Crystallography Open Database

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1547384 CIFC62 H45 Au Cl O3 P Si2P 21 21 219.7873; 12.8393; 39.6173
90; 90; 90		4978.4Nicolas Delpont; Imma Escofet; Patricia Perez-Galen; Dirk Spiegl; Mihai Raducan; Christophe Bour; Riccardo Sinisi; Antonio M. Echavarrena
Modular chiral gold(i) phosphite complexes
Catalysis Science & Technology, 2013, 3, 3007-3012
1547385 CIFC32 H25 Au Cl Fe PP 4113.2861; 13.2861; 14.7974
90; 90; 90		2612Nicolas Delpont; Imma Escofet; Patricia Perez-Galen; Dirk Spiegl; Mihai Raducan; Christophe Bour; Riccardo Sinisi; Antonio M. Echavarrena
Modular chiral gold(i) phosphite complexes
Catalysis Science & Technology, 2013, 3, 3007-3012
1547386 CIFC28 H33 Au Cl Fe PP 319.7478; 9.7478; 23.296
90; 90; 120		1917Nicolas Delpont; Imma Escofet; Patricia Perez-Galen; Dirk Spiegl; Mihai Raducan; Christophe Bour; Riccardo Sinisi; Antonio M. Echavarrena
Modular chiral gold(i) phosphite complexes
Catalysis Science & Technology, 2013, 3, 3007-3012
1547387 CIFC32 H38 Fe O SP 21 21 219.6442; 15.8547; 17.74
90; 90; 90		2712.6Nicolas Delpont; Imma Escofet; Patricia Perez-Galen; Dirk Spiegl; Mihai Raducan; Christophe Bour; Riccardo Sinisi; Antonio M. Echavarrena
Modular chiral gold(i) phosphite complexes
Catalysis Science & Technology, 2013, 3, 3007-3012
1547388 CIFC30 H57 Au Cl O3 PC 1 2 119.461; 9.2739; 20.008
90; 112.325; 90		3340.4Nicolas Delpont; Imma Escofet; Patricia Perez-Galen; Dirk Spiegl; Mihai Raducan; Christophe Bour; Riccardo Sinisi; Antonio M. Echavarrena
Modular chiral gold(i) phosphite complexes
Catalysis Science & Technology, 2013, 3, 3007-3012
1547389 CIFC63 H47 O4 P Si2P 21 21 2111.6873; 13.7576; 34.499
90; 90; 90		5547.1Nicolas Delpont; Imma Escofet; Patricia Perez-Galen; Dirk Spiegl; Mihai Raducan; Christophe Bour; Riccardo Sinisi; Antonio M. Echavarrena
Modular chiral gold(i) phosphite complexes
Catalysis Science & Technology, 2013, 3, 3007-3012
1548338 CIFC108 H36 Cd6 Cl3 N24 O48F m -3 m38.527; 38.527; 38.527
90; 90; 90		57187Chun-Yi Sun; Xin-Long Wang; Xiao Zhang; Chao Qin; Peng Li; Zhong-Min Su; Dong-Xia Zhu; Guo-Gang Shan; Kui-Zhan Shao; Han Wu; Jing Li
Efficient and tunable white-light emission of metal-organic frameworks by iridium-complex encapsulation
Nature Communications, 2013, 3, 2717
1548339 CIFC10 H27 Al2 N2 O15 P3P 1 21/c 19.2188; 28.76; 9.2188
90; 112.73; 90		2254.4Jiancong Liu; Ning Wang; Yue Yu; Yan Yan; Hongyue Zhang; Jiyang Li; Jihong Yu
Carbon dots in zeolites: A new class of thermally activated delayed fluorescence materials with ultralong lifetimes
Science Advances, 2017, 3, 1603171
1548604 CIFC12 H20 N2 O7C 1 2/c 119.957; 9.858; 15.78
90; 99.02; 90		3066.1Yu-Qiang Zhou; Nai-Xing Wang; Yalan Xing; Yan-Jing Wang; Xiao-Wei Hong; Jia-Xiang Zhang; Dong-Dong Chen; Jing-Bo Geng; Yanfeng Dang; Zhi-Xiang Wang
Stable acyclic aliphatic solid enols: synthesis, characterization, X-ray structure analysis and calculations
Scientific Reports, 2013, 3, 1058
1548605 CIFC11 H18 N2 O6P -18.6838; 8.8343; 10.114
80.33; 72.94; 67.07		681.9Yu-Qiang Zhou; Nai-Xing Wang; Yalan Xing; Yan-Jing Wang; Xiao-Wei Hong; Jia-Xiang Zhang; Dong-Dong Chen; Jing-Bo Geng; Yanfeng Dang; Zhi-Xiang Wang
Stable acyclic aliphatic solid enols: synthesis, characterization, X-ray structure analysis and calculations
Scientific Reports, 2013, 3, 1058
1548666 CIF
HKL
Paper		C36 H56 Fe O4 P Si4I -412.589; 12.589; 13.689
90; 90; 90		2169Hay, Michael T.; Yennawar, Hemant P.
Tetraphenylphosphonium tetrakis(trimethylsilanolato)ferrate(III)
IUCrData, 2018, 3, x171823
1548667 CIF
HKL
Paper		C17 H10 Cl4 OF d d 228.1477; 17.3385; 26.1837
90; 90; 90		12778.7Dravida Thendral, Era; Mohamooda Sumaya, U.; Gomathi, S.; Biruntha, K.; Usha, G.
(1<i>E</i>,4<i>E</i>)-1,5-Bis(2,6-dichlorophenyl)penta-1,4-dien-3-one
IUCrData, 2018, 3, x171822
1548668 CIF
HKL		C26 H27 N5 OP 1 21/c 111.9896; 18.4215; 10.9903
90; 110.153; 90		2278.8Singh, Vikram. D.; Anthal, Sumati; Desai, N. R.; Arunakumar, D. B.; Sreenivasa, S.; Kamni; Kant, Rajni
3-[6-(4-Methoxyphenyl)-2-methylpyrimidin-4-yl]-2-(4-methylpiperazin-1-yl)quinoline
IUCrData, 2018, 3, x180030
1548669 CIF
HKL
Paper		C15 H16 N4 O3 SP 21 21 215.6487; 16.7479; 16.9726
90; 90; 90		1605.67El-Hiti, Gamal A.; Mohamed, Hanan A.; Abdel-Wahab, Bakr F.; Alotaibi, Mohammad Hayal; Hegazy, Amany S.; Kariuki, Benson M.
Ethyl (<i>Z</i>)-2-[2-(4-methylphenyl)hydrazin-1-ylidene]-3-oxo-3-(thiazol-2-ylamino)propanoate
IUCrData, 2018, 3, x171852
1548670 CIF
HKL
Paper		C19 H16 N2 O2P n a 2132.387; 9.8559; 5.0043
90; 90; 90		1597.4El-Hiti, Gamal A.; Mohamed, Hanan A.; Abdel-Wahab, Bakr F.; Alotaibi, Mohammad Hayal; Hegazy, Amany S.; Kariuki, Benson M.
Ethyl 1-phenyl-1,4-dihydroindeno[1,2-<i>c</i>]pyrazole-3-carboxylate
IUCrData, 2018, 3, x171840
1548671 CIF
HKL
Paper		C37 H28 Br Cl N8 SP 1 21/n 110.422; 13.4232; 23.8943
90; 90.198; 90		3342.7El-Hiti, Gamal A.; Mohamed, Hanan A.; Abdel-Wahab, Bakr F.; Alotaibi, Mohammad Hayal; Hegazy, Amany S.; Kariuki, Benson M.
4-(4-Bromophenyl)-2-(3-(4-chlorophenyl)-5-{3-[5-methyl-1-(4-methylphenyl)-1<i>H</i>-1,2,3-triazol-4-yl]-1-phenyl-1<i>H</i>-pyrazol-4-yl}-4,5-dihydro-1<i>H</i>-pyrazol-1-yl)thiazole
IUCrData, 2018, 3, x180036
1548672 CIF
HKL
Paper		C21 H24 N2 O2P 1 21 18.5395; 8.9377; 23.444
90; 91.066; 90		1789Guerrab, Walid; Mague, Joel T.; Taoufik, Jamal; Ramli, Youssef
3-Hexyl-5,5-diphenylimidazolidine-2,4-dione
IUCrData, 2018, 3, x180057
1548673 CIF
HKL
Paper		C19 H20 N2 O2P -18.492; 8.5213; 12.6353
91.9; 99.41; 115.117		811.33Guerrab, Walid; Mague, Joel T.; Akrad, Rachida; Ansar, Mhammed; Taoufik, Jamal; Ramli, Youssef
3-Butyl-5,5-diphenylimidazolidine-2,4-dione
IUCrData, 2018, 3, x180050
1548674 CIF
HKL
Paper		C22 H18 N2 O2P -18.8897; 13.2911; 16.6864
67.9; 81.027; 74.294		1755.27Guerrab, Walid; Akrad, Rachida; Ansar, Mhammed; Taoufik, Jamal; Mague, Joel T.; Ramli, Youssef
3-Benzyl-5,5-diphenylimidazolidine-2,4-dione
IUCrData, 2018, 3, x171832
1548675 CIF
HKL
Paper		C7 H3 Br2 NP 1 21/m 14.0047; 13.2585; 7.3356
90; 97.44; 90		386.21Noland, Wayland E.; Tritch, Kenneth J.
3,5-Dibromobenzonitrile
IUCrData, 2018, 3, x180059
1548676 CIF
HKL
Paper		C7 H2 Br2 Cl NP 1 21/m 14.7215; 10.0181; 8.7689
90; 93.023; 90		414.2Noland, Wayland E.; Tritch, Kenneth J.
2,6-Dibromo-4-chlorophenyl isocyanide
IUCrData, 2018, 3, x171819
1548677 CIF
HKL
Paper		C5 H3 Cl N2 O3P b c a5.9238; 9.735; 22.444
90; 90; 90		1294.3Shafer, Sarah K.; Lynch, Will E.; Padgett, Clifford W.
2-Chloro-4-nitropyridine <i>N</i>-oxide
IUCrData, 2018, 3, x180016
1548678 CIF
HKL
Paper		C11 H19 N O7 SP 1 21 18.0762; 6.2486; 14.5096
90; 92.161; 90		731.71Prabu, P.; Thiruvalluvar, A.; Ramachandra Raja, C.
1-Carboxy-2-hydroxypropan-1-aminium 4-methylbenzenesulfonate monohydrate
IUCrData, 2018, 3, x171848
1548679 CIF
HKL		C10 H13 Br N2 SP 1 21/n 112.2617; 8.0222; 12.7397
90; 112.38; 90		1158.76El-Hiti, Gamal A.; Smith, Keith; Hegazy, Amany S.; Alshammari, Mohammed B.; Kariuki, Benson M.
1-(2-Bromo-4-methylphenyl)-3,3-dimethylthiourea
IUCrData, 2018, 3, x180045
1548680 CIF
HKL
Paper		C19 H14 O5P 1 21/n 19.1617; 10.2307; 16.8581
90; 92.812; 90		1578.22Cao, Yi; Mai, Wenpeng; Yuan, Jinwei
3-Benzoyl-4-methyl-2-oxo-2<i>H</i>-chromen-7-yl acetate
IUCrData, 2018, 3, x180015
1548681 CIF
HKL
Paper		C8 H7 Br Cl N O2P -14.6637; 9.4598; 11.9898
111.639; 101.035; 93.712		477.25El-Hiti, Gamal A.; Smith, Keith; Hegazy, Amany S.; Alshammari, Mohammed B.; Kariuki, Benson M.
Methyl <i>N</i>-(2-bromo-4-chlorophenyl)carbamate
IUCrData, 2018, 3, x180054
1548682 CIF
HKL
Paper		C18 H13 F2 N3 OP -18.1891; 14.1804; 14.505
68.075; 84.22; 74.627		1506.65El-Hiti, Gamal A.; Abdel-Wahab, Bakr F.; Alotaibi, Mohammad Hayal; Hegazy, Amany S.; Kariuki, Benson M.
(<i>E</i>)-3-(4-Fluorophenyl)-1-[1-(4-fluorophenyl)-5-methyl-1<i>H</i>-1,2,3-triazol-4-yl]prop-2-en-1-one
IUCrData, 2018, 3, x171841
1548683 CIF
HKL
Paper		C19 H18 N2 O3 SP 1 21/c 17.6756; 13.6762; 17.6561
90; 110.442; 90		1736.7Balakumaran, K.; Mosesbabu, J.; Anireddy, Jayashree; Chakkaravarthi, G.
(<i>E</i>)-5-{4-[2-(5-Ethylpyridin-2-yl)ethoxy]benzylidene}thiazolidine-2,4-dione
IUCrData, 2018, 3, x171839
1548684 CIF
HKL
Paper		C10 H8 Br N3 O2P 1 21/n 17.5971; 9.9501; 28.569
90; 95.086; 90		2151.08Mohamed Abdelahi, Mohamed Mokhtar; El Bakri, Youness; Benchidmi, Mohammed; Essassi, El Mokhtar; Mague, Joel T.
3-Bromo-6-nitro-1-(prop-2-en-1-yl)-1<i>H</i>-indazole
IUCrData, 2018, 3, x171837
1548685 CIF
HKL
Paper		C10 H11 F3 N2 OP b c a9.8152; 10.0783; 22.512
90; 90; 90		2226.9El-Hiti, Gamal A.; Smith, Keith; Hegazy, Amany S.; Alshammari, Mohammed B.; Kariuki, Benson M.
1,1-Dimethyl-3-[4-(trifluoromethyl)phenyl]urea
IUCrData, 2018, 3, x180040
1548726 CIF
HKL		C17 H19 N O3P 1 21/n 111.172; 8.532; 16.287
90; 106.54; 90		1488.2Ait Elhad, Mustapha; Benharref, Ahmed; El Ammari, Lahcen; Saadi, Mohamed; Mazoir, Noureddine; Berraho, Moha
1-(2-Isopropyl-4,7-dimethyl-3-nitronaphthalen-1-yl)ethanone
IUCrData, 2018, 3, x180083
1548727 CIF
HKL
Paper		C40 H24 F4 N4 S2P -17.57; 10.206; 11.549
113.4; 90.01; 108.607		767.8Fujii, Takuya; Yamakado, Hideo
The 2:1 charge-transfer complex of 4,6-dimethyldibenzothiophene and 7,7,8,8-tetracyano-2,3,5,6-tetrafluoroquinodimethane
IUCrData, 2018, 3, x180077
1548728 CIF
HKL
Paper		C7 H5 N O3P 1 21 13.7363; 7.0071; 12.5877
90; 94.8144; 90		328.39Engwerda, Antonius H.J.; Brugman, Sander J.T.; Tinnemans, Paul; Vlieg, Elias
3-Nitrobenzaldehyde
IUCrData, 2018, 3, x180092
1548729 CIF
HKL
Paper		C71 H71 N33 O S8P 1 21/c 118.3427; 13.5855; 16.9385
90; 110.393; 90		3956.4El-Hiti, Gamal A.; Abdel-Wahab, Bakr F.; Alotaibi, Mohammad Hayal; Hegazy, Amany S.; Kariuki, Benson M.
2-({6-[5-Methyl-1-(4-methylphenyl)-1<i>H</i>-1,2,3-triazol-4-yl]imidazo[2,1-<i>b</i>]thiazol-5-yl}methylidene)hydrazinecarbothioamide dimethylformamide 0.25-solvate
IUCrData, 2018, 3, x180087
1548730 CIF
HKL
Paper		C27 H20 Br N5 OP 1 21/n 115.0387; 6.8105; 24.385
90; 106.473; 90		2395El-Hiti, Gamal A.; Abdel-Wahab, Bakr F.; Alotaibi, Mohammad Hayal; Hegazy, Amany S.; Kariuki, Benson M.
(<i>E</i>)-1-(4-Bromophenyl)-3-[3-(5-methyl-1-phenyl-1<i>H</i>-1,2,3-triazol-4-yl)-1-phenyl-1<i>H</i>-pyrazol-4-yl]prop-2-en-1-one
IUCrData, 2018, 3, x180069
1548731 CIF
HKL
Paper		C14 H10 O2 SP 1 21/n 110.4355; 8.6955; 25.7106
90; 95.42; 90		2322.6Elumalai, K.; Raja, R.; Karunakaran, Jayachandran; Mohanakrishnan, Arasambattu K.; Murugesan, K. Sakthi
(<i>E</i>)-2-(3-Oxo-3-phenylprop-1-enyl)thiophene-3-carbaldehyde
IUCrData, 2018, 3, x180041
1548830 CIF
HKL
Paper		C17 H11 Cl N2 O2P -18.7208; 8.7703; 9.6278
86.035; 80.227; 79.352		712.65Baral, Nilofar; Nayak, Sabita; Pal, Satyanarayan; Mohapatra, Seetaram
5-(2-Chlorophenyl)-3-(2<i>H</i>-chromen-3-yl)-1,2,4-oxadiazole
IUCrData, 2018, 3, x180129
1548831 CIF
HKL
Paper		C19 H24 O2P -16.36; 11.0807; 11.5351
114.539; 91.465; 93.401		737.06Kotha, Sambasivarao; Cheekatla, Subba Rao; Gunta, Rama
7-Hydroxyhexacyclo[7.5.1.0^1,7^.0^6,13^.0^8,12^.0^10,14^]pentadecan-15-one-11-spirocyclopentane
IUCrData, 2018, 3, x180090
1548832 CIF
HKL
Paper		C14 H8 N2 S SeP n a 2120.8533; 9.9698; 23.4151
90; 90; 90		4868.1Schollmeyer, Dieter; Detert, Heiner
Dibenzo[2,3:6,7]thiepino[4,5-<i>d</i>][1,2,3]selenadiazole
IUCrData, 2018, 3, x180070
1548840 CIF
HKL
Paper		C6 H12 O6P 1 21/a 112.8152; 6.29489; 18.9482
90; 108.347; 90		1450.85Taguchi, Hiroaki; Sogo, Kouta; Ishii, Tomohiko; Yoshihara, Akihide; Fukada, Kazuhiro
α-<small>D</small>,<small>L</small>-Sorbose
IUCrData, 2018, 3, x180114
1548841 CIF
HKL
Paper		C24 H26 O4P b c n15.1185; 11.0273; 24.141
90; 90; 90		4024.7Kalaivanan, R.; Sughanya, V.; Sureshbabu, N.
9-(4-Formylphenyl)-3,3,6,6-tetramethyl-3,4,5,6,7,9-hexahydro-1<i>H</i>-xanthene-1,8(2<i>H</i>)-dione
IUCrData, 2018, 3, x180105
1548842 CIF
HKL
Paper		C23 H15 N3 O SP 1 21/n 119.2666; 9.7769; 20.3265
90; 94.423; 90		3817.5El-Hiti, Gamal A.; Abdel-Wahab, Bakr F.; Alotaibi, Mohammad Hayal; Hegazy, Amany S.; Kariuki, Benson M.
(<i>E</i>)-2-Benzoyl-3-[1-phenyl-3-(thiophen-2-yl)-1<i>H</i>-pyrazol-4-yl]acrylonitrile
IUCrData, 2018, 3, x180171
1548843 CIF
HKL
Paper		C14 H11 N3 O2P 1 21/n 14.489; 19.77; 13.308
90; 93.608; 90		1178.7Mohamed Abdelahi, Mohamed Mokhtar; El Bakri, Youness; Benchidmi, Mohammed; Essassi, El Mokhtar; Mague, Joel T.
2-Benzyl-6-nitro-2<i>H</i>-indazole
IUCrData, 2018, 3, x180151
1548889 CIF
HKL
Paper		C6 Cl3 N9I 1 2/a 122.2914; 14.1339; 23.1869
90; 115.732; 90		6580.9Limbach, Daniel; Detert, Heiner; Schollmeyer, Dieter
2,6,10-Trichlorotris[1,2,4]triazolo[1,5-<i>a</i>:1',5'-<i>c</i>:1'',5''-<i>e</i>][1,3,5]triazine
IUCrData, 2018, 3, x180212
1548890 CIF
HKL
Paper		C24 H23 N3 O2P 1 21/c 19.1066; 19.6406; 11.2901
90; 94.343; 90		2013.54Tamam, Asmaa H. A.; Kaur, Manpreet; Akkurt, Mehmet; Mohamed, Shaaban K.; Jasinski, Jerry P.; Hussain, Faiq H. S.
2-Amino-4-(4-methoxyphenyl)-1-(4-methylphenyl)-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carbonitrile
IUCrData, 2018, 3, x180167
1548891 CIF
HKL
Paper		C22 H17 N3 OP 1 21/c 19.1084; 10.8314; 17.2226
90; 94.06; 90		1694.9Mohamed, Shaaban K.; Mague, Joel T.; Akkurt, Mehmet; Said, Awad I.; Hawaiz, Farouq E.; Elgarhy, Sahar M. I.
(<i>Z</i>)-1-(1,3-Diphenyl-1<i>H</i>-pyrazol-4-yl)-<i>N</i>-phenylmethanimine <i>N</i>-oxide
IUCrData, 2018, 3, x180208
1548892 CIF
HKL
Paper		Al4 CrC 1 m 15.1574; 17.413; 5.1107
90; 100.357; 90		451.49Fan, Changzeng; Liu, Cong
Crystal structure of ω-Al~4~Cr
IUCrData, 2018, 3, x180216
1548930 CIF
HKL
Paper		C26 H19 Br N4 O2 SC 1 2/c 125.289; 10.076; 19.05
90; 98.89; 90		4795.9Muthuselvi, C.; Muthu, M.; Athimoolam, S.; Ravikumar, B.; Pandiarajan, S.; Krishnakumar, R. V.
6'-(3-Bromophenyl)-7'-nitro-1',6',7',7a'-tetrahydro-3'<i>H</i>-spiro[indeno[1,2-<i>b</i>]quinoxaline-11,5'-pyrrolo[1,2-<i>c</i>]thiazole]
IUCrData, 2018, 3, x180238
1548931 CIF
HKL
Paper		Al10 Fe0.83 Ni3P 63/m m c7.6981; 7.6981; 7.6231
90; 90; 120		391.227Wang, Sai; Liu, Cong; Fan, Changzeng
Al~10~Ni~3~Fe~0.83~, an Fe-depleted phase in the Al‒Ni‒Fe system
IUCrData, 2018, 3, x180237
1548932 CIF
HKL
Paper		C19 H17 Cl2 N S SiP -110.073; 10.37; 10.547
105.029; 115.48; 90.3532		951.7Umezono, Satoru; Okuno, Tsunehisa
10-[1,1-Dichloro-4-(trimethylsilyl)but-1-en-3-yn-2-yl]-10<i>H</i>-phenothiazine
IUCrData, 2018, 3, x180232
1548972 CIF
HKL
Paper		C8 H13 Br N O0.5C 1 2/c 130.7456; 5.0266; 12.0636
90; 98.43; 90		1844.24Aarthi, R.; Thiruvalluvar, A.; Ramachandra Raja, C.
(4-Methylphenyl)methanaminium bromide hemihydrate
IUCrData, 2018, 3, x180270
1548973 CIF
HKL
Paper		C9 H5 I3 O2P 1 21/n 14.7121; 18.752; 13.856
90; 92.379; 90		1223.3Szell, Patrick M.J.; Gabidullin, Bulat; Bryce, David L.
3-(1,2,2-Triiodoethenyl)benzoic acid
IUCrData, 2018, 3, x180258
1548985 CIF
HKL
Paper		C22 H16 Br N3 O3C 1 2/c 134.0146; 4.9522; 23.4539
90; 111.578; 90		3673.9Filali Baba, Yassir; Kandri Rodi, Youssef; Mague, Joel T.; Ouzidan, Younes; Ouazzani Chahdi, Fouad; Essassi, El Mokhtar
(Pyridin-2-yl)methyl 6-bromo-2-oxo-1-[(pyridin-2-yl)methyl]-1,2-dihydroquinoline-4-carboxylate
IUCrData, 2018, 3, x180288
1548986 CIF
HKL
Paper		C22 H14 O6P -18.1833; 15.4412; 15.525
110.657; 104.919; 90.516		1762.9Mohamed, Shaaban K.; Mague, Joel T.; Akkurt, Mehmet; Hawaiz, Farouq E.; Ayoob, Mzgin M.; Hussein, Awaz J.
Bis(2-formylphenyl) benzene-1,2-dicarboxylate
IUCrData, 2018, 3, x180251
1548987 CIF
HKL
Paper		C13 H8 Br N3 O2P 1 21/c 110.1922; 17.347; 7.0216
90; 92.382; 90		1240.37Sikine, Meriem; Kandri Rodi, Youssef; Ouzidan, Younes; Jasinski, Jerry P.; Kaur, Manpreet; Essassi, El Mokhtar
7-Bromo-1,4-bis(prop-2-ynyl)pyrido[2,3-<i>b</i>]pyrazine-2,3(1<i>H</i>,4<i>H</i>)-dione
IUCrData, 2018, 3, x180266
1548988 CIF
HKL		C15 H17 N O2C 1 2/c 129.001; 4.8412; 20.474
90; 113.16; 90		2642.9Dakir, Mohamed; Benharref, Ahmed; El Ammari, Lahcen; Saadi, Mohamed; Oukhrib, Abdelouahd; Berraho, Moha
6-Methyl-1-(nitromethyl)-4-(propan-2-yl)naphthalene
IUCrData, 2018, 3, x180274
1549006 CIF
HKL
Paper		C19 H18 N2 O2P 1 21/n 18.9229; 18.8922; 9.7147
90; 104.879; 90		1582.73Samba, Mohamed; Minnih, Mohamed Said; El Bakri, Youness; Essassi, El Mokhtar; Mague, Joel T.
A monoclinic modification of (4<i>Z</i>)-1-benzyl-4-(2-oxopropylidene)-2,3,4,5-tetrahydro-1<i>H</i>-1,5-benzodiazepin-2-one
IUCrData, 2018, 3, x180326
1549007 CIF
HKL
Paper		C10 H13 N OP n m a10.4838; 6.8965; 12.8538
90; 90; 90		929.35Bosch, Eric; Jeffries, Laura
1-(2-Amino-4,5-dimethylphenyl)ethanone
IUCrData, 2018, 3, x180313
1549019 CIF
HKL
Paper		C10 H10 N2 O4 S2P 21 21 211.232; 12.283; 4.401
90; 90; 90		607.2Lynch, Will; Padgett, Clifford W.
2,2′-Disulfanediylbis(pyridine N-oxide)–hydrogen peroxide (1/1)
IUCrData, 2018, 3, x180320
1549037 CIF
HKL
Paper		C16 H14 N2 OP -17.3502; 17.3508; 17.9449
118.226; 100.042; 92.294		1965.63Ramli, Youssef; El Bakri, Youness; El Ghayati, L'houssaine; Essassi, El Mokhtar; Mague, Joel T.
1-Benzyl-3-methylquinoxalin-2(1<i>H</i>)-one
IUCrData, 2018, 3, x180390
1549038 CIF
HKL
Paper		C13 H18 F N O5P 1 21 110.561; 5.156; 12.504
90; 90.606; 90		680.8Mossine, Valeri V.; Barnes, Charles L.; Mawhinney, Thomas P.
1-Deoxy-1-(<i>N</i>-methyl-4-fluorophenylamino)-<small>D</small>-<i>arabino</i>-hexulose
IUCrData, 2018, 3, x180369
1549065 CIF
HKL
Paper		C14 H11 Br2 N O2P 1 21/n 116.7219; 6.90389; 23.0811
90; 99.502; 90		2628.07Pal, Tarun Kumar; Hossain, Md Dulal; Sheikh, Md Chanmiya; Miyatake, Ryuta; Alam, Md Ashraful
2,4-Dibromo-6-[(2-hydroxy-5-methylanilino)methylidene]cyclohexa-2,4-dienone
IUCrData, 2018, 3, x180388
1549066 CIF
HKL
Paper		C15 H21 N3 O2 SP c c n29.5823; 15.1971; 7.4303
90; 90; 90		3340.4Chaurasia, Rahul; Bharti, Akhilesh; Butcher, Ray J.; Wikaira, Jan L.; Bharty, Manoj K.
4-Cyclohexyl-1-(2-methoxybenzoyl)thiosemicarbazide with an unknown solvent
IUCrData, 2018, 3, x180383
1549074 CIF
HKL
Paper		C14 H7 Br2 N O2P n m a15.116; 6.8728; 12.7492
90; 90; 90		1324.5El-Hiti, Gamal A.; Smith, Keith; Alamri, Mesfer; Morris, Ceri A.; Kille, Peter; Kariuki, Benson M.
5-Bromo-1-(4-bromophenyl)isatin
IUCrData, 2018, 3, x180426
1549075 CIF
HKL
Paper		C24 H22 N4 O2 SP 1 21/c 16.2938; 10.9254; 31.229
90; 90.221; 90		2147.4El-Hiti, Gamal A.; Abdel-Wahab, Bakr F.; Khidre, Rizk E.; Mostafa, Mohamed S.; Hegazy, Amany S.; Kariuki, Benson M.
1-{2-Anilino-4-methyl-5-[5-methyl-1-(4-methylphenyl)-1<i>H</i>-1,2,3-triazole-4-carbonyl]thiophen-3-yl}ethanone
IUCrData, 2018, 3, x180402
1549076 CIF
HKL
Paper		C20 H18 N8 O2C 1 2/c 161.5399; 11.8988; 8.2661
90; 93.301; 90		6042.8El-Hiti, Gamal A.; Abdel-Wahab, Bakr F.; Mostafa, Mohamed S.; Khidre, Rizk E.; Hegazy, Amany S.; Kariuki, Benson M.
5-Methyl-<i>N</i>'-(5-methyl-1-phenyl-1<i>H</i>-1,2,3-triazole-4-carbonyl)-1-phenyl-1<i>H</i>-1,2,3-triazole-4-carbohydrazide
IUCrData, 2018, 3, x180424
1549125 CIF
HKL
Paper		C16 H12 N2 OP -14.0205; 11.316; 13.781
85.067; 88.517; 84.335		621.5Umezono, Satoru; Okuno, Tsunehisa
5-[Phenyl(pyridin-4-yl)amino]penta-2,4-diyn-1-ol
IUCrData, 2018, 3, x180454
1549126 CIF
HKL		C20 H20 N2 O2P 1 21/c 115.6203; 8.6349; 13.9758
90; 108.948; 90		1782.9Yousufuddin, Muhammed; Morales, Ruth; Cassis, Waleed; Brown, Gary W.; Singh, Ravi P.; Lovely, Carl J.
[1,4-Bis(4-methoxyphenyl)but-3-yn-2-yl](cyano)methylamine
IUCrData, 2018, 3, x180389
1549127 CIF
HKL
Paper		C33 H40 N4 O9 S3P -110.5058; 12.8929; 14.0425
80.187; 73.218; 89.188		1793.17Amirthakumar, C.; Pandi, P.; Kumar, R. Mohan; Chakkaravarthi, G.
2-Aminoanilinium benzene-1,2-diaminium tris(4-methylbenzene-1-sulfonate)
IUCrData, 2018, 3, x180437
1549128 CIF
HKL
Paper		C37 H28 Br Cl N8 SP 1 21/n 110.4422; 13.3065; 24.0683
90; 90.181; 90		3344.25El-Hiti, Gamal A.; Abdel-Wahab, Bakr F.; Khidre, Rizk E.; Mostafa, Mohamed S.; Hegazy, Amany S.; Kariuki, Benson M.
4-(4-Bromophenyl)-2-(3-(4-chlorophenyl)-5-{3-[5-methyl-1-(4-methylphenyl)-1<i>H</i>-1,2,3-triazol-4-yl]-1-phenyl-1<i>H</i>-pyrazol-4-yl}-4,5-dihydro-1<i>H</i>-pyrazol-1-yl)-1,3-thiazole
IUCrData, 2018, 3, x180443
1549129 CIF
HKL
Paper		C2 H6 Ni O6P 1 21/c 18.5806; 7.0202; 9.2257
90; 97.551; 90		550.91Weil, Matthias
Redetermination of nickel(II) formate dihydrate
IUCrData, 2018, 3, x180428
1549130 CIF
HKL
Paper		C6 H5 F N2 O2P 1 21/n 112.1967; 3.7559; 14.4539
90; 102.143; 90		647.31Moorthy, K.; NizamMohideen, M.; Vetrivel, S.; Vinoth, E.; Arun, A.
2-Fluoro-5-nitroaniline
IUCrData, 2018, 3, x180425
1549131 CIF
HKL
Paper		C37 H28 Br2 N8 SP 1 21/n 110.3624; 13.5082; 24.0262
90; 90.457; 90		3363.02El-Hiti, Gamal A.; Abdel-Wahab, Bakr F.; Khidre, Rizk E.; Mostafa, Mohamed S.; Hegazy, Amany S.; Kariuki, Benson M.
4-(4-Bromophenyl)-2-(3-(4-bromophenyl)-5-{3-[5-methyl-1-(4-methylphenyl)-1<i>H</i>-1,2,3-triazol-4-yl]-1-phenyl-1<i>H</i>-pyrazol-4-yl}-4,5-dihydro-1<i>H</i>-pyrazol-1-yl)-1,3-thiazole
IUCrData, 2018, 3, x180449
1549173 CIF
HKL
Paper		C8 H5 Cl N2 SeP 1 21/c 110.3353; 14.0058; 5.954
90; 97.32; 90		854.84Ravichandran, K.; Ranjith, S.; Sankari, S.; Beemarao, M.; Ponnuswamy, M. N.
4-(4-Chlorophenyl)-1,2,3-selenadiazole
IUCrData, 2018, 3, x180462
1549174 CIF
HKL
Paper		C14 H13 N OP 1 21/n 14.6976; 19.3656; 12.3116
90; 95.831; 90		1114.21Swetha, G.; Ida Malarselvi, R.; Ramachandra Raja, C.; Thiruvalluvar, A.; Priscilla, J.
(<i>E</i>)-4-Methyl-2-(<i>N</i>-phenylcarboximidoyl)phenol
IUCrData, 2018, 3, x180464
1549176 CIF
HKL
Paper		C6 H6 N4 OP -13.8342; 5.5701; 15.0346
93.396; 92.812; 92.361		319.83El Hafi, Mohamed; Lahmidi, Sanae; Boulhaoua, Mohammed; Ramli, Youssef; Essassi, El Mokhtar; Mague, Joel T.
1-Methyl-1<i>H</i>-pyrazolo[3,4-<i>d</i>]pyrimidin-4(5<i>H</i>)-one
IUCrData, 2018, 3, x180483
1549177 CIF
HKL
Paper		C21 H14 N6P 1 21/c 18.556; 8.982; 22.13
90; 98.28; 90		1683Wang, Jianwei; Yuan, Caixia
4-(1<i>H</i>-Indol-3-yl)-2,6-bis(pyrazin-2-yl)pyridine
IUCrData, 2018, 3, x180492
1549178 CIF
HKL
Paper		C17 H41 B Co N O P2P 1 21/n 18.0249; 27.32; 10.3546
90; 97.101; 90		2252.73Junge, Kathrin; Cingolani, Andrea; Spannenberg, Anke; Beller, Matthias
{Bis[2-(diisopropylphosphanyl)ethyl]amine}carbonyl(tetrahydroborato)cobalt(I)
IUCrData, 2018, 3, x180471
1549340 CIF
HKL
Paper		C11 H6 F5 N OP b c m13.1081; 11.1491; 7.1798
90; 90; 90		1049.3Zhao, Hui
3-Difluoromethyl-5-[4-(trifluoromethyl)phenyl]isoxazole
IUCrData, 2018, 3, x180445
1549341 CIF
HKL
Paper		C56 H50 N2P -110.4026; 13.6115; 16.5769
105.502; 105.796; 94.038		2150.3Adas, Sonya K.; Peloquin, Andrew J.; Iacono, Scott T.; Balaich, Gary J.
9-(3,5-Dimethylbenzylidene)-8-(3,5-dimethylphenyl)-1,3,5,7-tetraphenyl-2,4,7,8-tetrahydro-4,7-methanoazulene acetonitrile disolvate
IUCrData, 2018, 3, x180553
1549342 CIF
HKL
Paper		C16 H19 N5 OP 1 21/c 115.8299; 10.627; 9.2041
90; 98.084; 90		1532.97Abad, Nadeem; Ramli, Youssef; Sebbar, Nada Kheira; Kaur, Manpreet; Essassi, El Mokhtar; Jasinski, Jerry P.
1-[(1-Butyl-1<i>H</i>-1,2,3-triazol-5-yl)methyl]-3-methylquinoxalin-2(1<i>H</i>)-one
IUCrData, 2018, 3, x180482
1549343 CIF
HKL
Paper		C18 H22P -17.9315; 8.2047; 12.3474
108.513; 98.09; 103.805		719.18Brieger, Lukas; Unkelbach, Christian; Strohmann, Carsten
1,2-Bis(3,5-dimethylphenyl)ethane
IUCrData, 2018, 3, x180636
1549344 CIF
HKL
Paper		C15 H14 Br2P 1 21 17.4526; 5.8441; 16.278
90; 101.808; 90		694Peloquin, Andrew J.; Godman, Nicholas P.; Allison, Bruce D.; Balaich, Gary J.; Iacono, Scott T.
1,3-Bis(4-bromophenyl)propane
IUCrData, 2018, 3, x180563
1549345 CIF
HKL
Paper		C15 H12 Cl N O2P -17.2162; 8.0068; 11.65
80.123; 84.57; 88.084		660.1Zhong, Ling; Shi, Jianyou; Zhong, Lei; Wei, Xin; Xhang, Hongjia; Cheng, Liang; Bai, Lan
2-(3-Chlorophenyl)-3,4-dihydrobenzo[<i>f</i>][1,4]oxazepin-5(2<i>H</i>)-one
IUCrData, 2018, 3, x180587
1549346 CIF
HKL
Paper		C16 H20 N2 O2P -18.8546; 8.9841; 9.5523
98.481; 96.412; 106.772		710El Foujji, Laila; Sebhaoui, Jihad; El Bakri, Youness; El Ghayati, L'houssaine; Essassi, El Mokhtar; Mague, Joel T.
(3<i>R</i>,4<i>Z</i>)-1,3-Diethyl-4-(2-oxopropylidene)-2,3,4,5-tetrahydro-1<i>H</i>-1,5-benzodiazepin-2-one
IUCrData, 2018, 3, x180515
1549347 CIF
HKL
Paper		C17 H16 OP 1 21/c 19.6483; 10.606; 13.4332
90; 104.034; 90		1333.59Seidel, Nadine; Seichter, Wilhelm; Weber, Edwin
1-Methoxy-1,1-diphenylbut-2-yne
IUCrData, 2018, 3, x180415
1549348 CIF
HKL
Paper		C13 H15 N5 O2 SP b c a18.2763; 7.5909; 20.0571
90; 90; 90		2782.59Choudhury, Manisha; Viswanathan, Vijayan; Timiri, Ajay Kumar; Sinha, Barij Nayan; Jeyaprakash, Venkatesan; Velmurugan, Devadasan
2-[(4,6-Diaminopyrimidin-2-yl)sulfanyl]-<i>N</i>-(4-methoxyphenyl)acetamide
IUCrData, 2018, 3, x180600
1549349 CIF
HKL
Paper		C18 H16 N2 O3P 1 21/c 118.171; 4.9012; 16.9492
90; 91.923; 90		1508.64Abad, Nadeem; El Bakri, Youness; Sebhaoui, Jihad; Ramli, Youssef; Essassi, El Mokhtar; Mague, Joel T.
Ethyl 2-(2-oxo-3-phenyl-1,2-dihydroquinoxalin-1-yl)acetate
IUCrData, 2018, 3, x180519
1549350 CIF
HKL
Paper		C27 H37 Cl N2 O4P c c n11.0729; 12.6284; 19.6141
90; 90; 90		2742.7Minaker, Samuel A.; Wang, Ruiyao; Aquino, Manuel A. S.
1,3-Bis(2,6-diisopropylphenyl)imidazolium perchlorate
IUCrData, 2018, 3, x180516
1549351 CIF
HKL
Paper		C12 H14 N2 O3P -14.8082; 8.26; 14.413
84.072; 81.473; 85.14		561.7Abad, Nadeem; Sebhaoui, Jihad; El Bakri, Youness; Ramli, Youssef; Essassi, El Mokhtar; Mague, Joel T.
Ethyl 2-(3-oxo-1,2,3,4-tetrahydroquinoxalin-2-yl)acetate
IUCrData, 2018, 3, x180596
1549352 CIF
HKL
Paper		C47.8 H42 Au Co2 F12.6 Fe2 N6 O5.4 P1.2 S1.8P -112.1395; 13.8587; 17.366
85.994; 80.863; 66.136		2637.9Vanicek, Stefan; Wurst, Klaus; Kopacka, Holger; Bildstein, Benno
Bis(4-cobaltoceniumyl-1-ferrocenyl-3-methyl-1,2,3-triazolylidene)gold(I) hexafluoridophosphate‒trifluoromethanesulfonate (1.2/1.8)
IUCrData, 2018, 3, x180623
1549353 CIF
HKL
Paper		C21.2 H22.4 Cl6.4 Co3P -118.1419; 19.9967; 20.3048
79.631; 78.398; 63.844		6441.7Shaw, Michael J.; Xu, Nan; Caveny, Ian E.; Abucayon, Erwin G.; Ramuglia, Anthony R.; Richter-Addo, George B.
Bis(cobaltocenium) tetrachloridocobaltate(II) dichloromethane 1.2-solvate
IUCrData, 2018, 3, x180552
1549354 CIF
HKL
Paper		C17 H14 N2 O2P 1 21 112.7853; 7.0167; 15.4215
90; 95.718; 90		1376.59Abad, Nadeem; El Bakri, Youness; Sebhaoui, Jihad; Ramli, Youssef; Essassi, El Mokhtar; Mague, Joel T.
1-[(Oxiran-2-yl)methyl]-3-phenyl-1,2-dihydroquinoxalin-2-one
IUCrData, 2018, 3, x180610
1549355 CIF
HKL
Paper		C28 H20 Br2 OP 21 21 219.4301; 9.4561; 24.8572
90; 90; 90		2216.6Seidel, Nadine; Seichter, Wilhelm; Weber, Edwin
3,4-Dibromo-2,2,5,5-tetraphenyl-2,5-dihydrofuran
IUCrData, 2018, 3, x180416
1549356 CIF
HKL
Paper		C56 H52 As2 Cl6 N4 ZrP 1 21/c 19.6505; 19.378; 15.1026
90; 97.849; 90		2797.8Borjas, Rosendo; Mariappan Balasekaran, Samundeeswari; Poineau, Frederic
Bis(tetraphenylarsonium) hexachloridozirconate(IV) acetonitrile tetrasolvate
IUCrData, 2018, 3, x180528
1549358 CIF
HKL
Paper		C16 H24 Br4 N2 ZnP n a 2111.0702; 26.0585; 7.7302
90; 90; 90		2229.95Aarthi, Ramkumar; Thiruvalluvar, Aravazhi Amalan; Ramachandra Raja, Chidambaram
Bis(4-methylbenzylammonium) tetrabromidozincate
IUCrData, 2018, 3, x180648
1549359 CIF
HKL
Paper		Br F4 KI 4/m c m6.0999; 6.0999; 11.0509
90; 90; 90		411.19Ivlev, Sergei I.; Kraus, Florian
Redetermination of the crystal structure of K[BrF4] from single-crystal X-ray diffraction data
IUCrData, 2018, 3, x180646
1549381 CIF
HKL
Paper		C15 H11 N3 O4P 1 21/c 112.8698; 8.1365; 13.0309
90; 107.275; 90		1302.98AaminaNaaz, Y.; Kamalraja, Jayabal; Perumal, Paramasivam T.; SubbiahPandi, A.
5'-Nitro-1,4-dihydrospiro[3,1-benzoxazine-2,3'-indolin]-2'-one
IUCrData, 2018, 3, x180664
1549393 CIF
HKL
Paper		C24 H22 N2 O2 P2P -18.6901; 10.1547; 12.6282
71.352; 84.442; 81.817		1043.56Höhne, Martha; Aluri, Bhaskar R.; Spannenberg, Anke; Müller, Bernd H.; Peulecke, Normen; Rosenthal, Uwe
1,1-Bis(diphenylphosphoryl)hydrazine
IUCrData, 2018, 3, x180679
1549394 CIF
HKL
Paper		C22 H32 N2 O3P 1 21/c 128.061; 4.765; 15.3667
90; 91.503; 90		2053.98Abad, Nadeem; El Bakri, Youness; Ramli, Youssef; Essassi, El Mokhtar; Mague, Joel T.
Ethyl 2-[(2<i>E</i>)-4-decyl-3-oxo-1,2,3,4-tetrahydroquinoxalin-2-ylidene]acetate
IUCrData, 2018, 3, x180680
1549412 CIF
HKL
Paper		C18 H16 Cu Na2 O16P -16.9048; 7.0555; 11.8449
105.071; 93.073; 109.955		517.26Yang, Annabeth P.; LaDuca, Robert L.
Poly[diaquabis(μ-hydrogen benzene-1,2,4-tricarboxylato)copper(II)disodium]: a novel 4,5,6-connected trinodal net
IUCrData, 2018, 3, x180676
1549413 CIF
HKL
Paper		C14 H21 N O4P 1 21/c 18.16; 14.876; 12.549
90; 93.192; 90		1520.9Seye, Dame; Diop, Libasse; Diop, Cheikh Abdoul Khadir; Geiger, David K.
Diisopropylammonium hydrogen phthalate
IUCrData, 2018, 3, x180704
1549439 CIF
HKL
Paper		C61 H81 B F15 N3 ZrP 1 21/c 123.493; 11.9942; 21.8489
90; 104.259; 90		5966.9Frerichs, Nils; Adler, Christian; Schmidtmann, Marc; Beckhaus, Rüdiger
Crystal structure of a zwitterionic azaallyl zirconiumamide complex bearing a Zr^+^-μ-CH~3~—B^{-^} moiety and one equivalent of <i>n</i>-hexane as a solvent
IUCrData, 2018, 3, x180644
1549440 CIF
HKL
Paper		C23 H18 Fe2 O S2P -19.8525; 10.6407; 19.272
98.867; 95.255; 105.512		1904.76Sánchez García, Jessica J.; Flores-Alamo, Marcos; Klimova, Elena I.
4,5-Diferrocenyl-1,2-dithiol-3-one
IUCrData, 2018, 3, x180685
1549494 CIF
HKL
Paper		C10 H23 Cl3 N2 PdP 1 21/c 17.286; 17.379; 12.95
90; 102.769; 90		1599.2Oberley, Alan J.; Kadel, Lava R.; Senaratne, Nilmini K.; Eichhorn, David M.
Tetraethylammonium (acetonitrile)trichloridopalladate(II)
IUCrData, 2018, 3, x180750
1549518 CIF
HKL
Paper		C17 H19 NP 1 21/n 16.7724; 7.1774; 26.793
90; 93.184; 90		1300.3Peloquin, Andrew J.; Smith, Madelyn B.; Balaich, Gary J.; Iacono, Scott T.
(<i>E</i>)-1-[1-(3-Phenylcyclopenta-2,4-dien-1-ylidene)ethyl]pyrrolidine
IUCrData, 2018, 3, x180764
1549520 CIF
HKL
Paper		C19 H19 N3 O3P -17.5867; 10.268; 11.4684
95.592; 102.147; 109.987		806.72Koh, Dongsoo; Lee, Ji Hye
4-(3,5-Dimethoxyphenyl)-6-(2-methoxyphenyl)pyrimidin-2-amine
IUCrData, 2018, 3, x180796
1549521 CIF
HKL
Paper		C16 H24 Br4 Cd N2 O2P 1 21/n 116.7564; 7.9403; 17.9303
90; 103.777; 90		2317Umarani, Parthasarathy; Thiruvalluvar, Aravazhi Amalan; Ramachandra Raja, Chidambaram
Bis(4-methoxybenzylammonium) tetrabromidocadmate(II)
IUCrData, 2018, 3, x180795
1549528 CIF
HKL
Paper		C19 H16 O3P -16.8573; 7.4073; 15.55
87.843; 78.892; 72.347		738.4Biruntha, K.; Reuben Jonathan, D.; Mohamooda Sumaya, U.; Dravida Thendral, E. R. A.; Usha, G.
(3<i>E</i>)-3-[(2<i>E</i>)-3-(4-Methoxyphenyl)prop-2-enylidene]-2,3-dihydro-4<i>H</i>-chromen-4-one
IUCrData, 2018, 3, x180829
1549529 CIF
HKL
Paper		C19.83 H29 Cl3 N4 O2.17P -111.0118; 11.7295; 11.7453
66.009; 67.12; 66.057		1220.4Van Erdewyk, Martha L.; Oshin, Kayode D.
Crystal structure of tris[(pyridin-1-ium-2-yl)methyl]amine trichloride‒methanol‒water (1/1.829/0.342)
IUCrData, 2018, 3, x180826
1549562 CIF
HKL
Paper		C5 H17 I N Na O5P -15.8131; 7.6682; 26.7168
90.221; 91.168; 91.44		1190.29Nazarenko, Alexander Y.
Betaine (trimethylammonioacetate) binary compound with sodium iodide
IUCrData, 2018, 3, x180864
1549563 CIF
HKL
Paper		C19 H16 N4 O3P 1 21/c 137.0489; 13.3154; 6.917
90; 93.771; 90		3404.9El-Hiti, Gamal A.; Abdel-Wahab, Bakr F.; Mostafa, Mohamed S.; Khidre, Rizk E.; Hegazy, Amany S.; Kariuki, Benson M.
(<i>E</i>)-1-[5-Methyl-1-(4-methylphenyl)-1<i>H</i>-1,2,3-triazol-4-yl]-3-(4-nitrophenyl)prop-2-en-1-one
IUCrData, 2018, 3, x180841
1549576 CIF
Paper		C14 H12 O3P 21 21 217.4539; 7.8553; 17.2286
90; 90; 90		1008.78Kotha, Sambasivarao; Cheekatla, Subba Rao; Gunta, Rama
Hexacyclo[6.5.1.0^1,5^.0^5,12^.0^7,11^.0^9,13^]tetradecane-4,6,14-trione
IUCrData, 2018, 3, x180852
1549584 CIF
HKL
Paper		C18 H16 N4 O2P 1 21/n 19.2366; 10.2045; 16.1922
90; 92.144; 90		1525.1Moussaif, Ahmed; Ramli, Youssef; El Ghayati, Lhoussaine; Essassi, El Mokhtar; Mague, Joel T.
Ethyl 5-(4-methylphenyl)-2,4,5,7-tetraazatricyclo[6.4.0.0^2,6^]dodeca-1(8),3,6,9,11-pentaene-3-carboxylate
IUCrData, 2018, 3, x180892
1549585 CIF
HKL
Paper		C11 H14 N2 O5P 1 21/n 17.7306; 16.8048; 9.3113
90; 102.001; 90		1183.2Missioui, Mohcine; El Fal, Mohammed; Taoufik, Jamal; Essassi, El Mokhtar; Mague, Joel T.; Ramli, Youssef
2-(3-Methyl-2-oxo-1,2-dihydroquinoxalin-1-yl)acetic acid dihydrate
IUCrData, 2018, 3, x180882
1549586 CIF
HKL
Paper		C17 H13 Cl O3 SP 1 21/c 113.1301; 11.9592; 10.3738
90; 112.041; 90		1509.9Piontek, Aleksandra; Siodłak, Dawid; Zarychta, Bartosz
4-Chloronaphthalen-1-yl 4-methylbenzenesulfonate
IUCrData, 2018, 3, x180889
1549587 CIF
HKL
Paper		C24 H20 O6 S2P 1 21/n 112.227; 5.7229; 15.9353
90; 109.869; 90		1048.68Piontek, Aleksandra; Siodłak, Dawid; Zarychta, Bartosz
Naphthalene-2,6-diyl bis(4-methylbenzenesulfonate)
IUCrData, 2018, 3, x180890
1549604 CIF
HKL
Paper		C45 H39 F6 Fe O4 P3P 1 21/n 19.10074; 17.7897; 24.9408
90; 97.7826; 90		4000.71Ma, Yuzhi; Lindeman, Sergey; Donaldson, William A.
Dicarbonyl{[(<i>E</i>,<i>E</i>)-(2,3,4,5-η)-6-methoxy-6-oxo-2,4-hexadienyl]triphenylphosphonium}(triphenylphosphane-κ<i>P</i>)iron(1+) hexafluoridophosphate
IUCrData, 2018, 3, x180902
1549605 CIF
HKL
Paper		C12 H21 N O3 SP 1 21/c 111.737; 8.8719; 14.3722
90; 106.616; 90		1434.1Seye, Dame; Diop, Cheikh Abdoul Khadir; Diop, Libasse; Geiger, David K.
Diisopropylammonium benzenesulfonate
IUCrData, 2018, 3, x180876
1549606 CIF
HKL
Paper		C28 H30 Mo N2 O4 P2P b c a15.634; 17.716; 21.661
90; 90; 90		5999Höhne, Martha; Gongoll, Marc; Spannenberg, Anke; Müller, Bernd H.; Peulecke, Normen; Rosenthal, Uwe
Tetracarbonyl[<i>N</i>-(diphenylphosphanyl-κ<i>P</i>)-<i>N</i>,<i>N</i>'-diisopropyl-<i>P</i>-phenylphosphorus diamide-κ<i>P</i>]molybdenum(0) with an unknown solvent
IUCrData, 2018, 3, x180846
1549607 CIF
HKL
Paper		C19 H13 F3 N4P 1 21/c 115.0553; 15.7338; 6.9701
90; 99.54; 90		1628.2El Hafi, Mohamed; Boulhaoua, Mohammed; Lahmidi, Sanae; Ramli, Youssef; Essassi, El Mokhtar; Mague, Joel T.
1-Methyl-4-phenyl-3-[4-(trifluoromethyl)phenyl]-1<i>H</i>-pyrazolo[3,4-<i>d</i>]pyrimidine
IUCrData, 2018, 3, x180875
1549608 CIF
HKL
Paper		C12 H15 N O4 SP 1 21/c 18.834; 18.6849; 7.6927
90; 91.478; 90		1269.35Baryala, Yamna; El Bakri, Youness; Anouar, El Hassane; Zerzouf, Abdelfettahb; Essassi, El Mokhtar; Mague, Joel T.
Ethyl 3-methyl-1-oxo-4<i>H</i>-1,4-benzothiazine-2-carboxylate monohydrate
IUCrData, 2018, 3, x180887
1549628 CIF
HKL
Paper		C14 H16 N2 Na O10 Rb S2P n m a14.2754; 6.5831; 21.5365
90; 90; 90		2023.9Nazarenko, Alexander Y.
Sodium rubidium disaccharinate tetrahydrate
IUCrData, 2018, 3, x180867
1549664 CIF
HKL
Paper		C21 H24 N2 O SP 1 21/c 114.898; 14.878; 8.4007
90; 96.78; 90		1849Akrad, Rachida; Guerrab, Walid; Lazrak, Fatima; Ansar, Mhammed; Taoufik, Jamal; Mague, Joel T.; Ramli, Youssef
4,4-Diphenyl-1-propyl-2-propylsulfanyl-4,5-dihydro-1<i>H</i>-imidazol-5-one
IUCrData, 2018, 3, x180934
1549665 CIF
HKL
Paper		C15 H13 N3P 1 21/n 15.9642; 17.7004; 11.3963
90; 100.695; 90		1182.2El Ghayati, Lhoussaine; Ramli, Youssef; Moussaif, Ahmed; Koubachi, Jamal; Taha, Mohamed Labd; Essassi, El Mokhtar; Mague, Joel T.
2-Methyl-4-(pyridin-2-yl)-3<i>H</i>-1,5-benzodiazepine
IUCrData, 2018, 3, x180953
1549666 CIF
HKL
Paper		C17 H12 O4P 1 c 15.7029; 4.0346; 28.9081
90; 90.751; 90		665.09Djandé, Abdoulaye; Abou, Akoun; Kini, Félix; Kambo, Konan René; Giorgi, Michel
2-Oxo-2<i>H</i>-chromen-7-yl 4-methylbenzoate
IUCrData, 2018, 3, x180927
1549667 CIF
HKL
Paper		C16 H16 Cd2 O8P 1 21/n 19.8377; 7.07; 24.268
90; 100.12; 90		1661.6LaDuca, Andrew R.; LaDuca, Robert L.
Poly[(μ5-cis-cyclohex-4-ene-1,2-dicarboxylato)(μ3-cis-cyclohex-4-ene-1,2-dicarboxylato)dicadmium(II)]
IUCrData, 2018, 3, x180924
1549674 CIF
HKL
Paper		C25 H20 N2 O5P -111.5219; 14.2321; 14.7033
72.201; 73.469; 73.647		2150.18Mahfoud, Asmae; Al Houari, Ghali; El Yazidi, Mohamed; Saadi, Mohamed; El Ammari, Lahcen
2-Methyl-3'-(4-methylphenyl)-4'-(2-nitrophenyl)-4'<i>H</i>-spiro[chroman-3,5'-isoxazol]-4-one
IUCrData, 2018, 3, x180962
1549675 CIF
HKL
Paper		C17 H13 N5 OP c a 2123.5234; 10.5928; 23.4895
90; 90; 90		5853.1El-Hiti, Gamal A.; Abdel-Wahab, Bakr F.; Mostafa, Mohamed S.; Khidre, Rizk E.; Hegazy, Amany S.; Kariuki, Benson M.
2-(5-Methyl-1-phenyl-1<i>H</i>-1,2,3-triazol-4-yl)-5-phenyl-1,3,4-oxadiazole
IUCrData, 2018, 3, x180966
1549702 CIF
HKL
Paper		C17 H18 N2 O2 S2P 1 21/n 17.3167; 15.5894; 15.5627
90; 101.82; 90		1737.49Aziz, Hamid; Saeed, Aamer; Simpson, Jim
5,5-Diphenyl-2-thioxoimidazolidin-4-one dimethyl sulfoxide monosolvate
IUCrData, 2018, 3, x181010
1549703 CIF
HKL
Paper		C15 H18 N2 OP 1 21/c 111.4283; 9.2294; 12.3632
90; 96.89; 90		1294.6Al Garadi, Wedad; Ramli, Youssef; El Ghayati, Lhoussaine; Moussaif, Ahmed; Essassi, El Mokhtar; Mague, Joel T.
4-Phenyl-5a,6,7,8,9,9a-hexahydro-1<i>H</i>-1,5-benzodiazepin-2(5<i>H</i>)-one
IUCrData, 2018, 3, x181011
1549714 CIF
HKL
Paper		C22 H15 N O2 SP b c a9.265; 10.3523; 36.0698
90; 90; 90		3459.6Bakhouch, Mohamed; El Yazidi, Mohamed; Al Houari, Ghali; Saadi, Mohamed; El Ammari, Lahcen
3',4'-Diphenyl-3<i>H</i>,4'<i>H</i>-spiro[benzo[<i>b</i>]thiophene-2,5'-isoxazol]-3-one
IUCrData, 2018, 3, x181019
1549720 CIF
HKL
Paper		C14 H18 N2 O3P n a 2112.2836; 14.5343; 7.8596
90; 90; 90		1403.2Rasheeda, Kedila; Samshuddin, Seranthimata; Swathi, Phadke N.; Alva, Vijaya D. P.; Mague, Joel T.; Ramli, Youssef
2-(4-Hydroxyphenyl)-4,6-dimethyl-2,3-dihydropyrimidin-1-ium acetate
IUCrData, 2018, 3, x181046
1549721 CIF
HKL
Paper		C19 H16 O5P 21 21 214.6852; 17.5786; 18.8573
90; 90; 90		1553.07Goyal, Navneet; Do, Camilla; Donahue, James P.; Mague, Joel T.; Foroozesh, Maryam
Ethyl 2-[2-(4-oxo-4<i>H</i>-chromen-2-yl)phenoxy]acetate
IUCrData, 2018, 3, x180993
1549779 CIF
HKL
Paper		C25 H24 N4 O3 SP 1 2/c 18.3287; 13.8956; 20.3124
90; 90.635; 90		2350.7El-Hiti, Gamal A.; Abdel-Wahab, Bakr F.; Alotaibi, Mohammad Hayal; Yousif, Emad; Hegazy, Amany S.; Kariuki, Benson M.
Ethyl 2-anilino-4-methyl-5-[5-methyl-1-(4-methylphenyl)-1<i>H</i>-1,2,3-triazole-4-carbonyl]thiophene-3-carboxylate
IUCrData, 2018, 3, x181106
1549780 CIF
HKL
Paper		H4 N O3 VP b c m4.9045; 11.7945; 5.8231
90; 90; 90		336.84Pérez-Benítez, Aarón; Bernès, Sylvain
Redetermination of ammonium metavanadate
IUCrData, 2018, 3, x181080
1549781 CIF
HKL
Paper		C19 H14 O2P b c n19.7403; 9.3294; 15.0595
90; 90; 90		2773.4Devassia, Tomson; Mathew, Eason M.; Sithambaresan, M.; Unnikrishnan, P. A.; Kurup, M. R. Prathapachandra
10-Methyl-9,11-annulated dibenzobarrelene
IUCrData, 2018, 3, x181102
1549793 CIF
HKL
Paper		C10 H7 Cl N3 Na O2P 1 21/c 111.6462; 6.3754; 14.7003
90; 92.711; 90		1090.26El-Hiti, Gamal A.; Abdel-Wahab, Bakr F.; Alotaibi, Mohammad Hayal; Yousif, Emad; Hegazy, Amany S.; Kariuki, Benson M.
Sodium 1-(4-chlorophenyl)-5-methyl-1<i>H</i>-1,2,3-triazole-4-carboxylate
IUCrData, 2018, 3, x181127
1549794 CIF
HKL
Paper		C37 H31 B Cl3 F4 N P2P -19.6306; 10.813; 17.0381
91.826; 95.619; 90.734		1764.6Manandhar, Rachana; Rath, Nigam P.; Jones, Myron W.
Bis(triphenylphosphine)iminium tetrafluoroborate chloroform monosolvate
IUCrData, 2018, 3, x181108
1549795 CIF
HKL
Paper		C15 H22 I NP b c a15.631; 11.614; 16.976
90; 90; 90		3082da Costa Duarte, Rodrigo; Kommers Reimann, Louise; Severo Rodembusch, Fabiano; Gustavo Teixeira Alves Duarte, Luís
1-Butyl-2,3,3-trimethylindol-1-ium iodide
IUCrData, 2018, 3, x181130
1549803 CIF
HKL
Paper		C16 H12 O3P 1 21/n 113.2958; 5.1981; 18.8162
90; 109.212; 90		1228.02Padgett, Clifford W.; Lynch, Will E.; Sheriff, Kirkland; Dean, Raven; Zingales, Sarah
3-Hydroxy-2-(4-methylphenyl)-4<i>H</i>-chromen-4-one
IUCrData, 2018, 3, x181138
1549804 CIF
HKL
Paper		C18 H18 Cl N3 OP 659.9013; 9.9013; 28.981
90; 90; 120		2460.5Lee, Ji Hye; Koh, Dongsoo
2-Amino-4-(4-methoxyphenyl)-6-(4-methylphenyl)pyrimidin-1-ium chloride
IUCrData, 2018, 3, x181152
1549819 CIF
HKL		C17 H20 N6 O2P -17.3968; 10.6475; 12.7769
106.577; 100.809; 108.208		872.83El-Hiti, Gamal A.; Abdel-Wahab, Bakr F.; Alotaibi, Mohammad Hayal; Yousif, Emad; Hegazy, Amany S.; Kariuki, Benson M.
5-Methyl-1-(4-methylphenyl)-<i>N</i>'-[1-(1<i>H</i>-pyrrol-2-yl)ethylidene]-1<i>H</i>-1,2,3-triazole-4-carbohydrazide monohydrate
IUCrData, 2018, 3, x181162
1549869 CIF
HKL
Paper		C25 H47 N O7P 21 21 217.9093; 13.3712; 25.3669
90; 90; 90		2682.72Eitel, Michael; Schollmeyer, Dieter; Gross, Harald; Koch, Pierre
(2<i>S</i>,3<i>S</i>)-2-Azaniumyl-4-[(1<i>S</i>,4a<i>S</i>,4b<i>S</i>,6<i>S</i>,7<i>S</i>,8a<i>S</i>,10a<i>S</i>)-6,7-dihydroxy-2,4b,8,8,10a-pentamethyl-1,4,4a,4b,5,6,7,8,8a,9,10,10a-dodecahydrophenanthren-1-yl]-3-methoxybutanoate–methanol–water (1/1/1)
IUCrData, 2018, 3, x181194
1549870 CIF
HKL
Paper		C9 H14 Br4 Co N4C 1 2/c 115.7782; 7.4076; 28.567
90; 95.7271; 90		3322.2Peppel, Tim; Spannenberg, Anke
3,3'-Dimethyl-1,1'-methylenediimidazolium tetrabromidocobaltate(II)
IUCrData, 2018, 3, x181212
1549871 CIF
HKL
Paper		C18 H13 Cl2 N O2P -17.4005; 10.4272; 10.5704
86.076; 72.382; 81.325		768.3Grinev, Vyacheslav S.; Osipov, Alexander K.; Yegorova, Alevtina Yu.
(<i>Z</i>)-3-[(3,5-Dichloroanilino)methylidene]-5-(4-methylphenyl)furan-2(3<i>H</i>)-one
IUCrData, 2018, 3, x181224
1549872 CIF
HKL
Paper		C13 H13 N2 O7P -17.2618; 8.9419; 11.0001
85.545; 86.177; 75.248		687.84Dziuk, Błażej; Jezuita, Anna
2,2'-Bipyridin-1-ium hemioxalate oxalic acid monohydrate
IUCrData, 2018, 3, x181219
1549898 CIF
HKL
Paper		C22 H36 N2P 1 21/n 15.6271; 21.1764; 8.2787
90; 105.86; 90		948.95Grace, P. Selvarathy; Nirmalram, Jeyaraman Selvaraj; Nayagam, B. Ravindran Durai; Schollmeyer, Dieter
1,1'-[(2,3,5,6-Tetramethyl-1,4-phenylene)bis(methylene)]dipiperidine
IUCrData, 2018, 3, x181237
1549899 CIF
HKL
Paper		C15 H14 N4 O3P 15.859; 7.479; 16.329
93.818; 91.29; 94.252		711.7Wang, Zhaodong; Ni, Haitao
Methyl 4-{<i>N</i>'-[(1<i>E</i>)-1-(pyrazin-2-yl)ethylidene]hydrazinecarbonyl}benzoate
IUCrData, 2018, 3, x181230
1549950 CIF
HKL
Paper		C20 H19 N O2P 1 21/c 19.362; 11.6073; 15.0732
90; 98.859; 90		1618.43Biruntha, K.; Reuben Jonathan, D.; Mohamooda Sumaya, U.; Dravida Thendral, E. R. A.; Usha, G.
Crystal structure of (3<i>E</i>)-3-{(2<i>E</i>)-3-[4-(dimethylamino)phenyl]prop-2-enylidene}-3,4-dihydro-2<i>H</i>-chromen-4-one
IUCrData, 2018, 3, x181273
1549951 CIF
HKL
Paper		C17 H24 N2 O SP 1 21/n 112.0255; 8.9303; 15.8822
90; 95.813; 90		1696.84Al Garadi, Wedad; Ramli, Youssef; El Ghayati, Lhoussaine; El Hafi, Mohamed; Moussaif, Ahmed; Essassi, El Mokhtar; Mague, Joel T.
4-Phenyl-2,5,5a,6,7,8,9,9a-hexahydro-1<i>H</i>-1,5-benzodiazepine-2-thione ethanol monosolvate
IUCrData, 2018, 3, x181276
1549952 CIF
HKL
Paper		C21 H16 O4P -17.9937; 9.3819; 12.2131
72.552; 86.895; 67.288		804.06Sung, Jiha
6-Methoxy-2-(2-methoxynaphthalen-1-yl)-4<i>H</i>-chromen-4-one
IUCrData, 2018, 3, x181277
1549966 CIF
HKL
Paper		C30 H24 N4 O2 SC 1 2/c 118.6131; 18.2243; 15.8867
90; 110.757; 90		5039.2Muthuselvi, C.; Athimoolam, S.; Srinivasan, N.; Ravikumar, B.; Pandiarajan, S.; Krishnakumar, R. V.
Ethyl 6'-cyano-7'-phenyl-1',6',7',7a'-tetrahydro-3'<i>H</i>-spiro[indeno[1,2-<i>b</i>]quinoxaline-11,5'-pyrrolo[1,2-<i>c</i>]thiazole-6'-carboxylate
IUCrData, 2018, 3, x181286
1549978 CIF
HKL
Paper		C15 H9 F O3P 1 21/c 122.3701; 6.8836; 15.7987
90; 106.058; 90		2337.88Koh, Dongsoo
2-(2-Fluorophenyl)-3-hydroxy-4<i>H</i>-chromen-4-one
IUCrData, 2018, 3, x181332
1549979 CIF
HKL
Paper		C8 H12 N2 O8C 1 2/c 116.805; 8.3008; 15.7976
90; 100.259; 90		2168.5Seidel, Rüdiger W.
Revision of the crystal structure of `bis(glycine) squaric acid'
IUCrData, 2018, 3, x181324
1549980 CIF
HKL
Paper		C18 H14 O2 SP 1 21/n 113.0062; 5.9631; 18.3801
90; 104.019; 90		1383.05Hemanathan, K.; Raja, R.; Murugesan, K. Sakthi
8,9-Dimethoxybenzo[<i>b</i>]naphtho[2,3-<i>d</i>]thiophene
IUCrData, 2018, 3, x181257
1549981 CIF
HKL
Paper		C27 H22 N4 O2P 1 21/c 18.0233; 16.877; 17.013
90; 101.021; 90		2261.2Liu, Gang; Liu, Qingsong; Zhang, Huihui; Yu, Jianhua
2-(4-Aminophenyl)-3-[3,4-bis(pyridin-2-ylmethoxy)phenyl]acrylonitrile
IUCrData, 2018, 3, x181329
1549982 CIF
HKL
Paper		C13 H16 N4 O2P 1 21/n 19.069; 13.319; 11.851
90; 112.161; 90		1325.7Lahmidi, Sanae; El Hafi, Mohamed; Moussaif, Ahmed; Benchidmi, Mohammed; Essassi, El Mokhtar; Mague, Joel T.
Ethyl 2-(5-methyl-1,2,4-triazolo[1,5-<i>a</i>]pyrimidin-7-yl)pent-4-enoate
IUCrData, 2018, 3, x181280
1549983 CIF
HKL
Paper		C17 H19 N O5P 1 21/c 18.462; 16.243; 11.477
90; 93.091; 90		1575.2Wang, Junjun; Zhu, Yin; Wang, Haiyan; Yang, Mingdi
3-Acetyl-7-(2-morpholin-4-yl-ethoxy)-chromen-2-one
IUCrData, 2018, 3, x181327
1549987 CIF
HKL
Paper		C17 H18 O2P -17.841; 8.203; 11.08
79.131; 85.616; 74.077		672.8Goyal, Navneet; Donahue, James P.; Do, Camilla; Perry, Timothy; Bongay-Williams, Kyla; Foroozesh, Maryam
A dibenzofuran derivative: 2-(pentyloxy)dibenzo[<i>b</i>,<i>d</i>]furan
IUCrData, 2018, 3, x181306
1549988 CIF
HKL
Paper		C21 H15 N3 O3P 1 21/c 110.1759; 23.521; 7.4038
90; 95.674; 90		1763.4Rao, Qingpeng; Wang, Zepeng; Yang, Mingdi; Wu, Zhichao
(<i>Z</i>)-2-(4-Nitrophenyl)-3-[4-(pyridin-4-ylmethoxy)phenyl]acrylonitrile
IUCrData, 2018, 3, x181328
1549989 CIF
HKL
Paper		C11 H11 N3 O4P -110.1251; 11.1335; 15.9006
102.745; 101.1; 101.52		1659.74Marten, Jan; Seichter, Wilhelm; Weber, Edwin
3-[2-(3-Nitrophenyl)hydrazin-1-ylidene]pentane-2,4-dione
IUCrData, 2018, 3, x181344
1550027 CIF
HKL
Paper		C21.5 H20.5 Br N6.5 O0.5 SP -19.9957; 14.5325; 15.8353
81.671; 81.344; 80.469		2225.6El-Hiti, Gamal A.; Abdel-Wahab, Bakr F.; Alotaibi, Mohammad Hayal; Yousif, Emad; Hegazy, Amany S.; Kariuki, Benson M.
5-[(4-Bromophenyl)diazenyl]-2-{2-[1-(1<i>H</i>-indol-3-yl)ethylidene]hydrazinyl}-4-methylthiazole dimethylformamide hemisolvate
IUCrData, 2018, 3, x181378
1550028 CIF
HKL
Paper		C17 H17 N5 O SP -19.0292; 9.864; 10.8754
111.021; 105.103; 96.945		847.86El-Hiti, Gamal A.; Abdel-Wahab, Bakr F.; Alotaibi, Mohammad Hayal; Yousif, Emad; Hegazy, Amany S.; Kariuki, Benson M.
5-Methyl-1-(4-methylphenyl)-N′-[1-(thiophen-2-yl)ethylidene]-1H-1,2,3-triazole-4-carbohydrazide
IUCrData, 2018, 3, x181379
1550078 CIF
HKL
Paper		C24 H23 N3 O2P -18.6962; 8.7349; 14.559
106.468; 92.949; 111.771		969.6Jouha, Jabrane; Loubidi, Mohamed; El Hafi, Mohamed; Tber, Zahira; Essassi, El Mokhtar; Mague, Joel T.
Ethyl 4-(3,4,6-trimethyl-1-phenyl-1<i>H</i>-pyrazolo[3,4-<i>b</i>]pyridin-5-yl)benzoate
IUCrData, 2018, 3, x181449
1550079 CIF
HKL
Paper		C11 H23 N10 O15 SmP 1 21/c 110.0164; 22.7494; 15.0848
90; 138.151; 90		2293.3Gioia, Michael; Crundwell, Guy; Westcott, Barry L.
Tetraaqua[2,6-diacetylpyridine bis(semicarbazone)]samarium(III) trinitrate
IUCrData, 2018, 3, x181454
1550080 CIF
HKL
Paper		C18 H19 N O7P -14.9417; 7.6157; 23.4472
94.49; 92.997; 98.136		869.06Bouzian, Younos; Hlimi, Fouzia; kheira Sebbar, Nada; El Hafi, Mohamed; Hni, Brahim; Essassi, El Mokhtar; Mague, Joel T.
Ethyl 2-{[2-(2-ethoxy-2-oxoethoxy)quinolin-4-yl]carbonyloxy}acetate
IUCrData, 2018, 3, x181438
1550081 CIF
HKL
Paper		C8 H20 Cl6 N2 SnC 1 2/m 116.3784; 7.3134; 7.1566
90; 91.205; 90		857.04Gotoh, Kazuma; Ishida, Hiroyuki
Bis(pyrrolidinium) hexachloridostannate: a redetermination
IUCrData, 2018, 3, x181397
1550082 CIF
HKL
Paper		C19 H28 Cl N3 O5P 438.5308; 8.5308; 31.893
90; 90; 90		2321Rasheeda, Kedila; Samshuddin, Seranthimata; Swathi, Phadke N.; Alva, Vijaya D. P.; Mague, Joel T.; Ramli, Youssef
Diethyl 4-(4-chloro-2-propyl-1<i>H</i>-imidazol-5-yl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate monohydrate
IUCrData, 2018, 3, x181470
1550129 CIF
HKL
Paper		C12 H8 Br2 N2 OP 1 21/n 13.8938; 5.8223; 25.8645
90; 92.044; 90		586Goswami, Shailesh K.; Hanton, Lyall R.; McAdam, C. John; Moratti, Stephen C.; Simpson, Jim
(<i>Z</i>)-1,2-Bis(3-bromophenyl)diazene 1-oxide
IUCrData, 2018, 3, x181486
1550130 CIF
HKL
Paper		C13 H10 Cl N OP -19.7335; 10.6473; 24.7554
87.443; 84.272; 62.978		2274.1Javed, Saleem; Faizi, Md. Serajul Haque; Nazia, Siddiqui; Iskenderov, Turganbay
2-Amino-5-chlorobenzophenone
IUCrData, 2018, 3, x181444
1550169 CIF
HKL
Paper		C10 H28 Cl6 N6 TeF d d d7.3899; 22.447; 28.512
90; 90; 90		4729.6Giltzau, Niels Ole; Köckerling, Martin
Bis(tetramethylguanidinium) hexachloridotellurate(IV)
IUCrData, 2018, 3, x181488
1550200 CIF
HKL
Paper		C7 H9 I N2 SC 1 2/c 119.6249; 7.2198; 14.9117
90; 108.592; 90		2002.5Shotonwa, Ibukun O.; Boeré, René T.
1-Methyl-4-thiocarbamoylpyridin-1-ium iodide
IUCrData, 2018, 3, x181491
1550216 CIF
HKL
Paper		C19 H37 Cl2 Co Li N2 O3P 1 21/n 110.0535; 12.3705; 19.236
90; 104.476; 90		2316.4Vinocour, Felipe A.; Soto-Navarro, Andrea; Pineda, Leslie W.
μ2-Chlorido-chlorido(μ2-4-{[2-(diethylamino)ethyl]imino}pent-2-en-2-olato)bis(tetrahydrofuran-κO)cobalt(II)lithium
IUCrData, 2018, 3, x181577
1550217 CIF
HKL
Paper		C16 H14 O2P 1 21 110.1497; 5.1276; 11.6896
90; 99.541; 90		599.95Detert, Heiner; Schollmeyer, Dieter
The <i>rel-R</i>,<i>R</i>-enantiomer of 7-[7-hydroxybicyclo[4.2.0]octa-1(6),2,4-trien-7-yl]bicyclo[4.2.0]octa-1(6),2,4-trien-7-ol
IUCrData, 2018, 3, x181550
1550273 CIF
HKL
Paper		C16 H14 OP 21 21 217.485; 9.173; 16.995
90; 90; 90		1166.9Umaña, Christian A.; Pineda, Leslie W.; Cabezas, Jorge A.
Homopropargyl alcohol 1,1-diphenylbut-3-yn-1-ol
IUCrData, 2018, 3, x181619
1550274 CIF
HKL		C19 H18 O7P 1 21/c 112.1143; 9.8134; 14.2602
90; 95.116; 90		1688.53Abou, Akoun; Akonan, Ludovic; Koblavi-Mansilla, Frédérica; N'gouan, Aka Joseph; Kambo, Konan René
3-Hydroxy-3-methylisochroman-1-one–2-(carboxymethyl)benzoic acid (1/1)
IUCrData, 2018, 3, x181653
1550275 CIF
HKL
Paper		C20 H16 O SP 1 21/n 19.424; 16.0262; 20.8913
90; 99.042; 90		3116Umaña, Christian A.; Pineda, Leslie W.; Cabezas, Jorge A.
1,1-Diphenyl-4-(thiophen-2-yl)but-3-yn-1-ol
IUCrData, 2018, 3, x181616
1550276 CIF
HKL
Paper		C2 H10 N4 O8 S4P -15.1371; 9.5237; 12.9884
106.521; 96.067; 95.618		600.32Zouihri, Hafid; El Korchi, Khadija; Yamni, Khalid; Tijani, Najib
Dithiobis(formamidinium) bis(hydrogen sulfate)
IUCrData, 2018, 3, x181540
1550277 CIF
HKL
Paper		C17 H16 O2P 1 21/c 17.9772; 22.8528; 7.3075
90; 92.791; 90		1330.59Umaña, Christian A.; Pineda, Leslie W.; Cabezas, Jorge A.
Homopropargyl alcohol 5,5-diphenylpent-2-yne-1,5-diol
IUCrData, 2018, 3, x181618
1550278 CIF
HKL
Paper		C6 H7 N5 OP -16.5921; 8.3935; 13.185
92.023; 98.309; 99.741		710.1Lahmidi, Sanae; El Hafi, Mohamed; kheira Sebbar, Nada; Abad, Nadeem; Essassi, El Mokhtar; Mague, Joel T.
2-Amino-5-methyl-1,2,4-triazolo[1,5-<i>a</i>]pyrimidin-7(4<i>H</i>)-one
IUCrData, 2018, 3, x181500
1550294 CIF
HKL
Paper		C19 H22 O2P 1 21/c 110.865; 14.3936; 9.8008
90; 111.68; 90		1424.3Kotha, Sambasivarao; Gunta, Rama; Cheekatla, Subba Rao; Mhatre, Darshan S.
Spiro[cyclopentane-1,11'-hexacyclo[7.6.0.0^1,6^.0^6,13^.0^8,12^.0^10,14^]pentadecane]-7',15'-dione
IUCrData, 2018, 3, x181590
1550295 CIF
HKL
Paper		Ca2 Cl2 Cu O2I 4/m m m3.868; 3.868; 15.0321
90; 90; 90		224.9Baptiste, Benoît; Azuma, Masaki; Yu, Runze; Giura, Paola; d'Astuto, Matteo
Ca2CuO2Cl2, a redetermination from single-crystal X-ray diffraction data
IUCrData, 2018, 3, x181645
1550311 CIF
HKL
Paper		C17 H16 N2 O2P 1 21/n 18.1914; 9.5151; 17.781
90; 94.88; 90		1380.9Abad, Nadeem; Ramli, Youssef; Lahmidi, Sanae; El Hafi, Mohamed; Essassi, El Mokhtar; Mague, Joel T.
1-(3-Hydroxypropyl)-3-phenylquinoxalin-2(1<i>H</i>)-one
IUCrData, 2018, 3, x181633
1550312 CIF
HKL
Paper		C19 H17 N3 SP -17.6672; 9.9098; 11.4101
82.548; 78.176; 76.607		822.39Loubidi, Mohamed; Jouha, Jabrane; Tber, Zahira; El Hafi, Mohamed; Essassi, El Mokhtar; Mague, Joel T.
3,4,6-Trimethyl-1-phenyl-5-(thiophen-3-yl)-1<i>H</i>-pyrazolo[3,4-<i>b</i>]pyridine
IUCrData, 2018, 3, x181593
1550313 CIF
HKL
Paper		C13 H12 Cl N3 O2P 21 21 216.4405; 7.266; 28.081
90; 90; 90		1314.1Stondus, Jigmat; Anthal, Sumati; Jayashree, A.; Narayana, B.; Sarojini, B. K.; Kant, Rajni
Polymorph of (<i>E</i>)-<i>N</i>'-(4-chlorobenzylidene)isonicotinohydrazide monohydrate
IUCrData, 2018, 3, x181634
1550314 CIF
HKL
Paper		C10 H12 O3P 21 21 215.4774; 11.1557; 14.561
90; 90; 90		889.74Abdou, Moaz M.; Matziari, Magdalini; O'Neill, Paul M.; Amigues, Eric; Zhou, Ruixue; Wang, Ruiyao; Ali, Basem F.
Methyl 3-(4-hydroxyphenyl)propionate
IUCrData, 2018, 3, x181662
1550336 CIF
HKL
Paper		C9 H11 N O3P 14.8011; 6.5522; 7.5052
93.618; 107.044; 95.658		223.575Baillargeon, Pierre; Rahem, Tarik; Amigo, Carl; Fortin, Daniel; Dory, Yves L.
Polar crystal of vanillylformamide through replacement of the alkene by an isosteric formamide group
IUCrData, 2018, 3, x181630
1550356 CIF
HKL
Paper		C11 H11 N O2P b c m8.3019; 16.628; 6.7622
90; 90; 90		933.5Furuya, Tetsundo; Yagi, Shiomi; Yamazaki, Shu; Haraguchi, Tomoyuki; Akitsu, Takashiro; Mahesha, Ninganayaka; Sagar, Belakavadi K.; Yathirajan, Hemmige S.
Methyl 1-methyl-1<i>H</i>-indole-3-carboxylate
IUCrData, 2018, 3, x181728
1550362 CIF
HKL
Paper		C188 H140 Cl12 N16 O8 Zn3P 1 21/n 120.216; 21.275; 20.821
90; 115.414; 90		8088Makino, Masatomo; Matsubayashi, Kazuhiko; Kodama-Oda, Yukiko; Imawaka, Naoto; Mizuno, Nobuhiro; Kumasaka, Takashi; Yoshino, Katsumi
Construction of a supramolecule comprising [2,3,9,10,16,17,23,24-octakis(2,6-dimethylphenoxy)phthalocyaninato]zinc(II) and (5,10,15,20-tetraphenylporphyrinato)zinc(II)
IUCrData, 2018, 3, x181741
1550363 CIF
HKL
Paper		C10 H13 N O4P 1 21/c 112.996; 9.2813; 8.665
90; 105.503; 90		1007.1Suresh, S.; Pandi, P.; Akilan, R.; Kumar, R. Mohan; Chakkaravarthi, G.
4-Methylanilinium 2-carboxyacetate
IUCrData, 2018, 3, x181714
1550364 CIF
HKL		C11 H8 Cl2 N2 O3P 1 21/c 17.8233; 7.4705; 20.1932
90; 94.866; 90		1175.92Stondus, Jigmat; Anthal, Sumati; Karanth, S.; Narayana, B.; Sarojini, B. K.; Kant, Rajni
2,4-Dichloro-<i>N</i>-(2,5-dioxopyrrolidin-1-yl)benzamide
IUCrData, 2018, 3, x181740
1550365 CIF
HKL
Paper		C10 H10 N2 OP 21 21 217.5676; 10.7802; 11.4092
90; 90; 90		930.77Dioukhane, Khadim; Aouine, Younas; Faraj, Hassane; Alami, Anouar; Essassi, El Mokhtar; Zouihri, Hafid
4-Methyl-1<i>H</i>-1,5-benzodiazepin-2(3<i>H</i>)-one
IUCrData, 2018, 3, x181718
1550374 CIF
HKL
Paper		C22 H28 Cl18 N2 Nb6 O2 S2P 1 21/c 18.711; 24.171; 11.0653
90; 102.598; 90		2273.75Sperlich, Eric; Köckerling, Martin
(C~7~H~6~NS)~2~[Nb~6~Cl~18~]·2C~4~H~8~O: first niobium cluster with an <i>N</i>,<i>S</i>-heterocyclic cation
IUCrData, 2018, 3, x181760
1550385 CIF
HKL
Paper		C5 H10 N2 O3 SP 1 21/n 110.1891; 7.4627; 11.4884
90; 111.635; 90		812.02Hmissa, Taha; Mathivathanan, Logesh; Thompson, Alexander P.; Mirjafari, Arsalan
1-Methyl-1<i>H</i>-imidazol-3-ium methanesulfonate
IUCrData, 2018, 3, x181781
1550386 CIF
Paper		C10 H12 O4P 1 21/n 17.818; 17.017; 8.189
90; 117.459; 90		966.7Xiong, Huiping; Mao, Shilong; Lv, Qianzhou; Zhang, Ning
Crystal structure of the ethyl 2,4-dihydroxy-6-methylbenzoate from <i>Illicium difengpi</i> K.I.B et K.I.M.
IUCrData, 2018, 3, x181776
1550387 CIF
HKL
Paper		C24 H22 N2 O P2P -18.4464; 10.4163; 13.488
71.55; 76.477; 71.75		1057.04Höhne, Martha; Aluri, Bhaskar R.; Spannenberg, Anke; Müller, Bernd H.; Peulecke, Normen; Rosenthal, Uwe
1-Diphenylphosphanyl-2-(diphenylphosphoryl)hydrazine
IUCrData, 2018, 3, x181784
1550389 CIFCo Li0.37 O2R -3 m :H2.812; 2.812; 14.437
90; 90; 120		98.86Rosolen JM; Ballirano P; Berrettoni M; Decker F; Gregorkiewitz M
Structural Assessment of the Electrochemical Performance of LixCoO2 Membrane Electrodes by X-Ray Diffraction and Absorpion Refinements
Ionics, 1997, 3, 345-354
1550390 CIFCo Li0.42 O2R -3 m :H2.8149; 2.8149; 14.3429
90; 90; 120		98.42Rosolen JM; Ballirano P; Berrettoni M; Decker F; Gregorkiewitz M
Structural Assessment of the Electrochemical Performance of LixCoO2 Membrane Electrodes by X-Ray Diffraction and Absorpion Refinements
Ionics, 1997, 3, 345-354
1550391 CIFCo Li0.48 O2R -3 m :H2.8127; 2.8127; 14.3151
90; 90; 120		98.078Rosolen JM; Ballirano P; Berrettoni M; Decker F; Gregorkiewitz M
Structural Assessment of the Electrochemical Performance of LixCoO2 Membrane Electrodes by X-Ray Diffraction and Absorpion Refinements
Ionics, 1997, 3, 345-354
1550392 CIFCo Li0.5 O2R -3 m :H2.8127; 2.8127; 14.2754
90; 90; 120		97.806Rosolen JM; Ballirano P; Berrettoni M; Decker F; Gregorkiewitz M
Structural Assessment of the Electrochemical Performance of LixCoO2 Membrane Electrodes by X-Ray Diffraction and Absorpion Refinements
Ionics, 1997, 3, 345-354
1550393 CIFCo Li0.58 O2R -3 m :H2.8145; 2.8145; 14.2475
90; 90; 120		97.74Rosolen JM; Ballirano P; Berrettoni M; Decker F; Gregorkiewitz M
Structural Assessment of the Electrochemical Performance of LixCoO2 Membrane Electrodes by X-Ray Diffraction and Absorpion Refinements
Ionics, 1997, 3, 345-354
1550394 CIFCo Li0.79 O2R -3 m :H2.8165; 2.8165; 14.093
90; 90; 120		96.817Rosolen JM; Ballirano P; Berrettoni M; Decker F; Gregorkiewitz M
Structural Assessment of the Electrochemical Performance of LixCoO2 Membrane Electrodes by X-Ray Diffraction and Absorpion Refinements
Ionics, 1997, 3, 345-354
1550395 CIFCo Li0.89 O2R -3 m :H2.8175; 2.8175; 14.0598
90; 90; 120		96.658Rosolen JM; Ballirano P; Berrettoni M; Decker F; Gregorkiewitz M
Structural Assessment of the Electrochemical Performance of LixCoO2 Membrane Electrodes by X-Ray Diffraction and Absorpion Refinements
Ionics, 1997, 3, 345-354
1550396 CIFCo Li0.98 O2R -3 m :H2.8178; 2.8178; 14.0621
90; 90; 120		96.694Rosolen JM; Ballirano P; Berrettoni M; Decker F; Gregorkiewitz M
Structural Assessment of the Electrochemical Performance of LixCoO2 Membrane Electrodes by X-Ray Diffraction and Absorpion Refinements
Ionics, 1997, 3, 345-354
1550397 CIFCo Li O2R -3 m :H2.8185; 2.8185; 14.0664
90; 90; 120		96.772Rosolen JM; Ballirano P; Berrettoni M; Decker F; Gregorkiewitz M
Structural Assessment of the Electrochemical Performance of LixCoO2 Membrane Electrodes by X-Ray Diffraction and Absorpion Refinements
Ionics, 1997, 3, 345-354
1550398 CIFCo Li1.16 O2R -3 m :H2.8176; 2.8176; 14.061
90; 90; 120		96.673Rosolen JM; Ballirano P; Berrettoni M; Decker F; Gregorkiewitz M
Structural Assessment of the Electrochemical Performance of LixCoO2 Membrane Electrodes by X-Ray Diffraction and Absorpion Refinements
Ionics, 1997, 3, 345-354
1550399 CIFCo Li1.43 O2R -3 m :H2.8503; 2.8503; 14.139
90; 90; 120		99.48Rosolen JM; Ballirano P; Berrettoni M; Decker F; Gregorkiewitz M
Structural Assessment of the Electrochemical Performance of LixCoO2 Membrane Electrodes by X-Ray Diffraction and Absorpion Refinements
Ionics, 1997, 3, 345-354
1552859 CIF
HKL
Paper		C36 H38 Cl4 Cu2 N6 O2P 1 21/n 112.004; 9.7942; 17.4116
90; 107.633; 90		1950.9Naugle, Mercedes S.; Keller, Brittany T.; Zeller, Matthias; Zaleski, Curtis M.
Di-μ-chlorido-bis[chlorido(dimethylformamide-κ<i>N</i>)(3,5-diphenyl-1<i>H</i>-pyrazole-κ<i>N</i>^2^)copper(II)]
IUCrData, 2018, 3, x181186
1552860 CIF
HKL
Paper		C34 H45 Li Mo N4 O4 P2P -111.7633; 12.5731; 13.7249
87.283; 75.537; 67.45		1812.66Höhne, Martha; Spannenberg, Anke; Müller, Bernd H.; Peulecke, Normen; Rosenthal, Uwe
Tetracarbonyl-2κ^4^<i>C</i>-[μ-5-methyl-1,1,3-triphenyl-2-(propan-2-yl)-2,4-diaza-1,3-diphosphahexan-4-ido-1κ<i>N</i>^4^:2κ<i>P</i>^1^,<i>P</i>^3^](<i>N</i>,<i>N</i>,<i>N</i>',<i>N</i>'-tetramethylethane-1,2-diamine-1κ^2^<i>N</i>,<i>N</i>')lithiummolybdenum
IUCrData, 2018, 3, x181149
1553182 CIFC20 H19 N O7P 1 21/c 111.3454; 13.013; 12.3899
90; 91.009; 90		1828.93Kulkarni, Anand M.; Srinivas, Kolluru; Deshpande, Mukund V.; Ramana, Chepuri V.
Cu-catalyzed sequential C–N bond formations: expeditious synthesis of tetracyclic indoloindol-3-ones
Organic Chemistry Frontiers, 2016, 3, 43
1553195 CIFC24 H22 N4 O4P 21 21 217.6889; 15.5382; 16.4272
90; 90; 90		1962.58Mao, Zhong-Yi; Geng, Hui; Zhang, Tian-Tian; Ruan, Yuan-Ping; Ye, Jian-Liang; Huang, Pei-Qiang
Stereodivergent and enantioselective total syntheses of isochaetominines A–C and four pairs of isochaetominine C enantiomers: a six-step approach
Organic Chemistry Frontiers, 2016, 3, 24
1553196 CIFC24 H26 N4 O6P -19.32; 10.5489; 12.1772
95.818; 90.49; 111.805		1104.44Mao, Zhong-Yi; Geng, Hui; Zhang, Tian-Tian; Ruan, Yuan-Ping; Ye, Jian-Liang; Huang, Pei-Qiang
Stereodivergent and enantioselective total syntheses of isochaetominines A–C and four pairs of isochaetominine C enantiomers: a six-step approach
Organic Chemistry Frontiers, 2016, 3, 24
1553197 CIFC15 H24 Br N O5P -18.8508; 10.0352; 10.7879
116.066; 107.114; 90.5266		811.83Acharya, A.; Eickhoff, J. A.; Chen, K.; Catalano, V. J.; Jeffrey, C. S.
Access to bicyclic hydroxamate macrocycles via intramolecular aza-(4 + 3) cyloaddition reactions of aza-oxyallylic cation intermediates
Organic Chemistry Frontiers, 2016, 3, 330
1553198 CIFC14 H23 Cl2 N O5P 1 21/n 111.7775; 8.7429; 16.8595
90; 105.852; 90		1670Acharya, A.; Eickhoff, J. A.; Chen, K.; Catalano, V. J.; Jeffrey, C. S.
Access to bicyclic hydroxamate macrocycles via intramolecular aza-(4 + 3) cyloaddition reactions of aza-oxyallylic cation intermediates
Organic Chemistry Frontiers, 2016, 3, 330
1553199 CIFC13 H19 N O4P 1 21/n 111.3134; 9.429; 12.7345
90; 110.991; 90		1268.29Acharya, A.; Eickhoff, J. A.; Chen, K.; Catalano, V. J.; Jeffrey, C. S.
Access to bicyclic hydroxamate macrocycles via intramolecular aza-(4 + 3) cyloaddition reactions of aza-oxyallylic cation intermediates
Organic Chemistry Frontiers, 2016, 3, 330
1553200 CIFC15 H21 N O4P 1 21/c 117.0197; 16.271; 10.1414
90; 99.0774; 90		2773.26Acharya, A.; Eickhoff, J. A.; Chen, K.; Catalano, V. J.; Jeffrey, C. S.
Access to bicyclic hydroxamate macrocycles via intramolecular aza-(4 + 3) cyloaddition reactions of aza-oxyallylic cation intermediates
Organic Chemistry Frontiers, 2016, 3, 330
1553201 CIFC13 H19 N O5P 1 21/n 110.9816; 9.2222; 13.0751
90; 107.689; 90		1261.57Acharya, A.; Eickhoff, J. A.; Chen, K.; Catalano, V. J.; Jeffrey, C. S.
Access to bicyclic hydroxamate macrocycles via intramolecular aza-(4 + 3) cyloaddition reactions of aza-oxyallylic cation intermediates
Organic Chemistry Frontiers, 2016, 3, 330
1553202 CIFC25 H32 Cl Ir N2P 1 21/n 113.083; 9.848; 18.876
90; 93.26; 90		2428.1Tang, Guo-Dong; Pan, Cheng-Ling; Li, Xingwei
Iridium(iii)- and rhodium(iii)-catalyzed coupling of anilines with α-diazoesters via chelation-assisted C‒H activation
Organic Chemistry Frontiers, 2016, 3, 87
1553203 CIFC27 H29 N O2P 1 21/c 115.5737; 12.7774; 11.4615
90; 91.399; 90		2280.06Roy, Tony; Bhojgude, Sachin Suresh; Kaicharla, Trinadh; Thangaraj, Manikandan; Garai, Bikash; Biju, Akkattu T.
Employing carboxylic acids in aryne multicomponent coupling triggered by aziridines/azetidines
Organic Chemistry Frontiers, 2016, 3, 71
1553204 CIFC12 H14 O2P 1 21/c 19.8964; 7.7982; 13.421
90; 91.267; 90		1035.5Ling, Jesse; Lam, Sze Kui; Lo, Brian; Lam, Sarah; Wong, Wing-Tak; Sun, Jian; Chen, Guanhua; Chiu, Pauline
Epoxy and aziridinyl enolsilanes in diastereoselective inter- and intramolecular Friedel–Crafts alkylations
Organic Chemistry Frontiers, 2016, 3, 457
1553205 CIFC22 H20 Cl N O2 SI 1 a 111.4861; 14.0594; 13.486
90; 111.393; 90		2027.77Prabagar, B.; Nayak, Sanatan; Mallick, Rajendra K.; Prasad, Rangu; Sahoo, Akhila K.
Triphenylphosphine promoted regio and stereoselective α-halogenation of ynamides
Organic Chemistry Frontiers, 2016, 3, 110
1553206 CIFC27 H28 Br N3 O7 SP 1 21 111.0065; 8.788; 14.4392
90; 99.424; 90		1377.78Gerten, Anthony L.; Stanley, Levi M.
Enantioselective dearomative [3 + 2] cycloadditions of indoles with azomethine ylides derived from alanine imino esters
Organic Chemistry Frontiers, 2016, 3, 339
1553207 CIFC36 H29 Cl O6P 21 21 216.2154; 20.2473; 22.9882
90; 90; 90		2893Fu, Zhenqian; Wu, Xingxing; Chi, Yonggui Robin
Rapid access to bicyclic δ-lactones via carbene-catalyzed activation and cascade reaction of unsaturated carboxylic esters
Organic Chemistry Frontiers, 2016, 3, 145
1553208 CIFC24 H25 N3 O2P -17.1121; 8.5933; 18.426
94.339; 100.719; 105.418		1057.3Yang, Xiu-Long; Long, Yan; Chen, Fei; Han, Bing
Synthesis of isoxazoline-featured oxindoles by iminoxyl radical-promoted cascade oxyalkylation/alkylarylation of alkenes
Organic Chemistry Frontiers, 2016, 3, 184
1553209 CIFC28 H26 N2 O3P 1 21/c 115.8733; 11.8466; 12.3385
90; 99.402; 90		2289Yang, Xiu-Long; Long, Yan; Chen, Fei; Han, Bing
Synthesis of isoxazoline-featured oxindoles by iminoxyl radical-promoted cascade oxyalkylation/alkylarylation of alkenes
Organic Chemistry Frontiers, 2016, 3, 184
1553210 CIFC22 H24 Br2 N2P -19.1241; 10.2171; 11.3635
78.194; 82.379; 72.418		985.63Ma, Can-Liang; Li, Xiao-Hua; Yu, Xiao-Long; Zhu, Xiao-Long; Hu, Yong-Zhou; Dong, Xiao-Wu; Tan, Bin; Liu, Xin-Yuan
Gold-catalyzed tandem synthesis of bioactive spiro-dipyrroloquinolines and its application in the one-step synthesis of incargranine B aglycone and seneciobipyrrolidine (I)
Organic Chemistry Frontiers, 2016, 3, 324
1553211 CIFC20 H22 N2P -17.4987; 7.9073; 14.5997
77.721; 79.566; 69.529		787.06Ma, Can-Liang; Li, Xiao-Hua; Yu, Xiao-Long; Zhu, Xiao-Long; Hu, Yong-Zhou; Dong, Xiao-Wu; Tan, Bin; Liu, Xin-Yuan
Gold-catalyzed tandem synthesis of bioactive spiro-dipyrroloquinolines and its application in the one-step synthesis of incargranine B aglycone and seneciobipyrrolidine (I)
Organic Chemistry Frontiers, 2016, 3, 324
1553212 CIFC22 H32 N2 O4P 21 21 2110.016; 10.025; 21.596
90; 90; 90		2168.5Fu, Jian-Guo; Xu, Guang-Qiang; Ding, Rui; Lin, Guo-Qiang; Sun, Bing-Feng
Asymmetric total synthesis of Lycopodium alkaloids α-obscurine, N-desmethyl-α-obscurine, β-obscurine and N-desmethyl-β-obscurine
Organic Chemistry Frontiers, 2016, 3, 62
1553213 CIFC17 H25 Cl N2 O2C 2 2 2110.351; 11.942; 26.963
90; 90; 90		3332.9Fu, Jian-Guo; Xu, Guang-Qiang; Ding, Rui; Lin, Guo-Qiang; Sun, Bing-Feng
Asymmetric total synthesis of Lycopodium alkaloids α-obscurine, N-desmethyl-α-obscurine, β-obscurine and N-desmethyl-β-obscurine
Organic Chemistry Frontiers, 2016, 3, 62
1553214 CIFC23 H27 Cl6 I N2P 1 21/n 112.0005; 9.4272; 25.9285
90; 101.178; 90		2877.7Desens, Willi; Kohrt, Christina; Spannenberg, Anke; Werner, Thomas
A novel zinc based binary catalytic system for CO2utilization under mild conditions
Organic Chemistry Frontiers, 2016, 3, 156
1553215 CIFC16 H17 Cl2 N O4P 21 21 218.3061; 9.701; 20.7173
90; 90; 90		1669.35Yang, Li; Song, Liqiang; Huang, Chong; Huang, Mingzheng; Liu, Bo
Exploiting ortho-substitution effect on formation of oxygen-containing [10]paracyclophane through ring-closing metathesis
Organic Chemistry Frontiers, 2016, 3, 319
1553216 CIFC16 H17 Br2 N O4P 1 21 18.3327; 9.5492; 11.4501
90; 108.133; 90		865.84Yang, Li; Song, Liqiang; Huang, Chong; Huang, Mingzheng; Liu, Bo
Exploiting ortho-substitution effect on formation of oxygen-containing [10]paracyclophane through ring-closing metathesis
Organic Chemistry Frontiers, 2016, 3, 319
1553217 CIFC20 H16 O5P -17.1154; 11.1585; 11.1645
107.811; 95.51; 91.238		838.83Zhang, Wen-Zhen; Yang, Ming-Wang; Yang, Xu-Tong; Shi, Ling-Long; Wang, Hui-Bo; Lu, Xiao-Bing
Double carboxylation of o-alkynyl acetophenone with carbon dioxide
Organic Chemistry Frontiers, 2016, 3, 217
1553218 CIFC25 H27 N O2 SP 1 21/n 18.6446; 10.8046; 24.326
90; 99.922; 90		2238.1Li, Jiawen; Qin, Guiping; Liu, Yang; Huang, Hanmin
Palladium-catalysed coupling reaction of aminals with N-sulfonyl hydrazones to give allylic sulfones
Organic Chemistry Frontiers, 2016, 3, 259
1553219 CIFC20 H28 O2 SiP 1 21/n 17.5687; 30.831; 8.0907
90; 90.916; 90		1887.7Cai, Shujun; Xiao, Zheming; Ou, Jinjie; Shi, Yingbo; Gao, Shuanhu
A photo-induced C–C bond formation methodology to construct tetrahydrofluorenones and their related structures
Organic Chemistry Frontiers, 2016, 3, 354
1553220 CIFC14 H11 F3 OP -17.3733; 11.2959; 14.9182
109.524; 92.663; 101.436		1139.24Cai, Shujun; Xiao, Zheming; Ou, Jinjie; Shi, Yingbo; Gao, Shuanhu
A photo-induced C–C bond formation methodology to construct tetrahydrofluorenones and their related structures
Organic Chemistry Frontiers, 2016, 3, 354
1553221 CIFC14 H12 O3P 1 2/c 115.9874; 10.2887; 13.7969
90; 108.28; 90		2154.92Cai, Shujun; Xiao, Zheming; Ou, Jinjie; Shi, Yingbo; Gao, Shuanhu
A photo-induced C–C bond formation methodology to construct tetrahydrofluorenones and their related structures
Organic Chemistry Frontiers, 2016, 3, 354
1553222 CIFC14 H13 F OP b c a34.01; 9.158; 7.196
90; 90; 90		2241Cai, Shujun; Xiao, Zheming; Ou, Jinjie; Shi, Yingbo; Gao, Shuanhu
A photo-induced C–C bond formation methodology to construct tetrahydrofluorenones and their related structures
Organic Chemistry Frontiers, 2016, 3, 354
1553223 CIFC34 H24 N PP -19.9764; 11.8382; 12.5698
115.716; 100.125; 93.876		1299.22Fu, Wai Chung; Zhou, Zhongyuan; Kwong, Fuk Yee
A benzo[c]carbazolyl-based phosphine ligand for Pd-catalyzed tetra-ortho-substituted biaryl syntheses
Organic Chemistry Frontiers, 2016, 3, 273
1553224 CIFC19 H16 F N O5 SP 21 21 2110.342; 12.672; 13.549
90; 90; 90		1775.6Yu, Jin-Sheng; Zhou, Jian
Organocatalytic enantioselective Mukaiyama–Mannich reaction of fluorinated enol silyl ethers and cyclic N-sulfonyl ketimines
Organic Chemistry Frontiers, 2016, 3, 298
1553225 CIFC17 H14 F2 N2 O4 SP 21 21 217.1956; 9.6833; 23.2873
90; 90; 90		1622.59Yu, Jin-Sheng; Zhou, Jian
Organocatalytic enantioselective Mukaiyama–Mannich reaction of fluorinated enol silyl ethers and cyclic N-sulfonyl ketimines
Organic Chemistry Frontiers, 2016, 3, 298
1553226 CIFC23 H14 Cl2 N2 OP 1 21/c 18.9936; 20.9137; 10.6975
90; 112.585; 90		1857.78Zhang, Zhiguo; Qian, Jingjing; Zhang, Guisheng; Ma, Nana; Liu, Qingfeng; Liu, Tongxin; Sun, Kai; Shi, Lei
Copper(i) catalyzed C(sp2)–N bond formation: synthesis of pyrrolo[3,2-c]quinolinone derivatives
Organic Chemistry Frontiers, 2016, 3, 344
1553227 CIFC24 H14 Cl2 N2 O2P -16.3775; 12.1686; 13.4121
80.819; 88.955; 75.537		994.7Zhang, Zhiguo; Qian, Jingjing; Zhang, Guisheng; Ma, Nana; Liu, Qingfeng; Liu, Tongxin; Sun, Kai; Shi, Lei
Copper(i) catalyzed C(sp2)–N bond formation: synthesis of pyrrolo[3,2-c]quinolinone derivatives
Organic Chemistry Frontiers, 2016, 3, 344
1553228 CIFC24 H14 Cl2 N2 O2P -15.2005; 13.556; 15.6215
73.584; 85.49; 87.12		1052.7Zhang, Zhiguo; Qian, Jingjing; Zhang, Guisheng; Ma, Nana; Liu, Qingfeng; Liu, Tongxin; Sun, Kai; Shi, Lei
Copper(i) catalyzed C(sp2)–N bond formation: synthesis of pyrrolo[3,2-c]quinolinone derivatives
Organic Chemistry Frontiers, 2016, 3, 344
1553229 CIFC24 H17 Cl N2 O2P 21 21 218.0462; 9.2337; 26.6656
90; 90; 90		1981.2Zhang, Zhiguo; Qian, Jingjing; Zhang, Guisheng; Ma, Nana; Liu, Qingfeng; Liu, Tongxin; Sun, Kai; Shi, Lei
Copper(i) catalyzed C(sp2)–N bond formation: synthesis of pyrrolo[3,2-c]quinolinone derivatives
Organic Chemistry Frontiers, 2016, 3, 344
1553230 CIFC20 H15 N3 O3I 1 2/a 113.6461; 10.723; 22.268
90; 90.915; 90		3258Nack, W. A.; Wang, B.; Wu, X.; Jiao, R.; He, G.; Chen, G.
Palladium-catalyzed arylation of β-methylene C(sp3)–H bonds at room temperature: desymmetrization of simple cycloalkyl carboxylic acids
Organic Chemistry Frontiers, 2016, 3, 561
1553231 CIFC23 H18 N2 O5P 1 21 17.6839; 11.0556; 12.4153
90; 106.486; 90		1011.32Jiao, Lihui; Zhao, Xiaowei; Liu, Huixin; Ye, Xinyi; Li, Yun; Jiang, Zhiyong
Organocatalytic asymmetric conjugate addition of diaryloxazolidin-2,4-diones to nitroolefins: an efficient approach to chiral α-aryl-α-hydroxy carboxylic acids
Organic Chemistry Frontiers, 2016, 3, 470
1553232 CIFC38 H34 N O4 P SP 1 21/c 113.83; 21.2702; 14.1309
90; 119.452; 90		3619.6Zhu, Yi-Long; Wang, De-Cai; Jiang, Bo; Hao, Wen-Juan; Wei, Ping; Wang, Ai-Fang; Qiu, Jiang-Kai; Tu, Shu-Jiang
Metal-free oxidative hydrophosphinylation of 1,7-enynes
Organic Chemistry Frontiers, 2016, 3, 385
1553233 CIFC13 H14 Br N O3 SP 1 21/c 120.218; 9.2121; 15.306
90; 95.315; 90		2838.5Song, Lu; Luo, Sanzhong; Cheng, Jin-Pei
Visible-light promoted intermolecular halofunctionalization of alkenes with N-halogen saccharins
Organic Chemistry Frontiers, 2016, 3, 447
1553234 CIFC13 H14 Br N O3 SP -17.8592; 9.0905; 9.748
79.19; 89.1; 77.31		667.1Song, Lu; Luo, Sanzhong; Cheng, Jin-Pei
Visible-light promoted intermolecular halofunctionalization of alkenes with N-halogen saccharins
Organic Chemistry Frontiers, 2016, 3, 447
1553235 CIFC16 H14 Br N O3 SP 1 21/c 111.83; 9.2659; 14.59
90; 97.6; 90		1585.2Song, Lu; Luo, Sanzhong; Cheng, Jin-Pei
Visible-light promoted intermolecular halofunctionalization of alkenes with N-halogen saccharins
Organic Chemistry Frontiers, 2016, 3, 447
1553236 CIFC16 H14 Br N O3 SP -18.3045; 9.415; 11.19
87.089; 73.797; 70.74		792.3Song, Lu; Luo, Sanzhong; Cheng, Jin-Pei
Visible-light promoted intermolecular halofunctionalization of alkenes with N-halogen saccharins
Organic Chemistry Frontiers, 2016, 3, 447
1553237 CIFC16 H14 Br N O3 SP 1 21/c 115.825; 8.982; 11.426
90; 109.905; 90		1527.1Song, Lu; Luo, Sanzhong; Cheng, Jin-Pei
Visible-light promoted intermolecular halofunctionalization of alkenes with N-halogen saccharins
Organic Chemistry Frontiers, 2016, 3, 447
1553238 CIFC22 H25 N O3P 1 21 18.1343; 27.626; 8.8172
90; 97.223; 90		1965.7Mu, Yucheng; Tan, Xiaodong; Zhang, Yemin; Jing, Xiaobi; Shi, Zhuangzhi
Pd(ii)-catalyzed β-C–H arylation of O-methyl ketoximes with iodoarenes
Organic Chemistry Frontiers, 2016, 3, 380
1553418 CIFC21 H15 Br F N OP -15.9396; 11.302; 13.413
96.05; 99.59; 101.21		862Sheng, Jinyu; Su, Xiang; Cao, Chengyao; Chen, Chao
Synthesis of benzo[1,3]oxazines via copper(i)-catalyzed cascade annulation of nitriles, aldehydes and diaryliodonium salts
Organic Chemistry Frontiers, 2016, 3, 501
1553419 CIFC28 H22 F3 N O5P 21 21 219.1158; 9.8126; 28.3116
90; 90; 90		2532.46Gao, Tai-Ping; Liu, Dan; Lin, Jun-Bing; Hu, Xiu-Qin; Wang, Zhu-Yin; Xu, Peng-Fei
Direct construction of chiral quaternary dihydropyranones through highly enantioselective organocatalytic hetero-Diels–Alder reactions of olefinic azlactones
Organic Chemistry Frontiers, 2016, 3, 598
1553420 CIFC25 H48 N2 O5 S SiP 1 21 112.5809; 8.9728; 13.319
90; 93.554; 90		1500.64Ye, Jian-Liang; Chen, Hang; Zhang, Yu-Feng; Huang, Pei-Qiang
A versatile access to vicinal diamine motifs by highly anti-selective asymmetric vinylogous Mannich reactions: an efficient total synthesis of (+)-absouline
Organic Chemistry Frontiers, 2016, 3, 683
1553421 CIFC20 H28 Cl N2 O4.5 SP 21 21 2111.701; 14.628; 25.939
90; 90; 90		4439.8Ye, Jian-Liang; Chen, Hang; Zhang, Yu-Feng; Huang, Pei-Qiang
A versatile access to vicinal diamine motifs by highly anti-selective asymmetric vinylogous Mannich reactions: an efficient total synthesis of (+)-absouline
Organic Chemistry Frontiers, 2016, 3, 683
1553422 CIFC250 H238 F24 N18 O12 P4 Ru2P n n n :222.824; 22.583; 47.813
90; 90; 90		24644.5Klosterman, Jeremy K.; Veliks, Janis; Frantz, Derik K.; Yasui, Yoshizumi; Loepfe, Michael; Zysman-Colman, Eli; Linden, Anthony; Siegel, Jay S.
Conformations of large macrocycles and ring-in-ring complexes
Organic Chemistry Frontiers, 2016, 3, 661
1553423 CIFC90 H102 F12 N10 O8 P2 RuP 1 21/n 120.3614; 15.5902; 30.5936
90; 94.4504; 90		9682.3Klosterman, Jeremy K.; Veliks, Janis; Frantz, Derik K.; Yasui, Yoshizumi; Loepfe, Michael; Zysman-Colman, Eli; Linden, Anthony; Siegel, Jay S.
Conformations of large macrocycles and ring-in-ring complexes
Organic Chemistry Frontiers, 2016, 3, 661
1553424 CIFC102 H130 F12 N10 O26 S4 Zn2P -111.0301; 12.3939; 21.8715
76.878; 78.788; 87.305		2856.3Klosterman, Jeremy K.; Veliks, Janis; Frantz, Derik K.; Yasui, Yoshizumi; Loepfe, Michael; Zysman-Colman, Eli; Linden, Anthony; Siegel, Jay S.
Conformations of large macrocycles and ring-in-ring complexes
Organic Chemistry Frontiers, 2016, 3, 661
1553425 CIFC155 H166 Cl22 F24 N12 O12 P4 Ru2P -115.004; 15.1525; 21.5611
98.4023; 98.0121; 108.321		4512.9Klosterman, Jeremy K.; Veliks, Janis; Frantz, Derik K.; Yasui, Yoshizumi; Loepfe, Michael; Zysman-Colman, Eli; Linden, Anthony; Siegel, Jay S.
Conformations of large macrocycles and ring-in-ring complexes
Organic Chemistry Frontiers, 2016, 3, 661
1553426 CIFC98 H98 Br2 F12 N16 O10 P2 RuP 1 21/n 114.556; 24.668; 26.949
90; 93.27; 90		9660.8Veliks, Janis; Seifert, Helen M.; Frantz, Derik K.; Klosterman, Jeremy K.; Tseng, Jui-Chang; Linden, Anthony; Siegel, Jay S.
Towards the molecular Borromean link with three unequal rings: double-threaded ruthenium(ii) ring-in-ring complexes
Organic Chemistry Frontiers, 2016, 3, 667
1553427 CIFC180 H194 F24 N22 O18 P4 Ru2P -113.6711; 16.967; 22.4266
71.073; 82.622; 68.288		4571.45Veliks, Janis; Seifert, Helen M.; Frantz, Derik K.; Klosterman, Jeremy K.; Tseng, Jui-Chang; Linden, Anthony; Siegel, Jay S.
Towards the molecular Borromean link with three unequal rings: double-threaded ruthenium(ii) ring-in-ring complexes
Organic Chemistry Frontiers, 2016, 3, 667
1553428 CIFC14 H16 O5P 1 21/c 119.5895; 7.0388; 9.2405
90; 91.626; 90		1273.63Yu, Jingxun; Ma, Haichen; Yao, Hongliang; Cheng, Hang; Tong, Rongbiao
Diastereoselective and regiodivergent oxa-[3 + 2] cycloaddition of Achmatowicz products and cyclic 1,3-dicarbonyl compounds
Organic Chemistry Frontiers, 2016, 3, 714
1553429 CIFC14 H16 O5P 1 21/c 18.144; 14.5913; 11.013
90; 94.901; 90		1303.91Yu, Jingxun; Ma, Haichen; Yao, Hongliang; Cheng, Hang; Tong, Rongbiao
Diastereoselective and regiodivergent oxa-[3 + 2] cycloaddition of Achmatowicz products and cyclic 1,3-dicarbonyl compounds
Organic Chemistry Frontiers, 2016, 3, 714
1553430 CIFC17 H16 Cl N O2P 21 21 218.1449; 10.8999; 16.4545
90; 90; 90		1460.81Vyas, Vijyesh K.; Bhanage, Bhalchandra M.
Asymmetric transfer hydrogenation of seven membered tricyclic ketones: N-substituted dibenzo[b,e]azepine-6,11-dione driven by nonclassical CH/O interactions
Organic Chemistry Frontiers, 2016, 3, 614
1553431 CIFC31 H28 N4 O3P 1 21 19.837; 10.113; 14.456
90; 106.063; 90		1382Zhu, Yi; Li, Yao; Meng, Qingbin; Li, Xin
An organocatalytic enantioselective vinylogous Mannich reaction of α,α-dicyanoolefins with isatin N-Boc ketimines
Organic Chemistry Frontiers, 2016, 3, 709
1553432 CIFC23 H15 Cl3 N2 O2P c a 217.7032; 16.441; 14.9629
90; 90; 90		1895Zhang, Zeyuan; Dai, Zhen; Ma, Xinkun; Liu, Yihan; Ma, Xiaojun; Li, Wanli; Ma, Chen
Cu-catalyzed one-pot synthesis of fused oxazepinone derivatives via sp2 C–H and O–H cross-dehydrogenative coupling
Organic Chemistry Frontiers, 2016, 3, 799
1553433 CIFC21 H12 Cl N3 O2P -17.147; 7.9449; 16.405
101.767; 96.018; 106.731		859.9Zhang, Zeyuan; Dai, Zhen; Ma, Xinkun; Liu, Yihan; Ma, Xiaojun; Li, Wanli; Ma, Chen
Cu-catalyzed one-pot synthesis of fused oxazepinone derivatives via sp2 C–H and O–H cross-dehydrogenative coupling
Organic Chemistry Frontiers, 2016, 3, 799
1553434 CIFC16 H11 Br O2P 1 21/c 19.986; 15.521; 8.74
90; 101.027; 90		1329.6Qiu, Guanyinsheng; Liu, Tong; Ding, Qiuping
Tandem oxidative radical brominative addition of activated alkynes and spirocyclization: switchable synthesis of 3-bromocoumarins and 3-bromo spiro-[4,5] trienone
Organic Chemistry Frontiers, 2016, 3, 510
1553435 CIFC37 H24 O3P -16.3266; 11.3868; 18.6894
94.305; 99.144; 100.166		1301Wang, Lei; Zhang, Jianwei; Lang, Ming; Wang, Jian
Palladium-catalyzed ring contraction reaction of naphthoquinones upon reaction with alkynes
Organic Chemistry Frontiers, 2016, 3, 603
1553436 CIFC37 H26 O2P -16.514; 11.9444; 17.215
93.28; 94.949; 104.241		1289.2Wang, Lei; Zhang, Jianwei; Lang, Ming; Wang, Jian
Palladium-catalyzed ring contraction reaction of naphthoquinones upon reaction with alkynes
Organic Chemistry Frontiers, 2016, 3, 603
1553437 CIFC38 H27 N O3.5P -112.8713; 12.9061; 18.4438
83.491; 70.221; 87.197		2864.3Wang, Lei; Zhang, Jianwei; Lang, Ming; Wang, Jian
Palladium-catalyzed ring contraction reaction of naphthoquinones upon reaction with alkynes
Organic Chemistry Frontiers, 2016, 3, 603
1553438 CIFC41 H34 O6P 1 21/c 19.5936; 9.4163; 34.688
90; 93.15; 90		3128.8Wang, Lei; Zhang, Jianwei; Lang, Ming; Wang, Jian
Palladium-catalyzed ring contraction reaction of naphthoquinones upon reaction with alkynes
Organic Chemistry Frontiers, 2016, 3, 603
1553439 CIFC38 H26 O2P -19.837; 10.766; 13.71
87.68; 77.4; 71.54		1343.4Wang, Lei; Zhang, Jianwei; Lang, Ming; Wang, Jian
Palladium-catalyzed ring contraction reaction of naphthoquinones upon reaction with alkynes
Organic Chemistry Frontiers, 2016, 3, 603
1553440 CIFC29 H20 OC 1 2/c 126.128; 8.1552; 21.487
90; 119.724; 90		3976Wang, Lei; Zhang, Jianwei; Lang, Ming; Wang, Jian
Palladium-catalyzed ring contraction reaction of naphthoquinones upon reaction with alkynes
Organic Chemistry Frontiers, 2016, 3, 603
1553441 CIFC71 H64 O24P 1 21/c 119.7803; 8.925; 17.1219
90; 93.062; 90		3018.37Leowanawat, Pawaret; Nowak-Król, Agnieszka; Würthner, Frank
Tetramethoxy-bay-substituted perylene bisimides by copper-mediated cross-coupling
Organic Chemistry Frontiers, 2016, 3, 537
1553442 CIFC20 H24 N2P 1 21/n 113.1094; 8.943; 14.6031
90; 105.214; 90		1652.03Peng, Xingao; Kaga, Atsushi; Hirao, Hajime; Chiba, Shunsuke
Hydroamination of alkenyl N-arylhydrazones mediated by t-BuOK for the synthesis of nitrogen heterocycles
Organic Chemistry Frontiers, 2016, 3, 609
1553443 CIFC23 H24 N2 SP 1 21/n 111.6939; 9.4598; 16.9069
90; 91.481; 90		1869.65Peng, Xingao; Kaga, Atsushi; Hirao, Hajime; Chiba, Shunsuke
Hydroamination of alkenyl N-arylhydrazones mediated by t-BuOK for the synthesis of nitrogen heterocycles
Organic Chemistry Frontiers, 2016, 3, 609
1553444 CIFC16 H16 O3 SP 21 21 215.9262; 8.0475; 31.957
90; 90; 90		1524.06Phanindrudu, Mandalaparthi; Tiwari, Dipak Kumar; Sridhar, B.; Likhar, Pravin R.; Tiwari, Dharmendra Kumar
Magnetically separable nano-copper catalyzed unprecedented stereoselective synthesis of E-vinyl sulfones from tosylmethyl isocyanide and alkynes: TosMIC as a source of the sulfonyl group
Organic Chemistry Frontiers, 2016, 3, 795
1553445 CIFC23 H20 Br2 N2 O2P 1 21/n 113.4028; 11.2931; 14.0439
90; 91.99; 90		2124.4Hu, Haoxiang; Wang, Yidong; Qian, Deyun; Zhang, Zhan-Ming; Liu, Lu; Zhang, Junliang
Enantioselective gold-catalyzed intermolecular [2 + 2]-cycloadditions of 3-styrylindoles with N-allenyl oxazolidinone
Organic Chemistry Frontiers, 2016, 3, 759
1553446 CIFC36 H56 Au Cl N O P SP 1 21 112.5457; 22.382; 12.6621
90; 92.052; 90		3553.2Hu, Haoxiang; Wang, Yidong; Qian, Deyun; Zhang, Zhan-Ming; Liu, Lu; Zhang, Junliang
Enantioselective gold-catalyzed intermolecular [2 + 2]-cycloadditions of 3-styrylindoles with N-allenyl oxazolidinone
Organic Chemistry Frontiers, 2016, 3, 759
1553447 CIFC26 H21 N O3 SC 1 2/c 121.51; 10.73; 19.7
90; 113.492; 90		4170Gong, Xinxing; Xia, Hongguang; Wu, Jie
A palladium-catalyzed tandem reaction of 2-alkynylbenzenesulfonamides with 2-(2-bromoarylidene)cyclobutanones
Organic Chemistry Frontiers, 2016, 3, 697
1553448 CIFC23 H21 F N4P -110.5273; 11.4221; 34.217
90.072; 98.137; 105.697		3917.7Jiang, Yu; Wang, Qiang; Sun, Run; Tang, Xiang-Ying; Shi, Min
Base-induced synthesis of N-dialkylaminomethyl-2H-1,2,3-triazoles from N-sulfonyl-1,2,3-triazoles
Organic Chemistry Frontiers, 2016, 3, 744
1553449 CIFC32 H25 N O6P 21 21 219.02156; 9.44417; 30.948
90; 90; 90		2636.81Ran, Guang-Yao; Wang, Pan; Du, Wei; Chen, Ying-Chun
α-Regioselective [3 + 2] annulations with Morita‒Baylis‒Hillman carbonates of isatins and 2-nitro-1,3-enynes
Organic Chemistry Frontiers, 2016, 3, 861
1553450 CIFC21 H13 N SP -17.187; 10.356; 11.075
66.214; 86.273; 89.284		752.6Wen, Li-Rong; Shen, Qiang-Yu; Guo, Wei-Si; Li, Ming
Copper-catalyzed tandem arylation–cyclization of 2-alkynylaryl isothiocyanates with diaryliodonium salts: an efficient synthesis of thiochromeno[2,3-b]indoles
Organic Chemistry Frontiers, 2016, 3, 870
1553451 CIFC22 H17 N O2 SP -111.0789; 11.6353; 16.29
93.084; 106.29; 115.259		1786.1Wen, Li-Rong; Shen, Qiang-Yu; Guo, Wei-Si; Li, Ming
Copper-catalyzed tandem arylation–cyclization of 2-alkynylaryl isothiocyanates with diaryliodonium salts: an efficient synthesis of thiochromeno[2,3-b]indoles
Organic Chemistry Frontiers, 2016, 3, 870
1553452 CIFC19 H17 N O5P 1 21/n 113.5013; 18.6052; 13.6121
90; 106.649; 90		3275.9Görgen née Boersch, Christina; Lutsenko, Kiril; Merkul, Eugen; Frank, Walter; Müller, Thomas J. J.
Catalytic one-pot synthesis of 4-(hetero)aryl substituted 5-(2-oxoethyl) oxazol-2(3H)-ones by coupling–isomerization–elimination (CIE) sequence
Organic Chemistry Frontiers, 2016, 3, 887
1553453 CIFC48 H53 Cl2 N3 O6 Ru SP 1 21/c 18.4973; 40.566; 26.516
90; 97.469; 90		9063Sabbasani, Venkata R.; Yun, Sang Young; Lee, Daesung
Structure and reactivity of sulfonamide- and acetate-chelated ruthenium alkylidene complexes
Organic Chemistry Frontiers, 2016, 3, 939
1553454 CIFC44 H49 Cl2 N3 O3 Ru SP n a 2116.8326; 12.2762; 20.4575
90; 90; 90		4227.3Sabbasani, Venkata R.; Yun, Sang Young; Lee, Daesung
Structure and reactivity of sulfonamide- and acetate-chelated ruthenium alkylidene complexes
Organic Chemistry Frontiers, 2016, 3, 939
1553455 CIFC40 H47 Cl2 N3 O4 Ru SP 1 21/c 111.3136; 21.889; 16.102
90; 97.063; 90		3957.3Sabbasani, Venkata R.; Yun, Sang Young; Lee, Daesung
Structure and reactivity of sulfonamide- and acetate-chelated ruthenium alkylidene complexes
Organic Chemistry Frontiers, 2016, 3, 939
1553456 CIFC36 H46 Cl2 N2 O3 RuP 1 21/c 120.114; 8.8782; 20.665
90; 105.736; 90		3552Sabbasani, Venkata R.; Yun, Sang Young; Lee, Daesung
Structure and reactivity of sulfonamide- and acetate-chelated ruthenium alkylidene complexes
Organic Chemistry Frontiers, 2016, 3, 939
1553457 CIFC22 H26 Cl3 N2 O RuP 21 21 212.073; 18.008; 10.7084
90; 90; 90		2328.1Sabbasani, Venkata R.; Yun, Sang Young; Lee, Daesung
Structure and reactivity of sulfonamide- and acetate-chelated ruthenium alkylidene complexes
Organic Chemistry Frontiers, 2016, 3, 939
1553458 CIFC42 H43 Cl2 N3 O4 Ru SR -3 :H40.354; 40.354; 14.657
90; 90; 120		20670Sabbasani, Venkata R.; Yun, Sang Young; Lee, Daesung
Structure and reactivity of sulfonamide- and acetate-chelated ruthenium alkylidene complexes
Organic Chemistry Frontiers, 2016, 3, 939
1553459 CIFC14 H10 F12 N2P 1 21/n 110.0639; 8.163; 20.469
90; 101.995; 90		1644.8Xie, Jin; Li, Jian; Wurm, Thomas; Weingand, Vanessa; Sung, Hui-Ling; Rominger, Frank; Rudolph, Matthias; Hashmi, A. Stephen K.
A general photoinduced electron transfer-directed chemoselective perfluoroalkylation of N,N-dialkylhydrazones
Organic Chemistry Frontiers, 2016, 3, 841
1553460 CIFC27 H26 Cl2 F3 N7 SP b c a16.558; 17.307; 19.571
90; 90; 90		5608Wang, Fei; Zhao, Liang; You, Jingsong; Wang, Mei-Xiang
Synthesis of trifluoromethylthiolated azacalix[1]arene[3]pyridines from the Cu(ii)-mediated direct trifluoromethylthiolation reaction of arenes via reactive arylcopper(iii) intermediates
Organic Chemistry Frontiers, 2016, 3, 880
1553461 CIFC27 H23 F6 N7 S2P -19.817; 11.968; 13.149
102.73; 99.17; 104.43		1421.3Wang, Fei; Zhao, Liang; You, Jingsong; Wang, Mei-Xiang
Synthesis of trifluoromethylthiolated azacalix[1]arene[3]pyridines from the Cu(ii)-mediated direct trifluoromethylthiolation reaction of arenes via reactive arylcopper(iii) intermediates
Organic Chemistry Frontiers, 2016, 3, 880
1553462 CIFC27 H23 F6 N7 S2P 1 21/c 114.717; 15.564; 12.282
90; 103.48; 90		2735.8Wang, Fei; Zhao, Liang; You, Jingsong; Wang, Mei-Xiang
Synthesis of trifluoromethylthiolated azacalix[1]arene[3]pyridines from the Cu(ii)-mediated direct trifluoromethylthiolation reaction of arenes via reactive arylcopper(iii) intermediates
Organic Chemistry Frontiers, 2016, 3, 880
1553463 CIFC17 H25 Cl2 N3 O4 SP -110.82; 10.975; 11.163
74.634; 62.808; 65.132		1065.4Zhou, Kaida; Xia, Hongguang; Wu, Jie
Generation of (2-oxoindolin-3-yl)methanesulfonohydrazides via a photo-induced reaction of N-(2-iodoaryl)acrylamide, DABSO, and hydrazine
Organic Chemistry Frontiers, 2016, 3, 865
1553464 CIFC22 H18 F3 N O6P -111.266; 12.1474; 16.278
73.095; 73.52; 84.96		2043.8Li, Zong-Rui; Bao, Xing-Xing; Sun, Jian; Shen, Jing; Wu, Dun-Qi; Liu, Yan-Kai; Deng, Qing-Hai; Liu, Feng
Iron-catalyzed trifluoromethylation of vinylcyclopropanes: facile synthesis of CF3–containing dihydronaphthalene derivatives
Organic Chemistry Frontiers, 2016, 3, 934
1553465 CIFC16 H16 B N3 O2I 1 2/a 125.856; 5.37038; 21.5154
90; 101.646; 90		2926.05Zhai, Wenlei; Chapin, Brette M.; Yoshizawa, Akina; Wang, Hui-Chen; Hodge, Stephen A.; James, Tony D.; Anslyn, Eric V.; Fossey, John S.
“Click-fluors”: triazole-linked saccharide sensors
Organic Chemistry Frontiers, 2016, 3, 918
1553466 CIFC24 H24 B N3 O4P -17.1065; 9.0913; 17.685
81.994; 84.409; 68.79		1053.43Zhai, Wenlei; Chapin, Brette M.; Yoshizawa, Akina; Wang, Hui-Chen; Hodge, Stephen A.; James, Tony D.; Anslyn, Eric V.; Fossey, John S.
“Click-fluors”: triazole-linked saccharide sensors
Organic Chemistry Frontiers, 2016, 3, 918
1553467 CIFC14 H10 Br N O2P 21 21 214.4197; 11.6677; 22.915
90; 90; 90		1181.7Zhang, Xu; Xu, Bin; Xu, Ming-Hua
Rhodium-catalyzed asymmetric arylation of N- and O-containing cyclic aldimines: facile and efficient access to highly optically active 3,4-dihydrobenzo[1,4]oxazin-2-ones and dihydroquinoxalinones
Organic Chemistry Frontiers, 2016, 3, 944
1553468 CIFC14 H15 Cl N2 PdP 1 c 19.4647; 12.7252; 11.5908
90; 108.624; 90		1322.9Roffe, Gavin W.; Tizzard, Graham J.; Coles, Simon J.; Cox, Hazel; Spencer, John
Synthesis of unsymmetrical NCN′ and PCN pincer palladacycles and their catalytic evaluation compared with a related SCN pincer palladacycle
Organic Chemistry Frontiers, 2016, 3, 957
1553469 CIFC16 H19 Cl N2 PdP 1 21/c 19.6575; 11.675; 26.2578
90; 92.079; 90		2958.7Roffe, Gavin W.; Tizzard, Graham J.; Coles, Simon J.; Cox, Hazel; Spencer, John
Synthesis of unsymmetrical NCN′ and PCN pincer palladacycles and their catalytic evaluation compared with a related SCN pincer palladacycle
Organic Chemistry Frontiers, 2016, 3, 957
1553470 CIFC16 H17 Cl N2 O PdP 1 21/n 16.9704; 17.1706; 12.2014
90; 97.943; 90		1446.33Roffe, Gavin W.; Tizzard, Graham J.; Coles, Simon J.; Cox, Hazel; Spencer, John
Synthesis of unsymmetrical NCN′ and PCN pincer palladacycles and their catalytic evaluation compared with a related SCN pincer palladacycle
Organic Chemistry Frontiers, 2016, 3, 957
1553471 CIFC24 H19 Cl N O P PdP 1 21/n 112.2558; 9.9099; 17.4367
90; 109.768; 90		1992.95Roffe, Gavin W.; Tizzard, Graham J.; Coles, Simon J.; Cox, Hazel; Spencer, John
Synthesis of unsymmetrical NCN′ and PCN pincer palladacycles and their catalytic evaluation compared with a related SCN pincer palladacycle
Organic Chemistry Frontiers, 2016, 3, 957
1553472 CIFC23 H17 Cl N O P PdP -19.0641; 9.6782; 12.7031
91.535; 108.207; 112.231		966.47Roffe, Gavin W.; Tizzard, Graham J.; Coles, Simon J.; Cox, Hazel; Spencer, John
Synthesis of unsymmetrical NCN′ and PCN pincer palladacycles and their catalytic evaluation compared with a related SCN pincer palladacycle
Organic Chemistry Frontiers, 2016, 3, 957
1553473 CIFC25 H17 N O SP 1 21/n 15.4373; 22.5643; 15.678
90; 91.295; 90		1923Singh, Radhey M.; Kumar, Ritush; Bharadwaj, Kishor Chandra; Gupta, Tanu
Pd catalyzed facile synthesis of cyclopenta[b]quinolin-1-one via sequential Sonogashira coupling and annulation. An unusual mode of ring closure, using sulphur as a soft nucleophile
Organic Chemistry Frontiers, 2016, 3, 1100
1553474 CIFC36 H26P -19.2253; 12.0172; 12.8207
65.023; 76.245; 83.655		1251.4He, Bairong; Nie, Han; Luo, Wenwen; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
Synthesis, structure and optical properties of tetraphenylethene derivatives with through-space conjugation between benzene and various planar chromophores
Organic Chemistry Frontiers, 2016, 3, 1091
1553475 CIFC32 H24P 1 21/n 19.4248; 9.6366; 25.0543
90; 94.474; 90		2268.6He, Bairong; Nie, Han; Luo, Wenwen; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
Synthesis, structure and optical properties of tetraphenylethene derivatives with through-space conjugation between benzene and various planar chromophores
Organic Chemistry Frontiers, 2016, 3, 1091
1553476 CIFC40 H28P 1 21/c 116.4844; 9.1722; 19.225
90; 107.472; 90		2772.7He, Bairong; Nie, Han; Luo, Wenwen; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
Synthesis, structure and optical properties of tetraphenylethene derivatives with through-space conjugation between benzene and various planar chromophores
Organic Chemistry Frontiers, 2016, 3, 1091
1553477 CIFC40 H28P 1 21/n 111.3717; 15.9519; 15.1309
90; 93.429; 90		2739.83He, Bairong; Nie, Han; Luo, Wenwen; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
Synthesis, structure and optical properties of tetraphenylethene derivatives with through-space conjugation between benzene and various planar chromophores
Organic Chemistry Frontiers, 2016, 3, 1091
1553478 CIFC42 H28P 1 21/c 19.5798; 10.2198; 29.4004
90; 96.324; 90		2860.89He, Bairong; Nie, Han; Luo, Wenwen; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
Synthesis, structure and optical properties of tetraphenylethene derivatives with through-space conjugation between benzene and various planar chromophores
Organic Chemistry Frontiers, 2016, 3, 1091
1553479 CIFC28 H23 Cl N4 O7P 1 21 112.766; 16.24; 13.427
90; 107.96; 90		2648Li, Jun-Hua; Cui, Zhi-Hao; Du, Da-Ming
Diastereo- and enantioselective construction of cyclohexanone-fused spirospyrazolones containing four consecutive stereocenters through asymmetric sequential reactions
Organic Chemistry Frontiers, 2016, 3, 1087
1553480 CIFC17 H22 O2P 1 21/c 111.7876; 19.8876; 12.1607
90; 94.193; 90		2843.2Ondet, Pierrick; Lempenauer, Luisa; Duñach, Elisabet; Lemière, Gilles
Bismuth(iii) triflate-catalysed tandem cyclisations towards complex polycyclic ethers
Organic Chemistry Frontiers, 2016, 3, 999
1553481 CIFC17 H22 O2P 1 21/c 119.1606; 13.3348; 23.8068
90; 108.315; 90		5774.6Ondet, Pierrick; Lempenauer, Luisa; Duñach, Elisabet; Lemière, Gilles
Bismuth(iii) triflate-catalysed tandem cyclisations towards complex polycyclic ethers
Organic Chemistry Frontiers, 2016, 3, 999
1553482 CIFC23 H27 N O6 SP 1 21/n 18.2306; 9.8924; 26.999
90; 98.152; 90		2176.1Duan, Shuangshuang; Long, Dan; Zhao, Changgui; Zhao, Gaoyuan; Yuan, Ziyun; Xie, Xingang; Fang, Jianguo; She, Xuegong
Efficient construction of the A/C/D tricyclic skeleton of palhinine A
Organic Chemistry Frontiers, 2016, 3, 1137
1553483 CIFC23 H19 Br OP 1 21/n 110.005; 9.977; 18.125
90; 92.34; 90		1807.7Liu, Yu; Zhao, Peng; Zhang, Bo; Xi, Chanjuan
MeOTf-catalyzed annulation of aldehydes and arylalkynes leading to 2,3-disubstituted indanones
Organic Chemistry Frontiers, 2016, 3, 1116
1553484 CIFC23 H20 SP -19.756; 10.716; 10.881
65.921; 68.07; 63.361		902.7Ramesh, E.; Shankar, Majji; Dana, Suman; Sahoo, Akhila K.
Silver-mediated oxidative annulation of N-arylthio succinimides with alkynes: direct access to benzo[b]thiophenes
Organic Chemistry Frontiers, 2016, 3, 1126
1553485 CIFC20 H13 F SP 1 21/c 16.0606; 13.4845; 18.39
90; 91.36; 90		1502.5Ramesh, E.; Shankar, Majji; Dana, Suman; Sahoo, Akhila K.
Silver-mediated oxidative annulation of N-arylthio succinimides with alkynes: direct access to benzo[b]thiophenes
Organic Chemistry Frontiers, 2016, 3, 1126
1553486 CIFC20 H17 F3 I N OC 1 2/c 131.8; 8.994; 13.605
90; 110.595; 90		3642An, Yuanyuan; Kuang, Yunyan; Wu, Jie
Synthesis of trifluoromethylated 3,4-dihydroquinolin-2(1H)-ones via a photo-induced radical cyclization of benzene-tethered 1,7-enynes with Togni reagent
Organic Chemistry Frontiers, 2016, 3, 994
1553487 CIFC21 H19 Br N2 O4P 21 21 218.4058; 10.8659; 21.9188
90; 90; 90		2001.99Ma, Qiao; Gong, Lei; Meggers, Eric
Enantioselective β-alkylation of pyrroles with the formation of an all-carbon quaternary stereocenter
Organic Chemistry Frontiers, 2016, 3, 1319
1553488 CIFC20 H18 N6 OP 1 21/c 120.5231; 9.5667; 20.3255
90; 115.091; 90		3614.1Liu, Hou-Lu; Jiang, Yu; Hao, Jian; Tang, Xiang-Ying; Shi, Min
A new method to access triazole-fused spiro-guanidines from the reaction of isothiocyanates tethered N-sulfonyl-1,2,3-triazoles and amines
Organic Chemistry Frontiers, 2016, 3, 1447
1553489 CIFC18 H11 I N2 OP -17.504; 8.467; 13.179
95.607; 102.6; 110.95		748.8Wu, Yan-Dong; Geng, Xiao; Gao, Qinghe; Zhang, Jingjing; Wu, Xia; Wu, An-Xin
Iodine-promoted sequential dual oxidative Csp3–H amination/Csp3–H iodination reactions: efficient synthesis of 1-iodoimidazo[1,5-a]pyridines
Organic Chemistry Frontiers, 2016, 3, 1430
1553490 CIFC60 H44 N4 O4 Pd2P c c n20.2007; 25.2676; 31.3498
90; 90; 90		16001.7Naito, Masaya; Komiya, Naruyoshi; Naota, Takeshi
Homochiral association of binuclear trans-bis(β-iminoaryloxy)palladium(ii) complexes doubly linked with m-xylylene spacers: drastic linker-dependence of the association chirality of chiral clothespin-shaped molecules
Organic Chemistry Frontiers, 2016, 3, 1286
1553491 CIFC61 H45 Cl3 N4 O4 Pd2C 1 2/c 127.6181; 13.0551; 30.802
90; 113.65; 90		10173.2Naito, Masaya; Komiya, Naruyoshi; Naota, Takeshi
Homochiral association of binuclear trans-bis(β-iminoaryloxy)palladium(ii) complexes doubly linked with m-xylylene spacers: drastic linker-dependence of the association chirality of chiral clothespin-shaped molecules
Organic Chemistry Frontiers, 2016, 3, 1286
1553492 CIFC29 H44 O6 SiP 21 21 2111.5223; 14.9948; 16.4141
90; 90; 90		2835.9Pérez-Estrada, S.; Sayar, N.; Granja, J. R.
Towards taxane analogues synthesis by dienyne ring closing metathesis
Organic Chemistry Frontiers, 2016, 3, 1331
1553493 CIFC29 H40 O5 SiC 1 2 127.836; 7.8125; 14.1759
90; 92.711; 90		3079.4Pérez-Estrada, S.; Sayar, N.; Granja, J. R.
Towards taxane analogues synthesis by dienyne ring closing metathesis
Organic Chemistry Frontiers, 2016, 3, 1331
1553494 CIFC17 H14 O2P 1 21/c 113.6594; 5.9624; 17.4715
90; 106.688; 90		1363Cui, Fei-Hu; Su, Shi-Xia; Xu, Yan-li; Liang, Ying; Wang, Heng-shan; Pan, Ying-Ming
Capture of CO2 in air for 4,5-disubstituted furan-2(5H)-ones
Organic Chemistry Frontiers, 2016, 3, 1304
1553495 CIFC38 H24 Cl2 N2 O6P 1 21/c 114.2296; 6.2823; 33.8457
90; 90.358; 90		3025.56Wirtanen, T.; Muuronen, M.; Hurmalainen, J.; Tuononen, H. M.; Nieger, M.; Helaja, J.
Intermolecular oxidative dehydrogenative 3,3′-coupling of benzo[b]furans and benzo[b]thiophenes promoted by DDQ/H+: total synthesis of shandougenine B
Organic Chemistry Frontiers, 2016, 3, 1738
1553496 CIFC62 H61 N7 O20 S4P 1 21/n 113.909; 20.264; 22.762
90; 91.41; 90		6414Gaeta, Carmine; Della Sala, Paolo; Talotta, Carmen; De Rosa, Margherita; Soriente, Annunziata; Brancatelli, Giovanna; Geremia, Silvano; Neri, Placido
A tetrasulfate-resorcin[6]arene cavitand as the host for organic ammonium guests
Organic Chemistry Frontiers, 2016, 3, 1276
1553498 CIFC14 H17 N5 O4P 21 21 217.51038; 17.3551; 23.2172
90; 90; 90		3026.21Naik, Siddhi D.; Chandra, Girish; Sahu, Pramod K.; Kim, Hong-Rae; Qu, Shuhao; Yoon, Ji-seong; Jeong, Lak Shin
Stereo- and regio-selective synthesis of 3′-C-substituted-(N)-methanocarba adenosines as potential anticancer agents
Organic Chemistry Frontiers, 2016, 3, 1472
1553499 CIFC16 H12 F3 N O2P 1 21/c 112.057; 8.771; 14.736
90; 113.287; 90		1431.4Mizuta, Satoshi; Otaki, Hiroki; Kitamura, Kanami; Nishi, Kodai; Watanabe, Ken; Makau, Juliann Nzembi; Hashimoto, Ryo; Usui, Toshiya; Chiba, Kenya
3,3-Dibromo-2-trifluoromethyl acrylic acid ethyl ester: a versatile platform for the stereoselective preparation of functionalized-α-trifluoromethyl α,β-unsaturated lactones and trifluoromethyl pyrazolinones
Organic Chemistry Frontiers, 2016, 3, 1661
1553500 CIFC17 H10 Cl F3 N2 OP -18.165; 9.432; 10.126
85.485; 83.241; 73.145		740.3Jin, Li-Kun; Lu, Guo-Ping; Cai, Chun
Copper-catalyzed 8-amido chelation-induced regioselective C–H fluoroalkylation of quinolines
Organic Chemistry Frontiers, 2016, 3, 1309
1553501 CIFC24 H15 NP 21 21 214.8217; 10.1093; 31.14
90; 90; 90		1517.89Zagranyarski, Yulian; Skabeev, Artem; Ma, Yingjie; Müllen, Klaus; Li, Chen
Facile synthesis of annulated heterocyclic benzo[kl]acridine derivatives via one-pot N–H/C–H coupling
Organic Chemistry Frontiers, 2016, 3, 1520
1553502 CIFC22 H13 N SP c a 2116.3471; 11.2916; 8.0242
90; 90; 90		1481.15Zagranyarski, Yulian; Skabeev, Artem; Ma, Yingjie; Müllen, Klaus; Li, Chen
Facile synthesis of annulated heterocyclic benzo[kl]acridine derivatives via one-pot N–H/C–H coupling
Organic Chemistry Frontiers, 2016, 3, 1520
1553503 CIFC23 H24 N2P -16.202; 10.169; 14.7158
75.057; 85.343; 84.132		890.56Liu, Cheng-Guo; Gu, Zheng-Yang; Bai, Hui-Wen; Wang, Shun-Yi; Ji, Shun-Jun
An isocyanide insertion approach to substituted pyrrolo[2,3-b]quinolines under metal-free and azide-free conditions
Organic Chemistry Frontiers, 2016, 3, 1299
1553504 CIFC22 H25 N2 O4 PP -18.9115; 11.1099; 11.8272
83.858; 86.228; 67.922		1078.45Sun, Mengmeng; Sun, Suyan; Qiao, Huijie; Yang, Fan; Zhu, Yu; Kang, Jianxun; Wu, Yusheng; Wu, Yangjie
Silver(i)-promoted C5–H phosphonation of 8-aminoquinoline amides with H-phosphonates
Organic Chemistry Frontiers, 2016, 3, 1646
1553505 CIFC22 H25 N2 O4 PP c c n15.3031; 18.1046; 15.6855
90; 90; 90		4345.8Sun, Mengmeng; Sun, Suyan; Qiao, Huijie; Yang, Fan; Zhu, Yu; Kang, Jianxun; Wu, Yusheng; Wu, Yangjie
Silver(i)-promoted C5–H phosphonation of 8-aminoquinoline amides with H-phosphonates
Organic Chemistry Frontiers, 2016, 3, 1646
1553506 CIFC31 H27 N2 O2P 21 21 218.681; 17.323; 32.77
90; 90; 90		4928Chen, Zhen; Huo, Yuwen; An, Ping; Wang, Xichao; Song, Chun; Ma, Yudao
[2.2]Paracyclophane-based N-heterocyclic carbene as efficient catalyst or as ligand for copper catalyst for asymmetric α-silylation of N-tosylaldimines
Organic Chemistry Frontiers, 2016, 3, 1725
1553507 CIFC17 H31 N O4P 21 21 217.643; 16.144; 6.601
90; 90; 90		1880.2Cordero, F. M.; Vurchio, C.; Faggi, C.; Brandi, A.
Configuration-guided reactions: the case of highly decorated spiro[cyclopropane-1,2′(3′H)-pyrrolo[1,2-b]isoxazole] derivatives en route to polyhydroxyindolizidines
Organic Chemistry Frontiers, 2016, 3, 1651
1553508 CIFC17 H31 N O4P 21 21 216.03; 16.334; 18.224
90; 90; 90		1795Cordero, F. M.; Vurchio, C.; Faggi, C.; Brandi, A.
Configuration-guided reactions: the case of highly decorated spiro[cyclopropane-1,2′(3′H)-pyrrolo[1,2-b]isoxazole] derivatives en route to polyhydroxyindolizidines
Organic Chemistry Frontiers, 2016, 3, 1651
1553509 CIFC13 H21 N O3P 1 21 110.178; 21.78; 11.615
90; 90.547; 90		2574.7Cordero, F. M.; Vurchio, C.; Faggi, C.; Brandi, A.
Configuration-guided reactions: the case of highly decorated spiro[cyclopropane-1,2′(3′H)-pyrrolo[1,2-b]isoxazole] derivatives en route to polyhydroxyindolizidines
Organic Chemistry Frontiers, 2016, 3, 1651
1553510 CIFC13 H21 N O3P 21 21 216.078; 10.204; 19.957
90; 90; 90		1237.73Cordero, F. M.; Vurchio, C.; Faggi, C.; Brandi, A.
Configuration-guided reactions: the case of highly decorated spiro[cyclopropane-1,2′(3′H)-pyrrolo[1,2-b]isoxazole] derivatives en route to polyhydroxyindolizidines
Organic Chemistry Frontiers, 2016, 3, 1651
1553511 CIFC26 H42 N2 O6P 1 21 17.252; 25.57; 14.465
90; 100.17; 90		2640.2Cordero, F. M.; Vurchio, C.; Faggi, C.; Brandi, A.
Configuration-guided reactions: the case of highly decorated spiro[cyclopropane-1,2′(3′H)-pyrrolo[1,2-b]isoxazole] derivatives en route to polyhydroxyindolizidines
Organic Chemistry Frontiers, 2016, 3, 1651
1553512 CIFC41 H31 Cl2 N O2P -19.1392; 13.2716; 13.7699
77.608; 76.026; 84.909		1581.79Seifert, Sabine; Schmidt, David; Würthner, Frank
A cross-coupling-annulation cascade from peri-dibromonaphthalimide to pseudo-rylene bisimides
Organic Chemistry Frontiers, 2016, 3, 1435
1553513 CIFC79 H66 Cl2 N2 O4P 1 21/c 113.3641; 15.796; 14.8901
90; 112.839; 90		2896.9Seifert, Sabine; Schmidt, David; Würthner, Frank
A cross-coupling-annulation cascade from peri-dibromonaphthalimide to pseudo-rylene bisimides
Organic Chemistry Frontiers, 2016, 3, 1435
1553514 CIFC24 H20 O2 SP 1 21/n 19.2961; 10.1519; 20.823
90; 102.267; 90		1920.26Fu, Rong; Hao, Wen-Juan; Wu, Ya-Nan; Wang, Nan-Nan; Tu, Shu-Jiang; Li, Guigen; Jiang, Bo
Sulfonyl radical-enabled 6-endo-trig cyclization for regiospecific synthesis of unsymmetrical diaryl sulfones
Organic Chemistry Frontiers, 2016, 3, 1452
1553515 CIFC27 H20 O2 SP 1 21/c 17.0521; 28.03; 10.4649
90; 100.069; 90		2036.7Fu, Rong; Hao, Wen-Juan; Wu, Ya-Nan; Wang, Nan-Nan; Tu, Shu-Jiang; Li, Guigen; Jiang, Bo
Sulfonyl radical-enabled 6-endo-trig cyclization for regiospecific synthesis of unsymmetrical diaryl sulfones
Organic Chemistry Frontiers, 2016, 3, 1452
1553516 CIFC33 H35 N O4 SP 1 21/c 115.4186; 11.3388; 16.9081
90; 107.55; 90		2818.4Lv, Leiyang; Bai, Xiaohui; Yan, Xiaoyu; Li, Zhiping
Iron-catalyzed decarbonylation initiated [2 + 2 + m] annulation of benzene-linked 1,n-enynes with aliphatic aldehydes
Organic Chemistry Frontiers, 2016, 3, 1509
1553517 CIFC29 H26 N2 O5 SP -18.3151; 8.625; 18.7838
99.74; 96.686; 104.017		1270.61Sharma, Pankaj; Kumar, Niggula Praveen; Krishna, Namballa Hari; Prasanna, Daasi; Sridhar, Balasubramanian; Shankaraiah, Nagula
Silver(i)-catalysed domino alkyne-annulation/Diels–Alder reaction: a mild synthetic approach to tetrahydrospiro[carbazole-4,3′-indoline] scaffolds
Organic Chemistry Frontiers, 2016, 3, 1503
1553518 CIFC14 H17 F3 N2 O3 SP 1 21/n 18.849; 10.773; 17.758
90; 91.599; 90		1692.2Li, Yuewen; Xiang, Yuanchao; Li, Zhiming; Wu, Jie
Direct vicinal difunctionalization of alkynes through trifluoromethylation and aminosulfonylation via insertion of sulfur dioxide under catalyst-free conditions
Organic Chemistry Frontiers, 2016, 3, 1493
1553528 CIFC22 H32 O2 SiP b c a12.7034; 11.6077; 28.683
90; 90; 90		4229.5Liu, Zhen; Xia, Ying; Feng, Sheng; Zhang, Yan; Wang, Jianbo
Rh(i)-Catalyzed coupling of 2-bromoethyl aryldiazoacetates with tertiary propargyl alcohols through carbene migratory insertion
Organic Chemistry Frontiers, 2016, 3, 1691
1553529 CIFC24 H19 N O3P -19.3034; 9.6541; 11.6687
101.875; 106.962; 96.397		964.39Duan, Jindian; Cheng, Yuyu; Li, Rou; Li, Pengfei
Synthesis of spiro[indane-1,3-dione-1-pyrrolines] via copper-catalyzed heteroannulation of ketoxime acetates with 2-arylideneindane-1,3-diones
Organic Chemistry Frontiers, 2016, 3, 1614
1553532 CIFC18 H16 O SP b c a11.1348; 10.8734; 24.741
90; 90; 90		2995.5An, Zhenyu; She, Yue; Yang, Xiaodong; Pang, Xiaobo; Yan, Rulong
Metal-free synthesis of 3-methylthiofurans from homopropargylic alcohols and DMSO via a tandem sulfenylation/cyclization reaction in a one-pot manner
Organic Chemistry Frontiers, 2016, 3, 1746
1553533 CIFC24 H21 N OP 1 21/c 19.2943; 18.714; 20.557
90; 95.79; 90		3557.3Mahmood, Qaiser; Yue, Erlin; Zhang, Wenjuan; Solan, Gregory A.; Liang, Tongling; Sun, Wen-Hua
Bisimino-functionalized dibenzo[a,c]acridines as highly conjugated pincer frameworks for palladium(ii): synthesis, characterization and catalytic performance in Heck coupling
Organic Chemistry Frontiers, 2016, 3, 1668
1553534 CIFC24 H19 NP b c a11.335; 7.4991; 37.869
90; 90; 90		3219Mahmood, Qaiser; Yue, Erlin; Zhang, Wenjuan; Solan, Gregory A.; Liang, Tongling; Sun, Wen-Hua
Bisimino-functionalized dibenzo[a,c]acridines as highly conjugated pincer frameworks for palladium(ii): synthesis, characterization and catalytic performance in Heck coupling
Organic Chemistry Frontiers, 2016, 3, 1668
1553535 CIFC42 H34 Cl7 N3 PdP -110.641; 10.978; 17.744
100.04; 106.43; 93.41		1944.7Mahmood, Qaiser; Yue, Erlin; Zhang, Wenjuan; Solan, Gregory A.; Liang, Tongling; Sun, Wen-Hua
Bisimino-functionalized dibenzo[a,c]acridines as highly conjugated pincer frameworks for palladium(ii): synthesis, characterization and catalytic performance in Heck coupling
Organic Chemistry Frontiers, 2016, 3, 1668
1553536 CIFC44 H40 Cl N3 PdR -3 :H36.49; 36.49; 21.305
90; 90; 120		24567Mahmood, Qaiser; Yue, Erlin; Zhang, Wenjuan; Solan, Gregory A.; Liang, Tongling; Sun, Wen-Hua
Bisimino-functionalized dibenzo[a,c]acridines as highly conjugated pincer frameworks for palladium(ii): synthesis, characterization and catalytic performance in Heck coupling
Organic Chemistry Frontiers, 2016, 3, 1668
1553537 CIFC33 H25 Cl3 N2 O PdP 1 21/c 111.611; 19.188; 13.466
90; 113.15; 90		2758.5Mahmood, Qaiser; Yue, Erlin; Zhang, Wenjuan; Solan, Gregory A.; Liang, Tongling; Sun, Wen-Hua
Bisimino-functionalized dibenzo[a,c]acridines as highly conjugated pincer frameworks for palladium(ii): synthesis, characterization and catalytic performance in Heck coupling
Organic Chemistry Frontiers, 2016, 3, 1668
1553538 CIFC34 H27 Cl N2 O PdP 1 21/n 114.187; 12.38; 14.674
90; 92.59; 90		2574.6Mahmood, Qaiser; Yue, Erlin; Zhang, Wenjuan; Solan, Gregory A.; Liang, Tongling; Sun, Wen-Hua
Bisimino-functionalized dibenzo[a,c]acridines as highly conjugated pincer frameworks for palladium(ii): synthesis, characterization and catalytic performance in Heck coupling
Organic Chemistry Frontiers, 2016, 3, 1668
1553539 CIFC40 H33 N3 O0P 1 21/c 111.91; 32.793; 9.4655
90; 113.37; 90		3393.6Mahmood, Qaiser; Yue, Erlin; Zhang, Wenjuan; Solan, Gregory A.; Liang, Tongling; Sun, Wen-Hua
Bisimino-functionalized dibenzo[a,c]acridines as highly conjugated pincer frameworks for palladium(ii): synthesis, characterization and catalytic performance in Heck coupling
Organic Chemistry Frontiers, 2016, 3, 1668
1553540 CIFC50 H50 N2 O6 S2P 1 21/c 112.0255; 18.091; 10.1121
90; 105.935; 90		2115.4Michelet, Bastien; Tang, Shun; Thiery, Guillaume; Monot, Julien; Li, Huijing; Guillot, Régis; Bour, Christophe; Gandon, Vincent
Catalytic applications of [IPr·GaX2][SbF6] and related species
Organic Chemistry Frontiers, 2016, 3, 1603
1553541 CIFC18 H22 O4P b c a7.6825; 17.5861; 22.9639
90; 90; 90		3102.5Michelet, Bastien; Tang, Shun; Thiery, Guillaume; Monot, Julien; Li, Huijing; Guillot, Régis; Bour, Christophe; Gandon, Vincent
Catalytic applications of [IPr·GaX2][SbF6] and related species
Organic Chemistry Frontiers, 2016, 3, 1603
1553542 CIFC20 H13 F SP 1 21/c 16.0149; 13.4117; 18.2153
90; 91.601; 90		1468.86Wang, Xiaoming; Gensch, Tobias; Glorius, Frank
Highly selective synthesis of 6-substituted benzothiophenes by Sc(OTf)3-catalyzed intermolecular cyclization and sulfur migration
Organic Chemistry Frontiers, 2016, 3, 1619
1553546 CIFC24 H28 O8P 1 21/c 116.1503; 8.3426; 18.1574
90; 108.184; 90		2324.3Cao, Tao; Ma, Shengming
Nickel-catalyzed alkyl-zincation and carboxylation of diynes
Organic Chemistry Frontiers, 2016, 3, 1711
1553553 CIFC19 H17 Cl OP 1 21 15.828; 8.2327; 16.8844
90; 98.492; 90		801.23Luo, Hongwen; Yu, Yihua; Ma, Shengming
Suzuki coupling for preparation of allenes – ligand effects and chirality transfer
Organic Chemistry Frontiers, 2016, 3, 1705
1553655 CIFC72 H84 N12R -3 :H24.741; 24.741; 19.826
90; 90; 120		10510Slater, A. G.; Little, M. A.; Briggs, M. E.; Jelfs, K. E.; Cooper, A. I.
A solution-processable dissymmetric porous organic cage
Molecular Systems Design & Engineering, 2018, 3, 223
1553656 CIFC73.1 H89.96 Cl1.55 N12 O1.89R -3 :H24.483; 24.483; 19.6123
90; 90; 120		10181Slater, A. G.; Little, M. A.; Briggs, M. E.; Jelfs, K. E.; Cooper, A. I.
A solution-processable dissymmetric porous organic cage
Molecular Systems Design & Engineering, 2018, 3, 223
1553657 CIFC4 H18 N2 O22 Se6 V3P -110.0027; 10.4765; 12.2924
74.478; 72.643; 79.707		1177.8Xu, Rosalind J.; Olshansky, Jacob H.; Adler, Philip D. F.; Huang, Yongjia; Smith, Matthew D.; Zeller, Matthias; Schrier, Joshua; Norquist, Alexander J.
Understanding structural adaptability: a reactant informatics approach to experiment design
Molecular Systems Design & Engineering, 2018, 3, 473
1553658 CIFC4 H12 N2 O10 Se2 V2P 1 21/c 110.0879; 6.2047; 10.6765
90; 116.566; 90		597.71Xu, Rosalind J.; Olshansky, Jacob H.; Adler, Philip D. F.; Huang, Yongjia; Smith, Matthew D.; Zeller, Matthias; Schrier, Joshua; Norquist, Alexander J.
Understanding structural adaptability: a reactant informatics approach to experiment design
Molecular Systems Design & Engineering, 2018, 3, 473
1553659 CIFC8 H44 N4 O48 Se12 V6C 1 2/c 118.816; 7.934; 34.439
90; 95.85; 90		5114Xu, Rosalind J.; Olshansky, Jacob H.; Adler, Philip D. F.; Huang, Yongjia; Smith, Matthew D.; Zeller, Matthias; Schrier, Joshua; Norquist, Alexander J.
Understanding structural adaptability: a reactant informatics approach to experiment design
Molecular Systems Design & Engineering, 2018, 3, 473
1553660 CIFC8 H58.67 N6 O65.33 Se16 V8P 1 21/c 117.999; 15.658; 26.0344
90; 113.803; 90		6713.1Xu, Rosalind J.; Olshansky, Jacob H.; Adler, Philip D. F.; Huang, Yongjia; Smith, Matthew D.; Zeller, Matthias; Schrier, Joshua; Norquist, Alexander J.
Understanding structural adaptability: a reactant informatics approach to experiment design
Molecular Systems Design & Engineering, 2018, 3, 473
1553661 CIFC8 H43 N4 O47 Se12 V6P 1 21/c 124.713; 7.9212; 34.399
90; 130.376; 90		5129.9Xu, Rosalind J.; Olshansky, Jacob H.; Adler, Philip D. F.; Huang, Yongjia; Smith, Matthew D.; Zeller, Matthias; Schrier, Joshua; Norquist, Alexander J.
Understanding structural adaptability: a reactant informatics approach to experiment design
Molecular Systems Design & Engineering, 2018, 3, 473
1554236 CIFC25 H20 SP 18.886; 10.971; 11.261
64.477; 78.704; 77.452		960.5Wang, Can; Yu, Yun; Chai, Zhaofei; He, Fangdi; Wu, Chaozheng; Gong, Yanbin; Han, Mengmeng; Li, Qianqian; Li, Zhen
Recyclable mechanoluminescent luminogen: different polymorphs, different self-assembly effects of the thiophene moiety and recovered molecular packing via simple thermal-treatment
Materials Chemistry Frontiers, 2019, 3, 32
1554237 CIFC25 H20 SP 21 21 215.988; 7.36; 45.02
90; 90; 90		1984.1Wang, Can; Yu, Yun; Chai, Zhaofei; He, Fangdi; Wu, Chaozheng; Gong, Yanbin; Han, Mengmeng; Li, Qianqian; Li, Zhen
Recyclable mechanoluminescent luminogen: different polymorphs, different self-assembly effects of the thiophene moiety and recovered molecular packing via simple thermal-treatment
Materials Chemistry Frontiers, 2019, 3, 32
1554238 CIFC61 H55 N5 O2 SP -113.5619; 13.7951; 15.3779
110.309; 101.188; 97.849		2581.1Yu, Hai-Xia; Zhi, Junge; Chang, Zheng-Feng; Shen, Tianjiao; Ding, Wei-Lu; Zhang, Xiaoling; Wang, Jin-Liang
Rational design of aggregation-induced emission sensor based on Rhodamine B for turn-on sensing of trivalent metal cations, reversible data protection, and bioimaging
Materials Chemistry Frontiers, 2019, 3, 151
1554239 CIFC40 H37 F6 N O2 PP 1 21/c 111.951; 15.59; 18.828
90; 97.29; 90		3479.6Ren, Fei; Liu, Pai; Gao, Yu; Shi, Jianbing; Tong, Bin; Cai, Zhengxu; Dong, Yuping
Real time bioimaging for mitochondria by taking the aggregation process of aggregation-induced emission near-infrared dyes with wash-free staining
Materials Chemistry Frontiers, 2019, 3, 57
1554240 CIFC25 H14 N4 O SP 1 21/c 117.804; 9.217; 12.5258
90; 107.795; 90		1957.1Wang, Ya-Kun; Huang, Chen-Chao; Kumar, Sarvendra; Wu, Sheng-Fan; Yuan, Yi; Aziz Khan, Aziz Khan; Jiang, Zuo-Quan; Fung, Man-Keung; Liao, Liang-Sheng
The roles of thermally activated delayed fluorescence sensitizers for efficient red fluorescent organic light-emitting diodes with D–A–A type emitters
Materials Chemistry Frontiers, 2019, 3, 161
1554241 CIFC109 H80 N16 O10 S4P -111.8289; 20.0485; 21.3871
105.379; 102.037; 99.001		4660.7Wang, Ya-Kun; Huang, Chen-Chao; Kumar, Sarvendra; Wu, Sheng-Fan; Yuan, Yi; Aziz Khan, Aziz Khan; Jiang, Zuo-Quan; Fung, Man-Keung; Liao, Liang-Sheng
The roles of thermally activated delayed fluorescence sensitizers for efficient red fluorescent organic light-emitting diodes with D‒A‒A type emitters
Materials Chemistry Frontiers, 2019, 3, 161
1554242 CIFC23 H17 N3 O3P 1 21 110.83; 7.65; 12.063
90; 103.07; 90		973.5He, Yanling; Li, Yuanyuan; Su, Huifang; Si, Yue; Liu, Yuanyuan; Peng, Qiuchen; He, Juan; Hou, Hongwei; Li, Kai
An o-phthalimide-based multistimuli-responsive aggregation-induced emission (AIE) system
Materials Chemistry Frontiers, 2019, 3, 50
1554243 CIFC47 H38 Cl2 N2 OP 1 21/c 120.728; 11.337; 17.818
90; 107.633; 90		3990Lin, Tingting; Su, Xing; Wang, Kai; Li, Minjie; Guo, Hongwei; Liu, Lulu; Zou, Bo; Zhang, Yu-Mo; Liu, Yifei; Zhang, Sean Xiao-An
An AIE fluorescent switch with multi-stimuli responsive properties and applications for quantitatively detecting pH value, sulfite anion and hydrostatic pressure
Materials Chemistry Frontiers, 2019, 3, 1052
1554244 CIFC41 H33 N3 O2P 1 21/c 115.538; 13.276; 16.39
90; 101.907; 90		3308.2Shimizu, Masaki; Tamagawa, Tomokazu; Nishimura, Kenta
4,5-Diaminophthalimides: highly efficient solid-state fluorophores and turn-on type fluorescent probes for hydrazine
Materials Chemistry Frontiers, 2019, 3, 563
1554245 CIFC29 H20 N2P c a 218.7745; 11.508; 20.298
90; 90; 90		2049.6Lei, Yunxiang; Dai, Wenbo; Liu, Zhiqi; Guo, Shuai; Cai, Zhengxu; Shi, Jianbing; Zheng, Xiaoyan; Zhi, Junge; Tong, Bin; Dong, Yuping
A novel strategy for realizing dual state fluorescence and low-temperature phosphorescence
Materials Chemistry Frontiers, 2019, 3, 284
1554246 CIFC29 H23 N OP c a 2145.21; 6.1483; 7.449
90; 90; 90		2070.6Lei, Yunxiang; Dai, Wenbo; Liu, Zhiqi; Guo, Shuai; Cai, Zhengxu; Shi, Jianbing; Zheng, Xiaoyan; Zhi, Junge; Tong, Bin; Dong, Yuping
A novel strategy for realizing dual state fluorescence and low-temperature phosphorescence
Materials Chemistry Frontiers, 2019, 3, 284
1554247 CIFC31 H27 NC 1 c 142.454; 11.064; 9.786
90; 94.49; 90		4582.5Lei, Yunxiang; Dai, Wenbo; Liu, Zhiqi; Guo, Shuai; Cai, Zhengxu; Shi, Jianbing; Zheng, Xiaoyan; Zhi, Junge; Tong, Bin; Dong, Yuping
A novel strategy for realizing dual state fluorescence and low-temperature phosphorescence
Materials Chemistry Frontiers, 2019, 3, 284
1554248 CIFC29 H23 N OC 1 2/c 131.66; 5.901; 22.932
90; 100.11; 90		4217.8Lei, Yunxiang; Dai, Wenbo; Liu, Zhiqi; Guo, Shuai; Cai, Zhengxu; Shi, Jianbing; Zheng, Xiaoyan; Zhi, Junge; Tong, Bin; Dong, Yuping
A novel strategy for realizing dual state fluorescence and low-temperature phosphorescence
Materials Chemistry Frontiers, 2019, 3, 284
1554249 CIFC32 H27 N3 OP 1 21/c 123.528; 6.0582; 17.914
90; 93.56; 90		2548.5Lei, Yunxiang; Dai, Wenbo; Liu, Zhiqi; Guo, Shuai; Cai, Zhengxu; Shi, Jianbing; Zheng, Xiaoyan; Zhi, Junge; Tong, Bin; Dong, Yuping
A novel strategy for realizing dual state fluorescence and low-temperature phosphorescence
Materials Chemistry Frontiers, 2019, 3, 284
1554250 CIFC29 H20 N2P -18.4662; 15.145; 17.692
106.62; 95.32; 91.57		2160.9Lei, Yunxiang; Dai, Wenbo; Liu, Zhiqi; Guo, Shuai; Cai, Zhengxu; Shi, Jianbing; Zheng, Xiaoyan; Zhi, Junge; Tong, Bin; Dong, Yuping
A novel strategy for realizing dual state fluorescence and low-temperature phosphorescence
Materials Chemistry Frontiers, 2019, 3, 284
1554251 CIFC37 H36 N4 O4 SP 1 21/n 111.695; 19.14; 15.289
90; 111.7; 90		3179.8Liu, Xuedan; Li, Aisen; Xu, Weiqing; Ma, Zhiyong; Jia, Xinru
An ESIPT-based fluorescent switch with AIEE, solvatochromism, mechanochromism and photochromism
Materials Chemistry Frontiers, 2019, 3, 620
1554252 CIFC45 H29 N5P -18.9145; 13.2762; 14.5859
110.467; 98.648; 96.716		1571.88Cao, Chen; Chen, Wen-Cheng; Tian, Shuang; Chen, Jia-Xiong; Wang, Zhong-Yi; Zheng, Xu-Hui; Ding, Chong-Wei; Li, Jing-Hong; Zhu, Jie-Ji; Zhu, Ze-Lin; Tong, Qing-Xiao; Lee, Chun-Sing
A novel D–π–A blue fluorophore based on [1,2,4]triazolo[1,5-a]pyridine as an electron acceptor and its application in organic light-emitting diodes
Materials Chemistry Frontiers, 2019, 3, 1071
1554611 CIFC63 H46 Cu F6 N4 O P3P -111.2628; 12.4158; 21.9828
83.055; 78.448; 87.667		2989.2Giereth, Robin; Reim, Immanuel; Frey, Wolfgang; Junge, Henrik; Tschierlei, Stefanie; Karnahl, Michael
Remarkably long-lived excited states of copper photosensitizers containing an extended π-system based on an anthracene moiety
Sustainable Energy & Fuels, 2019, 3, 692
1554612 CIFC48 H28 Cu F6 N8 PP -18.1362; 10.6863; 22.4625
86.186; 81.28; 87.085		1924.5Giereth, Robin; Reim, Immanuel; Frey, Wolfgang; Junge, Henrik; Tschierlei, Stefanie; Karnahl, Michael
Remarkably long-lived excited states of copper photosensitizers containing an extended π-system based on an anthracene moiety
Sustainable Energy & Fuels, 2019, 3, 692
1554613 CIFC22.5 H28 K0.5 N6 Ni0.5 O3P -112.9939; 13.5751; 14.0727
78.667; 85.315; 77.907		2377.8Dubrawski, Zachary; Heidebrecht, Joshua; Puerta Lombardi, Braulio M.; Hyla, Alexander S.; Willkomm, Janina; Radford, Chase L.; Lin, Jian-Bin; Welch, Gregory C.; Ponnurangam, Sathish; Roesler, Roland; Prokopchuk, Demyan E.; Piers, Warren E.
Ligand-centered electrochemical processes enable CO2 reduction with a nickel bis(triazapentadienyl) complex
Sustainable Energy & Fuels, 2019, 3, 1172
1554614 CIFC36 H44 K2 N10 O3P 1 21/c 123.3268; 7.362; 22.2054
90; 94.794; 90		3800Dubrawski, Zachary; Heidebrecht, Joshua; Puerta Lombardi, Braulio M.; Hyla, Alexander S.; Willkomm, Janina; Radford, Chase L.; Lin, Jian-Bin; Welch, Gregory C.; Ponnurangam, Sathish; Roesler, Roland; Prokopchuk, Demyan E.; Piers, Warren E.
Ligand-centered electrochemical processes enable CO2 reduction with a nickel bis(triazapentadienyl) complex
Sustainable Energy & Fuels, 2019, 3, 1172
1554615 CIFC24 H20 N10 NiP 1 21/n 17.7492; 16.392; 8.8505
90; 101.096; 90		1103.2Dubrawski, Zachary; Heidebrecht, Joshua; Puerta Lombardi, Braulio M.; Hyla, Alexander S.; Willkomm, Janina; Radford, Chase L.; Lin, Jian-Bin; Welch, Gregory C.; Ponnurangam, Sathish; Roesler, Roland; Prokopchuk, Demyan E.; Piers, Warren E.
Ligand-centered electrochemical processes enable CO2 reduction with a nickel bis(triazapentadienyl) complex
Sustainable Energy & Fuels, 2019, 3, 1172
1554632 CIFC39 H32 F6 Ir N3 O0 S2C 1 2/c 126.026; 12.94; 22.386
90; 97.214; 90		7479.4Lu, Guang-Zhao; Wu, Ruixia; Liu, Liang; Zhou, Liang; Zheng, You-Xuan; Zhang, Wen-Wei; Zuo, Jing-Lin; Zhang, Hongjie
A series of red iridium(iii) complexes using flexible dithiocarbamate derivatives as ancillary ligands for highly efficient phosphorescent OLEDs
Materials Chemistry Frontiers, 2019, 3, 860
1554633 CIFC53 H42 F6 Ir N3 S2P -111.3; 15.22; 16.31
79.22; 79.11; 82.46		2693Lu, Guang-Zhao; Wu, Ruixia; Liu, Liang; Zhou, Liang; Zheng, You-Xuan; Zhang, Wen-Wei; Zuo, Jing-Lin; Zhang, Hongjie
A series of red iridium(iii) complexes using flexible dithiocarbamate derivatives as ancillary ligands for highly efficient phosphorescent OLEDs
Materials Chemistry Frontiers, 2019, 3, 860
1554634 CIFC45 H28 F6 Ir N3 S2P 1 21/c 115.5226; 12.6925; 20.61
90; 97.559; 90		4025.3Lu, Guang-Zhao; Wu, Ruixia; Liu, Liang; Zhou, Liang; Zheng, You-Xuan; Zhang, Wen-Wei; Zuo, Jing-Lin; Zhang, Hongjie
A series of red iridium(iii) complexes using flexible dithiocarbamate derivatives as ancillary ligands for highly efficient phosphorescent OLEDs
Materials Chemistry Frontiers, 2019, 3, 860
1554635 CIFC72 H46 Co6 N12 O39P 1 21/c 17.237; 18.371; 62.028
90; 92.02; 90		8242Li, Ang; Qian, Binbin; Zhong, Ming; Liu, Yingying; Chang, Ze; Bu, Xian-He
An insight into the pyrolysis process of metal‒organic framework templates/precursors to construct metal oxide anode materials for lithium-ion batteries
Materials Chemistry Frontiers, 2019, 3, 1398
1554636 CIFC42 H36 N4 O2 Pt2P 1 21/c 111.768; 17.4213; 17.5279
90; 97.615; 90		3561.77Qu, Lang; Li, Chunbo; Shen, Guangyu; Gou, Fei; Song, Jintong; Wang, Man; Xu, Xuemei; Zhou, Xiangge; Xiang, Haifeng
Syntheses, crystal structures, chirality and aggregation-induced phosphorescence of stacked binuclear platinum(ii) complexes with bridging Salen ligands
Materials Chemistry Frontiers, 2019, 3, 1199
1554637 CIFC43 H38 Cl2 N4 O2 Pt2P 21 21 2111.0565; 16.7748; 20.3659
90; 90; 90		3777.3Qu, Lang; Li, Chunbo; Shen, Guangyu; Gou, Fei; Song, Jintong; Wang, Man; Xu, Xuemei; Zhou, Xiangge; Xiang, Haifeng
Syntheses, crystal structures, chirality and aggregation-induced phosphorescence of stacked binuclear platinum(ii) complexes with bridging Salen ligands
Materials Chemistry Frontiers, 2019, 3, 1199
1554638 CIFC42 H28 Cl2 N4 O2 Pt2P 1 21/n 19.6783; 18.7346; 19.5011
90; 100.777; 90		3473.6Qu, Lang; Li, Chunbo; Shen, Guangyu; Gou, Fei; Song, Jintong; Wang, Man; Xu, Xuemei; Zhou, Xiangge; Xiang, Haifeng
Syntheses, crystal structures, chirality and aggregation-induced phosphorescence of stacked binuclear platinum(ii) complexes with bridging Salen ligands
Materials Chemistry Frontiers, 2019, 3, 1199
1554639 CIFC51 H35 Cl3 N4 O2 Pt2P 21 21 2110.7354; 20.1891; 21.7815
90; 90; 90		4720.9Qu, Lang; Li, Chunbo; Shen, Guangyu; Gou, Fei; Song, Jintong; Wang, Man; Xu, Xuemei; Zhou, Xiangge; Xiang, Haifeng
Syntheses, crystal structures, chirality and aggregation-induced phosphorescence of stacked binuclear platinum(ii) complexes with bridging Salen ligands
Materials Chemistry Frontiers, 2019, 3, 1199
1554640 CIFC43 H38 Cl2 N4 O2 Pt2P 21 21 2111.05822; 16.7782; 20.3868
90; 90; 90		3782.51Qu, Lang; Li, Chunbo; Shen, Guangyu; Gou, Fei; Song, Jintong; Wang, Man; Xu, Xuemei; Zhou, Xiangge; Xiang, Haifeng
Syntheses, crystal structures, chirality and aggregation-induced phosphorescence of stacked binuclear platinum(ii) complexes with bridging Salen ligands
Materials Chemistry Frontiers, 2019, 3, 1199
1554641 CIFC17 H19 N O2 SP 1 21/n 111.377; 9.712; 13.362
90; 95.331; 90		1470Yang, Jie; Gao, Heqi; Wang, Yunsheng; Yu, Yun; Gong, Yanbin; Fang, Manman; Ding, Dan; Hu, Wenping; Tang, Ben Zhong; Li, Zhen
The odd–even effect of alkyl chain in organic room temperature phosphorescence luminogens and the corresponding in vivo imaging
Materials Chemistry Frontiers, 2019, 3, 1391
1554642 CIFC14 H13 N O2 SP 1 21/n 17.9027; 11.1576; 13.5298
90; 93.338; 90		1190.97Yang, Jie; Gao, Heqi; Wang, Yunsheng; Yu, Yun; Gong, Yanbin; Fang, Manman; Ding, Dan; Hu, Wenping; Tang, Ben Zhong; Li, Zhen
The odd–even effect of alkyl chain in organic room temperature phosphorescence luminogens and the corresponding in vivo imaging
Materials Chemistry Frontiers, 2019, 3, 1391
1554643 CIFC13 H11 N O2 SP 1 21/n 18.78316; 11.4642; 11.1048
90; 91.3006; 90		1117.88Yang, Jie; Gao, Heqi; Wang, Yunsheng; Yu, Yun; Gong, Yanbin; Fang, Manman; Ding, Dan; Hu, Wenping; Tang, Ben Zhong; Li, Zhen
The odd–even effect of alkyl chain in organic room temperature phosphorescence luminogens and the corresponding in vivo imaging
Materials Chemistry Frontiers, 2019, 3, 1391
1554644 CIFC16 H17 N O2 SP 1 21/c 118.9325; 9.4253; 17.2146
90; 114.976; 90		2784.59Yang, Jie; Gao, Heqi; Wang, Yunsheng; Yu, Yun; Gong, Yanbin; Fang, Manman; Ding, Dan; Hu, Wenping; Tang, Ben Zhong; Li, Zhen
The odd–even effect of alkyl chain in organic room temperature phosphorescence luminogens and the corresponding in vivo imaging
Materials Chemistry Frontiers, 2019, 3, 1391
1554645 CIFC18 H21 N O2 SR 3 c :H26.477; 26.477; 12.475
90; 90; 120		7574Yang, Jie; Gao, Heqi; Wang, Yunsheng; Yu, Yun; Gong, Yanbin; Fang, Manman; Ding, Dan; Hu, Wenping; Tang, Ben Zhong; Li, Zhen
The odd–even effect of alkyl chain in organic room temperature phosphorescence luminogens and the corresponding in vivo imaging
Materials Chemistry Frontiers, 2019, 3, 1391
1554646 CIFC15 H15 N O2 SP -17.7584; 9.0839; 10.0043
109.128; 97.408; 103.752		630.4Yang, Jie; Gao, Heqi; Wang, Yunsheng; Yu, Yun; Gong, Yanbin; Fang, Manman; Ding, Dan; Hu, Wenping; Tang, Ben Zhong; Li, Zhen
The odd–even effect of alkyl chain in organic room temperature phosphorescence luminogens and the corresponding in vivo imaging
Materials Chemistry Frontiers, 2019, 3, 1391
1554647 CIFC44 H46 N2 O4P -16.3304; 7.2037; 20.473
89.41; 89.13; 76.08		906.1Dai, Shuangxiong; Cai, Zhengxu; Peng, Zhe; Wang, Zhi; Tong, Bin; Shi, Jianbing; Gan, Shenglong; He, Qiming; Chen, Wei; Dong, Yuping
A stabilized lamellar liquid crystalline phase with aggregation-induced emission features based on pyrrolopyrrole derivatives
Materials Chemistry Frontiers, 2019, 3, 1105
1554648 CIFC4 H14 Br3 N3 OP b c m6.70475; 13.3306; 13.1204
90; 90; 90		1172.68Li, Kai; Dong, Li-Yuan; Xu, Hao-Xiang; Qin, Yan; Li, Zhi-Gang; Azeem, Muhammad; Li, Wei; Bu, Xian-He
Electronic structures and elastic properties of a family of metal-free perovskites
Materials Chemistry Frontiers, 2019, 3, 1678
1554649 CIFC4 H14 I3 N3 OP b c m7.064; 14.089; 13.684
90; 90; 90		1361.9Li, Kai; Dong, Li-Yuan; Xu, Hao-Xiang; Qin, Yan; Li, Zhi-Gang; Azeem, Muhammad; Li, Wei; Bu, Xian-He
Electronic structures and elastic properties of a family of metal-free perovskites
Materials Chemistry Frontiers, 2019, 3, 1678
1554650 CIFC30 H29 N5 OP 1 21/c 122.0567; 7.7405; 15.5138
90; 102.762; 90		2583.2Yang, Jinfeng; Gu, Kaizhi; Shi, Chuanxing; Li, Meng; Zhao, Ping; Zhu, Wei-Hong
Fluorescent thermometer based on a quinolinemalononitrile copolymer with aggregation-induced emission characteristics
Materials Chemistry Frontiers, 2019, 3, 1503
1554651 CIFC20 H22 B F2 N3 OC 1 2/c 112.8894; 9.0135; 31.806
90; 93.146; 90		3689.6Yu, Changjiang; Huang, Zhenlong; Gu, Wei; Wu, Qinghua; Hao, Erhong; Xiao, Yi; Jiao, Lijuan; Wong, Wai-Yeung
A novel family of AIE-active meso-2-ketopyrrolyl BODIPYs: bright solid-state red fluorescence, morphological properties and application as viscosimeters in live cells
Materials Chemistry Frontiers, 2019, 3, 1823
1554652 CIFC26 H34 B F2 N3 OC 1 2/c 126.649; 9.8463; 19.4482
90; 101.393; 90		5002.5Yu, Changjiang; Huang, Zhenlong; Gu, Wei; Wu, Qinghua; Hao, Erhong; Xiao, Yi; Jiao, Lijuan; Wong, Wai-Yeung
A novel family of AIE-active meso-2-ketopyrrolyl BODIPYs: bright solid-state red fluorescence, morphological properties and application as viscosimeters in live cells
Materials Chemistry Frontiers, 2019, 3, 1823
1554653 CIFC24 H30 B F2 N3 OC 1 2/c 123.744; 12.2488; 19.0154
90; 101.276; 90		5423.6Yu, Changjiang; Huang, Zhenlong; Gu, Wei; Wu, Qinghua; Hao, Erhong; Xiao, Yi; Jiao, Lijuan; Wong, Wai-Yeung
A novel family of AIE-active meso-2-ketopyrrolyl BODIPYs: bright solid-state red fluorescence, morphological properties and application as viscosimeters in live cells
Materials Chemistry Frontiers, 2019, 3, 1823
1554654 CIFC20 H24P -14.7535; 6.1267; 13.209
96.215; 96.738; 91.369		379.53Zhang, Haoke; Liu, Junkai; Du, Lili; Ma, Chao; Leung, Nelson L. C.; Niu, Yingli; Qin, Anjun; Sun, Jingzhi; Peng, Qian; Sung, Herman H. Y.; Williams, Ian D.; Kwok, Ryan T. K.; Lam, Jacky W. Y.; Wong, Kam Sing; Phillips, David Lee; Tang, Ben Zhong
Drawing a clear mechanistic picture for the aggregation-induced emission process
Materials Chemistry Frontiers, 2019, 3, 1143
1554655 CIFC24 H26P 1 21/c 112.9394; 8.2851; 9.083
90; 106.48; 90		933.73Zhang, Haoke; Liu, Junkai; Du, Lili; Ma, Chao; Leung, Nelson L. C.; Niu, Yingli; Qin, Anjun; Sun, Jingzhi; Peng, Qian; Sung, Herman H. Y.; Williams, Ian D.; Kwok, Ryan T. K.; Lam, Jacky W. Y.; Wong, Kam Sing; Phillips, David Lee; Tang, Ben Zhong
Drawing a clear mechanistic picture for the aggregation-induced emission process
Materials Chemistry Frontiers, 2019, 3, 1143
1554656 CIFC24 H26P 1 21/n 17.9294; 7.3834; 16.2178
90; 90.745; 90		949.41Zhang, Haoke; Liu, Junkai; Du, Lili; Ma, Chao; Leung, Nelson L. C.; Niu, Yingli; Qin, Anjun; Sun, Jingzhi; Peng, Qian; Sung, Herman H. Y.; Williams, Ian D.; Kwok, Ryan T. K.; Lam, Jacky W. Y.; Wong, Kam Sing; Phillips, David Lee; Tang, Ben Zhong
Drawing a clear mechanistic picture for the aggregation-induced emission process
Materials Chemistry Frontiers, 2019, 3, 1143
1554657 CIFC20 H24P 1 21/n 14.8732; 10.6116; 15.5489
90; 90.251; 90		804.06Zhang, Haoke; Liu, Junkai; Du, Lili; Ma, Chao; Leung, Nelson L. C.; Niu, Yingli; Qin, Anjun; Sun, Jingzhi; Peng, Qian; Sung, Herman H. Y.; Williams, Ian D.; Kwok, Ryan T. K.; Lam, Jacky W. Y.; Wong, Kam Sing; Phillips, David Lee; Tang, Ben Zhong
Drawing a clear mechanistic picture for the aggregation-induced emission process
Materials Chemistry Frontiers, 2019, 3, 1143
1554658 CIFC44 H28 SP -19.7394; 9.8279; 16.0542
96.661; 100.097; 92.178		1499.99Kazantsev, Maxim S.; Sonina, Alina A.; Koskin, Igor P.; Sherin, Peter S.; Rybalova, Tatyana V.; Benassi, Enrico; Mostovich, Evgeny A.
Stimuli responsive aggregation-induced emission of bis(4-((9H-fluoren-9-ylidene)methyl)phenyl)thiophene single crystals
Materials Chemistry Frontiers, 2019, 3, 1545
1554659 CIFC44 H28 SP 1 21/c 115.4125; 9.8016; 20.9249
90; 105.66; 90		3043.7Kazantsev, Maxim S.; Sonina, Alina A.; Koskin, Igor P.; Sherin, Peter S.; Rybalova, Tatyana V.; Benassi, Enrico; Mostovich, Evgeny A.
Stimuli responsive aggregation-induced emission of bis(4-((9H-fluoren-9-ylidene)methyl)phenyl)thiophene single crystals
Materials Chemistry Frontiers, 2019, 3, 1545
1554660 CIFC40 H28 N4C 1 2/c 126.013; 12.858; 10.6428
90; 104.932; 90		3439.5Peng, Zhe; Dai, Shuangxiong; Ji, Yingchun; Tong, Bin; Shi, Jianbing; Cai, Zhengxu; Zhi, Junge; Dong, Yuping
Ionic liquid crystals with aggregation-induced emission properties based on pyrrolo[3,2-b]pyrrole salt compounds
Materials Chemistry Frontiers, 2019, 3, 1385
1554661 CIFC18 H15 Au F5 N OP 1 21/c 17.402; 19.562; 12.283
90; 97.32; 90		1764.1Dong, Yubao; Zhu, Fei; Chen, Zhao; Yin, Jun; Liu, Sheng Hua
Single-component gold(i)-containing highly white-emissive crystals based on a polymorph doping strategy
Materials Chemistry Frontiers, 2019, 3, 1866
1554662 CIFC18 H15 Au F5 N OP 1 21/c 17.3042; 19.814; 11.9572
90; 95.327; 90		1723Dong, Yubao; Zhu, Fei; Chen, Zhao; Yin, Jun; Liu, Sheng Hua
Single-component gold(i)-containing highly white-emissive crystals based on a polymorph doping strategy
Materials Chemistry Frontiers, 2019, 3, 1866
1554663 CIFC18 H15 Au F5 N OP 1 21/c 17.2889; 19.8254; 11.9641
90; 95.306; 90		1721.47Dong, Yubao; Zhu, Fei; Chen, Zhao; Yin, Jun; Liu, Sheng Hua
Single-component gold(i)-containing highly white-emissive crystals based on a polymorph doping strategy
Materials Chemistry Frontiers, 2019, 3, 1866
1554664 CIFC29 H14 N4 O2P 1 21 15.0052; 15.6076; 14.6006
90; 91.275; 90		1140.3Zhao, Na; Gao, Wangwang; Zhang, Min; Yang, Junfang; Zheng, Xiaoyan; Li, Yue; Cui, Rongrong; Yin, Wei; Li, Nan
Regulation of circular dichroism behavior and construction of tunable solid-state circularly polarized luminescence based on BINOL derivatives
Materials Chemistry Frontiers, 2019, 3, 1613
1554665 CIFC30 H16 N4 O2C 1 2 125.4902; 8.4676; 16.9657
90; 104.889; 90		3538.9Zhao, Na; Gao, Wangwang; Zhang, Min; Yang, Junfang; Zheng, Xiaoyan; Li, Yue; Cui, Rongrong; Yin, Wei; Li, Nan
Regulation of circular dichroism behavior and construction of tunable solid-state circularly polarized luminescence based on BINOL derivatives
Materials Chemistry Frontiers, 2019, 3, 1613
1554666 CIFC33 H22 N4 O2C 2 2 2112.0721; 17.9566; 12.2305
90; 90; 90		2651.3Zhao, Na; Gao, Wangwang; Zhang, Min; Yang, Junfang; Zheng, Xiaoyan; Li, Yue; Cui, Rongrong; Yin, Wei; Li, Nan
Regulation of circular dichroism behavior and construction of tunable solid-state circularly polarized luminescence based on BINOL derivatives
Materials Chemistry Frontiers, 2019, 3, 1613
1554667 CIFC36 H28 N4 O2P -18.8302; 18.7601; 19.027
110.64; 94.387; 93.845		2926Zhao, Na; Gao, Wangwang; Zhang, Min; Yang, Junfang; Zheng, Xiaoyan; Li, Yue; Cui, Rongrong; Yin, Wei; Li, Nan
Regulation of circular dichroism behavior and construction of tunable solid-state circularly polarized luminescence based on BINOL derivatives
Materials Chemistry Frontiers, 2019, 3, 1613
1554668 CIFC33 H22 Cl2 N4 O2P 1 21 17.9714; 22.5703; 9.1047
90; 115.426; 90		1479.42Zhao, Na; Gao, Wangwang; Zhang, Min; Yang, Junfang; Zheng, Xiaoyan; Li, Yue; Cui, Rongrong; Yin, Wei; Li, Nan
Regulation of circular dichroism behavior and construction of tunable solid-state circularly polarized luminescence based on BINOL derivatives
Materials Chemistry Frontiers, 2019, 3, 1613
1554669 CIFC48 H30 F6 N4 O2C 2 2 2118.4373; 25.7446; 11.6266
90; 90; 90		5518.7Zhao, Na; Gao, Wangwang; Zhang, Min; Yang, Junfang; Zheng, Xiaoyan; Li, Yue; Cui, Rongrong; Yin, Wei; Li, Nan
Regulation of circular dichroism behavior and construction of tunable solid-state circularly polarized luminescence based on BINOL derivatives
Materials Chemistry Frontiers, 2019, 3, 1613
1554670 CIFC11.67 H8.67 N1.33 O0.67P 1 21/c 18.5584; 18.7684; 17.4034
90; 94.951; 90		2785.03Zhao, Na; Gao, Wangwang; Zhang, Min; Yang, Junfang; Zheng, Xiaoyan; Li, Yue; Cui, Rongrong; Yin, Wei; Li, Nan
Regulation of circular dichroism behavior and construction of tunable solid-state circularly polarized luminescence based on BINOL derivatives
Materials Chemistry Frontiers, 2019, 3, 1613
1554671 CIFC33 H23 B F2 O3P -18.788; 10.446; 15.407
70.818; 88.67; 79.808		1313.8Wang, Yongtao; Liu, Wenjing; Ren, Litong; Ge, Guixian
Deep insights into polymorphism initiated by exploring multicolor conversion materials
Materials Chemistry Frontiers, 2019, 3, 1661
1554672 CIFC33 H23 B F2 O3C 1 c 153.109; 7.2441; 13.687
90; 97.371; 90		5222Wang, Yongtao; Liu, Wenjing; Ren, Litong; Ge, Guixian
Deep insights into polymorphism initiated by exploring multicolor conversion materials
Materials Chemistry Frontiers, 2019, 3, 1661
1554673 CIFC33 H23 B F2 O3P 1 21/n 115.955; 8.978; 19.823
90; 113.38; 90		2606.4Wang, Yongtao; Liu, Wenjing; Ren, Litong; Ge, Guixian
Deep insights into polymorphism initiated by exploring multicolor conversion materials
Materials Chemistry Frontiers, 2019, 3, 1661
1554674 CIFC33 H23 B F2 O3P 1 21/c 115.958; 8.99; 19.915
90; 113.62; 90		2617.7Wang, Yongtao; Liu, Wenjing; Ren, Litong; Ge, Guixian
Deep insights into polymorphism initiated by exploring multicolor conversion materials
Materials Chemistry Frontiers, 2019, 3, 1661
1554675 CIFC33 H23 B F2 O3P 1 21/c 115.957; 8.984; 19.969
90; 113.55; 90		2624.3Wang, Yongtao; Liu, Wenjing; Ren, Litong; Ge, Guixian
Deep insights into polymorphism initiated by exploring multicolor conversion materials
Materials Chemistry Frontiers, 2019, 3, 1661
1554676 CIFC30 H22 N2 O2 SP 112.1382; 12.8179; 15.1854
85.684; 78.373; 89.276		2307.59Chen, Yitong; Xu, Chao; Xu, Bingjia; Mao, Zhu; Li, Jian-An; Yang, Zhan; Peethani, Naga Raju; Liu, Cong; Shi, Guang; Gu, Feng Long; Zhang, Yi; Chi, Zhenguo
Chirality-activated mechanoluminescence from aggregation-induced emission enantiomers with high contrast mechanochromism and force-induced delayed fluorescence
Materials Chemistry Frontiers, 2019, 3, 1800
1554677 CIFC30 H22 N2 O2 SP 1 21/c 114.4773; 12.17882; 13.40691
90; 104.925; 90		2284.11Chen, Yitong; Xu, Chao; Xu, Bingjia; Mao, Zhu; Li, Jian-An; Yang, Zhan; Peethani, Naga Raju; Liu, Cong; Shi, Guang; Gu, Feng Long; Zhang, Yi; Chi, Zhenguo
Chirality-activated mechanoluminescence from aggregation-induced emission enantiomers with high contrast mechanochromism and force-induced delayed fluorescence
Materials Chemistry Frontiers, 2019, 3, 1800
1554678 CIFC30 H22 N2 O2 SP 112.135; 12.8327; 15.1864
85.785; 78.371; 89.345		2310.08Chen, Yitong; Xu, Chao; Xu, Bingjia; Mao, Zhu; Li, Jian-An; Yang, Zhan; Peethani, Naga Raju; Liu, Cong; Shi, Guang; Gu, Feng Long; Zhang, Yi; Chi, Zhenguo
Chirality-activated mechanoluminescence from aggregation-induced emission enantiomers with high contrast mechanochromism and force-induced delayed fluorescence
Materials Chemistry Frontiers, 2019, 3, 1800
1554679 CIFC30 H24 N4 O PtP -18.4381; 12.133; 23.3476
86.889; 81.757; 83.205		2347.31Ma, Huili; Shen, Kang; Wu, Yipei; Xia, Fang; Yu, Feiling; Sun, Zhengyi; Qian, Chunyue; Peng, Qiming; Zhang, Hong-Hai; You, Cong; Xie, Guohua; Hang, Xiao-Chun; Huang, Wei
High-color-purity and efficient solution-processable blue phosphorescent light-emitting diodes with Pt(ii) complexes featuring 3ππ* transitions
Materials Chemistry Frontiers, 2019, 3, 2448
1554680 CIFC27 H18 N4 O PtP 21 21 217.7277; 13.36; 20.072
90; 90; 90		2072.3Ma, Huili; Shen, Kang; Wu, Yipei; Xia, Fang; Yu, Feiling; Sun, Zhengyi; Qian, Chunyue; Peng, Qiming; Zhang, Hong-Hai; You, Cong; Xie, Guohua; Hang, Xiao-Chun; Huang, Wei
High-color-purity and efficient solution-processable blue phosphorescent light-emitting diodes with Pt(ii) complexes featuring 3ππ* transitions
Materials Chemistry Frontiers, 2019, 3, 2448
1554681 CIFC37 H28 N4 O3C 1 2/c 126.686; 16.726; 14.573
90; 107.7; 90		6197Ren, Fei; Shi, Jianbing; Tong, Bin; Cai, Zhengxu; Dong, Yuping
Effects of fused rings linked to the 2,5-position of pyrrole derivatives with near-infrared emission on their aggregation-enhanced emission properties
Materials Chemistry Frontiers, 2019, 3, 2072
1554682 CIFC18 H19 N3 OP 1 21/n 116.236; 7.7124; 25.238
90; 104.08; 90		3065.3Li, Aisen; Liu, Hao; Song, Chongping; Geng, Yijia; Xu, Shuping; Zhang, Hongyu; Zhang, Houyu; Cui, Haining; Xu, Weiqing
Flexible control of excited state transition under pressure/temperature: distinct stimuli-responsive behaviours of two ESIPT polymorphs
Materials Chemistry Frontiers, 2019, 3, 2128
1554683 CIFC18 H19 N3 OP 1 21/c 112.841; 10.286; 12.663
90; 111.023; 90		1561.2Li, Aisen; Liu, Hao; Song, Chongping; Geng, Yijia; Xu, Shuping; Zhang, Hongyu; Zhang, Houyu; Cui, Haining; Xu, Weiqing
Flexible control of excited state transition under pressure/temperature: distinct stimuli-responsive behaviours of two ESIPT polymorphs
Materials Chemistry Frontiers, 2019, 3, 2128
1554684 CIFC10 H26 Cl6 N2 ZnP 1 21/c 124.5577; 18.3997; 18.1621
90; 92.376; 90		8199.6Zhang, Yu-Wei; Wang, Qing; Shi, Ping-Ping; Zhang, Wan-Ying; Ye, Qiong; Fu, Da-Wei
Visual low-high interchange in a dielectric switch for trimethylchloroethylamine tetrachlorozincate with a large leap symmetry breaking
Materials Chemistry Frontiers, 2019, 3, 2077
1554685 CIFC10 H26 Cl6 N2 ZnI 41/a :212.7985; 12.7985; 25.8884
90; 90; 90		4240.6Zhang, Yu-Wei; Wang, Qing; Shi, Ping-Ping; Zhang, Wan-Ying; Ye, Qiong; Fu, Da-Wei
Visual low-high interchange in a dielectric switch for trimethylchloroethylamine tetrachlorozincate with a large leap symmetry breaking
Materials Chemistry Frontiers, 2019, 3, 2077
1554686 CIFC218 H276 O28 P2 PtP -112.2995; 12.7098; 38.043
80.979; 89.471; 65.725		5344.1Hu, Yang; Wang, Wei; Yao, Rui; Wang, Xu-Qing; Wang, Yu-Xuan; Sun, Bin; Chen, Li-Jun; Zhang, Ying; Zhao, Xiao-Li; Xu, Lin; Tan, Hong-Wei; Yu, Yihua; Li, Xiaopeng; Yang, Hai-Bo
Facile synthesis of diverse rotaxanes via successive supramolecular transformations
Materials Chemistry Frontiers, 2019, 3, 2397
1554687 CIFC52 H57.5 N4.5 O7P 1 21/c 115.215; 14.04; 23.048
90; 100.849; 90		4835Chan, Sing-Ming; Tang, Fung-Kit; Kwan, Chak-Shing; Lam, Ching-Yau; Hau, Sam C. K.; Leung, Ken Cham-Fai
Water-compatible fluorescent [2]rotaxanes for Au3+ detection and bioimaging
Materials Chemistry Frontiers, 2019, 3, 2388
1554688 CIFC37 H23 N O2 SP -18.9754; 11.9049; 13.8094
111.039; 90.487; 95.955		1368.09Huang, Lili; Wen, Xue; Liu, Jianwei; Chen, Mingxing; Ma, Zhiyong; Jia, Xinru
An AIE molecule featuring changeable triplet emission between phosphorescence and delayed fluorescence by an external force
Materials Chemistry Frontiers, 2019, 3, 2151
1554689 CIFC43 H31 N3P -112.995; 14.047; 18.771
85.928; 72.336; 78.362		3198Li, Aisen; Chu, Ning; Liu, Jianwei; Liu, Hao; Wang, Jing; Xu, Shuping; Cui, Haining; Zhang, Hongyu; Xu, Weiqing; Ma, Zhiyong
Pressure-induced remarkable luminescence switch of a dimer form of donor–acceptor–donor triphenylamine (TPA) derivative
Materials Chemistry Frontiers, 2019, 3, 2768
1554690 CIFC42 H30 N4P 1 21/c 117.2834; 10.2606; 18.3175
90; 96.618; 90		3226.74Li, Aisen; Chu, Ning; Liu, Jianwei; Liu, Hao; Wang, Jing; Xu, Shuping; Cui, Haining; Zhang, Hongyu; Xu, Weiqing; Ma, Zhiyong
Pressure-induced remarkable luminescence switch of a dimer form of donor–acceptor–donor triphenylamine (TPA) derivative
Materials Chemistry Frontiers, 2019, 3, 2768
1554691 CIFC15 H15 N O2P -16.2682; 7.1504; 28.857
94.165; 90.331; 90.002		1289.94Liu, Jianxun; Xing, Chang; Wei, Donghui; Deng, Qianqian; Yang, Cuiping; Peng, Qiuchen; Hou, Hongwei; Li, Yuanyuan; Li, Kai
Utilizing the aggregation-induced emission phenomenon to visualize spontaneous molecular directed motion in the solid state
Materials Chemistry Frontiers, 2019, 3, 2746
1554692 CIFC16 H17 N O2P -16.2328; 7.2129; 31.0245
92.777; 94.558; 90.014		1388.7Liu, Jianxun; Xing, Chang; Wei, Donghui; Deng, Qianqian; Yang, Cuiping; Peng, Qiuchen; Hou, Hongwei; Li, Yuanyuan; Li, Kai
Utilizing the aggregation-induced emission phenomenon to visualize spontaneous molecular directed motion in the solid state
Materials Chemistry Frontiers, 2019, 3, 2746
1554693 CIFC17 H19 N O2P -16.1745; 7.0411; 33.2296
86.545; 84.929; 89.992		1436.38Liu, Jianxun; Xing, Chang; Wei, Donghui; Deng, Qianqian; Yang, Cuiping; Peng, Qiuchen; Hou, Hongwei; Li, Yuanyuan; Li, Kai
Utilizing the aggregation-induced emission phenomenon to visualize spontaneous molecular directed motion in the solid state
Materials Chemistry Frontiers, 2019, 3, 2746
1555295 CIFC12 H21 I3 N3 O2 PbP -18.0816; 12.3906; 12.9013
97.876; 106.389; 104.083		1172.4Peng, Yong; Albero, Josep; Álvarez, Eleuterio; García, Hermenegildo
Hybrid benzidinium lead iodide perovskites with a 1D structure as photoinduced electron transfer photocatalysts
Sustainable Energy & Fuels, 2019, 3, 2356
1555297 CIFC20 H35 B N3 O P RuP b c a14.9558; 15.4562; 19.3998
90; 90; 90		4484.45Luconi, Lapo; Demirci, Umit B.; Peruzzini, Maurizio; Giambastiani, Giuliano; Rossin, Andrea
Ammonia borane and hydrazine bis(borane) dehydrogenation mediated by an unsymmetrical (PNN) ruthenium pincer hydride: metal‒ligand cooperation for hydrogen production
Sustainable Energy & Fuels, 2019, 3, 2583
1555298 CIFC45 H53 N3 O P2 RuP 1 21 110.512; 12.577; 16.003
90; 108.396; 90		2007.6Luconi, Lapo; Demirci, Umit B.; Peruzzini, Maurizio; Giambastiani, Giuliano; Rossin, Andrea
Ammonia borane and hydrazine bis(borane) dehydrogenation mediated by an unsymmetrical (PNN) ruthenium pincer hydride: metal‒ligand cooperation for hydrogen production
Sustainable Energy & Fuels, 2019, 3, 2583
1555299 CIFC22 H33 N4 O P RuP -18.4345; 14.1852; 20.2401
79.305; 86.313; 81.975		2354.42Luconi, Lapo; Demirci, Umit B.; Peruzzini, Maurizio; Giambastiani, Giuliano; Rossin, Andrea
Ammonia borane and hydrazine bis(borane) dehydrogenation mediated by an unsymmetrical (PNN) ruthenium pincer hydride: metal‒ligand cooperation for hydrogen production
Sustainable Energy & Fuels, 2019, 3, 2583
1555302 CIFC76 H92 S14P 1 21/c 116.8658; 24.1932; 9.164
90; 100.116; 90		3681.1Krishnan Jagadamma, Lethy; Taylor, Rupert G. D.; Kanibolotsky, Alexander L.; Sajjad, Muhammad Tariq; Wright, Iain A.; Horton, Peter N.; Coles, Simon J.; Samuel, Ifor D. W.; Skabara, Peter J.
Highly efficient fullerene and non-fullerene based ternary organic solar cells incorporating a new tetrathiocin-cored semiconductor
Sustainable Energy & Fuels, 2019, 3, 2087
1556100 CIFC13 H20 O2 SP -110.016; 11.499; 17.53
95.938; 100.417; 108.57		1854Dawid, M.; Mlostoñ, G; Warkentin, J.
The first 2,2-dialkoxythiirane.
Organic letters, 2001, 3, 2455-2456
1556325 CIFC15 H29 Cl2 N3 PdP -18.1051; 11.1155; 22.6264
77.784; 89.987; 71.894		1888.9Peral, Daniel; Gómez-Villarraga, Fernando; Sala, Xavier; Pons, Josefina; Carles Bayón, J.; Ros, Josep; Guerrero, Miguel; Vendier, Laure; Lecante, Pierre; García-Antón, Jordi; Philippot, Karine
Palladium catalytic systems with hybrid pyrazole ligands in C‒C coupling reactions. Nanoparticles versus molecular complexes
Catal. Sci. Technol., 2013, 3, 475
1556326 CIFC15 H28 Cl2 N2 Pd SP -18.1752; 15.2655; 15.457
94.321; 90.451; 93.185		1920.4Peral, Daniel; Gómez-Villarraga, Fernando; Sala, Xavier; Pons, Josefina; Carles Bayón, J.; Ros, Josep; Guerrero, Miguel; Vendier, Laure; Lecante, Pierre; García-Antón, Jordi; Philippot, Karine
Palladium catalytic systems with hybrid pyrazole ligands in C‒C coupling reactions. Nanoparticles versus molecular complexes
Catal. Sci. Technol., 2013, 3, 475
1556327 CIFC30 H56 Cl2 N4 O2 PdP 18.1693; 9.1162; 22.9935
93.592; 91.806; 89.939		1708.2Peral, Daniel; Gómez-Villarraga, Fernando; Sala, Xavier; Pons, Josefina; Carles Bayón, J.; Ros, Josep; Guerrero, Miguel; Vendier, Laure; Lecante, Pierre; García-Antón, Jordi; Philippot, Karine
Palladium catalytic systems with hybrid pyrazole ligands in C‒C coupling reactions. Nanoparticles versus molecular complexes
Catal. Sci. Technol., 2013, 3, 475
1556328 CIFC23 H45 Cl2 N3 PdP 1 21/c 115.7877; 21.0937; 8.109
90; 102.061; 90		2640.9Peral, Daniel; Gómez-Villarraga, Fernando; Sala, Xavier; Pons, Josefina; Carles Bayón, J.; Ros, Josep; Guerrero, Miguel; Vendier, Laure; Lecante, Pierre; García-Antón, Jordi; Philippot, Karine
Palladium catalytic systems with hybrid pyrazole ligands in C‒C coupling reactions. Nanoparticles versus molecular complexes
Catal. Sci. Technol., 2013, 3, 475
1556329 CIFC66 H64 Cl2 N4 O7.5 V2P 1 21/a 117.8598; 10.775; 31.054
90; 101.73; 90		5851.2Clowes, Lucy; Walton, Mark; Redshaw, Carl; Chao, Yimin; Walton, Alex; Elo, Pertti; Sumerin, Victor; Hughes, David L.
Vanadium(iii) phenoxyimine complexes for ethylene or ε-caprolactone polymerization: mononuclear versus binuclear pre-catalysts
Catal. Sci. Technol., 2013, 3, 152
1556330 CIFC44 H56 N2 O2P 1 21/a 19.6297; 12.1792; 16.2276
90; 100.851; 90		1869.18Clowes, Lucy; Walton, Mark; Redshaw, Carl; Chao, Yimin; Walton, Alex; Elo, Pertti; Sumerin, Victor; Hughes, David L.
Vanadium(iii) phenoxyimine complexes for ethylene or ε-caprolactone polymerization: mononuclear versus binuclear pre-catalysts
Catal. Sci. Technol., 2013, 3, 152
1556331 CIFC60 H86 Cl4 N2 O6 V2P b c a15.4851; 12.3449; 33.0323
90; 90; 90		6314.5Clowes, Lucy; Walton, Mark; Redshaw, Carl; Chao, Yimin; Walton, Alex; Elo, Pertti; Sumerin, Victor; Hughes, David L.
Vanadium(iii) phenoxyimine complexes for ethylene or ε-caprolactone polymerization: mononuclear versus binuclear pre-catalysts
Catal. Sci. Technol., 2013, 3, 152
1556332 CIFC42 H52 Cl2 N4 O3 VP 21 n b11.0873; 17.9157; 20.6832
90; 90; 90		4108.4Clowes, Lucy; Walton, Mark; Redshaw, Carl; Chao, Yimin; Walton, Alex; Elo, Pertti; Sumerin, Victor; Hughes, David L.
Vanadium(iii) phenoxyimine complexes for ethylene or ε-caprolactone polymerization: mononuclear versus binuclear pre-catalysts
Catal. Sci. Technol., 2013, 3, 152
1556333 CIFC54 H84 B Cl2 F4 P6 Rh3P 41 21 214.483; 14.483; 58.042
90; 90; 90		12175Preetz, Angelika; Kohrt, Christina; Meißner, Antje; Wei, Siping; Drexler, Hans-Joachim; Buschmann, Helmut; Heller, Detlef
Halide bridged trinuclear rhodium complexes and their inhibiting influence on catalysis
Catal. Sci. Technol., 2013, 3, 462
1556334 CIFC85 H86 B Cl4 F4 O6 P6 Rh3P 113.136; 13.405; 14.779
85.58; 68.44; 68.06		2239.6Preetz, Angelika; Kohrt, Christina; Meißner, Antje; Wei, Siping; Drexler, Hans-Joachim; Buschmann, Helmut; Heller, Detlef
Halide bridged trinuclear rhodium complexes and their inhibiting influence on catalysis
Catal. Sci. Technol., 2013, 3, 462
1556335 CIFC44 H72 Cl2 P4 Rh2P 21 21 2114.1975; 16.3823; 20.5561
90; 90; 90		4781.1Preetz, Angelika; Kohrt, Christina; Meißner, Antje; Wei, Siping; Drexler, Hans-Joachim; Buschmann, Helmut; Heller, Detlef
Halide bridged trinuclear rhodium complexes and their inhibiting influence on catalysis
Catal. Sci. Technol., 2013, 3, 462
1556336 CIFC135 H100 Cl6 F3 O3 P6 Rh3 SP 1 21 116.493; 23.276; 16.775
90; 118.1; 90		5681Preetz, Angelika; Kohrt, Christina; Meißner, Antje; Wei, Siping; Drexler, Hans-Joachim; Buschmann, Helmut; Heller, Detlef
Halide bridged trinuclear rhodium complexes and their inhibiting influence on catalysis
Catal. Sci. Technol., 2013, 3, 462
1556337 CIFC54 H84 B Br0.8 Cl1.2 F4 P6 Rh3P 21 21 2116.431; 20.348; 21.116
90; 90; 90		7060Preetz, Angelika; Kohrt, Christina; Meißner, Antje; Wei, Siping; Drexler, Hans-Joachim; Buschmann, Helmut; Heller, Detlef
Halide bridged trinuclear rhodium complexes and their inhibiting influence on catalysis
Catal. Sci. Technol., 2013, 3, 462
1556338 CIFC36 H56 Br2 P4 Rh2P 1 21 111.2912; 16.6047; 11.4464
90; 105.766; 90		2065.32Preetz, Angelika; Kohrt, Christina; Meißner, Antje; Wei, Siping; Drexler, Hans-Joachim; Buschmann, Helmut; Heller, Detlef
Halide bridged trinuclear rhodium complexes and their inhibiting influence on catalysis
Catal. Sci. Technol., 2013, 3, 462
1556339 CIFC36 H86 B F4 O2 P6 Rh3P 112.416; 12.444; 18.186
95.81; 94.37; 111.98		2572.3Preetz, Angelika; Kohrt, Christina; Meißner, Antje; Wei, Siping; Drexler, Hans-Joachim; Buschmann, Helmut; Heller, Detlef
Halide bridged trinuclear rhodium complexes and their inhibiting influence on catalysis
Catal. Sci. Technol., 2013, 3, 462
1556340 CIFC37 H86 B Cl4 F4 P6 Rh3P 19.6676; 12.005; 12.658
109.83; 94.19; 90.56		1377.3Preetz, Angelika; Kohrt, Christina; Meißner, Antje; Wei, Siping; Drexler, Hans-Joachim; Buschmann, Helmut; Heller, Detlef
Halide bridged trinuclear rhodium complexes and their inhibiting influence on catalysis
Catal. Sci. Technol., 2013, 3, 462
1556341 CIFC30.5 H30 Cl2 F6 N6 O3 P2 RuC 1 2/c 129.0844; 15.042; 16.3344
90; 108.315; 90		6784.1Vaquer, Lydia; Riente, Paola; Sala, Xavier; Jansat, Susanna; Benet-Buchholz, Jordi; Llobet, Antoni; Pericàs, Miquel A.
Molecular ruthenium complexes anchored on magnetic nanoparticles that act as powerful and magnetically recyclable stereospecific epoxidation catalysts
Catal. Sci. Technol., 2013, 3, 706
1556342 CIFC30.5 H30.5 Cl2 F6 N6 O3.25 P2 RuP -110.9643; 11.9921; 15.491
110.491; 99.026; 107.666		1737.2Vaquer, Lydia; Riente, Paola; Sala, Xavier; Jansat, Susanna; Benet-Buchholz, Jordi; Llobet, Antoni; Pericàs, Miquel A.
Molecular ruthenium complexes anchored on magnetic nanoparticles that act as powerful and magnetically recyclable stereospecific epoxidation catalysts
Catal. Sci. Technol., 2013, 3, 706
1556343 CIFC80 H102 Al Cl N4 O6 S2P 41 21 213.6143; 13.6143; 38.6616
90; 90; 90		7165.9Ternel, Jérémy; Roussel, Pascal; Agbossou-Niedercorn, Francine; Gauvin, Régis M.
Dismantling the salen framework: design of new asymmetric silylcyanation catalysts
Catal. Sci. Technol., 2013, 3, 580
1556344 CIFC108 H253 Br7 Co6 O75 Ti27P 1 21/c 123.8831; 20.6857; 20.2699
90; 92.546; 90		10004.2Lv, Yaokang; Willkomm, Janina; Steiner, Alexander; Gan, Lihua; Reisner, Erwin; Wright, Dominic S.
Encapsulation of a ‘naked’ Br− anion in a polyoxotitanate host
Chemical Science, 2012, 3, 2470
1556345 CIFC22.5 H27 Cl F6 I N2 O2 Os PP -111.3168; 13.0498; 19.2278
95.398; 103.654; 97.2625		2714.5Fu, Ying; Romero, María J.; Habtemariam, Abraha; Snowden, Michael E.; Song, Lijiang; Clarkson, Guy J.; Qamar, Bushra; Pizarro, Ana M.; Unwin, Patrick R.; Sadler, Peter J.
The contrasting chemical reactivity of potent isoelectronic iminopyridine and azopyridine osmium(ii) arene anticancer complexes
Chemical Science, 2012, 3, 2485
1556346 CIFC6 H14 N4 O6 SP 41 21 27.9553; 7.9553; 18.7605
90; 90; 90		1187.29Cliffe, Matthew J.; Mottillo, Cristina; Stein, Robin S.; Bučar, Dejan-Krešimir; Friščić, Tomislav
Accelerated aging: a low energy, solvent-free alternative to solvothermal and mechanochemical synthesis of metal–organic materials
Chemical Science, 2012, 3, 2495
1556347 CIFC144 Cu6 O42 P3C 2 2 217.5328; 30.3514; 49.1818
90; 90; 90		26171.9Zheng, Min; Liu, Yan; Wang, Cheng; Liu, Shubin; Lin, Wenbin
Cavity-induced enantioselectivity reversal in a chiral metal‒organic framework Brønsted acid catalyst
Chemical Science, 2012, 3, 2623
1556348 CIFC48 H24 Cu2 O14 PI 41 2 224.4616; 24.4616; 71.8721
90; 90; 90		43006.1Zheng, Min; Liu, Yan; Wang, Cheng; Liu, Shubin; Lin, Wenbin
Cavity-induced enantioselectivity reversal in a chiral metal‒organic framework Brønsted acid catalyst
Chemical Science, 2012, 3, 2623
1556349 CIFC26 Cu O5P 42 2 218.744; 18.744; 29.259
90; 90; 90		10279.8Zheng, Min; Liu, Yan; Wang, Cheng; Liu, Shubin; Lin, Wenbin
Cavity-induced enantioselectivity reversal in a chiral metal‒organic framework Brønsted acid catalyst
Chemical Science, 2012, 3, 2623
1556350 CIFC79 H75 K N7 Nd O10P 1 21/c 114.7976; 23.2598; 20.8144
90; 92.145; 90		7159.1Camp, Clément; Guidal, Valentin; Biswas, Biplab; Pécaut, Jacques; Dubois, Lionel; Mazzanti, Marinella
Multielectron redox chemistry of lanthanide Schiff-base complexes
Chemical Science, 2012, 3, 2433
1556351 CIFC108.1 H150.89 K N4 Nd O12P -116.1709; 17.5403; 19.5362
90.671; 113.704; 96.867		5026.5Camp, Clément; Guidal, Valentin; Biswas, Biplab; Pécaut, Jacques; Dubois, Lionel; Mazzanti, Marinella
Multielectron redox chemistry of lanthanide Schiff-base complexes
Chemical Science, 2012, 3, 2433
1556352 CIFC177.5 H141.5 K9 N23.5 Nd3 O12P 1 21 115.6191; 27.7932; 19.045
90; 97.395; 90		8198.8Camp, Clément; Guidal, Valentin; Biswas, Biplab; Pécaut, Jacques; Dubois, Lionel; Mazzanti, Marinella
Multielectron redox chemistry of lanthanide Schiff-base complexes
Chemical Science, 2012, 3, 2433
1556353 CIFC65 H53 K3 N9 O4 TbP 1 21/c 114.5693; 30.262; 14.6011
90; 108.494; 90		6105.1Camp, Clément; Guidal, Valentin; Biswas, Biplab; Pécaut, Jacques; Dubois, Lionel; Mazzanti, Marinella
Multielectron redox chemistry of lanthanide Schiff-base complexes
Chemical Science, 2012, 3, 2433
1556354 CIFC64 H78 I K2 N4 Nd O16P 1 2/n 114.0578; 12.1559; 19.078
90; 89.466; 90		3260Camp, Clément; Guidal, Valentin; Biswas, Biplab; Pécaut, Jacques; Dubois, Lionel; Mazzanti, Marinella
Multielectron redox chemistry of lanthanide Schiff-base complexes
Chemical Science, 2012, 3, 2433
1556355 CIFC39.5 H45.5 K N3.5 Nd O8P 1 21/n 113.3718; 15.0596; 19.3034
90; 102.603; 90		3793.54Camp, Clément; Guidal, Valentin; Biswas, Biplab; Pécaut, Jacques; Dubois, Lionel; Mazzanti, Marinella
Multielectron redox chemistry of lanthanide Schiff-base complexes
Chemical Science, 2012, 3, 2433
1556356 CIFC65 H112 Ni2 P10P -111.3941; 12.6121; 14.341
66.008; 82.323; 66.713		1728.51Tofan, Daniel; Cummins, Christopher C.
Bicyclic dinuclear tris-(ditopic diphosphane) complexes of zerovalent group 10 metals
Chemical Science, 2012, 3, 2474
1556357 CIFC87 H114 O2 P8 Pt2C 1 c 120.4091; 16.3489; 26.2219
90; 111.97; 90		8114Tofan, Daniel; Cummins, Christopher C.
Bicyclic dinuclear tris-(ditopic diphosphane) complexes of zerovalent group 10 metals
Chemical Science, 2012, 3, 2474

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