10 of 11
HAN ET AL.
4
H), 7.62 (d, 4H, J = 8.4 Hz), 7.35 (d, 4H, J = 8.4 Hz), 2.76
Shinde, R. Banerjee, S. Kurungot, Chem. Mater. 2016, 28,
13
4375. c)J. Q. Zhang, Y. S. Peng, W. G. Leng, Y. A. Gao, F. F.
(
(
q, 4H, J = 7.6 Hz), 1.34 (t, 6H, J = 7.6 Hz) ppm. C NMR
100 MHz, CDCl ) δ 143.4, 139.8, 138.2, 128.4, 127.3,
Xu, J. L. Chai, Chin. J. Catal. 2016, 37, 468.
3
[
14] a)J. P. Wan, S. Cao, C. F. Hu, C. P. Wen, Asian J. Org. Chem.
1
26.9, 28.5, 15.6 ppm.
2
018, 7, 328. b)M. Zhang, Q. Y. Fu, G. Gao, H. Y. He, Y. Zhang,
Y. S. Wu, Z. H. Zhang, ACS Sustainable Chem. Eng. 2017, 5,
175. c)L. Wei, X. W. Chen, Y. Y. Liu, J. P. Wan, Chin. J. Org.
[
1,1′:4′,1”‐Terphenyl]‐4,4″‐dicarbonitrile (6c)
6
White solid; m.p. 296–297 °C; IR (KBr): 3033, 2215, 1625,
Chem. 2016, 36, 954. d)G. Gao, Y. Han, Z. H. Zhang,
ChemistrySelect 2017, 2, 11561. e)G. Gao, M.‐N. Chen, L.‐P.
Mo, Z.‐H. Zhang, Phosphorus, Sulfur Silicon Relat. Elem. 2019,
194, 528.
1
1
500, 832; H NMR (400 MHz, CDCl ) δ 7.77 (t, 4H,
3
J = 7.6 Hz), 7.70–7.64 (m, 6H), 7.49 (d, 2H, J = 8.8 Hz)
ppm. C NMR (100 MHz, CDCl ) δ 144.5, 138.1, 132.7,
13
3
1
32.3, 128.8, 127.6, 111.4 ppm.
[
[
[
15] a)A. Biffis, P. Centomo, A. Del Zotto, M. Zeccal, Chem. Rev.
2
018, 118, 2249. b)F. S. Han, Chem. Soc. Rev. 2013, 42, 5270.
16] M. Adib, R. Karimi‐Nami, H. Veisi, New J. Chem. 2016, 40,
945.
ACKNOWLEDGEMENTS
4
Financial support from the National Natural Science
Foundation of China (No. 21272053) and the Science
Technology Research Foundation of Hebei Normal
University (No. L2018Z06) is gratefully acknowledged.
17] a)K. Bahrami, S. N. Kamrani, Appl. Organomet. Chem. 2018,
32, e4102. b)B. Heidari, M. M. Heravi, M. R. Nabid, R. Sedghi,
S. E. Hooshmand, Appl. Organomet. Chem. 2019, 33, e4632.
[18] a)N. Y. Baran, T. Baran, A. Mentes, Appl. Catal. A: Gen. 2017,
31, 36. b)T. Baran, I. Sargin, A. Mentes, M. Kaya, Appl. Catal.
5
Gen. 2016, 523, 12.
AUTHOR CONTRIBUTIONS
[
19] a)T. Baran, N. Y. Baran, A. Mentes, Appl. Organomet. Chem.
2018, 32, e4075. b)T. Baran, N. Y. Baran, A. Mentes, Appl.
Organomet. Chem. 2018, 32, e4076. c)T. Baran, A. Inanan,
Mentes, Carbohydr. Polym. 2016, 145, 20. d)T. Baran, J. Colloid
Interface Sci. 2017, 496, 446. e)T. Baran, E. Aciksoz, A. Mentes,
J. Mol. Catal. A: Chem. 2015, 407, 47. f)T. Baran, I. Sargin, M.
Kaya, A. Mentes, J. Mol. Catal. A: Chem. 2016, 420, 216. g)T.
Baran, J. Mol. Struct. 2017, 1141, 535. h)T. Baran, A. Mentes,
J. Mol. Struct. 2016, 1122, 111. i)T. Baran, A. Mentes, J. Mol.
Struct. 2017, 1134, 591.
Yi Han and Jia‐Qi Di contributed equally to this work.
ORCID
REFERENCES
[
[
1] Z. H. Xiang, D. P. Cao, L. M. Dai, Polym. Chem. 2015, 6, 1896.
[
20] T. Baran, Carbohydr. Polym. 2018, 195, 45.
2] W. Chen, L. Huang, X. F. Yi, A. M. Zheng, Phys. Chem. Chem.
Phys. 2018, 20, 6487.
[21] T. Baran, I. Sargin, M. Kaya, A. Mentes, Carbohydr. Polym.
2
016, 152, 181.
22] a)T. Baran, N. Y. Baran, A. Mentes, Int. J. Biol. Macromol. 2018,
15, 249. b)T. Baran, Ultrason. Sonochem. 2018, 45, 231.
[
[
[
[
[
[
[
3] H. R. Wang, W. W. Zhu, J. J. Liu, Z. L. Dong, Z. Liu, ACS Appl.
Mater. Interfaces 2018, 10, 14475.
[
[
[
1
4] S. Bhowmik, R. G. Jadhav, A. K. Das, J. Phys. Chem. C 2018,
23] T. Baran, I. Sargin, M. Kaya, A. Mentes, T. Ceter, J. Colloid
Interface Sci. 2017, 486, 194.
1
22, 274.
5] Z. H. Xiang, Q. B. Dai, J. F. Chen, L. M. Dai, Adv. Mater. 2016,
8, 6253.
6] R. Gomes, P. Bhanja, A. Bhaumik, Chem. Commun. 2015, 51,
0050.
24] a)T. Baran, N. Y. Baran, A. Mentes, J. Mol. Struct. 2018, 1160,
2
154. b)N. Y. Baran, T. Baran, A. Mentes, M. Karakisla, M.
Sacak, J. Organomet. Chem. 2018, 866, 87.
1
[
[
25] M. Nasrollahzadeh, S. M. Sajadi, J. Colloid Interface Sci. 2016,
7] R. Khatioda, D. Talukdar, B. Saikia, K. K. Bania, B. Sarma, Cat.
Sci. Technol. 2017, 7, 3143.
465, 121.
26] A. Mahanta, P. K. Raul, S. Saikia, U. Bora, A. J. Thakur, Appl.
Organomet. Chem. 2018, 32, e4192.
8] R. Khatioda, D. Pathak, B. Sarma, ChemistrySelect 2018, 3,
6
309.
9] V. Sadhasivam, M. Mariyappan, A. Siva, ChemistrySelect 2018,
, 13442.
[27] A. Tadjarodi, M. Dehghani, M. Imani, Appl. Organomet. Chem.
2018, 32, e4594.
3
[
[
[
[
10] V. Sadhasivam, R. Balasaravanan, C. Chithiraikumar, A. Siva,
[28] B. Van Vaerenbergh, K. De Vlieger, K. Claeys, G. Vanhoutte, J.
ChemCatChem 2018, 10, 3833.
De Clercq, P. Vermeir, A. Verberckmoes, Appl. Catal. A: Gen.
2018, 550, 236.
11] P. Y. Ju, S. J. Wu, Q. Su, X. D. Li, Z. Q. Liu, G. H. Li, Q. L. Wu,
J. Mater. Chem. A 2019, 7, 2660.
[29] G. J. Lichtenegger, M. Maier, M. Hackl, J. G. Khinast, W.
Gossler, T. Griesser, V. S. P. Kumar, H. Gruber‐Woelfler, P.
A. Deshpande, J. Mol. Catal. A: Chem. 2017, 426, 39.
12] Y. Sim, Y. X. Shi, R. Ganguly, Y. X. Li, F. Garcia, Chem. Eur. J.
2
017, 23, 11279.
13] a)E. M. Johnson, R. Haiges, S. C. Marinescu, ACS Appl. Mater.
Interfaces 2018, 10, 37919. b)H. B. Aiyappa, J. Thote, D. B.
[30] C. Schmoger, T. Szuppa, A. Tied, F. Schneider, A. Stolle, B.
Ondruschka, ChemSusChem 2008, 1, 339.