-
12
-
-
0032529961
-
-
I.D. Figueroa, M. El Baraka, E. Quiñones, O. Rosario, and M. Deumié Anal. Chem. 70 1998 3974
-
(1998)
Anal. Chem.
, vol.70
, pp. 3974
-
-
Figueroa, I.D.1
El Baraka, M.2
Quiñones, E.3
Rosario, O.4
Deumié, M.5
-
17
-
-
0242337186
-
-
A.P. de Silva, H.Q.N. Gunaratne, K.R. Jayasekera, S. O'Callaghan, and K.R.A.S. Sandanayake Chem. Lett. 1995 123
-
(1995)
Chem. Lett.
, pp. 123
-
-
De Silva, A.P.1
Gunaratne, H.Q.N.2
Jayasekera, K.R.3
O'Callaghan, S.4
Sandanayake, K.R.A.S.5
-
18
-
-
33748224820
-
-
N. Sabbatini, M. Guardigli, F. Bolletta, I. Manet, and R. Ziessel Angew. Chem., Int. Ed. Engl. 33 1994 1501
-
(1994)
Angew. Chem., Int. Ed. Engl.
, vol.33
, pp. 1501
-
-
Sabbatini, N.1
Guardigli, M.2
Bolletta, F.3
Manet, I.4
Ziessel, R.5
-
19
-
-
0036500524
-
-
Reversible D-A reactions have been utilized for the studies of macromolecular architectures, thermally cleavable/reassembling dendrons and dendrimers, and NLO functional materials: X. Chen, M. Dam, K. Ono, A. Mal, H. Shen, S.R. Nutt, K. Sheran, and F. Wudl Science 295 2002 1698
-
(2002)
Science
, vol.295
, pp. 1698
-
-
Chen, X.1
Dam, M.2
Ono, K.3
Mal, A.4
Shen, H.5
Nutt, S.R.6
Sheran, K.7
Wudl, F.8
-
20
-
-
1342283744
-
-
M. Haller, J. Luo, H. Li, T.-D. Kim, Y. Liao, B.H. Robinson, L.R. Dalton, and A.K.-Y. Jen Macromolecules 37 2004 688
-
(2004)
Macromolecules
, vol.37
, pp. 688
-
-
Haller, M.1
Luo, J.2
Li, H.3
Kim, T.-D.4
Liao, Y.5
Robinson, B.H.6
Dalton, L.R.7
Jen, A.K.-Y.8
-
21
-
-
0142169428
-
-
J. Luo, M. Haller, H. Li, T.-D. Kim, and A.K.-Y. Jen Adv. Mater. 15 2003 1635
-
(2003)
Adv. Mater.
, vol.15
, pp. 1635
-
-
Luo, J.1
Haller, M.2
Li, H.3
Kim, T.-D.4
Jen, A.K.-Y.5
-
26
-
-
20344380287
-
-
note
-
Reduction potential of 4-methoxyarylmaleimide (5, see Supporting data) was measured with the differential pulse voltammetry to be -1.03 V in DMF (potential are reported by reference to SCE), no reduction wave was not detected for the D-A adduct of 5 with furan (compound 6, see Supplementary data) under identical conditions
-
-
-
-
27
-
-
4644317800
-
-
X. Zhang, Z.-C. Li, K.-B. Li, F.-S. Du, and F.-M. Li J. Am. Chem. Soc. 126 2004 12200
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 12200
-
-
Zhang, X.1
Li, Z.-C.2
Li, K.-B.3
Du, F.-S.4
Li, F.-M.5
-
29
-
-
0002475372
-
-
1H NMR spectrum, the endo and exo isomers of 4 exist in 1:1 ratio, and the sample was not separated and used for reaction
-
(1991)
Chin. J. Pharm.
, vol.22
, pp. 8
-
-
Liu, Y.1
Ling, Y.-Z.2
-
30
-
-
20344392757
-
-
note
-
Characterization data of endo and exo 2 are provided in Supporting data
-
-
-
-
32
-
-
20344393234
-
-
note
-
Characterization data of dyad 1 are provided in Supporting data
-
-
-
-
33
-
-
20344389631
-
-
note
-
The quantum yields presented in this letter were calculated by reference to 9,10-diphenylanthracene; the excitation wavelength is 370 nm
-
-
-
-
34
-
-
20344406579
-
-
note
-
For each fluorescence measurement, a 2 ml solution of endo 2 in DMF was prepared and carefully sealed. The solution was kept in a constant temperature trough for 10 min (the temperature was controlled with a thermocouple). After that, the fluorescence spectrum of endo 2 was measured using a Hitachi-4500 spectrometer in a quartz cell. The fluorescence spectra of exo 2 were measured similarly
-
-
-
-
35
-
-
20344408706
-
-
note
-
1H NMR data
-
-
-
|