28044455218
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Inagaki, A.; Edure, S.; Yatsuda, S.; Akita, M. Chem. Commun. 2005, 5468.
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(2005)
Chem. Commun
, pp. 5468
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-
Inagaki, A.1
Edure, S.2
Yatsuda, S.3
Akita, M.4
-
17
-
-
34247168999
-
-
4 was used as a catalyst.
-
4 was used as a catalyst.
-
-
-
-
18
-
-
0039974931
-
-
(a) Sahai, R.; Rillema, D. P.; Shaver, R.; Van Wallendael, S.; Jackman, D. C.; Boldaji, M. Inorg. Chem. 1989, 28, 1022.
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Sahai, R.1
Rillema, D.P.2
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Van Wallendael, S.4
Jackman, D.C.5
Boldaji, M.6
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19
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0039382661
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(b) Tapolsky, G.; Duesing, R.; Meyer, T. J. Inorg. Chem. 1990, 29, 2285.
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Tapolsky, G.1
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20
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0001312842
-
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(c) Treadway, J. A.; Loeb, B.; Lopez, R.; Anderson, P. A.; Keene, F. R.; Meyer, T. J. Inorg. Chem. 1996, 35, 2242.
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Treadway, J.A.1
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Lopez, R.3
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Keene, F.R.5
Meyer, T.J.6
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21
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0035926256
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(d) Riesgo, E.; Hu, Y.-Z.; Bouvier, F.; Thummerl, R. P. Inorg. Chem. 2001, 40, 2541.
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Riesgo, E.1
Hu, Y.-Z.2
Bouvier, F.3
Thummerl, R.P.4
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22
-
-
0010861035
-
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(e) Cola, D. L.; Balzani, V.; Barigelletti, F.; Flamigni, L.; Belser, P.; von Zelewsky, A.; Frank, M.; Vögtle, F. Inorg. Chem. 1993, 32, 5228.
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Cola, D.L.1
Balzani, V.2
Barigelletti, F.3
Flamigni, L.4
Belser, P.5
von Zelewsky, A.6
Frank, M.7
Vögtle, F.8
-
23
-
-
0033526308
-
-
(f) Schlicke, B.; Belser, P.; Cola, D. L.; Sabbioni, E.; Balzani, V. J. Am. Chem. Soc. 1999, 121, 4207.
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Schlicke, B.1
Belser, P.2
Cola, D.L.3
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Balzani, V.5
-
24
-
-
0034725543
-
-
Ji, A.; Huang, S. D.; Guadalupe, A. R. Inorg. Chim. Acta 2000, 305, 127.
-
(2000)
Inorg. Chim. Acta
, vol.305
, pp. 127
-
-
Ji, A.1
Huang, S.D.2
Guadalupe, A.R.3
-
25
-
-
34247147987
-
-
9 but no spectroscopic data were provided.
-
9 but no spectroscopic data were provided.
-
-
-
-
27
-
-
34247129036
-
-
4 anion as its counterion.
-
4 anion as its counterion.
-
-
-
-
28
-
-
0039413542
-
-
(a) Ferrari, M. B.; Fava, G. G.; Pelosi, G.; Predieri, G.; Vignali, C.; Denti, G.; Serroni, S. Inorg. Chim. Acta 1998, 275-276, 320.
-
(1998)
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, pp. 320
-
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Ferrari, M.B.1
Fava, G.G.2
Pelosi, G.3
Predieri, G.4
Vignali, C.5
Denti, G.6
Serroni, S.7
-
29
-
-
0343004213
-
-
(b) Fletcher, N. C.; Junk, P. C.; Reitsma, D. A.; Keene, F. R. J. Chem. Soc., Dalton Trans. 1998, 133.
-
(1998)
J. Chem. Soc., Dalton Trans
, pp. 133
-
-
Fletcher, N.C.1
Junk, P.C.2
Reitsma, D.A.3
Keene, F.R.4
-
30
-
-
34247114121
-
-
Plane I: Ru-N5-N6. Plane II: N5-C24-C25-N6. Plane III: N5-C24-N7. Plane IV: N6-C25-N8.
-
Plane I: Ru-N5-N6. Plane II: N5-C24-C25-N6. Plane III: N5-C24-N7. Plane IV: N6-C25-N8.
-
-
-
-
31
-
-
34247106156
-
-
2+.
-
2+.
-
-
-
-
32
-
-
34247147539
-
-
Redox data for 11 are not shown in the table because 11 is electrochemically too unstable to detect peaks of the dinuclear compound.
-
Redox data for 11 are not shown in the table because 11 is electrochemically too unstable to detect peaks of the dinuclear compound.
-
-
-
-
33
-
-
27544506369
-
-
Rillema, D. P.; Allen, G.; Meyer, T. J.; Conrad, D. Inorg. Chem. 1983, 22, 1617.
-
(1983)
Inorg. Chem
, vol.22
, pp. 1617
-
-
Rillema, D.P.1
Allen, G.2
Meyer, T.J.3
Conrad, D.4
-
34
-
-
0000225972
-
-
Milkevitch, M.; Brauns, E.; Brewer, K. J. Inorg. Chem. 1996, 35, 1737.
-
(1996)
Inorg. Chem
, vol.35
, pp. 1737
-
-
Milkevitch, M.1
Brauns, E.2
Brewer, K.J.3
-
35
-
-
34247097842
-
-
See the Supporting Information for the spectra
-
See the Supporting Information for the spectra.
-
-
-
-
36
-
-
18844456039
-
-
Ioachim, E.; Medlycott, E. A.; Hana, G. S.; Loiseau, F.; Ricevuto, V.; Campagna, S. Inorg. Chem. Commun. 2005, 8, 559.
-
(2005)
Inorg. Chem. Commun
, vol.8
, pp. 559
-
-
Ioachim, E.1
Medlycott, E.A.2
Hana, G.S.3
Loiseau, F.4
Ricevuto, V.5
Campagna, S.6
-
37
-
-
12044252836
-
-
Brookhart, M.; Wagner, M. I.; Balavoine, G. G. A.; Haddou, H. A. J. Am. Chem. Soc. 1994, 116, 3641.
-
(1994)
J. Am. Chem. Soc
, vol.116
, pp. 3641
-
-
Brookhart, M.1
Wagner, M.I.2
Balavoine, G.G.A.3
Haddou, H.A.4
-
39
-
-
34247101032
-
-
The average Mulliken charge values of the noncoordinated bipyrimidine N atoms, which have been calculated using the optimized structures obtained in the DFT calculation, were 0.518 (3) < 0.520 (1) < 0.533 (2) < 0.559 (4) < 0.561 (5). The data indicate the presence of a larger electronic repulsion among the free lone pairs for 4 and 5.
-
The average Mulliken charge values of the noncoordinated bipyrimidine N atoms, which have been calculated using the optimized structures obtained in the DFT calculation, were 0.518 (3) < 0.520 (1) < 0.533 (2) < 0.559 (4) < 0.561 (5). The data indicate the presence of a larger electronic repulsion among the free lone pairs for 4 and 5.
-
-
-
-
40
-
-
34247128161
-
-
Synthesized and measured by our group
-
Synthesized and measured by our group.
-
-
-
-
41
-
-
34247169877
-
-
Frisch, M. J, Trucks, G. W, Schlegel, H. B, Scuseria, G. E, Robb, M. A, Cheeseman, J. R, Montgomery, J. A, Vreven, J, Kudin, T. K. N, Burant, J. C, Millam, J. M, Iyengar, S. S, Tomasi, J, Barone, V, Mennucci, B, Cossi, M, Scalmani, G, Rega, N, Petersson, G. A, Nakatsuji, H, Hada, M, Ehara, M, Toyota, K, Fukuda, R, Hasegawa, J, Ishida, M, Nakajima, T, Honda, Y, Kitao, O, Nakai, H, Klene, M, Li, X, Knox, J. E, Hratchian, H. P, Cross, J. B, Adamo, C, Jaramillo, J, Gomperts, R, Stratmann, R. E, Yazyev, O, Austin, A. J, Cammi, R, Pomelli, C, Ochterski, J. W, Ayala, P. Y, Morokuma, K, Voth, G. A, Salvador, P, Dannenberg, J. J, Zakrzewski, V. G, Dapprich, S, Daniels, A. D, Strain, M. C, Farkas, O, Malick, D. K, Rabuck, A. D, Raghavachari, K, Foresman, J. B, Ortiz, J. V, Cui, Q, Baboul, A. G, Clifford, S, Cioslowski, J, Stefanov, B. B, Liu, G, Liashenko, A, Piskorz, P, Komaromi, I, Martin, R. L, Fox, D. J, Keith, T, Al-Laha
-
Frisch, M. J.; Trucks, G. W.; Schlegel, H. B.; Scuseria, G. E.; Robb, M. A.; Cheeseman, J. R.; Montgomery, J. A.; Vreven, J.; Kudin, T. K. N.; Burant, J. C.; Millam, J. M.; Iyengar, S. S.; Tomasi, J.; Barone, V.; Mennucci, B.; Cossi, M.; Scalmani, G.; Rega, N.; Petersson, G. A.; Nakatsuji, H.; Hada, M.; Ehara, M.; Toyota, K.; Fukuda, R.; Hasegawa, J.; Ishida, M.; Nakajima, T.; Honda, Y.; Kitao, O.; Nakai, H.; Klene, M.; Li, X.; Knox, J. E.; Hratchian, H. P.; Cross, J. B.; Adamo, C.; Jaramillo, J.; Gomperts, R.; Stratmann, R. E.; Yazyev, O.; Austin, A. J.; Cammi, R.; Pomelli, C.; Ochterski, J. W.; Ayala, P. Y.; Morokuma, K.; Voth, G. A.; Salvador, P.; Dannenberg, J. J.; Zakrzewski, V. G.; Dapprich, S.; Daniels, A. D.; Strain, M. C.; Farkas, O.; Malick, D. K.; Rabuck, A. D.; Raghavachari, K.; Foresman, J. B.; Ortiz, J. V.; Cui, Q.; Baboul, A. G.; Clifford, S.; Cioslowski, J.; Stefanov, B. B.; Liu, G.; Liashenko, A.; Piskorz, P.; Komaromi, I.; Martin, R. L.; Fox, D. J.; Keith, T.; Al-Laham, M. A.; Peng, C. Y.; Nanayakkara, A.; Challacombe, M.; Gill, P. M. W.; Johnson, B.; Chen, B. W.; Wong, M. W.; Gonzalez, C.; Pople, J. A. Gaussian 03, revision B.04; Gaussian, Inc.: Pittsburgh, PA, 2003.
-
-
-
-
42
-
-
34247144458
-
-
I au (atomic unit) = 27.21 eV.
-
I au (atomic unit) = 27.21 eV.
-
-
-
-
43
-
-
0001526490
-
-
Biner, M.; Bürgi, H.-B.; Ludi, A.; Röhr, C. J. Am. Chem. Soc. 1992, 114, 5197.
-
(1992)
J. Am. Chem. Soc
, vol.114
, pp. 5197
-
-
Biner, M.1
Bürgi, H.-B.2
Ludi, A.3
Röhr, C.4
-
44
-
-
34247099652
-
-
4 and a subsequent reaction with CO gas. All of the complexes have been fully characterized by NMR and IR spectroscopies. The synthetic procedure and NMR data are shown in the Supporting Information.
-
4 and a subsequent reaction with CO gas. All of the complexes have been fully characterized by NMR and IR spectroscopies. The synthetic procedure and NMR data are shown in the Supporting Information.
-
-
-
-
46
-
-
34247132096
-
-
The products were analyzed by GC-MS spectra
-
The products were analyzed by GC-MS spectra.
-
-
-
-
47
-
-
34247167021
-
-
X-ray diffraction studies clarified that substituents on the 5 and 5′ positions did not cause substantial sterical hinderance on both Ru and Pd centers.
-
X-ray diffraction studies clarified that substituents on the 5 and 5′ positions did not cause substantial sterical hinderance on both Ru and Pd centers.
-
-
-
-
48
-
-
34247140102
-
-
9]*}).
-
9]*}).
-
-
-
-
49
-
-
0037169106
-
-
Schwab, P. F. H.; Fleischer, F.; Michl, J. J. Org. Chem. 2002, 67, 443.
-
(2002)
J. Org. Chem
, vol.67
, pp. 443
-
-
Schwab, P.F.H.1
Fleischer, F.2
Michl, J.3
-
50
-
-
84987505493
-
-
Mukkala, V.-M.; Sund, C.; Kwiatkowski, M.; Pasanen, P.; Högberg, M.; Kankare, J.; Takalo, H. Helv. Chem. Acta 1992, 75, 1621.
-
(1992)
Helv. Chem. Acta
, vol.75
, pp. 1621
-
-
Mukkala, V.-M.1
Sund, C.2
Kwiatkowski, M.3
Pasanen, P.4
Högberg, M.5
Kankare, J.6
Takalo, H.7
-
51
-
-
0021143098
-
-
(a) Tiecco, M.; Testaferri, L.; Tingoli, M.; Chianelli, D.; Montanucci, M. Synthesis 1984, 736.
-
(1984)
Synthesis
, pp. 736
-
-
Tiecco, M.1
Testaferri, L.2
Tingoli, M.3
Chianelli, D.4
Montanucci, M.5
-
52
-
-
0041025238
-
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(b) Semelhack, M. F.; Helquist, P. M.; Jones, L. D. J. Am. Chem. Soc. 1971, 93, 5908.
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(1971)
J. Am. Chem. Soc
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, pp. 5908
-
-
Semelhack, M.F.1
Helquist, P.M.2
Jones, L.D.3
-
53
-
-
0020115658
-
-
Synthesis of 2-chloro-5-methylpyrimidine: Hannout, I. B.; Johnson, A. Dyes Pigm. 1982, 3, 173.
-
Synthesis of 2-chloro-5-methylpyrimidine: Hannout, I. B.; Johnson, A. Dyes Pigm. 1982, 3, 173.
-
-
-
-
58
-
-
0041825628
-
DIRDIF99: The DIRDIF-99 program system
-
University of Nijmegen: Nijmegen, The Netherlands
-
Beurskens, P. T.; Admiraal, G.; Beurskens, G.; Bosman, W. P.; de Gelder, R.; Israel, R.; Smits, J. M. M. DIRDIF99: The DIRDIF-99 program system; Technical Report of the Crystallography Laboratory; University of Nijmegen: Nijmegen, The Netherlands, 1999.
-
(1999)
Technical Report of the Crystallography Laboratory
-
-
Beurskens, P.T.1
Admiraal, G.2
Beurskens, G.3
Bosman, W.P.4
de Gelder, R.5
Israel, R.6
Smits, J.M.M.7
|