Crystallography Open Database
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Searching journal of publication like 'New J. Chem.' volume of publication is 41
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 7055946 | CIF | C18 H20 Cl2 N4 O6 Zn | C 1 2/c 1 | 32.755; 10.5714; 13.5063 90; 110.305; 90 | 4386.2 | Bolotin, Dmitrii S.; Il'in, Mikhail V.; Novikov, Alexander S.; Bokach, Nadezhda A.; Suslonov, Vitalii V.; Kukushkin, Vadim Yu. Trinuclear (aminonitrone)ZnII complexes as key intermediates in zinc(ii)-mediated generation of 1,2,4-oxadiazoles from amidoximes and nitriles New J. Chem., 2017, 41, 1940 |
| 7055947 | CIF | C24 H32 Cl2 F6 N8 O9 S2 Zn | P -1 | 8.7052; 12.9506; 17.0474 108.023; 90.814; 95.484 | 1817.27 | Bolotin, Dmitrii S.; Il'in, Mikhail V.; Novikov, Alexander S.; Bokach, Nadezhda A.; Suslonov, Vitalii V.; Kukushkin, Vadim Yu. Trinuclear (aminonitrone)ZnII complexes as key intermediates in zinc(ii)-mediated generation of 1,2,4-oxadiazoles from amidoximes and nitriles New J. Chem., 2017, 41, 1940 |
| 7055948 | CIF | C14 H28 F6 N8 O8 S2 Zn | P n a 21 | 16.8415; 20.4363; 16.1946 90; 90; 90 | 5573.82 | Bolotin, Dmitrii S.; Il'in, Mikhail V.; Novikov, Alexander S.; Bokach, Nadezhda A.; Suslonov, Vitalii V.; Kukushkin, Vadim Yu. Trinuclear (aminonitrone)ZnII complexes as key intermediates in zinc(ii)-mediated generation of 1,2,4-oxadiazoles from amidoximes and nitriles New J. Chem., 2017, 41, 1940 |
| 7055949 | CIF | C9 H19 F3 N4 O4 S | P 1 21/c 1 | 11.8893; 18.4419; 7.2746 90; 103.177; 90 | 1553 | Bolotin, Dmitrii S.; Il'in, Mikhail V.; Novikov, Alexander S.; Bokach, Nadezhda A.; Suslonov, Vitalii V.; Kukushkin, Vadim Yu. Trinuclear (aminonitrone)ZnII complexes as key intermediates in zinc(ii)-mediated generation of 1,2,4-oxadiazoles from amidoximes and nitriles New J. Chem., 2017, 41, 1940 |
| 7055950 | CIF | C11 H15 F3 N4 O4 S | C 1 2/c 1 | 16.7859; 8.3599; 21.9907 90; 90.745; 90 | 3085.66 | Bolotin, Dmitrii S.; Il'in, Mikhail V.; Novikov, Alexander S.; Bokach, Nadezhda A.; Suslonov, Vitalii V.; Kukushkin, Vadim Yu. Trinuclear (aminonitrone)ZnII complexes as key intermediates in zinc(ii)-mediated generation of 1,2,4-oxadiazoles from amidoximes and nitriles New J. Chem., 2017, 41, 1940 |
| 7055951 | CIF | C18 H22 N4 O6 Zn | P 1 21/c 1 | 11.955; 17.5685; 15.782 90; 139.46; 90 | 2154.5 | Bolotin, Dmitrii S.; Il'in, Mikhail V.; Novikov, Alexander S.; Bokach, Nadezhda A.; Suslonov, Vitalii V.; Kukushkin, Vadim Yu. Trinuclear (aminonitrone)ZnII complexes as key intermediates in zinc(ii)-mediated generation of 1,2,4-oxadiazoles from amidoximes and nitriles New J. Chem., 2017, 41, 1940 |
| 7055952 | CIF | C36 H50 F12 N8 O26 S4 Zn3 | P -1 | 9.9101; 17.0394; 18.2463 74.733; 89.846; 82.485 | 2945.2 | Bolotin, Dmitrii S.; Il'in, Mikhail V.; Novikov, Alexander S.; Bokach, Nadezhda A.; Suslonov, Vitalii V.; Kukushkin, Vadim Yu. Trinuclear (aminonitrone)ZnII complexes as key intermediates in zinc(ii)-mediated generation of 1,2,4-oxadiazoles from amidoximes and nitriles New J. Chem., 2017, 41, 1940 |
| 7055953 | CIF | C18 H15 Cu N5 O8 | P 1 21/n 1 | 10.0651; 12.301; 16.281 90; 93.537; 90 | 2011.9 | Hu, Kun; Li, Feiyan; Zhang, Zhong; Liang, Fupei Synthesis of two potential anticancer copper(ii) complex drugs: their crystal structure, human serum albumin/DNA binding and anticancer mechanism New J. Chem., 2017, 41, 2062 |
| 7055954 | CIF | C18 H16 Cu N4 O5 | P 1 21/n 1 | 7.854; 10.712; 21.44 90; 97.575; 90 | 1788 | Hu, Kun; Li, Feiyan; Zhang, Zhong; Liang, Fupei Synthesis of two potential anticancer copper(ii) complex drugs: their crystal structure, human serum albumin/DNA binding and anticancer mechanism New J. Chem., 2017, 41, 2062 |
| 7055955 | CIF | C14 H37 Cu2 N6 O12 | P -1 | 11.3213; 11.3226; 22.7583 76.496; 84.96; 60.21 | 2460.4 | Sama, Farasha; Ansari, Istikhar A.; Raizada, Mukul; Ahmad, Musheer; Nagaraja, C. M.; Shahid, M.; Kumar, Abhinav; Khan, Kulsum; Siddiqi, Zafar A. Design, structures and study of non-covalent interactions of mono-, di-, and tetranuclear complexes of a bifurcated quadridentate tripod ligand, N-(aminopropyl)-diethanolamine New J. Chem., 2017, 41, 1959 |
| 7055956 | CIF | C9 H19 N4 Ni O2.5 S2 | P 1 21/c 1 | 16.48; 13.6513; 14.4161 90; 115.185; 90 | 2934.9 | Sama, Farasha; Ansari, Istikhar A.; Raizada, Mukul; Ahmad, Musheer; Nagaraja, C. M.; Shahid, M.; Kumar, Abhinav; Khan, Kulsum; Siddiqi, Zafar A. Design, structures and study of non-covalent interactions of mono-, di-, and tetranuclear complexes of a bifurcated quadridentate tripod ligand, N-(aminopropyl)-diethanolamine New J. Chem., 2017, 41, 1959 |
| 7055957 | CIF | C11 H23 N3 O5 S Zn2 | P -1 | 8.6719; 10.0649; 11.3026 89.096; 79.802; 65.87 | 884.33 | Sama, Farasha; Ansari, Istikhar A.; Raizada, Mukul; Ahmad, Musheer; Nagaraja, C. M.; Shahid, M.; Kumar, Abhinav; Khan, Kulsum; Siddiqi, Zafar A. Design, structures and study of non-covalent interactions of mono-, di-, and tetranuclear complexes of a bifurcated quadridentate tripod ligand, N-(aminopropyl)-diethanolamine New J. Chem., 2017, 41, 1959 |
| 7055958 | CIF | C14 H39 Co2 N7 O16 | P b c a | 15.2182; 14.6493; 23.9361 90; 90; 90 | 5336.22 | Sama, Farasha; Ansari, Istikhar A.; Raizada, Mukul; Ahmad, Musheer; Nagaraja, C. M.; Shahid, M.; Kumar, Abhinav; Khan, Kulsum; Siddiqi, Zafar A. Design, structures and study of non-covalent interactions of mono-, di-, and tetranuclear complexes of a bifurcated quadridentate tripod ligand, N-(aminopropyl)-diethanolamine New J. Chem., 2017, 41, 1959 |
| 7055959 | CIF | C16 H36 Co2 N7 O8.5 S2 | P -1 | 8.795; 12.132; 14.2294 103.245; 96.276; 111.032 | 1348.4 | Sama, Farasha; Ansari, Istikhar A.; Raizada, Mukul; Ahmad, Musheer; Nagaraja, C. M.; Shahid, M.; Kumar, Abhinav; Khan, Kulsum; Siddiqi, Zafar A. Design, structures and study of non-covalent interactions of mono-, di-, and tetranuclear complexes of a bifurcated quadridentate tripod ligand, N-(aminopropyl)-diethanolamine New J. Chem., 2017, 41, 1959 |
| 7055960 | CIF | C12 H13 Ag0.87 N2 Na0.13 O6 S | P b c a | 7.0886; 11.8816; 32.9373 90; 90; 90 | 2774.1 | Dodds, Christopher A.; Hobday, Claire L.; Kennedy, Alan R.; McKellar, Scott C.; Smillie, Katy; Walls, Aiden Ag(i) bipyridyl coordination polymers containing functional anions New J. Chem., 2017, 41, 1574 |
| 7055961 | CIF | C12 H9 Ag N2 O4 S | P 1 21/n 1 | 8.3838; 9.7225; 14.934 90; 94.352; 90 | 1213.78 | Dodds, Christopher A.; Hobday, Claire L.; Kennedy, Alan R.; McKellar, Scott C.; Smillie, Katy; Walls, Aiden Ag(i) bipyridyl coordination polymers containing functional anions New J. Chem., 2017, 41, 1574 |
| 7055962 | CIF | C42 H35 Ag Cl4 N6 O4 | P -1 | 13.3362; 16.5265; 20.1331 66.518; 75.035; 89.409 | 3910.3 | Dodds, Christopher A.; Hobday, Claire L.; Kennedy, Alan R.; McKellar, Scott C.; Smillie, Katy; Walls, Aiden Ag(i) bipyridyl coordination polymers containing functional anions New J. Chem., 2017, 41, 1574 |
| 7055963 | CIF | C19 H15 Ag N4 O3 | P 1 21/n 1 | 8.12; 9.7869; 21.6736 90; 97.433; 90 | 1707.9 | Dodds, Christopher A.; Hobday, Claire L.; Kennedy, Alan R.; McKellar, Scott C.; Smillie, Katy; Walls, Aiden Ag(i) bipyridyl coordination polymers containing functional anions New J. Chem., 2017, 41, 1574 |
| 7055964 | CIF | C27.5 H25.5 Ag Cl0.99 N6.51 O4 S | P -1 | 11.1773; 11.6004; 12.188 81.629; 73.899; 70.341 | 1427.43 | Dodds, Christopher A.; Hobday, Claire L.; Kennedy, Alan R.; McKellar, Scott C.; Smillie, Katy; Walls, Aiden Ag(i) bipyridyl coordination polymers containing functional anions New J. Chem., 2017, 41, 1574 |
| 7055965 | CIF | C25 H19 Ag N6 O3 | P -1 | 7.1538; 12.9587; 13.2859 67.835; 82.451; 76.606 | 1108.3 | Dodds, Christopher A.; Hobday, Claire L.; Kennedy, Alan R.; McKellar, Scott C.; Smillie, Katy; Walls, Aiden Ag(i) bipyridyl coordination polymers containing functional anions New J. Chem., 2017, 41, 1574 |
| 7055966 | CIF | C26.64 H21.14 Ag Cl2.72 N5.14 O2 | P -1 | 6.8116; 13.5608; 28.7557 95.438; 95.833; 96.716 | 2608.96 | Dodds, Christopher A.; Hobday, Claire L.; Kennedy, Alan R.; McKellar, Scott C.; Smillie, Katy; Walls, Aiden Ag(i) bipyridyl coordination polymers containing functional anions New J. Chem., 2017, 41, 1574 |
| 7055967 | CIF | C12 H13 N2 Na O6 S | P b c a | 7.1227; 11.9399; 32.5608 90; 90; 90 | 2769.11 | Dodds, Christopher A.; Hobday, Claire L.; Kennedy, Alan R.; McKellar, Scott C.; Smillie, Katy; Walls, Aiden Ag(i) bipyridyl coordination polymers containing functional anions New J. Chem., 2017, 41, 1574 |
| 7055968 | CIF | C19 H15 Ag N4 O3 | P -1 | 10.0038; 13.377; 14.2918 71.64; 78.179; 78.327 | 1757.03 | Dodds, Christopher A.; Hobday, Claire L.; Kennedy, Alan R.; McKellar, Scott C.; Smillie, Katy; Walls, Aiden Ag(i) bipyridyl coordination polymers containing functional anions New J. Chem., 2017, 41, 1574 |
| 7055969 | CIF | C28 H26 Ag N7 O4 S | P -1 | 7.1356; 14.0212; 15.4526 109.697; 101.688; 98.473 | 1385.86 | Dodds, Christopher A.; Hobday, Claire L.; Kennedy, Alan R.; McKellar, Scott C.; Smillie, Katy; Walls, Aiden Ag(i) bipyridyl coordination polymers containing functional anions New J. Chem., 2017, 41, 1574 |
| 7055970 | CIF | C6 H8 N10 O10 | P -1 | 6.7135; 6.7702; 8.1378 80.267; 76.307; 74.335 | 343.82 | Tian, Jiawei; Xiong, Hualin; Lin, Qiuhan; Cheng, Guangbin; Yang, Hongwei Energetic compounds featuring bi(1,3,4-oxadiazole): a new family of insensitive energetic materials New J. Chem., 2017, 41, 1918 |
| 7055971 | CIF | C8 H16 N18 O10 | P b c n | 24.125; 8.0141; 10.8158 90; 90; 90 | 2091.1 | Tian, Jiawei; Xiong, Hualin; Lin, Qiuhan; Cheng, Guangbin; Yang, Hongwei Energetic compounds featuring bi(1,3,4-oxadiazole): a new family of insensitive energetic materials New J. Chem., 2017, 41, 1918 |
| 7055972 | CIF | C10 H8 N14 O10 | P -1 | 7.6518; 7.7243; 9.0083 95.49; 106.941; 117.039 | 437.09 | Tian, Jiawei; Xiong, Hualin; Lin, Qiuhan; Cheng, Guangbin; Yang, Hongwei Energetic compounds featuring bi(1,3,4-oxadiazole): a new family of insensitive energetic materials New J. Chem., 2017, 41, 1918 |
| 7055973 | CIF | C14 H22 Mo4 N6 O17 Zn | P -1 | 9.8239; 11.5351; 12.3691 91.417; 102.778; 96.494 | 1356.4 | Wang, Xiu-Li; Zhang, Shan; Wang, Xiang; Zhang, Hui-Xiu; Xu, Na; Li, Tian-Jiao Three β-octamolybdate-based supramolecular hybrids constructed from a bis-imidazolyl-bis-amide ligand: fast and selective adsorption activities of organic dyes New J. Chem., 2017, 41, 2178 |
| 7055974 | CIF | C14 H22 Co Mo4 N6 O17 | P -1 | 9.8153; 11.6524; 12.3272 90.58; 103.212; 97.069 | 1361.06 | Wang, Xiu-Li; Zhang, Shan; Wang, Xiang; Zhang, Hui-Xiu; Xu, Na; Li, Tian-Jiao Three β-octamolybdate-based supramolecular hybrids constructed from a bis-imidazolyl-bis-amide ligand: fast and selective adsorption activities of organic dyes New J. Chem., 2017, 41, 2178 |
| 7055975 | CIF | C28 H46 Cu2 Mo8 N12 O35 | P 1 21/c 1 | 10.4739; 24.6254; 21.3617 90; 90.085; 90 | 5509.7 | Wang, Xiu-Li; Zhang, Shan; Wang, Xiang; Zhang, Hui-Xiu; Xu, Na; Li, Tian-Jiao Three β-octamolybdate-based supramolecular hybrids constructed from a bis-imidazolyl-bis-amide ligand: fast and selective adsorption activities of organic dyes New J. Chem., 2017, 41, 2178 |
| 7055976 | CIF | C10 H16 Br2 Cl3 Fe N4 O | P b c n | 23.654; 8.738; 8.595 90; 90; 90 | 1776.5 | Govor, Evgen V.; Sanakis, Yiannis; Raptis, Raphael G. Synthesis of pyrazole (hemi)aminals via the cleavage of saturated aliphatic ether C‒O bonds in the presence of ferric halides New J. Chem., 2017, 41, 2220 |
| 7055977 | CIF | C24 H28 Br8 Cl16 Fe2 N8 O | I 41/a :2 | 19.167; 19.167; 16.153 90; 90; 90 | 5934 | Govor, Evgen V.; Sanakis, Yiannis; Raptis, Raphael G. Synthesis of pyrazole (hemi)aminals via the cleavage of saturated aliphatic ether C‒O bonds in the presence of ferric halides New J. Chem., 2017, 41, 2220 |
| 7055978 | CIF | C16 H24 Cl6 Fe2 N4 O2 | C 1 2/c 1 | 8.5983; 20.475; 14.989 90; 100.778; 90 | 2592.3 | Govor, Evgen V.; Sanakis, Yiannis; Raptis, Raphael G. Synthesis of pyrazole (hemi)aminals via the cleavage of saturated aliphatic ether C‒O bonds in the presence of ferric halides New J. Chem., 2017, 41, 2220 |
| 7055979 | CIF | C14 H20 Cl4 Fe2 I2 N4 O2 | P 1 2/n 1 | 8.595; 9.6865; 15.7769 90; 99.35; 90 | 1296.06 | Govor, Evgen V.; Sanakis, Yiannis; Raptis, Raphael G. Synthesis of pyrazole (hemi)aminals via the cleavage of saturated aliphatic ether C‒O bonds in the presence of ferric halides New J. Chem., 2017, 41, 2220 |
| 7055980 | CIF | C14 H20 Br6 Fe2 N4 O2 | P 1 2/n 1 | 8.6395; 9.7711; 15.8621 90; 103.665; 90 | 1301.13 | Govor, Evgen V.; Sanakis, Yiannis; Raptis, Raphael G. Synthesis of pyrazole (hemi)aminals via the cleavage of saturated aliphatic ether C‒O bonds in the presence of ferric halides New J. Chem., 2017, 41, 2220 |
| 7055981 | CIF | C12 H16 Br2 Cl2 Fe N4 | P 1 21/n 1 | 12.1777; 8.7316; 17.3452 90; 92.407; 90 | 1842.7 | Govor, Evgen V.; Sanakis, Yiannis; Raptis, Raphael G. Synthesis of pyrazole (hemi)aminals via the cleavage of saturated aliphatic ether C‒O bonds in the presence of ferric halides New J. Chem., 2017, 41, 2220 |
| 7055982 | CIF | C12 H16 Br4 Fe N4 | P 1 21/n 1 | 12.247; 8.932; 17.42 90; 91.93; 90 | 1904.5 | Govor, Evgen V.; Sanakis, Yiannis; Raptis, Raphael G. Synthesis of pyrazole (hemi)aminals via the cleavage of saturated aliphatic ether C‒O bonds in the presence of ferric halides New J. Chem., 2017, 41, 2220 |
| 7055983 | CIF | C10 H16 Cl5 Fe N4 O | C 1 2/c 1 | 24.487; 8.7651; 8.5302 90; 110.281; 90 | 1717.3 | Govor, Evgen V.; Sanakis, Yiannis; Raptis, Raphael G. Synthesis of pyrazole (hemi)aminals via the cleavage of saturated aliphatic ether C‒O bonds in the presence of ferric halides New J. Chem., 2017, 41, 2220 |
| 7055984 | CIF | C30 H25 B F2 N2 | P -1 | 7.1985; 11.4552; 14.805 78.169; 81.599; 88.276 | 1182.1 | Maity, Apurba; Sarkar, Anirban; Sil, Amit; B. N., Shivakiran Bhaktha; Patra, Sanjib K. Synthesis, photophysical and concentration-dependent tunable lasing behavior of 2,6-diacetylenyl-functionalized BODIPY dyes New J. Chem., 2017, 41, 2296 |
| 7055985 | CIF | C21 H36 N6 O5 S | P -1 | 9.666; 9.761; 14.448 104.97; 108.43; 91.04 | 1241.9 | Ke, Ya-Ting; Chou, Wei-Tzu; Chiang, Yi-Fen; Hsieh, Chang-Chih; Horng, Yih-Chern Efficient and selective separation of aqueous sulfate through recognition and precipitation New J. Chem., 2017, 41, 2249 |
| 7055986 | CIF | C27 H37 N7 O2 | P 1 21/n 1 | 12.605; 16.671; 13.147 90; 99.243; 90 | 2726.8 | Ke, Ya-Ting; Chou, Wei-Tzu; Chiang, Yi-Fen; Hsieh, Chang-Chih; Horng, Yih-Chern Efficient and selective separation of aqueous sulfate through recognition and precipitation New J. Chem., 2017, 41, 2249 |
| 7055987 | CIF | C50 H72 N14 O6 S | R -3 c :H | 23.541; 23.541; 59.81 90; 90; 120 | 28705 | Ke, Ya-Ting; Chou, Wei-Tzu; Chiang, Yi-Fen; Hsieh, Chang-Chih; Horng, Yih-Chern Efficient and selective separation of aqueous sulfate through recognition and precipitation New J. Chem., 2017, 41, 2249 |
| 7055988 | CIF | C51 H60 Br2 O10 | P -1 | 11.8851; 12.1025; 21.045 82.412; 76.788; 60.595 | 2566.6 | Chen, Jin-Fa; Cheng, Xiao-Bin; Li, Hui; Lin, Qi; Yao, Hong; Zhang, You-Ming; Wei, Tai-Bao A copillar[5]arene-based fluorescence “on‒off‒on” sensor is applied in sequential recognition of an iron cation and a fluoride anion New J. Chem., 2017, 41, 2148 |
| 7055989 | CIF | C53 H36 Br2 | P 1 | 8.3886; 9.0069; 14.5283 76.634; 89.729; 64.661 | 959.66 | Khasanov, Albert F.; Kopchuk, Dmitry S.; Kovalev, Igor S.; Taniya, Olga S.; Giri, Kousik; Slepukhin, Pavel A.; Santra, Sougata; Rahman, Matiur; Majee, Adinath; Charushin, Valery N.; Chupakhin, Oleg N. Extended cavity pyrene-based iptycenes for the turn-off fluorescence detection of RDX and common nitroaromatic explosives New J. Chem., 2017, 41, 2309 |
| 7055990 | CIF | C221 H140 Br8 N4 O8 | P -1 | 13.0874; 15.5471; 22.686 70.666; 88.978; 67.069 | 3978.5 | Khasanov, Albert F.; Kopchuk, Dmitry S.; Kovalev, Igor S.; Taniya, Olga S.; Giri, Kousik; Slepukhin, Pavel A.; Santra, Sougata; Rahman, Matiur; Majee, Adinath; Charushin, Valery N.; Chupakhin, Oleg N. Extended cavity pyrene-based iptycenes for the turn-off fluorescence detection of RDX and common nitroaromatic explosives New J. Chem., 2017, 41, 2309 |
| 7055991 | CIF | C70 H108 Al2 Cl6 N4 O4 | P -1 | 10.6582; 11.7546; 15.703 86.775; 82.638; 84.317 | 1939.6 | Zhang, Jie; Liu, Shaofeng; Zuo, Weiwei; Ye, Hongqi; Li, Zhibo Synthesis of dinuclear aluminum complexes bearing bis-phenolate ligand and application in ring-opening polymerization of ε-caprolactone New J. Chem., 2017, 41, 2358 |
| 7055992 | CIF | C38 H58 Al Cl N2 O2 | I 1 2/a 1 | 22.5443; 12.9305; 25.5225 90; 93.527; 90 | 7425.95 | Beament, James; Mahon, Mary F.; Buchard, Antoine; Jones, Matthew D. Salan group 13 complexes ‒ structural study and lactide polymerisation New J. Chem., 2017, 41, 2198 |
| 7055993 | CIF | C38 H58 Cl Ga N2 O2 | I 1 2/a 1 | 22.4184; 12.9111; 25.8038 90; 93.354; 90 | 7456.02 | Beament, James; Mahon, Mary F.; Buchard, Antoine; Jones, Matthew D. Salan group 13 complexes ‒ structural study and lactide polymerisation New J. Chem., 2017, 41, 2198 |
| 7055994 | CIF | C38 H58 Cl In N2 O2 | P 1 21/c 1 | 12.3467; 15.823; 19.2186 90; 94.865; 90 | 3741.05 | Beament, James; Mahon, Mary F.; Buchard, Antoine; Jones, Matthew D. Salan group 13 complexes ‒ structural study and lactide polymerisation New J. Chem., 2017, 41, 2198 |
| 7055995 | CIF | C38.5 H64.5 Al Cl N2 O2 | C 1 2/c 1 | 33.7559; 13.9577; 17.7422 90; 102.82; 90 | 8150.9 | Beament, James; Mahon, Mary F.; Buchard, Antoine; Jones, Matthew D. Salan group 13 complexes ‒ structural study and lactide polymerisation New J. Chem., 2017, 41, 2198 |
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