Crystallography Open Database

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1542543 CIFC9 H6.2 N6 O0.1R -3 m :H12.657; 12.657; 9.296
90; 90; 120
1289.7Zhou, Dong-Dong; Xu, Yan-Tong; Lin, Rui-Biao; Mo, Zong-Wen; Zhang, Wei-Xiong; Zhang, Jie-Peng
High-symmetry hydrogen-bonded organic frameworks: air separation and crystal-to-crystal structural transformation.
Chemical communications (Cambridge, England), 2016, 52, 4991-4994
1542544 CIFC12 H17 F9 N6 O7P b c n12.335; 21.047; 7.89
90; 90; 90
2048.4Zhou, Dong-Dong; Xu, Yan-Tong; Lin, Rui-Biao; Mo, Zong-Wen; Zhang, Wei-Xiong; Zhang, Jie-Peng
High-symmetry hydrogen-bonded organic frameworks: air separation and crystal-to-crystal structural transformation.
Chemical communications (Cambridge, England), 2016, 52, 4991-4994
1542545 CIFC14 H3.5 F10.5 N7P 41 3 215.8427; 15.8427; 15.8427
90; 90; 90
3976.4Zhou, Dong-Dong; Xu, Yan-Tong; Lin, Rui-Biao; Mo, Zong-Wen; Zhang, Wei-Xiong; Zhang, Jie-Peng
High-symmetry hydrogen-bonded organic frameworks: air separation and crystal-to-crystal structural transformation.
Chemical communications (Cambridge, England), 2016, 52, 4991-4994
7118161 CIFC9 H15 Dy N2 O14P 1 21/n 110.1045; 15.4994; 10.4754
90; 102.207; 90
1603.5Liang Qin; Li-Xian Lin; Zhi-Ping Fang; Shui-Ping Yang; Gui-Hua Qiu; Jin-Xiang Chen; Wen-Hua Chen
A water-stable metal-organic framework of a zwitterionic carboxylate with dysprosium: a sensing platform for Ebolavirus RNA sequences
Chem.Commun., 2016, 52, 132
7118162 CIFC12 H16 N2 O4P 1 21 15.1412; 26.4969; 9.2776
90; 105.207; 90
1219.59Abigail E. Hooper; Stuart R. Kennedy; Christopher D. Jones; Jonathan W. Steed
Gelation by supramolecular dimerization of mono(urea)s
Chem.Commun., 2016, 52, 198
7118163 CIFC11 H14 N2 O4P -14.6214; 8.2787; 14.248
92.962; 94.351; 95.33
540.25Abigail E. Hooper; Stuart R. Kennedy; Christopher D. Jones; Jonathan W. Steed
Gelation by supramolecular dimerization of mono(urea)s
Chem.Commun., 2016, 52, 198
7118164 CIFC12 H16 N2 O4P -14.529; 9.009; 15.234
101.869; 93.598; 101.742
592Abigail E. Hooper; Stuart R. Kennedy; Christopher D. Jones; Jonathan W. Steed
Gelation by supramolecular dimerization of mono(urea)s
Chem.Commun., 2016, 52, 198
7118165 CIFC93 H14 N O2 S2 Sc3P n a 2119.9441; 15.7417; 14.9924
90; 90; 90
4706.9Maira R. Ceron; Marta Izquierdo; Nuria Alegret; Juan A. Valdez; Antonio Rodriguez-Fortea; Marilyn M. Olmstead; Alan L. Balch; Josep M. Poblet; Luis Echegoyen
Reactivity differences of Sc3N at C2n (2n = 68 and 80). Synthesis of the first methanofullerene derivatives of Sc3N at D5h-C80
Chem.Commun., 2016, 52, 64
7118166 CIFC30 H49 B Fe N4 O2 Si2P 1 21/n 116.807; 12.849; 17.795
90; 114.07; 90
3509Holger Braunschweig; Rian D. Dewhurst; Katharina Ferkinghoff
Carbene-induced synthesis of the first borironium cations using the [(eta^5^-C5Me5)Fe(CO)2]^-^ anion as an unlikely leaving group
Chem.Commun., 2016, 52, 183
7118167 CIFC34 H57 B Fe N4 O2 Si2P 1 21/c 110.5605; 17.2867; 20.8645
90; 99.455; 90
3757.2Holger Braunschweig; Rian D. Dewhurst; Katharina Ferkinghoff
Carbene-induced synthesis of the first borironium cations using the [(eta^5^-C5Me5)Fe(CO)2]^-^ anion as an unlikely leaving group
Chem.Commun., 2016, 52, 183
7118168 CIFC71 H58 Cl4 N2 S2P 21 21 2113.4055; 15.0828; 29.1775
90; 90; 90
5899.5Ping Chen; Sheng-mei Lu; Wengang Guo; Yan Liu; Can Li
A highly enantioselective thiolation of sulfonyl indoles to access 3-sec-sulfur-substituted indoles in water
Chem.Commun., 2016, 52, 96
7118169 CIFC17 H19 Cl O5C 1 2 121.41; 9.115; 8.678
90; 90.827; 90
1693.4Qiang Sha; Hadi Arman; Michael P. Doyle
Asymmetric synthesis of 1H-pyrrol-3(2H)-ones from 2,3-diketoesters by combination of aldol condensation with benzilic acid rearrangement
Chem.Commun., 2016, 52, 108
7118170 CIFC23 H22 Cl N O3P 21 21 219.258; 9.554; 22.789
90; 90; 90
2015.7Qiang Sha; Hadi Arman; Michael P. Doyle
Asymmetric synthesis of 1H-pyrrol-3(2H)-ones from 2,3-diketoesters by combination of aldol condensation with benzilic acid rearrangement
Chem.Commun., 2016, 52, 108
7118171 CIFC96 H104 N7 O ReP -115.7923; 16.6247; 21.4456
70.8548; 70.4554; 71.4233
4872.6Jan Paulo T. Zaragoza; Maxime A. Siegler; David P. Goldberg
Rhenium(V)-oxo corrolazines: isolating redox-active ligand reactivity
Chem.Commun., 2016, 52, 167
7118172 CIFC18 H26 N3 Ni O2P 21 21 215.79; 10.095; 29.897
90; 90; 90
1747.5Jan Wenz; Christoph A. Rettenmeier; Hubert Wadepohl; Lutz H. Gade
Catalytic C-F bond activation of geminal difluorocyclopropanes by nickel(I) complexes via a radical mechanism
Chem.Commun., 2016, 52, 202
7118173 CIFC24 H23 F2 N3 Ni O2P 21 21 2110.148; 11.913; 17.409
90; 90; 90
2104.6Jan Wenz; Christoph A. Rettenmeier; Hubert Wadepohl; Lutz H. Gade
Catalytic C-F bond activation of geminal difluorocyclopropanes by nickel(I) complexes via a radical mechanism
Chem.Commun., 2016, 52, 202
7118174 CIFC21.5 H31 F N3 Ni O2.5P 21 21 2110.777; 10.97; 36.58
90; 90; 90
4325Jan Wenz; Christoph A. Rettenmeier; Hubert Wadepohl; Lutz H. Gade
Catalytic C-F bond activation of geminal difluorocyclopropanes by nickel(I) complexes via a radical mechanism
Chem.Commun., 2016, 52, 202
7118175 CIFC15 H12 F2C 1 2/c 124.87; 5.944; 16.266
90; 107.995; 90
2287Jan Wenz; Christoph A. Rettenmeier; Hubert Wadepohl; Lutz H. Gade
Catalytic C-F bond activation of geminal difluorocyclopropanes by nickel(I) complexes via a radical mechanism
Chem.Commun., 2016, 52, 202
7118176 CIFC15 H13 FC 1 c 17.74284; 17.2689; 8.39473
90; 91.1751; 90
1122.23Jan Wenz; Christoph A. Rettenmeier; Hubert Wadepohl; Lutz H. Gade
Catalytic C-F bond activation of geminal difluorocyclopropanes by nickel(I) complexes via a radical mechanism
Chem.Commun., 2016, 52, 202
7118177 CIFC20 H26 N2 O6 SP 21 21 214.0216; 21.3117; 6.4976
90; 90; 90
1941.64Pedras, M. S. C.; To, Q. H.; Schatte, G.
Divergent reactivity of an indole glucosinolate yields Lossen or Neber rearrangement products: the phytoalexin rapalexin A or a unique β-d-glucopyranose fused heterocycle.
Chemical communications (Cambridge, England), 2016, 52, 2505-2508
7118178 CIFC60 H90 Li2 O12 ThR -3 :H14.8737; 14.8737; 24.3175
90; 90; 120
4658.9Pedrick, Elizabeth A.; Hrobárik, Peter; Seaman, Lani A.; Wu, Guang; Hayton, Trevor W.
Synthesis, structure and bonding of hexaphenyl thorium(iv): observation of a non-octahedral structure.
Chemical communications (Cambridge, England), 2015, 52, 689-692
7118179 CIFC60 H78 Li2 O10 ThP 1 21/n 116.5641; 16.7043; 21.3854
90; 108.682; 90
5605.4Pedrick, Elizabeth A.; Hrobárik, Peter; Seaman, Lani A.; Wu, Guang; Hayton, Trevor W.
Synthesis, structure and bonding of hexaphenyl thorium(iv): observation of a non-octahedral structure.
Chemical communications (Cambridge, England), 2015, 52, 689-692
7118185 CIFC29 H21 N OP 21 21 219.002; 13.225; 17.293
90; 90; 90
2058.8Barsu, Nagaraju; Sen, Malay; Premkumar, J. Richard; Sundararaju, Basker
Cobalt(iii) catalyzed C-8 selective C-H and C-O coupling of quinoline N-oxide with internal alkynes via C-H activation and oxygen atom transfer.
Chemical communications (Cambridge, England), 2016, 52, 1338-1341
7118186 CIFC12 H14 N6 O6P 1 21/n 19.22642; 9.71725; 18.0546
90; 101.605; 90
1585.6Erhardt, Hellmuth; Mohr, Fabian; Kirsch, Stefan F.
Synthesis of geminal bis- and tristriazoles: exploration of unconventional azide chemistry.
Chemical communications (Cambridge, England), 2016, 52, 545-548
7118187 CIFC31 H25 N9 O6P 1 21/n 114.6712; 12.489; 17.0137
90; 106.677; 90
2986.3Erhardt, Hellmuth; Mohr, Fabian; Kirsch, Stefan F.
Synthesis of geminal bis- and tristriazoles: exploration of unconventional azide chemistry.
Chemical communications (Cambridge, England), 2016, 52, 545-548
7118188 CIFC33 H35 Cl2 I N4 O PdP -110.7622; 12.8238; 13.4282
114.432; 100.558; 93.044
1641.4Vicente-Hernández, Inmaculada; Chicote, María-Teresa; Vicente, José; Bautista, Delia
A new type of oxidative addition of an iodoarene to a Pd(ii) complex.
Chemical communications (Cambridge, England), 2016, 52, 594-596
7118189 CIFC40 H38 Cu2 N9 O12 S2P 4/n c c11.4766; 11.4766; 30.5554
90; 90; 90
4024.5Abrahams, C. T.; Abrahams, B. F.; Hudson, T. A.; Robson, R.
Templation of a square grid copper(ii) 4,4'-bipyridine network by a 3D PtS-related Cu(i)-Cu(ii) 4,4'-bipyridine crystal.
Chemical communications (Cambridge, England), 2016, 52, 609-612
7118190 CIFC20 H20 Cu N4 O8 S2P 4/n c c11.5095; 11.5095; 15.4286
90; 90; 90
2043.8Abrahams, C. T.; Abrahams, B. F.; Hudson, T. A.; Robson, R.
Templation of a square grid copper(ii) 4,4'-bipyridine network by a 3D PtS-related Cu(i)-Cu(ii) 4,4'-bipyridine crystal.
Chemical communications (Cambridge, England), 2016, 52, 609-612
7118196 CIFC77 H100 N4 O10 Pd SiP 1 21/c 124.3213; 10.002; 32.0407
90; 111.912; 90
7231.2Nisar Ahamed, B.; Duchêne, Roland; Robeyns, Koen; Fustin, Charles-André
Catenane-based mechanically-linked block copolymers.
Chemical communications (Cambridge, England), 2016, 52, 2149-2152
7118197 CIFC75 H96 N4 O10 Pd SiC 1 2/c 139.473; 12.053; 35.42
90; 114.26; 90
15364Nisar Ahamed, B.; Duchêne, Roland; Robeyns, Koen; Fustin, Charles-André
Catenane-based mechanically-linked block copolymers.
Chemical communications (Cambridge, England), 2016, 52, 2149-2152
7118198 CIFC75 H93 N4 O13 PdI 1 2/a 137.2375; 11.7434; 32.5955
90; 101.666; 90
13959.4Nisar Ahamed, B.; Duchêne, Roland; Robeyns, Koen; Fustin, Charles-André
Catenane-based mechanically-linked block copolymers.
Chemical communications (Cambridge, England), 2016, 52, 2149-2152
7118199 CIFC22 H29 O PP 1 21/c 115.6981; 7.4997; 16.6619
90; 93.155; 90
1958.65Krupski, Sergei; Kehr, Gerald; Daniliuc, Constantin G.; Erker, Gerhard
Cyclopropane formation under frustrated Lewis pair conditions.
Chemical communications (Cambridge, England), 2016, 52, 2695-2697
7118200 CIFC22 H29 PP -18.3322; 8.5865; 13.0867
87.833; 85.945; 86.322
931.49Krupski, Sergei; Kehr, Gerald; Daniliuc, Constantin G.; Erker, Gerhard
Cyclopropane formation under frustrated Lewis pair conditions.
Chemical communications (Cambridge, England), 2016, 52, 2695-2697
7118201 CIFC43 H37 B F15 O P SiP 1 21/c 110.8091; 25.3584; 16.9567
90; 96.133; 90
4621.25Krupski, Sergei; Kehr, Gerald; Daniliuc, Constantin G.; Erker, Gerhard
Cyclopropane formation under frustrated Lewis pair conditions.
Chemical communications (Cambridge, England), 2016, 52, 2695-2697
7118202 CIFC25 H6 B F15 OP -19.4516; 12.1427; 12.2399
110.414; 100.07; 97.111
1269.99Krupski, Sergei; Kehr, Gerald; Daniliuc, Constantin G.; Erker, Gerhard
Cyclopropane formation under frustrated Lewis pair conditions.
Chemical communications (Cambridge, England), 2016, 52, 2695-2697
7118203 CIFC96 H110 F12 N8 O18 P2P -112.01; 13.437; 16.32
106.161; 102.667; 98.007
2411Han, Ying; Meng, Zheng; Chen, Chuan-Feng
Acid/base controllable complexation of a triptycene-derived macrotricyclic host and protonated 4,4'-bipyridinium/pyridinium salts.
Chemical communications (Cambridge, England), 2016, 52, 590-593
7118204 CIFC90 H96 F12 N2 O16 P2P -113.799; 15.7; 22.416
104.6; 96.36; 107.93
4377Han, Ying; Meng, Zheng; Chen, Chuan-Feng
Acid/base controllable complexation of a triptycene-derived macrotricyclic host and protonated 4,4'-bipyridinium/pyridinium salts.
Chemical communications (Cambridge, England), 2016, 52, 590-593
7118205 CIFC80 H88 Cl6 F12 N2 O16 P2C 1 2/c 120.956; 17.451; 24.943
90; 109.498; 90
8599Han, Ying; Meng, Zheng; Chen, Chuan-Feng
Acid/base controllable complexation of a triptycene-derived macrotricyclic host and protonated 4,4'-bipyridinium/pyridinium salts.
Chemical communications (Cambridge, England), 2016, 52, 590-593
7118206 CIFC92 H104 F12 N2 O20 P2P -112.778; 12.983; 14.022
108.815; 93.025; 100.752
2147Han, Ying; Meng, Zheng; Chen, Chuan-Feng
Acid/base controllable complexation of a triptycene-derived macrotricyclic host and protonated 4,4'-bipyridinium/pyridinium salts.
Chemical communications (Cambridge, England), 2016, 52, 590-593
7118207 CIFC32 H29 N O2 SP 1 21/c 111.62; 11.0673; 21.125
90; 98.311; 90
2688.2Wang, Zhiming; Xu, Xingzhu; Gu, Zhanshou; Feng, Wei; Qian, Houjun; Li, Zhengyi; Sun, Xiaoqiang; Kwon, Ohyun
Nazarov cyclization of 1,4-pentadien-3-ols: preparation of cyclopenta[b]indoles and spiro[indene-1,4'-quinoline]s.
Chemical communications (Cambridge, England), 2016, 52, 2811-2814
7118208 CIFC26 H25 N O2 SP 1 21/n 113.926; 10.6835; 14.955
90; 92.243; 90
2223.3Wang, Zhiming; Xu, Xingzhu; Gu, Zhanshou; Feng, Wei; Qian, Houjun; Li, Zhengyi; Sun, Xiaoqiang; Kwon, Ohyun
Nazarov cyclization of 1,4-pentadien-3-ols: preparation of cyclopenta[b]indoles and spiro[indene-1,4'-quinoline]s.
Chemical communications (Cambridge, England), 2016, 52, 2811-2814
7118209 CIFC26 H27 N O3 SP 1 21/n 110.4657; 19.751; 12.477
90; 114.712; 90
2342.9Wang, Zhiming; Xu, Xingzhu; Gu, Zhanshou; Feng, Wei; Qian, Houjun; Li, Zhengyi; Sun, Xiaoqiang; Kwon, Ohyun
Nazarov cyclization of 1,4-pentadien-3-ols: preparation of cyclopenta[b]indoles and spiro[indene-1,4'-quinoline]s.
Chemical communications (Cambridge, England), 2016, 52, 2811-2814
7118210 CIFC24 H21 N O2 SP 1 21/c 110.6663; 10.8826; 18.121
90; 103.78; 90
2042.9Wang, Zhiming; Xu, Xingzhu; Gu, Zhanshou; Feng, Wei; Qian, Houjun; Li, Zhengyi; Sun, Xiaoqiang; Kwon, Ohyun
Nazarov cyclization of 1,4-pentadien-3-ols: preparation of cyclopenta[b]indoles and spiro[indene-1,4'-quinoline]s.
Chemical communications (Cambridge, England), 2016, 52, 2811-2814
7118211 CIFC24 H21 N O2 SP 1 21/c 114.001; 12.335; 11.587
90; 95.497; 90
1991.9Wang, Zhiming; Xu, Xingzhu; Gu, Zhanshou; Feng, Wei; Qian, Houjun; Li, Zhengyi; Sun, Xiaoqiang; Kwon, Ohyun
Nazarov cyclization of 1,4-pentadien-3-ols: preparation of cyclopenta[b]indoles and spiro[indene-1,4'-quinoline]s.
Chemical communications (Cambridge, England), 2016, 52, 2811-2814
7118212 CIFC24 H21 N O2 SP 1 21/c 18.9249; 9.9995; 22.944
90; 107.13; 90
1956.8Wang, Zhiming; Xu, Xingzhu; Gu, Zhanshou; Feng, Wei; Qian, Houjun; Li, Zhengyi; Sun, Xiaoqiang; Kwon, Ohyun
Nazarov cyclization of 1,4-pentadien-3-ols: preparation of cyclopenta[b]indoles and spiro[indene-1,4'-quinoline]s.
Chemical communications (Cambridge, England), 2016, 52, 2811-2814
7118213 CIFC54 H58 N3 P2 RhP 1 21/n 113.58; 21.768; 17.29
90; 111.548; 90
4754Hänninen, Mikko M; Zamora, Matthew T.; MacNeil, Connor S.; Knott, Jackson P.; Hayes, Paul G.
Elucidation of the resting state of a rhodium NNN-pincer hydrogenation catalyst that features a remarkably upfield hydride (1)H NMR chemical shift.
Chemical communications (Cambridge, England), 2016, 52, 586-589
7118214 CIFC48 H48 N3 P2 RhP 1 21/c 116.185; 18.144; 15.477
90; 118.406; 90
3998Hänninen, Mikko M; Zamora, Matthew T.; MacNeil, Connor S.; Knott, Jackson P.; Hayes, Paul G.
Elucidation of the resting state of a rhodium NNN-pincer hydrogenation catalyst that features a remarkably upfield hydride (1)H NMR chemical shift.
Chemical communications (Cambridge, England), 2016, 52, 586-589
7118215 CIFC72 H66 N3 P2 RhP 1 21/n 113.567; 28.198; 16.293
90; 109.213; 90
5886Hänninen, Mikko M; Zamora, Matthew T.; MacNeil, Connor S.; Knott, Jackson P.; Hayes, Paul G.
Elucidation of the resting state of a rhodium NNN-pincer hydrogenation catalyst that features a remarkably upfield hydride (1)H NMR chemical shift.
Chemical communications (Cambridge, England), 2016, 52, 586-589
7118216 CIFC98 H96 N6 P4 Rh2C 1 2/c 142.986; 17.237; 27.577
90; 119.527; 90
17779Hänninen, Mikko M; Zamora, Matthew T.; MacNeil, Connor S.; Knott, Jackson P.; Hayes, Paul G.
Elucidation of the resting state of a rhodium NNN-pincer hydrogenation catalyst that features a remarkably upfield hydride (1)H NMR chemical shift.
Chemical communications (Cambridge, England), 2016, 52, 586-589
7118217 CIFC60 H56 N3 P2 RhP 1 21/n 113.907; 27.103; 16.593
90; 112.133; 90
5793Hänninen, Mikko M; Zamora, Matthew T.; MacNeil, Connor S.; Knott, Jackson P.; Hayes, Paul G.
Elucidation of the resting state of a rhodium NNN-pincer hydrogenation catalyst that features a remarkably upfield hydride (1)H NMR chemical shift.
Chemical communications (Cambridge, England), 2016, 52, 586-589
7118218 CIFC36 H26 Br2 O4P 21 21 215.6288; 12.578; 41.669
90; 90; 90
2950.1Wang, Zhan-Yong; Ding, Ya-Li; Wang, Gang; Cheng, Ying
Chiral N-heterocyclic carbene/Lewis acid cooperative catalysis of the reaction of 2-aroylvinylcinnamaldehydes: a switch of the reaction pathway by Lewis acid activation.
Chemical communications (Cambridge, England), 2015, 52, 788-791
7118219 CIFC36 H28 O4P 21 21 219.263; 12.8186; 22.369
90; 90; 90
2656.1Wang, Zhan-Yong; Ding, Ya-Li; Wang, Gang; Cheng, Ying
Chiral N-heterocyclic carbene/Lewis acid cooperative catalysis of the reaction of 2-aroylvinylcinnamaldehydes: a switch of the reaction pathway by Lewis acid activation.
Chemical communications (Cambridge, England), 2015, 52, 788-791
7118220 CIFC36 H26 Br2 O4P 21 21 215.5911; 13.004; 40.623
90; 90; 90
2953.6Wang, Zhan-Yong; Ding, Ya-Li; Wang, Gang; Cheng, Ying
Chiral N-heterocyclic carbene/Lewis acid cooperative catalysis of the reaction of 2-aroylvinylcinnamaldehydes: a switch of the reaction pathway by Lewis acid activation.
Chemical communications (Cambridge, England), 2015, 52, 788-791
7118221 CIFC13 H11 F N2P -110.0641; 11.0425; 12.1824
114.924; 95.055; 111.476
1094.39Dey, Dhananjay; Thomas, Sajesh P.; Spackman, Mark A.; Chopra, Deepak
'Quasi-isostructural polymorphism' in molecular crystals: inputs from interaction hierarchy and energy frameworks.
Chemical communications (Cambridge, England), 2016, 52, 2141-2144
7118222 CIFC13 H10 F2 N2P 1 21/c 112.7028; 8.3775; 11.5509
90; 117.017; 90
1095.1Dey, Dhananjay; Thomas, Sajesh P.; Spackman, Mark A.; Chopra, Deepak
'Quasi-isostructural polymorphism' in molecular crystals: inputs from interaction hierarchy and energy frameworks.
Chemical communications (Cambridge, England), 2016, 52, 2141-2144
7118223 CIFC41 H33 N3 O6P 1 21/c 111.1829; 11.5006; 26.2259
90; 92.219; 90
3370.4Kim, Jeong Gyun; Noh, Tae Hwan; Cho, Yoonjung; Park, Jin Kyoon; Jung, Ok-Sang
A triple-function nanotube as a reactant reservoir, reaction platform, and byproduct scavenger for photo-cyclopropanation.
Chemical communications (Cambridge, England), 2016, 52, 2545-2548
7118224 CIFC41 H33 Cd Cl0 I2 N3 O6R -3 :H54.6374; 54.6374; 8.9458
90; 90; 120
23127.6Kim, Jeong Gyun; Noh, Tae Hwan; Cho, Yoonjung; Park, Jin Kyoon; Jung, Ok-Sang
A triple-function nanotube as a reactant reservoir, reaction platform, and byproduct scavenger for photo-cyclopropanation.
Chemical communications (Cambridge, England), 2016, 52, 2545-2548
7118225 CIFC42.17 H36 Br Cd I2 N3 O6.33R -3 :H54.5811; 54.5811; 8.9081
90; 90; 120
22982.7Kim, Jeong Gyun; Noh, Tae Hwan; Cho, Yoonjung; Park, Jin Kyoon; Jung, Ok-Sang
A triple-function nanotube as a reactant reservoir, reaction platform, and byproduct scavenger for photo-cyclopropanation.
Chemical communications (Cambridge, England), 2016, 52, 2545-2548
7118226 CIFC42 H35 Cd I4 N3 O6R -3 :H54.772; 54.772; 8.8733
90; 90; 120
23053.3Kim, Jeong Gyun; Noh, Tae Hwan; Cho, Yoonjung; Park, Jin Kyoon; Jung, Ok-Sang
A triple-function nanotube as a reactant reservoir, reaction platform, and byproduct scavenger for photo-cyclopropanation.
Chemical communications (Cambridge, England), 2016, 52, 2545-2548
7118227 CIFC41 H33 Cd I2 N3 O6R -3 :H54.8819; 54.8819; 8.8759
90; 90; 120
23152.7Kim, Jeong Gyun; Noh, Tae Hwan; Cho, Yoonjung; Park, Jin Kyoon; Jung, Ok-Sang
A triple-function nanotube as a reactant reservoir, reaction platform, and byproduct scavenger for photo-cyclopropanation.
Chemical communications (Cambridge, England), 2016, 52, 2545-2548
7118230 CIFC26 H18 Br Cl4 N2 O4P 1 21 113.0622; 8.2259; 13.1485
90; 106.33; 90
1355.79Cao, Zhong-Yan; Zhao, Yu-Lei; Zhou, Jian
Sequential Au(i)/chiral tertiary amine catalysis: a tandem C-H functionalization of anisoles or a thiophene/asymmetric Michael addition sequence to quaternary oxindoles.
Chemical communications (Cambridge, England), 2016, 52, 2537-2540
7118231 CIFC27 H21 Br Cl2 N2 O5P 21 21 2112.315; 13.9146; 15.2049
90; 90; 90
2605.49Cao, Zhong-Yan; Zhao, Yu-Lei; Zhou, Jian
Sequential Au(i)/chiral tertiary amine catalysis: a tandem C-H functionalization of anisoles or a thiophene/asymmetric Michael addition sequence to quaternary oxindoles.
Chemical communications (Cambridge, England), 2016, 52, 2537-2540
7118232 CIFC31 H30 Br N3 O5I 1 2 114.6406; 9.57209; 19.5953
90; 97.003; 90
2725.62Zhao, Kun; Zhi, Ying; Li, Xinyi; Puttreddy, Rakesh; Rissanen, Kari; Enders, Dieter
Asymmetric synthesis of 3,3'-pyrrolidinyl-dispirooxindoles via a one-pot organocatalytic Mannich/deprotection/aza-Michael sequence.
Chemical communications (Cambridge, England), 2016, 52, 2249-2252
7118241 CIFC40 H24 In N2 O8C 1 2/c 128.286; 20.9422; 27.5862
90; 120.798; 90
14037Li, Xingjun; Chen, Xueyuan; Jiang, Feilong; Chen, Lian; Lu, Shan; Chen, Qihui; Wu, Mingyan; Yuan, Daqiang; Hong, Maochun
The dynamic response of a flexible indium based metal-organic framework to gas sorption.
Chemical communications (Cambridge, England), 2016, 52, 2277-2280
7118242 CIFC40 H24 In N2 O8I 1 2/c 126.9793; 21.3293; 26.4721
90; 97.001; 90
15119.8Li, Xingjun; Chen, Xueyuan; Jiang, Feilong; Chen, Lian; Lu, Shan; Chen, Qihui; Wu, Mingyan; Yuan, Daqiang; Hong, Maochun
The dynamic response of a flexible indium based metal-organic framework to gas sorption.
Chemical communications (Cambridge, England), 2016, 52, 2277-2280
7118243 CIFC25 H32 B F6 I2 N8 O P WP 1 21/n 18.352; 22.5729; 18.2914
90; 100.772; 90
3387.69Helmdach, Kai; Rüger, Julia; Villinger, Alexander; Seidel, Wolfram W.
Dual nucleophilic substitution at a W(ii) η(2)-coordinated diiodo acetylene leading to an amidinium carbyne complex.
Chemical communications (Cambridge, England), 2016, 52, 2616-2619
7118244 CIFC33 H38 B F6 N8 O2 P WP 1 21/n 125.7178; 11.6201; 25.7435
90; 97.686; 90
7624.2Helmdach, Kai; Rüger, Julia; Villinger, Alexander; Seidel, Wolfram W.
Dual nucleophilic substitution at a W(ii) η(2)-coordinated diiodo acetylene leading to an amidinium carbyne complex.
Chemical communications (Cambridge, England), 2016, 52, 2616-2619
7118245 CIFC20 H21 Br O5P 1 21/c 112.3928; 8.3243; 18.5364
90; 95.888; 90
1902.15Yu, Zhunzhun; Qiu, Haile; Liu, Lu; Zhang, Junliang
Gold-catalyzed construction of two adjacent quaternary stereocenters via sequential C-H functionalization and aldol annulation.
Chemical communications (Cambridge, England), 2016, 52, 2257-2260
7118246 CIFC21 H23 Br O5P 1 21/c 19.2166; 9.0685; 23.2491
90; 99.08; 90
1918.83Yu, Zhunzhun; Qiu, Haile; Liu, Lu; Zhang, Junliang
Gold-catalyzed construction of two adjacent quaternary stereocenters via sequential C-H functionalization and aldol annulation.
Chemical communications (Cambridge, England), 2016, 52, 2257-2260
7118247 CIFC27 H24 N2 O3P -110.9476; 11.03; 11.0714
86.1003; 64.8281; 60.6087
1037.28Zhu, Xu; Chiba, Shunsuke
Construction of 1-pyrroline skeletons by Lewis acid-mediated conjugate addition of vinyl azides.
Chemical communications (Cambridge, England), 2016, 52, 2473-2476
7118249 CIFC31 H24 N2 O2P -19.365; 11.4265; 11.9971
74.104; 80.112; 71.016
1162.72Zhu, Xu; Chiba, Shunsuke
Construction of 1-pyrroline skeletons by Lewis acid-mediated conjugate addition of vinyl azides.
Chemical communications (Cambridge, England), 2016, 52, 2473-2476
7118250 CIFC25 H20 N3 OP 1 21/c 118.817; 10.53; 9.5207
90; 96.996; 90
1872.4Zhu, Xu; Chiba, Shunsuke
Construction of 1-pyrroline skeletons by Lewis acid-mediated conjugate addition of vinyl azides.
Chemical communications (Cambridge, England), 2016, 52, 2473-2476
7118251 CIFC28 H28 Cl N O3P -19.469; 10.0316; 13.1967
83.975; 70.468; 85.668
1173.8Zhu, Xu; Chiba, Shunsuke
Construction of 1-pyrroline skeletons by Lewis acid-mediated conjugate addition of vinyl azides.
Chemical communications (Cambridge, England), 2016, 52, 2473-2476
7118252 CIFC19 H15 N O4P 1 21/c 18.3566; 17.7311; 10.5304
90; 101.637; 90
1528.24Zhu, Xu; Chiba, Shunsuke
Construction of 1-pyrroline skeletons by Lewis acid-mediated conjugate addition of vinyl azides.
Chemical communications (Cambridge, England), 2016, 52, 2473-2476
7118253 CIFC27 H26 N2 O3P -18.2128; 12.0722; 12.1473
80.826; 73.356; 74.316
1106.54Zhu, Xu; Chiba, Shunsuke
Construction of 1-pyrroline skeletons by Lewis acid-mediated conjugate addition of vinyl azides.
Chemical communications (Cambridge, England), 2016, 52, 2473-2476
7118254 CIFC18 H19 N O3P n m a15.9415; 14.8517; 6.2573
90; 90; 90
1481.5Zhu, Xu; Chiba, Shunsuke
Construction of 1-pyrroline skeletons by Lewis acid-mediated conjugate addition of vinyl azides.
Chemical communications (Cambridge, England), 2016, 52, 2473-2476
7118255 CIFC14 H15 N O5P 1 21/c 19.5866; 19.5978; 7.6285
90; 111.316; 90
1335.17Baumann, A. N.; Music, A.; Karaghiosoff, K.; Didier, D.
Highly diastereoselective approach to methylenecyclopropanes via boron-homologation/allylboration sequences.
Chemical communications (Cambridge, England), 2016, 52, 2529-2532
7118256 CIFC45 H37 Cl N5 O P RuP 1 21/n 113.9666; 12.6444; 21.018
90; 95.457; 90
3694.9Tseng, Kuei-Nin T; Lin, Steve; Kampf, Jeff W.; Szymczak, Nathaniel K.
Upgrading ethanol to 1-butanol with a homogeneous air-stable ruthenium catalyst.
Chemical communications (Cambridge, England), 2016, 52, 2901-2904
7118257 CIFC39 H31 Cl N5 O3 P RuP 1 21/c 116.1333; 12.495; 16.9891
90; 98.709; 90
3385.27Tseng, Kuei-Nin T; Lin, Steve; Kampf, Jeff W.; Szymczak, Nathaniel K.
Upgrading ethanol to 1-butanol with a homogeneous air-stable ruthenium catalyst.
Chemical communications (Cambridge, England), 2016, 52, 2901-2904
7118258 CIFC38 H42 Cl6 Cu2 N6P -18.2153; 11.1662; 11.5343
85.272; 84.43; 77.543
1026.24Nitsch, Jörn; Lacemon, Frederick; Lorbach, Andreas; Eichhorn, Antonius; Cisnetti, Federico; Steffen, Andreas
Cuprophilic interactions in highly luminescent dicopper(i)-NHC-picolyl complexes - fast phosphorescence or TADF?
Chemical communications (Cambridge, England), 2016, 52, 2932-2935
7118259 CIFC38 H42 Cl6 Cu2 N6P -18.1887; 10.9691; 11.3579
85.0163; 85.1738; 77.5551
990.21Nitsch, Jörn; Lacemon, Frederick; Lorbach, Andreas; Eichhorn, Antonius; Cisnetti, Federico; Steffen, Andreas
Cuprophilic interactions in highly luminescent dicopper(i)-NHC-picolyl complexes - fast phosphorescence or TADF?
Chemical communications (Cambridge, England), 2016, 52, 2932-2935
7118260 CIFC40 H46 Cl6 Cu2 N6P -18.3056; 11.1055; 11.873
86.315; 89.284; 77.72
1067.9Nitsch, Jörn; Lacemon, Frederick; Lorbach, Andreas; Eichhorn, Antonius; Cisnetti, Federico; Steffen, Andreas
Cuprophilic interactions in highly luminescent dicopper(i)-NHC-picolyl complexes - fast phosphorescence or TADF?
Chemical communications (Cambridge, England), 2016, 52, 2932-2935
7118261 CIFC40 H46 Cl6 Cu2 N6P -18.3293; 10.9929; 11.7343
86.079; 89.732; 77.869
1047.9Nitsch, Jörn; Lacemon, Frederick; Lorbach, Andreas; Eichhorn, Antonius; Cisnetti, Federico; Steffen, Andreas
Cuprophilic interactions in highly luminescent dicopper(i)-NHC-picolyl complexes - fast phosphorescence or TADF?
Chemical communications (Cambridge, England), 2016, 52, 2932-2935
7118262 CIFC38 H40 Cl8 Cu2 N6P -18.253; 10.948; 11.802
85.792; 89.721; 78.477
1042Nitsch, Jörn; Lacemon, Frederick; Lorbach, Andreas; Eichhorn, Antonius; Cisnetti, Federico; Steffen, Andreas
Cuprophilic interactions in highly luminescent dicopper(i)-NHC-picolyl complexes - fast phosphorescence or TADF?
Chemical communications (Cambridge, England), 2016, 52, 2932-2935
7118263 CIFC40 H46 Cl6 Cu2 N6 O2P -18.292; 10.995; 12.277
84.743; 86.68; 78.394
1090.9Nitsch, Jörn; Lacemon, Frederick; Lorbach, Andreas; Eichhorn, Antonius; Cisnetti, Federico; Steffen, Andreas
Cuprophilic interactions in highly luminescent dicopper(i)-NHC-picolyl complexes - fast phosphorescence or TADF?
Chemical communications (Cambridge, England), 2016, 52, 2932-2935
7118264 CIFC18 H18 Cl Cu N4 O2P 21 21 219.0636; 9.6375; 20.925
90; 90; 90
1827.8Nitsch, Jörn; Lacemon, Frederick; Lorbach, Andreas; Eichhorn, Antonius; Cisnetti, Federico; Steffen, Andreas
Cuprophilic interactions in highly luminescent dicopper(i)-NHC-picolyl complexes - fast phosphorescence or TADF?
Chemical communications (Cambridge, England), 2016, 52, 2932-2935
7118265 CIFC21 H25 Cl Cu N3P 1 21/c 19.5545; 8.8034; 23.9329
90; 96.6239; 90
1999.61Nitsch, Jörn; Lacemon, Frederick; Lorbach, Andreas; Eichhorn, Antonius; Cisnetti, Federico; Steffen, Andreas
Cuprophilic interactions in highly luminescent dicopper(i)-NHC-picolyl complexes - fast phosphorescence or TADF?
Chemical communications (Cambridge, England), 2016, 52, 2932-2935
7118266 CIFC36 H38 Cl2 Cu2 N6P 1 21/n 110.0169; 15.969; 10.7209
90; 95.056; 90
1708.24Nitsch, Jörn; Lacemon, Frederick; Lorbach, Andreas; Eichhorn, Antonius; Cisnetti, Federico; Steffen, Andreas
Cuprophilic interactions in highly luminescent dicopper(i)-NHC-picolyl complexes - fast phosphorescence or TADF?
Chemical communications (Cambridge, England), 2016, 52, 2932-2935
7118267 CIFC43.5 H37 Al Au Cl F36 N2 O4 P4P 1 21/n 110.7137; 38.3822; 14.7478
90; 90.909; 90
6063.8Borger, Jaap E.; Bakker, Martijn S.; Ehlers, Andreas W.; Lutz, Martin; Chris Slootweg, J.; Lammertsma, Koop
Functionalization of P4 in the coordination sphere of coinage metal cations.
Chemical communications (Cambridge, England), 2016, 52, 3284-3287
7118268 CIFC94 H97 Al Au2 F36 N4 O4 P4C 1 2/c 139.9091; 25.1072; 22.5843
90; 100.38; 90
22259.3Borger, Jaap E.; Bakker, Martijn S.; Ehlers, Andreas W.; Lutz, Martin; Chris Slootweg, J.; Lammertsma, Koop
Functionalization of P4 in the coordination sphere of coinage metal cations.
Chemical communications (Cambridge, England), 2016, 52, 3284-3287
7118269 CIFC27 H24 Br N O3P 21 21 218.8669; 14.7074; 17.9059
90; 90; 90
2335.1Li, Mingfeng; Guo, Xin; Jin, Weifeng; Zheng, Qing; Liu, Shunying; Hu, Wenhao
An enantioselective three-component reaction of diazoacetates with indoles and enals by iridium/iminium co-catalysis.
Chemical communications (Cambridge, England), 2016, 52, 2736-2739
7118270 CIFC18 H32 O3 SiC 1 2/c 129.017; 11.4978; 12.6967
90; 111.472; 90
3942Stepherson, Jacob R.; Fronczek, Frank R.; Kartika, Rendy
An expedient synthesis of functionalized 1,4-diketone-derived compounds via silyloxyallyl cation intermediates.
Chemical communications (Cambridge, England), 2016, 52, 2300-2303
7118271 CIFC52 H44 N2 O20 Zn3P -19.4533; 18.614; 19.976
68.27; 82.61; 82.18
3223.2Chakraborty, Anindita; Bhattacharyya, Sohini; Hazra, Arpan; Ghosh, Ashta Chandra; Maji, Tapas Kumar
Post-synthetic metalation in an anionic MOF for efficient catalytic activity and removal of heavy metal ions from aqueous solution.
Chemical communications (Cambridge, England), 2016, 52, 2831-2834
7118272 CIFC15 H26 Cl N WP n a 2113.1669; 12.7572; 20.0394
90; 90; 90
3366.07Wright, Christopher M. R.; Turner, Zoë R; Buffet, Jean-Charles; O'Hare, Dermot
Tungsten imido catalysts for selective ethylene dimerisation.
Chemical communications (Cambridge, England), 2016, 52, 2850-2853
7118273 CIFC16 H25 Cl4 N O WP -18.5941; 14.1186; 17.4478
95.806; 98.562; 97.484
2059.88Wright, Christopher M. R.; Turner, Zoë R; Buffet, Jean-Charles; O'Hare, Dermot
Tungsten imido catalysts for selective ethylene dimerisation.
Chemical communications (Cambridge, England), 2016, 52, 2850-2853
7118274 CIFC22 H21 N O4P -111.0068; 18.8343; 19.829
72.08; 89.811; 77.711
3813.1Xiao, Jun-An; Xia, Peng-Ju; Zhang, Xing-Yu; Chen, Xiao-Qing; Ou, Guang-Chuan; Yang, Hua
Amide-assisted intramolecular [3+2] annulation of cyclopropane ring-opening: a facile and diastereoselective access to the tricyclic core of (±)-scandine.
Chemical communications (Cambridge, England), 2016, 52, 2177-2180
7118275 CIFC22 H21 N O4P -19.035; 13.258; 16.686
90.402; 103.495; 105.139
1871.2Xiao, Jun-An; Xia, Peng-Ju; Zhang, Xing-Yu; Chen, Xiao-Qing; Ou, Guang-Chuan; Yang, Hua
Amide-assisted intramolecular [3+2] annulation of cyclopropane ring-opening: a facile and diastereoselective access to the tricyclic core of (±)-scandine.
Chemical communications (Cambridge, England), 2016, 52, 2177-2180
7118276 CIFC24 H27 N O3C 1 2/c 144.225; 11.0988; 15.9916
90; 99.538; 90
7740.9Xiao, Jun-An; Xia, Peng-Ju; Zhang, Xing-Yu; Chen, Xiao-Qing; Ou, Guang-Chuan; Yang, Hua
Amide-assisted intramolecular [3+2] annulation of cyclopropane ring-opening: a facile and diastereoselective access to the tricyclic core of (±)-scandine.
Chemical communications (Cambridge, England), 2016, 52, 2177-2180
7118277 CIFC90 H187 O100P 1 21 115.517; 9.825; 21.953
90; 90.05; 90
3346.8Rutenberg, R.; Leitus, G.; Fallik, E.; Poverenov, E.
Discovery of a non classic host guest complexation mode in a β-cyclodextrin/propionic acid model.
Chemical communications (Cambridge, England), 2016, 52, 2565-2568
7118278 CIFC30 H25 F N2 O3 SP 1 21 15.552; 17.133; 13.413
90; 93.446; 90
1273.6Sun, Xiao-Xue; Zhang, Hong-Hao; Li, Guo-Hao; Meng, Li; Shi, Feng
Diastereo- and enantioselective construction of an indole-based 2,3-dihydrobenzofuran scaffold via catalytic asymmetric [3+2] cyclizations of quinone monoimides with 3-vinylindoles.
Chemical communications (Cambridge, England), 2016, 52, 2968-2971
7118279 CIFC16 H24 N2 O5P 1 21/n 16.9693; 12.1404; 19.3065
90; 90.623; 90
1633.43Eckshtain-Levi, Meital; Lavi, Ronit; Yufit, Dmitry S.; Daniel, Bareket; Green, Omer; Fleker, Ohad; Richman, Michal; Rahimipour, Shai; Gruzman, Arie; Benisvy, Laurent
A versatile water-soluble chelating and radical scavenging platform.
Chemical communications (Cambridge, England), 2016, 52, 2350-2353
7118280 CIFC32.5 H60 Cl N3 O5P 1 21/n 120.6006; 12.5488; 27.283
90; 92.36; 90
7047Eckshtain-Levi, Meital; Lavi, Ronit; Yufit, Dmitry S.; Daniel, Bareket; Green, Omer; Fleker, Ohad; Richman, Michal; Rahimipour, Shai; Gruzman, Arie; Benisvy, Laurent
A versatile water-soluble chelating and radical scavenging platform.
Chemical communications (Cambridge, England), 2016, 52, 2350-2353
7118281 CIFC32 H49 Cu N4 O11.5P -113.96; 14.092; 18.3587
89.637; 83.246; 85.326
3574.6Eckshtain-Levi, Meital; Lavi, Ronit; Yufit, Dmitry S.; Daniel, Bareket; Green, Omer; Fleker, Ohad; Richman, Michal; Rahimipour, Shai; Gruzman, Arie; Benisvy, Laurent
A versatile water-soluble chelating and radical scavenging platform.
Chemical communications (Cambridge, England), 2016, 52, 2350-2353
7118282 CIFC151 H146 Cl6 N8 O12P -114.438; 15.006; 16.156
104.214; 92.043; 94.227
3379Katoono, Ryo; Suzuki, Takanori
Planar chiral desymmetrization of a two-layered cyclophane and control of dynamic helicity through the arrangement of two nonstereogenic centers.
Chemical communications (Cambridge, England), 2016, 52, 1029-1031
7118283 CIFC27 H24 O3P 1 21/c 118.7438; 5.9398; 19.1345
90; 92.094; 90
2128.9Kumar, Atul; Maurya, Shivam; Pratap, Kemant; Srivastava, Suman
Betaine mediated synthesis of annulated dihydrofurans from oxobis(methylthio)ketene acetals and N-butyl-N'-methyl ethane-1,2-diamine as precursors via NHC elimination.
Chemical communications (Cambridge, England), 2016, 52, 2795-2798
7118284 CIFC2 H2 N4 O12P 1 21/c 17.5489; 7.2995; 8.3759
90; 97.935; 90
457.12Fischer, Dennis; Klapötke, Thomas M; Stierstorfer, Jörg
Tetranitratoethane.
Chemical communications (Cambridge, England), 2016, 52, 916-918
7118285 CIFC110 H108 Dy7 N24 O39 P3P 1 21/c 114.7481; 33.056; 25.607
90; 104.153; 90
12105Tian, Haiquan; Bao, Song-Song; Zheng, Li-Min
Cyclic single-molecule magnets: from the odd-numbered heptanuclear to a dimer of heptanuclear dysprosium clusters.
Chemical communications (Cambridge, England), 2016, 52, 2314-2317
7118286 CIFC212 H176 Dy14 N48 O70 P10C 1 2/c 122.068; 25.118; 44.977
90; 101.477; 90
24432Tian, Haiquan; Bao, Song-Song; Zheng, Li-Min
Cyclic single-molecule magnets: from the odd-numbered heptanuclear to a dimer of heptanuclear dysprosium clusters.
Chemical communications (Cambridge, England), 2016, 52, 2314-2317
7118287 CIFC40 H32 Br4 N2P b c a18.6729; 11.0827; 33.857
90; 90; 90
7006.58Greulich, Tobias W.; Suzuki, Naoya; Daniliuc, Constantin G.; Fukazawa, Aiko; Yamaguchi, Eriko; Studer, Armido; Yamaguchi, Shigehiro
A biphenyl containing two electron-donating and two electron-accepting moieties: a rigid and small donor-acceptor-donor ladder system.
Chemical communications (Cambridge, England), 2016, 52, 2374-2377
7118288 CIFC52 H42 N2 O2 P2C 1 2/c 128.1262; 8.5442; 20.5029
90; 109.719; 90
4638.24Greulich, Tobias W.; Suzuki, Naoya; Daniliuc, Constantin G.; Fukazawa, Aiko; Yamaguchi, Eriko; Studer, Armido; Yamaguchi, Shigehiro
A biphenyl containing two electron-donating and two electron-accepting moieties: a rigid and small donor-acceptor-donor ladder system.
Chemical communications (Cambridge, England), 2016, 52, 2374-2377
7118289 CIFC40 H34 Br2 N2P -111.0372; 12.6734; 13.6066
87.925; 67.674; 66.578
1600.69Greulich, Tobias W.; Suzuki, Naoya; Daniliuc, Constantin G.; Fukazawa, Aiko; Yamaguchi, Eriko; Studer, Armido; Yamaguchi, Shigehiro
A biphenyl containing two electron-donating and two electron-accepting moieties: a rigid and small donor-acceptor-donor ladder system.
Chemical communications (Cambridge, England), 2016, 52, 2374-2377
7118290 CIFC46 H39 N2 O PP 1 21/c 110.7866; 32.189; 10.4301
90; 99.194; 90
3574.9Greulich, Tobias W.; Suzuki, Naoya; Daniliuc, Constantin G.; Fukazawa, Aiko; Yamaguchi, Eriko; Studer, Armido; Yamaguchi, Shigehiro
A biphenyl containing two electron-donating and two electron-accepting moieties: a rigid and small donor-acceptor-donor ladder system.
Chemical communications (Cambridge, England), 2016, 52, 2374-2377
7118291 CIFC56 H66 N2 O2 P2C 1 2/c 129.5733; 8.868; 20.0015
90; 109.81; 90
4935.1Greulich, Tobias W.; Suzuki, Naoya; Daniliuc, Constantin G.; Fukazawa, Aiko; Yamaguchi, Eriko; Studer, Armido; Yamaguchi, Shigehiro
A biphenyl containing two electron-donating and two electron-accepting moieties: a rigid and small donor-acceptor-donor ladder system.
Chemical communications (Cambridge, England), 2016, 52, 2374-2377
7118292 CIFC40 H47 Cl Hg O4P -114.6684; 16.1503; 16.8665
109.87; 99.8419; 95.2508
3653.9Slavík, Petr; Kohout, Michal; Böhm, Stanislav; Eigner, Václav; Lhoták, Pavel
Synthesis of inherently chiral calixarenes via direct mercuration of the partial cone conformation.
Chemical communications (Cambridge, England), 2016, 52, 2366-2369
7118293 CIFC40 H47 Cl Hg O4C 1 2/c 136.8232; 9.7905; 26.7317
90; 131.016; 90
7271.6Slavík, Petr; Kohout, Michal; Böhm, Stanislav; Eigner, Václav; Lhoták, Pavel
Synthesis of inherently chiral calixarenes via direct mercuration of the partial cone conformation.
Chemical communications (Cambridge, England), 2016, 52, 2366-2369
7118294 CIFC40 H46 O4P -110.5111; 17.7963; 19.3271
110.342; 96.592; 101.212
3259.1Slavík, Petr; Kohout, Michal; Böhm, Stanislav; Eigner, Václav; Lhoták, Pavel
Synthesis of inherently chiral calixarenes via direct mercuration of the partial cone conformation.
Chemical communications (Cambridge, England), 2016, 52, 2366-2369
7118295 CIFC106 H135 Fe6 N6 O50 Tb3C 1 2/c 129.189; 26.117; 20.479
90; 124.572; 90
12855Kühne, Irina A; Mereacre, Valeriu; Anson, Christopher E.; Powell, Annie K.
Nine members of a family of nine-membered cyclic coordination clusters; Fe6Ln3 wheels (Ln = Gd to Lu and Y).
Chemical communications (Cambridge, England), 2016, 52, 1021-1024
7118296 CIFC109 H143 Dy3 Fe6 N6 O51C 1 2/c 129.2726; 26.0163; 20.8386
90; 125.139; 90
12977.8Kühne, Irina A; Mereacre, Valeriu; Anson, Christopher E.; Powell, Annie K.
Nine members of a family of nine-membered cyclic coordination clusters; Fe6Ln3 wheels (Ln = Gd to Lu and Y).
Chemical communications (Cambridge, England), 2016, 52, 1021-1024
7118297 CIFC109 H143 Fe6 Ho3 N6 O51C 1 2/c 129.211; 25.894; 20.7929
90; 124.97; 90
12888Kühne, Irina A; Mereacre, Valeriu; Anson, Christopher E.; Powell, Annie K.
Nine members of a family of nine-membered cyclic coordination clusters; Fe6Ln3 wheels (Ln = Gd to Lu and Y).
Chemical communications (Cambridge, England), 2016, 52, 1021-1024
7118298 CIFC108 H139 Fe6 N6 O50 Tm3C 1 2/c 129.069; 25.935; 20.683
90; 124.822; 90
12801Kühne, Irina A; Mereacre, Valeriu; Anson, Christopher E.; Powell, Annie K.
Nine members of a family of nine-membered cyclic coordination clusters; Fe6Ln3 wheels (Ln = Gd to Lu and Y).
Chemical communications (Cambridge, England), 2016, 52, 1021-1024
7118299 CIFC112 H151 Fe6 N6 O52 Yb3P -119.6191; 22.3573; 31.163
77.52; 80.86; 71.74
12612.6Kühne, Irina A; Mereacre, Valeriu; Anson, Christopher E.; Powell, Annie K.
Nine members of a family of nine-membered cyclic coordination clusters; Fe6Ln3 wheels (Ln = Gd to Lu and Y).
Chemical communications (Cambridge, England), 2016, 52, 1021-1024
7118300 CIFC109 H143 Fe6 Lu3 N6 O51C 1 2/c 129.1226; 25.811; 20.8572
90; 125.126; 90
12822.9Kühne, Irina A; Mereacre, Valeriu; Anson, Christopher E.; Powell, Annie K.
Nine members of a family of nine-membered cyclic coordination clusters; Fe6Ln3 wheels (Ln = Gd to Lu and Y).
Chemical communications (Cambridge, England), 2016, 52, 1021-1024
7118301 CIFC108 H139 Fe6 N6 O50 Y3C 1 2/c 129.172; 25.835; 20.884
90; 125.552; 90
12805Kühne, Irina A; Mereacre, Valeriu; Anson, Christopher E.; Powell, Annie K.
Nine members of a family of nine-membered cyclic coordination clusters; Fe6Ln3 wheels (Ln = Gd to Lu and Y).
Chemical communications (Cambridge, England), 2016, 52, 1021-1024
7118302 CIFC107 H125 Cl6 Fe6 Gd3 N6 O47P 1 21/n 123.721; 20.6579; 26.078
90; 100.61; 90
12560.4Kühne, Irina A; Mereacre, Valeriu; Anson, Christopher E.; Powell, Annie K.
Nine members of a family of nine-membered cyclic coordination clusters; Fe6Ln3 wheels (Ln = Gd to Lu and Y).
Chemical communications (Cambridge, England), 2016, 52, 1021-1024
7118303 CIFC24 H38 B N6 S3 ZnR -3 :H13.3984; 13.3984; 27.542
90; 90; 120
4281.9Kreider-Mueller, Ava; Quinlivan, Patrick J.; Rauch, Michael; Owen, Jonathan S.; Parkin, Gerard
Synthesis, structure and reactivity of [Tm(Bu(t))]ZnH, a monomeric terminal zinc hydride compound in a sulfur-rich coordination environment: access to a heterobimetallic compound.
Chemical communications (Cambridge, England), 2016, 52, 2358-2361
7118304 CIFC41 H57 B N6 S3 ZnR -3 c :H13.473; 13.473; 67.359
90; 90; 120
10589Kreider-Mueller, Ava; Quinlivan, Patrick J.; Rauch, Michael; Owen, Jonathan S.; Parkin, Gerard
Synthesis, structure and reactivity of [Tm(Bu(t))]ZnH, a monomeric terminal zinc hydride compound in a sulfur-rich coordination environment: access to a heterobimetallic compound.
Chemical communications (Cambridge, England), 2016, 52, 2358-2361
7118305 CIFC34 H47 B N6 O2 S3 ZnP 1 21 110.3568; 19.5721; 10.5278
90; 119.424; 90
1858.8Kreider-Mueller, Ava; Quinlivan, Patrick J.; Rauch, Michael; Owen, Jonathan S.; Parkin, Gerard
Synthesis, structure and reactivity of [Tm(Bu(t))]ZnH, a monomeric terminal zinc hydride compound in a sulfur-rich coordination environment: access to a heterobimetallic compound.
Chemical communications (Cambridge, England), 2016, 52, 2358-2361
7118306 CIFC41 H51 B Mo N6 O3 S3 ZnP -110.2866; 12.0489; 19.226
92.635; 93.904; 114.888
2149.3Kreider-Mueller, Ava; Quinlivan, Patrick J.; Rauch, Michael; Owen, Jonathan S.; Parkin, Gerard
Synthesis, structure and reactivity of [Tm(Bu(t))]ZnH, a monomeric terminal zinc hydride compound in a sulfur-rich coordination environment: access to a heterobimetallic compound.
Chemical communications (Cambridge, England), 2016, 52, 2358-2361
7118307 CIFC27 H38 B F N6 S4 ZnP 1 21/n 113.199; 17.979; 13.504
90; 92.785; 90
3201Kreider-Mueller, Ava; Quinlivan, Patrick J.; Rauch, Michael; Owen, Jonathan S.; Parkin, Gerard
Synthesis, structure and reactivity of [Tm(Bu(t))]ZnH, a monomeric terminal zinc hydride compound in a sulfur-rich coordination environment: access to a heterobimetallic compound.
Chemical communications (Cambridge, England), 2016, 52, 2358-2361
7118308 CIFCo6 H224 Li14 Na9 O250 P5 W36P -114.5199; 25.6135; 27.6975
94.512; 99.078; 93.145
10116.6Martin-Sabi, Mercè; Winter, Ross Stuart; Lydon, Claire; Cameron, Jamie M.; Long, De-Liang; Cronin, Leroy
Rearrangement of {α-P2W15} to {PW6} moieties during the assembly of transition-metal-linked polyoxometalate clusters.
Chemical communications (Cambridge, England), 2016, 52, 919-921
7118309 CIFH120 Li12 Mn6 Na11 O198 P5 W36P -114.0471; 21.9582; 30.7558
87.466; 88.627; 86.131
9453.6Martin-Sabi, Mercè; Winter, Ross Stuart; Lydon, Claire; Cameron, Jamie M.; Long, De-Liang; Cronin, Leroy
Rearrangement of {α-P2W15} to {PW6} moieties during the assembly of transition-metal-linked polyoxometalate clusters.
Chemical communications (Cambridge, England), 2016, 52, 919-921
7118310 CIFH137 Li20 Mn9 Na5 O245 P8 W45P -114.0535; 29.6184; 31.8218
74.118; 81.242; 89.716
12582Martin-Sabi, Mercè; Winter, Ross Stuart; Lydon, Claire; Cameron, Jamie M.; Long, De-Liang; Cronin, Leroy
Rearrangement of {α-P2W15} to {PW6} moieties during the assembly of transition-metal-linked polyoxometalate clusters.
Chemical communications (Cambridge, England), 2016, 52, 919-921
7118311 CIFC68 H162 Br Cr Mo6 N5 O26P 1 21 116.314; 15.3614; 18.1903
90; 92.867; 90
4552.9Zhang, Jiangwei; Li, Qi; Zeng, Mengyan; Huang, Yichao; Zhang, Jin; Hao, Jian; Wei, Yongge
The proton-controlled synthesis of unprecedented diol functionalized Anderson-type POMs.
Chemical communications (Cambridge, England), 2016, 52, 2378-2381
7118312 CIFC45 H109 Cr Mo6 N6 O29P -113.554; 13.7899; 21.0955
86.768; 88.944; 63.016
3508Zhang, Jiangwei; Li, Qi; Zeng, Mengyan; Huang, Yichao; Zhang, Jin; Hao, Jian; Wei, Yongge
The proton-controlled synthesis of unprecedented diol functionalized Anderson-type POMs.
Chemical communications (Cambridge, England), 2016, 52, 2378-2381
7118313 CIFC46 H108 Cr Mo6 N5 O28P -113.6865; 13.7366; 21.5248
86.727; 83.692; 62.304
3561.4Zhang, Jiangwei; Li, Qi; Zeng, Mengyan; Huang, Yichao; Zhang, Jin; Hao, Jian; Wei, Yongge
The proton-controlled synthesis of unprecedented diol functionalized Anderson-type POMs.
Chemical communications (Cambridge, England), 2016, 52, 2378-2381
7118314 CIFC68 H177 Br3 Cr Mo6 N6 O32.5P 1 21 123.7911; 15.3677; 28.4337
90; 96.193; 90
10335.1Zhang, Jiangwei; Li, Qi; Zeng, Mengyan; Huang, Yichao; Zhang, Jin; Hao, Jian; Wei, Yongge
The proton-controlled synthesis of unprecedented diol functionalized Anderson-type POMs.
Chemical communications (Cambridge, England), 2016, 52, 2378-2381
7118315 CIFC68 H176 Br3 Cr Mo6 N6 O31P 1 21 124.0231; 15.1457; 28.6632
90; 95.967; 90
10372.5Zhang, Jiangwei; Li, Qi; Zeng, Mengyan; Huang, Yichao; Zhang, Jin; Hao, Jian; Wei, Yongge
The proton-controlled synthesis of unprecedented diol functionalized Anderson-type POMs.
Chemical communications (Cambridge, England), 2016, 52, 2378-2381
7118316 CIFC67 H161 Br Cr Mo6 N4 O28P 1 21 116.5248; 15.1876; 18.3785
90; 93.071; 90
4605.9Zhang, Jiangwei; Li, Qi; Zeng, Mengyan; Huang, Yichao; Zhang, Jin; Hao, Jian; Wei, Yongge
The proton-controlled synthesis of unprecedented diol functionalized Anderson-type POMs.
Chemical communications (Cambridge, England), 2016, 52, 2378-2381
7118317 CIFC11 H12 N6 O2P 17; 7.1645; 13.4574
94.095; 93.302; 105.223
647.52Pathigoolla, Atchutarao; Sureshan, Kana M.
The topochemical synthesis of triazole-linked homobasic DNA.
Chemical communications (Cambridge, England), 2016, 52, 886-888
7118318 CIFC37 H53 Br3 Co2 N3 O PP 1 21/c 114.965; 24.298; 15.796
90; 110.07; 90
5395Simler, Thomas; Braunstein, Pierre; Danopoulos, Andreas A.
Cobalt PNC(NHC) 'pincers': ligand dearomatisation, formation of dinuclear and N2 complexes and promotion of C-H activation.
Chemical communications (Cambridge, England), 2016, 52, 2717-2720
7118319 CIFC33 H45 Br Co N3 PP 1 21/c 112.8384; 17.0917; 16.7231
90; 116.587; 90
3281.5Simler, Thomas; Braunstein, Pierre; Danopoulos, Andreas A.
Cobalt PNC(NHC) 'pincers': ligand dearomatisation, formation of dinuclear and N2 complexes and promotion of C-H activation.
Chemical communications (Cambridge, England), 2016, 52, 2717-2720
7118320 CIFC66 H90 Co2 N8 P2P -114.852; 16.6741; 18.3766
66.34; 84.429; 66.37
3807.8Simler, Thomas; Braunstein, Pierre; Danopoulos, Andreas A.
Cobalt PNC(NHC) 'pincers': ligand dearomatisation, formation of dinuclear and N2 complexes and promotion of C-H activation.
Chemical communications (Cambridge, England), 2016, 52, 2717-2720
7118321 CIFC33 H45 Co N5 PC 1 2/c 125.681; 15.695; 18.634
90; 113.151; 90
6906Simler, Thomas; Braunstein, Pierre; Danopoulos, Andreas A.
Cobalt PNC(NHC) 'pincers': ligand dearomatisation, formation of dinuclear and N2 complexes and promotion of C-H activation.
Chemical communications (Cambridge, England), 2016, 52, 2717-2720
7118322 CIFC9 H9 I N2 O3P -18.154; 11.633; 12.467
67.55; 76.11; 76.47
1047.6Puttreddy, Rakesh; Jurček, Ondřej; Bhowmik, Sandip; Mäkelä, Toni; Rissanen, Kari
Very strong (-)N-X(+)(-)O-N(+) halogen bonds.
Chemical communications (Cambridge, England), 2016, 52, 2338-2341
7118323 CIFC10 H12 I N2 O3.5P -19.7294; 11.427; 11.566
90.02; 110.88; 93.06
1199.5Puttreddy, Rakesh; Jurček, Ondřej; Bhowmik, Sandip; Mäkelä, Toni; Rissanen, Kari
Very strong (-)N-X(+)(-)O-N(+) halogen bonds.
Chemical communications (Cambridge, England), 2016, 52, 2338-2341
7118324 CIFC15 H13 I N2 O3P 21 21 215.7923; 8.4216; 29.71
90; 90; 90
1449.3Puttreddy, Rakesh; Jurček, Ondřej; Bhowmik, Sandip; Mäkelä, Toni; Rissanen, Kari
Very strong (-)N-X(+)(-)O-N(+) halogen bonds.
Chemical communications (Cambridge, England), 2016, 52, 2338-2341
7118325 CIFC12 H9 I N2 O4 SP 1 21/c 17.137; 22.707; 8.8248
90; 90.68; 90
1430Puttreddy, Rakesh; Jurček, Ondřej; Bhowmik, Sandip; Mäkelä, Toni; Rissanen, Kari
Very strong (-)N-X(+)(-)O-N(+) halogen bonds.
Chemical communications (Cambridge, England), 2016, 52, 2338-2341
7118326 CIFC13 H11 I N2 O4 SP -17.2705; 8.7631; 12.765
109.12; 99.97; 90.54
754.9Puttreddy, Rakesh; Jurček, Ondřej; Bhowmik, Sandip; Mäkelä, Toni; Rissanen, Kari
Very strong (-)N-X(+)(-)O-N(+) halogen bonds.
Chemical communications (Cambridge, England), 2016, 52, 2338-2341
7118327 CIFC18 H13 I N2 O4 SP 1 21/c 112.277; 10.283; 14.972
90; 106.71; 90
1810.3Puttreddy, Rakesh; Jurček, Ondřej; Bhowmik, Sandip; Mäkelä, Toni; Rissanen, Kari
Very strong (-)N-X(+)(-)O-N(+) halogen bonds.
Chemical communications (Cambridge, England), 2016, 52, 2338-2341
7118328 CIFC12 H10 N2 O4 SP -16.8571; 8.4482; 11.3117
98.755; 106.766; 93.582
616.19Puttreddy, Rakesh; Jurček, Ondřej; Bhowmik, Sandip; Mäkelä, Toni; Rissanen, Kari
Very strong (-)N-X(+)(-)O-N(+) halogen bonds.
Chemical communications (Cambridge, England), 2016, 52, 2338-2341
7118329 CIFC13 H12 N2 O4 SP 1 21/c 114.1204; 6.8482; 14.7897
90; 112.86; 90
1317.83Puttreddy, Rakesh; Jurček, Ondřej; Bhowmik, Sandip; Mäkelä, Toni; Rissanen, Kari
Very strong (-)N-X(+)(-)O-N(+) halogen bonds.
Chemical communications (Cambridge, England), 2016, 52, 2338-2341
7118330 CIFC21 H20 Cl N O6P 21 21 215.79637; 13.3106; 25.2934
90; 90; 90
1951.47Shu, Tao; Ni, Qijian; Song, Xiaoxiao; Zhao, Kun; Wu, Tianyu; Puttreddy, Rakesh; Rissanen, Kari; Enders, Dieter
Asymmetric synthesis of cyclopentanes bearing four contiguous stereocenters via an NHC-catalyzed Michael/Michael/esterification domino reaction.
Chemical communications (Cambridge, England), 2016, 52, 2609-2611
7118331 CIFC21 H23 N O7P -18.6216; 9.7362; 13.104
91.924; 104.975; 108.523
999.5Gao, Qian; Hao, Wen-Juan; Liu, Feng; Tu, Shu-Jiang; Wang, Shu-Liang; Li, Guigen; Jiang, Bo
Unexpected isocyanide-based three-component bicyclization for the stereoselective synthesis of densely functionalized pyrano[3,4-c]pyrroles.
Chemical communications (Cambridge, England), 2016, 52, 900-903
7118332 CIFC16 H12 N6 SP c c n12.0045; 10.8025; 11.0878
90; 90; 90
1437.9Wang, Ying; Yi, Jin-Min; Zhang, Meng-Yuan; Xu, Ping; Zhao, Xiao-Jun
I2-induced SC-SC transformation within two-dimensional Zn(ii)-triazole framework: an ideal detector of cyano-containing molecules.
Chemical communications (Cambridge, England), 2016, 52, 3099-3102
7118333 CIFC28.5 H30 N7.5 O6.5 S ZnP -19.0152; 12.4589; 13.9479
105.422; 91.756; 94.9
1502.37Wang, Ying; Yi, Jin-Min; Zhang, Meng-Yuan; Xu, Ping; Zhao, Xiao-Jun
I2-induced SC-SC transformation within two-dimensional Zn(ii)-triazole framework: an ideal detector of cyano-containing molecules.
Chemical communications (Cambridge, England), 2016, 52, 3099-3102
7118334 CIFC44 H33 I N12 O7.5 S2 Zn2P -18.94; 15.624; 18.684
65.286; 84.924; 74.295
2281.3Wang, Ying; Yi, Jin-Min; Zhang, Meng-Yuan; Xu, Ping; Zhao, Xiao-Jun
I2-induced SC-SC transformation within two-dimensional Zn(ii)-triazole framework: an ideal detector of cyano-containing molecules.
Chemical communications (Cambridge, England), 2016, 52, 3099-3102
7118335 CIFC70 H68 N4 O7 Zn2P n n a17.8685; 23.0557; 18.5326
90; 90; 90
7634.89He, Shixiong; Wang, Fuli; Tong, Wah-Leung; Yiu, Shek-Man; Chan, Michael C. W.
Topologically diverse shape-persistent bis-(Zn-salphen) catalysts: efficient cyclic carbonate formation under mild conditions.
Chemical communications (Cambridge, England), 2016, 52, 1017-1020
7118336 CIFC39 H36 N2 O SP 1 21/c 113.163; 9.4788; 25.5497
90; 96.7832; 90
3165.5Ikezawa, Takahiro; Mutoh, Katsuya; Kobayashi, Yoichi; Abe, Jiro
Thiophene-substituted phenoxyl-imidazolyl radical complexes with high photosensitivity.
Chemical communications (Cambridge, England), 2016, 52, 2465-2468
7118337 CIFC33 H32 N2 O SP -111.58; 14.496; 18.428
67.834; 89.295; 70.014
2668Ikezawa, Takahiro; Mutoh, Katsuya; Kobayashi, Yoichi; Abe, Jiro
Thiophene-substituted phenoxyl-imidazolyl radical complexes with high photosensitivity.
Chemical communications (Cambridge, England), 2016, 52, 2465-2468
7118338 CIFC39 H36 N2 O SP 1 21/c 112.934; 9.3801; 26.147
90; 97.1867; 90
3147.3Ikezawa, Takahiro; Mutoh, Katsuya; Kobayashi, Yoichi; Abe, Jiro
Thiophene-substituted phenoxyl-imidazolyl radical complexes with high photosensitivity.
Chemical communications (Cambridge, England), 2016, 52, 2465-2468
7118340 CIFC31 H29 Br N2 O5P 1 21 110.6073; 9.8229; 14.4413
90; 107.283; 90
1436.76Han, Jeng-Liang; Chang, Chia-Hao
An asymmetric assembly of spirooxindole dihydropyranones through a direct enantioselective organocatalytic vinylogous aldol-cyclization cascade reaction of 3-alkylidene oxindoles with isatins.
Chemical communications (Cambridge, England), 2016, 52, 2322-2325
7118341 CIFC16 H22 OP 1 c 15.6982; 18.9135; 13.0889
90; 95.097; 90
1405.05Pan, Jin-Long; Chen, Tao; Zhang, Zhi-Qiang; Li, Yi-Fan; Zhang, Xiao-Ming; Zhang, Fu-Min
A Cu-mediated one-pot Michael addition/α-arylation strategy using a diaryliodonium salt: a direct and efficient approach to α-aryl-β-substituted cyclic ketone scaffolds.
Chemical communications (Cambridge, England), 2016, 52, 2382-2385
7118342 CIFC42 H58 N2 O4.5 P SiP -111.473; 13.299; 13.766
85.201; 86.909; 86.437
2086.5Lin, Chao-Yang; Ma, Peng-Ju; Sun, Zhao; Lu, Chong-Dao; Xu, Yan-Jun
Carbamoyl anion-initiated cascade reaction for stereoselective synthesis of substituted α-hydroxy-β-amino amides.
Chemical communications (Cambridge, England), 2016, 52, 912-915
7118343 CIFC24 H31 Br N2 O3 SP 21 21 219.891; 16.14; 16.21
90; 90; 90
2588Lin, Chao-Yang; Ma, Peng-Ju; Sun, Zhao; Lu, Chong-Dao; Xu, Yan-Jun
Carbamoyl anion-initiated cascade reaction for stereoselective synthesis of substituted α-hydroxy-β-amino amides.
Chemical communications (Cambridge, England), 2016, 52, 912-915
7118344 CIFC184 H162 Co6 Mn6 N24 O32 S8R -323.1209; 23.1209; 27.281
90; 90; 120
12629.9Jeon, Ie-Rang; David Harris, T.
An S = 12 semiquinoid radical-bridged Mn6 wheel complex assembled from an asymmetric redox-active bridging ligand.
Chemical communications (Cambridge, England), 2016, 52, 1006-1008
7118345 CIFC29 H33 N2 PP 1 21/c 111.3578; 9.9307; 22.539
90; 102.838; 90
2478.6Majhi, Paresh Kumar; Chow, Keith C. F.; Hsieh, Tom H. H.; Bowes, Eric G.; Schnakenburg, Gregor; Kennepohl, Pierre; Streubel, Rainer; Gates, Derek P.
Even the normal is abnormal: N-heterocyclic carbene C(2) binding to a phosphaalkene without breaking the P[double bond, length as m-dash]C π-bond.
Chemical communications (Cambridge, England), 2016, 52, 998-1001
7118346 CIFC58 H72 B2 N4 O P2C 1 2/c 125.984; 9.734; 21.55
90; 108.32; 90
5174.3Majhi, Paresh Kumar; Chow, Keith C. F.; Hsieh, Tom H. H.; Bowes, Eric G.; Schnakenburg, Gregor; Kennepohl, Pierre; Streubel, Rainer; Gates, Derek P.
Even the normal is abnormal: N-heterocyclic carbene C(2) binding to a phosphaalkene without breaking the P[double bond, length as m-dash]C π-bond.
Chemical communications (Cambridge, England), 2016, 52, 998-1001
7118347 CIFC17 H23 N O6P 1 21 19.223; 7.1694; 13.3259
90; 92.731; 90
880.153Riaño, Iker; Díaz, Estibaliz; Uria, Uxue; Reyes, Efraím; Carrillo, Luisa; Vicario, Jose L.
Organocatalytic enantio- and diastereoselective synthesis of 3,5-disubstituted prolines.
Chemical communications (Cambridge, England), 2016, 52, 2330-2333
7118348 CIFC38 H70 Na3 O32 S3P -3 1 c27.0902; 27.0902; 30.1891
90; 90; 120
19186.9Garnett, Graham A. E.; Daze, Kevin D.; Peña Diaz, Jorge A; Fagen, Noah; Shaurya, Alok; Ma, Manuel C. F.; Collins, Mary S.; Johnson, Darren W.; Zakharov, Lev N.; Hof, Fraser
Attraction by repulsion: compounds with like charges undergo self-assembly in water that improves in high salt and persists in real biological fluids.
Chemical communications (Cambridge, England), 2016, 52, 2768-2771
7118349 CIFC29 H32 N2 O4 SP 1 21 112.959; 7.94026; 14.0403
90; 116.595; 90
1291.86Li, Guangxun; Liu, Hongxin; Wang, Yingwei; Zhang, Shiqi; Lai, Shujun; Tang, Ling; Zhao, Jinzhong; Tang, Zhuo
The catalytic enantioselective synthesis of tetrahydroquinolines containing all-carbon quaternary stereocenters via the formation of aza-ortho-xylylene with 1,2-dihydroquinoline as a precursor.
Chemical communications (Cambridge, England), 2016, 52, 2304-2306
7118350 CIFC23 H23 Br N2 O5P 1 21/n 114.4012; 10.1201; 15.5792
90; 97.623; 90
2250.47Zhang, Ya-Jun; Chen, Cheng; Tan, Bin; Cai, Li-Xuan; Yang, Xiao-Dong; Zhang, Jie
A dual-stimuli responsive small molecule organic material with tunable multi-state response showing turn-on luminescence and photocoloration.
Chemical communications (Cambridge, England), 2016, 52, 2835-2838
7118351 CIFC46 H58 Br2 N4 O16C 1 2/c 127.25; 13.662; 17.3
90; 110.04; 90
6051Zhang, Ya-Jun; Chen, Cheng; Tan, Bin; Cai, Li-Xuan; Yang, Xiao-Dong; Zhang, Jie
A dual-stimuli responsive small molecule organic material with tunable multi-state response showing turn-on luminescence and photocoloration.
Chemical communications (Cambridge, England), 2016, 52, 2835-2838
7118352 CIFC23 H21 F6 N2 O4 PP 1 21/c 16.821; 17.801; 19.7701
90; 98.215; 90
2375.9Zhang, Ya-Jun; Chen, Cheng; Tan, Bin; Cai, Li-Xuan; Yang, Xiao-Dong; Zhang, Jie
A dual-stimuli responsive small molecule organic material with tunable multi-state response showing turn-on luminescence and photocoloration.
Chemical communications (Cambridge, England), 2016, 52, 2835-2838
7118353 CIFC20 H18 Br N2 O2P 1 21/n 111.3148; 7.1192; 21.3182
90; 93.83; 90
1713.4Xu, Guo-Qiang; Li, Chen-Guang; Liu, Ming-Qian; Cao, Jian; Luo, Yong-Chun; Xu, Peng-Fei
Dual C-H functionalization of N-aryl tetrahydroisoquinolines: a highly diastereoselective synthesis of dibenzo[a,f]quinolizines via visible-light induced oxidation and inverse electron-demand aza-Diels-Alder reaction.
Chemical communications (Cambridge, England), 2016, 52, 1190-1193
7118354 CIFC20 H12 N O5.5 ZnP 65 2 215.9684; 15.9684; 33.649
90; 90; 120
7430.6Wen, Hui-Min; Li, Bin; Wang, Hailong; Krishna, Rajamani; Chen, Banglin
High acetylene/ethylene separation in a microporous zinc(ii) metal-organic framework with low binding energy.
Chemical communications (Cambridge, England), 2016, 52, 1166-1169
7118355 CIFC69 H87 Fe3 N6 S3P 63/m16.8444; 16.8444; 12.6713
90; 90; 120
3113.6Lee, Yousoon; Jeon, Ie-Rang; Abboud, Khalil A.; García-Serres, Ricardo; Shearer, Jason; Murray, Leslie J.
A [3Fe-3S](3+) cluster with exclusively μ-sulfide donors.
Chemical communications (Cambridge, England), 2016, 52, 1174-1177
7118356 CIFC4.5 H1.5 Eu0.25 In0.25 O4P 42/m c m12.6261; 12.6261; 29.234
90; 90; 90
4660.4Qian, Jinjie; Li, Qipeng; Liang, Linfeng; Yang, Yan; Cao, Zhen; Yu, Panpan; Huang, Shaoming; Hong, Maochun
A photoluminescent indium-organic framework with discrete cages and one-dimensional channels for gas adsorption.
Chemical communications (Cambridge, England), 2016, 52, 9032-9035
7118357 CIFC14 H7 F5 N2P 21 21 217.6294; 12.6995; 25.8239
90; 90; 90
2502.1Laubenstein, R.; Şerb, M-D; Englert, U.; Raabe, G.; Braun, T.; Braun, B.
Is it all in the hinge? A kryptoracemate and three of its alternative racemic polymorphs of an aminonitrile.
Chemical communications (Cambridge, England), 2016, 52, 1214-1217
7118358 CIFC14 H7 F5 N2P 1 21/c 17.6779; 23.7528; 13.8443
90; 90.3699; 90
2524.75Laubenstein, R.; Şerb, M-D; Englert, U.; Raabe, G.; Braun, T.; Braun, B.
Is it all in the hinge? A kryptoracemate and three of its alternative racemic polymorphs of an aminonitrile.
Chemical communications (Cambridge, England), 2016, 52, 1214-1217
7118359 CIFC14 H7 F5 N2P n a 2125.3241; 6.535; 29.874
90; 90; 90
4943.9Laubenstein, R.; Şerb, M-D; Englert, U.; Raabe, G.; Braun, T.; Braun, B.
Is it all in the hinge? A kryptoracemate and three of its alternative racemic polymorphs of an aminonitrile.
Chemical communications (Cambridge, England), 2016, 52, 1214-1217
7118360 CIFC14 H7 F5 N2P 1 21/c 113.9748; 7.4518; 11.8994
90; 104.487; 90
1199.77Laubenstein, R.; Şerb, M-D; Englert, U.; Raabe, G.; Braun, T.; Braun, B.
Is it all in the hinge? A kryptoracemate and three of its alternative racemic polymorphs of an aminonitrile.
Chemical communications (Cambridge, England), 2016, 52, 1214-1217
7118361 CIFC26 H19 O3 PC 1 2/c 116.295; 14.157; 18.637
90; 104.42; 90
4164Fukazawa, Aiko; Suda, Shinji; Taki, Masayasu; Yamaguchi, Eriko; Grzybowski, Marek; Sato, Yoshikatsu; Higashiyama, Tetsuya; Yamaguchi, Shigehiro
Phospha-fluorescein: a red-emissive fluorescein analogue with high photobleaching resistance.
Chemical communications (Cambridge, England), 2016, 52, 1120-1123
7118362 CIFC8 H5 Cl3 F N OP 1 21/c 19.1964; 11.7747; 9.7412
90; 98.134; 90
1044.21Ghosh, Monisankar; Saha, Suchandrima; Dutta, Samir Kumar
'Dual hit' metabolic modulator LDCA selectively kills cancer cells by efficient competitive inhibition of LDH-A.
Chemical communications (Cambridge, England), 2016, 52, 2401-2404
7118363 CIFC26 H22C 2 2 219.937; 17.673; 10.223
90; 90; 90
1795.3Iwahara, Hideaki; Kushida, Tomokatsu; Yamaguchi, Shigehiro
A planarized 9-phenylanthracene: a simple electron-donating building block for fluorescent materials.
Chemical communications (Cambridge, England), 2016, 52, 1124-1127
7118364 CIFC20 H14P -16.247; 10.259; 10.779
84.94; 76.39; 77.39
654.7Iwahara, Hideaki; Kushida, Tomokatsu; Yamaguchi, Shigehiro
A planarized 9-phenylanthracene: a simple electron-donating building block for fluorescent materials.
Chemical communications (Cambridge, England), 2016, 52, 1124-1127
7118365 CIFC186 H102 N8 O71 S3 Zn20R -3 :H25.299; 25.299; 166.828
90; 90; 120
92471Xie, Wei; He, Wen-Wen; Du, Dong-Ying; Li, Shun-Li; Qin, Jun-Sheng; Su, Zhong-Min; Sun, Chun-Yi; Lan, Ya-Qian
A stable Alq3@MOF composite for white-light emission.
Chemical communications (Cambridge, England), 2016, 52, 3288-3291
7118366 CIFC12 H16 N3 O5 PP -17.6832; 9.6923; 10.0668
89.063; 82.389; 80.144
732.07Gao, Ming; Li, Yi; Xie, Lijuan; Chauvin, Remi; Cui, Xiuling
Direct phosphonation of quinoxalin-2(1H)-ones under transition-metal-free conditions.
Chemical communications (Cambridge, England), 2016, 52, 2846-2849
7118367 CIFC25 H38 O5 SiP 1 21/n 110.5246; 7.1824; 33.424
90; 94.7154; 90
2518Yanai, Hikaru; Kobayashi, Osamu; Takada, Kenji; Isono, Takuya; Satoh, Toshifumi; Matsumoto, Takashi
Sequential Mukaiyama-Michael reaction induced by carbon acids.
Chemical communications (Cambridge, England), 2016, 52, 3280-3283
7118368 CIFC20 H23 Br O5P 1 21/c 17.1552; 17.356; 14.5825
90; 95.177; 90
1803.5Yanai, Hikaru; Kobayashi, Osamu; Takada, Kenji; Isono, Takuya; Satoh, Toshifumi; Matsumoto, Takashi
Sequential Mukaiyama-Michael reaction induced by carbon acids.
Chemical communications (Cambridge, England), 2016, 52, 3280-3283
7118369 CIFC22 H20 O6P c a 2134.732; 13.1317; 8.2791
90; 90; 90
3776Yanai, Hikaru; Kobayashi, Osamu; Takada, Kenji; Isono, Takuya; Satoh, Toshifumi; Matsumoto, Takashi
Sequential Mukaiyama-Michael reaction induced by carbon acids.
Chemical communications (Cambridge, England), 2016, 52, 3280-3283
7118370 CIFC23 H21 Br O6P 1 21/n 112.6704; 9.7676; 16.2166
90; 97.059; 90
1991.7Yanai, Hikaru; Kobayashi, Osamu; Takada, Kenji; Isono, Takuya; Satoh, Toshifumi; Matsumoto, Takashi
Sequential Mukaiyama-Michael reaction induced by carbon acids.
Chemical communications (Cambridge, England), 2016, 52, 3280-3283
7118371 CIFC18 H20 O5P c a 2125.583; 6.8787; 17.4038
90; 90; 90
3062.7Yanai, Hikaru; Kobayashi, Osamu; Takada, Kenji; Isono, Takuya; Satoh, Toshifumi; Matsumoto, Takashi
Sequential Mukaiyama-Michael reaction induced by carbon acids.
Chemical communications (Cambridge, England), 2016, 52, 3280-3283
7118372 CIFC18 H19 Br O5P 1 c 111.3068; 9.6829; 24.116
90; 103.091; 90
2571.7Yanai, Hikaru; Kobayashi, Osamu; Takada, Kenji; Isono, Takuya; Satoh, Toshifumi; Matsumoto, Takashi
Sequential Mukaiyama-Michael reaction induced by carbon acids.
Chemical communications (Cambridge, England), 2016, 52, 3280-3283
7118373 CIFC19 H22 O5P 1 21/c 115.1059; 7.0831; 16.4912
90; 114.08; 90
1610.9Yanai, Hikaru; Kobayashi, Osamu; Takada, Kenji; Isono, Takuya; Satoh, Toshifumi; Matsumoto, Takashi
Sequential Mukaiyama-Michael reaction induced by carbon acids.
Chemical communications (Cambridge, England), 2016, 52, 3280-3283
7118374 CIFC19 H21 Br O5P -18.854; 14.268; 14.396
94.289; 102.73; 95.207
1758.2Yanai, Hikaru; Kobayashi, Osamu; Takada, Kenji; Isono, Takuya; Satoh, Toshifumi; Matsumoto, Takashi
Sequential Mukaiyama-Michael reaction induced by carbon acids.
Chemical communications (Cambridge, England), 2016, 52, 3280-3283
7118375 CIFC20 H23 Br O5P 1 21/n 112.0177; 6.6196; 23.898
90; 93.302; 90
1898Yanai, Hikaru; Kobayashi, Osamu; Takada, Kenji; Isono, Takuya; Satoh, Toshifumi; Matsumoto, Takashi
Sequential Mukaiyama-Michael reaction induced by carbon acids.
Chemical communications (Cambridge, England), 2016, 52, 3280-3283
7118376 CIFC2 H10 N2 O12 S4 Zn3C 1 2/c 113.7379; 8.3487; 13.0277
90; 106.235; 90
1434.61Tiwari, Ranjay K.; Kumar, Jitendra; Behera, J. N.
The first organically templated open-framework metal-sulfites with layered and three-dimensional diamondoid structures.
Chemical communications (Cambridge, England), 2016, 52, 1282-1285
7118377 CIFC2 H12 N6 O6 S2 ZnF d d 214.4211; 12.1181; 14.0692
90; 90; 90
2458.7Tiwari, Ranjay K.; Kumar, Jitendra; Behera, J. N.
The first organically templated open-framework metal-sulfites with layered and three-dimensional diamondoid structures.
Chemical communications (Cambridge, England), 2016, 52, 1282-1285
7118378 CIFC28 H40 Cu I2 N8P 1 21/c 118.1909; 19.1754; 20.759
90; 112.85; 90
6672.9Roy, Subhasish; Sarma, Manas Jyoti; Kashyap, Bishwapran; Phukan, Prodeep
A quick Chan-Lam C-N and C-S cross coupling at room temperature in the presence of square pyramidal [Cu(DMAP)4I]I as a catalyst.
Chemical communications (Cambridge, England), 2016, 52, 1170-1173
7118379 CIFC20 H36 B6 Ir2P 1 21/n 19.1413; 19.4335; 28.6894
90; 98.911; 90
5035.1Borthakur, Rosmita; Mondal, Bijan; Nandi, Purbasha; Ghosh, Sundargopal
Hypoelectronic isomeric diiridaboranes [(Cp*Ir)2B6H6]: the "Rule-Breakers"(Cp* = η(5)-C5Me5).
Chemical communications (Cambridge, England), 2016, 52, 3199-3202
7118380 CIFC20 H37 B7 Ir2P -19.1768; 9.2116; 16.3496
99.379; 101.76; 102.741
1288.09Borthakur, Rosmita; Mondal, Bijan; Nandi, Purbasha; Ghosh, Sundargopal
Hypoelectronic isomeric diiridaboranes [(Cp*Ir)2B6H6]: the "Rule-Breakers"(Cp* = η(5)-C5Me5).
Chemical communications (Cambridge, England), 2016, 52, 3199-3202
7118381 CIFC20 H36 B6 Ir2P 1 21/c 116.4805; 19.9995; 16.6991
90; 117.242; 90
4893.5Borthakur, Rosmita; Mondal, Bijan; Nandi, Purbasha; Ghosh, Sundargopal
Hypoelectronic isomeric diiridaboranes [(Cp*Ir)2B6H6]: the "Rule-Breakers"(Cp* = η(5)-C5Me5).
Chemical communications (Cambridge, England), 2016, 52, 3199-3202
7118382 CIFC23 H26 N O3 PP -18.6783; 11.3201; 12.0032
111.032; 94.279; 105.86
1038.96Wang, Jieping; Siqueira, Gilberto; Müller, Georgina; Rentsch, Daniel; Huch, Anja; Tingaut, Philippe; Levalois-Grützmacher, Joëlle; Grützmacher, Hansjörg
Synthesis of new bis(acyl)phosphane oxide photoinitiators for the surface functionalization of cellulose nanocrystals.
Chemical communications (Cambridge, England), 2016, 52, 2823-2826
7118383 CIFC20 H15 N3 OP 1 21/n 19.7059; 15.7541; 10.525
90; 95.513; 90
1601.91Sadhu, Pradeep; Punniyamurthy, Tharmalingam
Copper(ii)-mediated regioselective N-arylation of pyrroles, indoles, pyrazoles and carbazole via dehydrogenative coupling.
Chemical communications (Cambridge, England), 2016, 52, 2803-2806
7118384 CIFC25 H17 F N2 O2P 1 21/c 110.9284; 18.6077; 10.9054
90; 118.516; 90
1948.6Rajkumar, Subramani; Antony Savarimuthu, S.; Senthil Kumaran, Rajendran; Nagaraja, C. M.; Gandhi, Thirumanavelan
Expedient synthesis of new cinnoline diones by Ru-catalyzed regioselective unexpected deoxygenation-oxidative annulation of propargyl alcohols with phthalazinones and pyridazinones.
Chemical communications (Cambridge, England), 2016, 52, 2509-2512
7118385 CIFC23 H15 N3 O4P 1 21/c 122.748; 10.773; 15.613
90; 102.346; 90
3737.7Rajkumar, Subramani; Antony Savarimuthu, S.; Senthil Kumaran, Rajendran; Nagaraja, C. M.; Gandhi, Thirumanavelan
Expedient synthesis of new cinnoline diones by Ru-catalyzed regioselective unexpected deoxygenation-oxidative annulation of propargyl alcohols with phthalazinones and pyridazinones.
Chemical communications (Cambridge, England), 2016, 52, 2509-2512
7118386 CIFC11 H14 O2 SP 1 21/c 123.952; 5.752; 14.804
90; 100.445; 90
2005.8Albarghouti, Ghassan; Kotikalapudi, Ramesh; Lankri, David; Valerio, Viviana; Tsvelikhovsky, Dmitry
Cascade Pd(ii)-catalyzed Wacker lactonization-Heck reaction: rapid assembly of spiranoid lactones.
Chemical communications (Cambridge, England), 2016, 52, 3095-3098
7118387 CIFC53 H100 N12 Ni2 O24P 1 2/c 118.257; 8.475; 28.615
90; 129.59; 90
3412Jiang, Xiang; Kou, Hui-Zhong
Solid state reconstructive phase transition from porous supramolecular network to porous coordination polymer.
Chemical communications (Cambridge, England), 2016, 52, 2952-2955
7118388 CIFC57 H92 N12 Ni2 O16I 41/a27.286; 27.286; 8.343
90; 90; 90
6212Jiang, Xiang; Kou, Hui-Zhong
Solid state reconstructive phase transition from porous supramolecular network to porous coordination polymer.
Chemical communications (Cambridge, England), 2016, 52, 2952-2955
7118389 CIFC20 H28 Cu N2 O4P -17.5787; 8.0875; 9.6138
72.4479; 68.0319; 85.0439
520.8Paquet, C.; Lacelle, T.; Deore, B.; Kell, A. J.; Liu, X.; Korobkov, I.; Malenfant, P. R. L.
Pyridine-copper(ii) formates for the generation of high conductivity copper films at low temperatures.
Chemical communications (Cambridge, England), 2016, 52, 2605-2608
7118392 CIFCs1.5 H130 Na14.5 Ni7 O180 P4 W30P -112.7488; 12.7765; 25.7791
92.399; 101.831; 104.172
3966Bassil, Bassem S.; Xiang, Yixian; Haider, Ali; Hurtado, Jaime; Novitchi, Ghenadie; Powell, Annie K.; Bossoh, A. Martin; Mbomekallé, Israël M; de Oliveira, Pedro; Kortz, Ulrich
Heptanickel(ii) double-cubane core in wells-dawson heteropolytungstate, [Ni7(OH)6(H2O)6(P2W15O56)2](16.).
Chemical communications (Cambridge, England), 2016, 52, 2601-2604
7118393 CIFC25 H17 N O2 S2P 1 21/c 111.3452; 17.9768; 10.1595
90; 110.197; 90
1944.63Ward, Jonathan S.; Nobuyasu, Roberto S.; Batsanov, Andrei S.; Data, Przemyslaw; Monkman, Andrew P.; Dias, Fernando B.; Bryce, Martin R.
The interplay of thermally activated delayed fluorescence (TADF) and room temperature organic phosphorescence in sterically-constrained donor-acceptor charge-transfer molecules.
Chemical communications (Cambridge, England), 2016, 52, 2612-2615
7118394 CIFC41 H32 Cl2 N2 O2 S3C 1 2/c 120.7971; 11.4101; 15.4184
90; 98.56; 90
3618Ward, Jonathan S.; Nobuyasu, Roberto S.; Batsanov, Andrei S.; Data, Przemyslaw; Monkman, Andrew P.; Dias, Fernando B.; Bryce, Martin R.
The interplay of thermally activated delayed fluorescence (TADF) and room temperature organic phosphorescence in sterically-constrained donor-acceptor charge-transfer molecules.
Chemical communications (Cambridge, England), 2016, 52, 2612-2615
7118395 CIFC42 H34 N2 O2 S3I 1 2/a 112.7719; 13.6832; 19.915
90; 98.962; 90
3437.9Ward, Jonathan S.; Nobuyasu, Roberto S.; Batsanov, Andrei S.; Data, Przemyslaw; Monkman, Andrew P.; Dias, Fernando B.; Bryce, Martin R.
The interplay of thermally activated delayed fluorescence (TADF) and room temperature organic phosphorescence in sterically-constrained donor-acceptor charge-transfer molecules.
Chemical communications (Cambridge, England), 2016, 52, 2612-2615
7118396 CIFC42 H34 N2 O3 S3P 1 21/c 111.6805; 15.8659; 19.4344
90; 98.323; 90
3563.68Ward, Jonathan S.; Nobuyasu, Roberto S.; Batsanov, Andrei S.; Data, Przemyslaw; Monkman, Andrew P.; Dias, Fernando B.; Bryce, Martin R.
The interplay of thermally activated delayed fluorescence (TADF) and room temperature organic phosphorescence in sterically-constrained donor-acceptor charge-transfer molecules.
Chemical communications (Cambridge, England), 2016, 52, 2612-2615
7118397 CIFC26 H26 N2 Ni O6P b c a11.4913; 18.0722; 22.1742
90; 90; 90
4605Shao, Haiyan; Muduli, Subas K.; Tran, Phong D.; Soo, Han Sen
Enhancing electrocatalytic hydrogen evolution by nickel salicylaldimine complexes with alkali metal cations in aqueous media.
Chemical communications (Cambridge, England), 2016, 52, 2948-2951
7118398 CIFC26 H26 F6 K N2 Ni O6 PP 1 21/n 19.4723; 18.6903; 15.7123
90; 96.0152; 90
2766.4Shao, Haiyan; Muduli, Subas K.; Tran, Phong D.; Soo, Han Sen
Enhancing electrocatalytic hydrogen evolution by nickel salicylaldimine complexes with alkali metal cations in aqueous media.
Chemical communications (Cambridge, England), 2016, 52, 2948-2951
7118399 CIFC160 H112 O34P -112.8218; 15.8756; 38.6736
93.295; 93.991; 102.38
7649.3Ichiro Hisaki; Nobuaki Ikenaka; Norimitsu Tohnai; Mikiji Miyata
Polymorphs of layered assemblies of hydrogen-bonded hexagonal networks caused by conformational frustration
Chem.Commun., 2016, 52, 300
7118400 CIFC80 H72 N4 O18P -114.5203; 16.0332; 18.9168
103.209; 94.7721; 106.869
4049.79Ichiro Hisaki; Nobuaki Ikenaka; Norimitsu Tohnai; Mikiji Miyata
Polymorphs of layered assemblies of hydrogen-bonded hexagonal networks caused by conformational frustration
Chem.Commun., 2016, 52, 300
7118401 CIFC166 H126 N2 O36P -115.3014; 20.3447; 28.1624
101.571; 99.3676; 103.554
8144.6Ichiro Hisaki; Nobuaki Ikenaka; Norimitsu Tohnai; Mikiji Miyata
Polymorphs of layered assemblies of hydrogen-bonded hexagonal networks caused by conformational frustration
Chem.Commun., 2016, 52, 300
7118402 CIFC68 H44 O14P -114.5303; 14.9461; 20.2579
102.355; 101.544; 99.0611
4117.4Ichiro Hisaki; Nobuaki Ikenaka; Norimitsu Tohnai; Mikiji Miyata
Polymorphs of layered assemblies of hydrogen-bonded hexagonal networks caused by conformational frustration
Chem.Commun., 2016, 52, 300
7118403 CIFC60 H36 O12P -115.4431; 20.9868; 28.0527
103.362; 98.9655; 105.805
8275.7Ichiro Hisaki; Nobuaki Ikenaka; Norimitsu Tohnai; Mikiji Miyata
Polymorphs of layered assemblies of hydrogen-bonded hexagonal networks caused by conformational frustration
Chem.Commun., 2016, 52, 300
7118404 CIFC68 H44 O14P -119.1278; 22.403; 22.3984
60.046; 87.4093; 81.0545
8209.05Ichiro Hisaki; Nobuaki Ikenaka; Norimitsu Tohnai; Mikiji Miyata
Polymorphs of layered assemblies of hydrogen-bonded hexagonal networks caused by conformational frustration
Chem.Commun., 2016, 52, 300
7118405 CIFC33 H39 Cl3 N2 O3 Ru SP 1 21 17.7787; 22.469; 9.7911
90; 104.593; 90
1656.08B. Vilhanova; J. Vaclavik; P. Sot; J. Pechacek; J. Zapal; R. Pazout; J. Maixner; M. Kuzmac; P. Kacer
Enantioselective hydrogenation of cyclic imines catalysed by Noyori-Ikariya half-sandwich complexes and their analogues
Chem.Commun., 2016, 52, 362
7118406 CIFC200 H274 Dy18 N18 O135 Zn12C 1 2/c 135.409; 30.501; 31.789
90; 115.52; 90
30983Nikoleta Stavgianoudaki; Milosz Siczek; Tadeusz Lis; Ross Inglis; Constantinos J. Milios
A triacontanuclear [Zn12Dy18] cluster: a ring of [Dy4] cubes
Chem.Commun., 2016, 52, 343
7118407 CIFC16 H13 NP b c a16.7246; 7.1468; 20.102
90; 90; 90
2402.7Kai Chen; Zi-Zhong Zhu; Jia-Xin Liu; Xiang-Ying Tang; Yin Wei; Min Shi
Substrate-controlled Rh(II)-catalyzed single-electron-transfer (SET): divergent synthesis of fused indoles
Chem.Commun., 2016, 52, 350
7118408 CIFC19 H17 N OP 1 21/n 19.2535; 14.994; 10.714
90; 101.697; 90
1455.7Kai Chen; Zi-Zhong Zhu; Jia-Xin Liu; Xiang-Ying Tang; Yin Wei; Min Shi
Substrate-controlled Rh(II)-catalyzed single-electron-transfer (SET): divergent synthesis of fused indoles
Chem.Commun., 2016, 52, 350
7118409 CIFC66 H49 N6 O8 TlP 1 21/n 114.4652; 17.501; 23.3205
90; 91.874; 90
5900.6Victoria Ndoyom; Luca Fusaro; Thierry Roisnel; Stephane Le Gac; Bernard Boitrel
Spontaneous Tl(I)-to-Tl(III) oxidation in dynamic heterobimetallic Hg(II)/Tl(I) porphyrin complexes
Chem.Commun., 2016, 52, 517
7118410 CIFC95.5 H129.25 F12 N3.75 O24 P2C 1 c 131.6051; 13.3823; 24.6753
90; 90.155; 90
10436.4Danyu Xia; Peifa Wei; Bingbing Shi; Feihe Huang
A pillar[6]arene-based [2]pseudorotaxane in solution and in the solid state and its photo-responsive self-assembly behavior in solution
Chem.Commun., 2016, 52, 513
7118411 CIFC19 H18 Eu N3 O10P 1 21 19.7675; 7.1607; 15.8901
90; 107.9; 90
1057.59Hai-Yang Li; Hong Xu; Shuang-Quan Zang; Thomas C. W. Mak
A viologen-functionalized chiral Eu-MOF as a platform for multifunctional switchable material
Chem.Commun., 2016, 52, 525
7118412 CIFC35 H48 F3 Ge N3 O3 SP 1 21/n 111.7454; 24.4796; 13.3037
90; 115.166; 90
3462Bochao Su; Rakesh Ganguly; Yongxin Li; Rei Kinjo
Synthesis, characterization, and electronic structures of a methyl germyliumylidene ion and germylone-group VI metal complexes
Chem.Commun., 2016, 52, 613
7118413 CIFC36 H47 Cr Ge N3 O6P 1 21/c 110.2157; 22.5884; 15.2996
90; 97.648; 90
3499.07Bochao Su; Rakesh Ganguly; Yongxin Li; Rei Kinjo
Synthesis, characterization, and electronic structures of a methyl germyliumylidene ion and germylone-group VI metal complexes
Chem.Commun., 2016, 52, 613
7118414 CIFC36 H47 Ge Mo N3 O6P 1 21/c 110.3172; 22.6231; 15.3939
90; 97.423; 90
3562.9Bochao Su; Rakesh Ganguly; Yongxin Li; Rei Kinjo
Synthesis, characterization, and electronic structures of a methyl germyliumylidene ion and germylone-group VI metal complexes
Chem.Commun., 2016, 52, 613
7118415 CIFC36 H47 Ge N3 O6 WP 1 21/c 110.3691; 22.617; 15.3476
90; 97.055; 90
3572Bochao Su; Rakesh Ganguly; Yongxin Li; Rei Kinjo
Synthesis, characterization, and electronic structures of a methyl germyliumylidene ion and germylone-group VI metal complexes
Chem.Commun., 2016, 52, 613
7118416 CIFC33 H33 N3P -18.299; 12.11; 13.39
76.13; 87.13; 87.08
1304Qitao Tan; Huanhuan Chen; Huaida Xia; Bingxin Liu; Bin Xu
Parent and trisubstituted triazacoronenes: synthesis, crystal structure and physicochemical properties
Chem.Commun., 2016, 52, 537
7118417 CIFC16 H23 F12 N3 Ru Sb2P 1 21/c 18.3829; 18.5671; 17.8534
90; 98.919; 90
2745.21Zhao, Yinsong; He, Zhen; Li, Shiqing; Tang, Junbin; Gao, Ge; Lan, Jingbo; You, Jingsong
An air-stable half-sandwich Ru(II) complex as an efficient catalyst for [3+2] annulation of 2-arylcyclo-2-enones with alkynes.
Chemical communications (Cambridge, England), 2016, 52, 4613-4616
7118418 CIFC20 H18 OP 1 21/c 19.7368; 8.7212; 17.6929
90; 97.34; 90
1490.11Zhao, Yinsong; He, Zhen; Li, Shiqing; Tang, Junbin; Gao, Ge; Lan, Jingbo; You, Jingsong
An air-stable half-sandwich Ru(II) complex as an efficient catalyst for [3+2] annulation of 2-arylcyclo-2-enones with alkynes.
Chemical communications (Cambridge, England), 2016, 52, 4613-4616
7118419 CIFC18 H14 Cl3 N SP -17.7687; 9.4304; 12.8027
101.342; 104.75; 102.507
853.44Yu, Liu-Zhu; Hu, Xu-Bo; Xu, Qin; Shi, Min
Thermally induced formal [3+2] cyclization of ortho-aminoaryl-tethered alkylidenecyclopropanes: facile synthesis of furoquinoline and thienoquinoline derivatives.
Chemical communications (Cambridge, England), 2016, 52, 2701-2704
7118420 CIFC17 H12 Cl N OP -18.277; 8.861; 20.949
78.278; 83.751; 64.58
1358.4Yu, Liu-Zhu; Hu, Xu-Bo; Xu, Qin; Shi, Min
Thermally induced formal [3+2] cyclization of ortho-aminoaryl-tethered alkylidenecyclopropanes: facile synthesis of furoquinoline and thienoquinoline derivatives.
Chemical communications (Cambridge, England), 2016, 52, 2701-2704
7118421 CIFC17 H13 Cl2 N OP -17.7899; 9.516; 11.134
99.138; 97.433; 109.903
751.1Yu, Liu-Zhu; Hu, Xu-Bo; Xu, Qin; Shi, Min
Thermally induced formal [3+2] cyclization of ortho-aminoaryl-tethered alkylidenecyclopropanes: facile synthesis of furoquinoline and thienoquinoline derivatives.
Chemical communications (Cambridge, England), 2016, 52, 2701-2704
7118422 CIFC18 H22 N2 O8 TiP 1 21/n 110.9669; 14.7049; 13.0353
90; 113.016; 90
1934.82Brennan, Bradley J.; Chen, Jeffrey; Rudshteyn, Benjamin; Chaudhuri, Subhajyoti; Mercado, Brandon Q.; Batista, Victor S.; Crabtree, Robert H.; Brudvig, Gary W.
Molecular titanium-hydroxamate complexes as models for TiO2 surface binding.
Chemical communications (Cambridge, England), 2016, 52, 2972-2975
7118423 CIFC54 H72 N6 O21 S6 Ti3R -3 c :H15.7049; 15.7049; 53.457
90; 90; 120
11418.4Brennan, Bradley J.; Chen, Jeffrey; Rudshteyn, Benjamin; Chaudhuri, Subhajyoti; Mercado, Brandon Q.; Batista, Victor S.; Crabtree, Robert H.; Brudvig, Gary W.
Molecular titanium-hydroxamate complexes as models for TiO2 surface binding.
Chemical communications (Cambridge, England), 2016, 52, 2972-2975
7118424 CIFC36 H40 Cl8 N4 O10 Ti2P 1 21/n 112.1927; 10.0654; 19.3484
90; 102.042; 90
2322.3Brennan, Bradley J.; Chen, Jeffrey; Rudshteyn, Benjamin; Chaudhuri, Subhajyoti; Mercado, Brandon Q.; Batista, Victor S.; Crabtree, Robert H.; Brudvig, Gary W.
Molecular titanium-hydroxamate complexes as models for TiO2 surface binding.
Chemical communications (Cambridge, England), 2016, 52, 2972-2975
7118425 CIFC24 O25 Zn4R -3 m :H18.2657; 18.2657; 22.3708
90; 90; 120
6463.8Bai, Linyi; Tu, Binbin; Qi, Yi; Gao, Qiang; Liu, Dong; Liu, Zhizhou; Zhao, Lingzhi; Li, Qiaowei; Zhao, Yanli
Enhanced performance in gas adsorption and Li ion batteries by docking Li(+) in a crown ether-based metal-organic framework.
Chemical communications (Cambridge, England), 2016, 52, 3003-3006
7118426 CIFC99 H152 Ge2 Si4P -116.3223; 17.6076; 18.3797
71.478; 77.643; 67.458
4600.3Nieder, David; Yildiz, Cem B.; Jana, Anukul; Zimmer, Michael; Huch, Volker; Scheschkewitz, David
Dimerization of a marginally stable disilenyl germylene to tricyclic systems: evidence for reversible NHC-coordination.
Chemical communications (Cambridge, England), 2016, 52, 2799-2802
7118427 CIFC95.5 H152 Ge2 Si4C 1 2/c 133.8499; 26.2285; 20.2919
90; 97.911; 90
17844.3Nieder, David; Yildiz, Cem B.; Jana, Anukul; Zimmer, Michael; Huch, Volker; Scheschkewitz, David
Dimerization of a marginally stable disilenyl germylene to tricyclic systems: evidence for reversible NHC-coordination.
Chemical communications (Cambridge, England), 2016, 52, 2799-2802
7118428 CIFC22 H18 F3 N O2P 1 21/c 113.9588; 8.5515; 16.218
90; 104.782; 90
1871.8Jiang, Quanbin; Guo, Tenglong; Wu, Kaikai; Yu, Zhengkun
Rhodium(iii)-catalyzed sp(2) C-H bond addition to CF3-substituted unsaturated ketones.
Chemical communications (Cambridge, England), 2016, 52, 2913-2915
7118429 CIFC18 H32 N O6 SiP 21 21 216.826; 9.791; 30.82
90; 90; 90
2059.8Jian-Liang Ye; Yang Liu; Zhi-Ping Yang; Pei-Qiang Huang
The asymmetric total synthesis of (+)-N-acetyl norloline
Chem.Commun., 2016, 52, 561
7118430 CIFC24 H21 B F2 N4P -18.4892; 8.7454; 14.2585
83.179; 79.851; 84.564
1031.68Dan Wu; Li Shao; Yang Li; Qinglian Hu; Feihe Huang; Guocan Yu; Guping Tang
A boron difluoride dye showing the aggregation-induced emission feature and high sensitivity to intra- and extra-cellular pH changes
Chem.Commun., 2016, 52, 541
7118431 CIFC43 H52 Ni P2 SiP 1 21/c 120.474; 22.468; 17.673
90; 110.92; 90
7594LaPierre, Etienne A.; Piers, Warren E.; Spasyuk, Denis M.; Bi, David W.
Activation of Si-H bonds across the nickel carbene bond in electron rich nickel PCcarbeneP pincer complexes.
Chemical communications (Cambridge, England), 2016, 52, 1361-1364
7118432 CIFC46 H58 Ni P2 SiP 1 21/c 115.1784; 13.3439; 21.4058
90; 110.73; 90
4054.82LaPierre, Etienne A.; Piers, Warren E.; Spasyuk, Denis M.; Bi, David W.
Activation of Si-H bonds across the nickel carbene bond in electron rich nickel PCcarbeneP pincer complexes.
Chemical communications (Cambridge, England), 2016, 52, 1361-1364
7118433 CIFC46 H58 Ni O3 P2 SiP 1 21/c 115.514; 13.3974; 21.723
90; 112.905; 90
4159.06LaPierre, Etienne A.; Piers, Warren E.; Spasyuk, Denis M.; Bi, David W.
Activation of Si-H bonds across the nickel carbene bond in electron rich nickel PCcarbeneP pincer complexes.
Chemical communications (Cambridge, England), 2016, 52, 1361-1364
7118434 CIFC33 H48 Ni P2 SiP 1 21/c 118.2625; 8.1482; 21.5259
90; 93.717; 90
3196.5LaPierre, Etienne A.; Piers, Warren E.; Spasyuk, Denis M.; Bi, David W.
Activation of Si-H bonds across the nickel carbene bond in electron rich nickel PCcarbeneP pincer complexes.
Chemical communications (Cambridge, England), 2016, 52, 1361-1364
7118435 CIFC31 H42 Ni O P2C 1 2/c 130.7146; 10.0835; 20.284
90; 114.295; 90
5725.82LaPierre, Etienne A.; Piers, Warren E.; Spasyuk, Denis M.; Bi, David W.
Activation of Si-H bonds across the nickel carbene bond in electron rich nickel PCcarbeneP pincer complexes.
Chemical communications (Cambridge, England), 2016, 52, 1361-1364
7118436 CIFC43 H52 Ni P2 SiP 21 21 2112.91; 15.492; 19.254
90; 90; 90
3850.8LaPierre, Etienne A.; Piers, Warren E.; Spasyuk, Denis M.; Bi, David W.
Activation of Si-H bonds across the nickel carbene bond in electron rich nickel PCcarbeneP pincer complexes.
Chemical communications (Cambridge, England), 2016, 52, 1361-1364
7118437 CIFC20 H24 Fe N5 O3 SP -18.394; 9.35; 13.675
82.26; 73.44; 82.14
1013.9Phonsri, Wasinee; Martinez, Victor; Davies, Casey G.; Jameson, Guy N. L.; Moubaraki, Boujemaa; Murray, Keith S.
Ligand effects in a heteroleptic bis-tridentate iron(iii) spin crossover complex showing a very high T1/2 value.
Chemical communications (Cambridge, England), 2016, 52, 1443-1446
7118438 CIFC30 H17 B F13 O3 P SP 1 21/c 110.0309; 16.5754; 17.784
90; 96.069; 90
2940.3Yu, Jiangang; Kehr, Gerald; Daniliuc, Constantin G.; Erker, Gerhard
Cooperative reaction chemistry derived from a borata-diene framework.
Chemical communications (Cambridge, England), 2016, 52, 1393-1396
7118439 CIFC29 H18 B F10 PP -111.8789; 12.5298; 12.6592
61.284; 72.907; 67.981
1516.86Yu, Jiangang; Kehr, Gerald; Daniliuc, Constantin G.; Erker, Gerhard
Cooperative reaction chemistry derived from a borata-diene framework.
Chemical communications (Cambridge, England), 2016, 52, 1393-1396
7118440 CIFC41 H19 B2 F20 PP 1 21/c 112.7173; 24.4025; 16.3076
90; 111.724; 90
4701.4Yu, Jiangang; Kehr, Gerald; Daniliuc, Constantin G.; Erker, Gerhard
Cooperative reaction chemistry derived from a borata-diene framework.
Chemical communications (Cambridge, England), 2016, 52, 1393-1396
7118441 CIFC41 H19 B2 F20 PC 1 2/c 124.6726; 20.3084; 19.6095
90; 124.093; 90
8136.8Yu, Jiangang; Kehr, Gerald; Daniliuc, Constantin G.; Erker, Gerhard
Cooperative reaction chemistry derived from a borata-diene framework.
Chemical communications (Cambridge, England), 2016, 52, 1393-1396
7118442 CIFC48 H25 B2 F20 O PP 1 21/n 113.2593; 22.2116; 19.2412
90; 101.101; 90
5560.7Yu, Jiangang; Kehr, Gerald; Daniliuc, Constantin G.; Erker, Gerhard
Cooperative reaction chemistry derived from a borata-diene framework.
Chemical communications (Cambridge, England), 2016, 52, 1393-1396
7118443 CIFC42 H19 B2 F20 O PP -111.3678; 11.6324; 16.8035
70.245; 82.445; 79.967
2052.93Yu, Jiangang; Kehr, Gerald; Daniliuc, Constantin G.; Erker, Gerhard
Cooperative reaction chemistry derived from a borata-diene framework.
Chemical communications (Cambridge, England), 2016, 52, 1393-1396
7118444 CIFC15 H21 N O SP 1 21/n 18.24752; 12.7555; 13.60131
90; 100.427; 90
1407.24Rayner, Peter J.; Smith, Joshua C.; Denneval, Charline; O'Brien, Peter; Clarke, Paul A.; Horan, Richard A. J.
Mechanistic interrogation of the asymmetric lithiation-trapping of N-thiopivaloyl azetidine and pyrrolidine.
Chemical communications (Cambridge, England), 2016, 52, 1354-1357
7118445 CIFC15 H21 N O SP 21 21 217.0524; 17.7693; 22.6194
90; 90; 90
2834.6Rayner, Peter J.; Smith, Joshua C.; Denneval, Charline; O'Brien, Peter; Clarke, Paul A.; Horan, Richard A. J.
Mechanistic interrogation of the asymmetric lithiation-trapping of N-thiopivaloyl azetidine and pyrrolidine.
Chemical communications (Cambridge, England), 2016, 52, 1354-1357
7118446 CIFC10 H17 N O2 SP 21 21 216.51691; 11.9691; 29.6051
90; 90; 90
2309.24Rayner, Peter J.; Smith, Joshua C.; Denneval, Charline; O'Brien, Peter; Clarke, Paul A.; Horan, Richard A. J.
Mechanistic interrogation of the asymmetric lithiation-trapping of N-thiopivaloyl azetidine and pyrrolidine.
Chemical communications (Cambridge, England), 2016, 52, 1354-1357
7118447 CIFC9 H15 N O2 SP 1 21 19.6985; 6.50545; 17.186
90; 94.266; 90
1081.31Rayner, Peter J.; Smith, Joshua C.; Denneval, Charline; O'Brien, Peter; Clarke, Paul A.; Horan, Richard A. J.
Mechanistic interrogation of the asymmetric lithiation-trapping of N-thiopivaloyl azetidine and pyrrolidine.
Chemical communications (Cambridge, England), 2016, 52, 1354-1357
7118448 CIFC14 H10 Cl F3 N2 O3 SP 21 21 2110.2939; 10.7278; 14.0751
90; 90; 90
1554.33Hou, Xuhe; Ma, Hongli; Zhang, Zhenhua; Xie, Lei; Qin, Zhaohai; Fu, Bin
An efficient approach for the construction of trifluoromethylated all-carbon quaternary stereocenters: enantioselective Ni(ii)-catalyzed Michael addition of 2-acetyl azaarene to β,β-disubstituted nitroalkenes.
Chemical communications (Cambridge, England), 2016, 52, 1470-1473
7118449 CIFC44 H63 Cl3 N2 O0.5 P2C 1 2/c 127.4838; 17.6558; 21.9216
90; 118.269; 90
9368.7Schwedtmann, Kai; Holthausen, Michael H.; Sala, Chris H.; Hennersdorf, Felix; Fröhlich, Roland; Weigand, Jan J.
[((Cl)Im(Dipp))P[double bond, length as m-dash]P(Dipp)][GaCl4]: a polarized, cationic diphosphene.
Chemical communications (Cambridge, England), 2016, 52, 1409-1412
7118450 CIFC45 H56 Cl6 F Ga N2 P2P 1 21/c 110.7484; 13.6179; 33.6481
90; 94.25; 90
4911.6Schwedtmann, Kai; Holthausen, Michael H.; Sala, Chris H.; Hennersdorf, Felix; Fröhlich, Roland; Weigand, Jan J.
[((Cl)Im(Dipp))P[double bond, length as m-dash]P(Dipp)][GaCl4]: a polarized, cationic diphosphene.
Chemical communications (Cambridge, England), 2016, 52, 1409-1412
7118451 CIFC53 H61 Cl3 F7 N2 O3 P2 SP 1 21/c 112.2639; 12.5384; 36.3192
90; 99.262; 90
5511.98Schwedtmann, Kai; Holthausen, Michael H.; Sala, Chris H.; Hennersdorf, Felix; Fröhlich, Roland; Weigand, Jan J.
[((Cl)Im(Dipp))P[double bond, length as m-dash]P(Dipp)][GaCl4]: a polarized, cationic diphosphene.
Chemical communications (Cambridge, England), 2016, 52, 1409-1412
7118452 CIFC42 H60 Cl6 Ga N2 P3P -113.8028; 17.4286; 21.7529
107.609; 98.701; 97.42
4844.6Schwedtmann, Kai; Holthausen, Michael H.; Sala, Chris H.; Hennersdorf, Felix; Fröhlich, Roland; Weigand, Jan J.
[((Cl)Im(Dipp))P[double bond, length as m-dash]P(Dipp)][GaCl4]: a polarized, cationic diphosphene.
Chemical communications (Cambridge, England), 2016, 52, 1409-1412
7118457 CIFC34 H33 Br N2 O7P 19.5019; 10.4381; 18.819
93.77; 102.375; 116.062
1610.3Zhang, Zhenhua; Sun, Wangsheng; Zhu, Gongming; Yang, Junxian; Zhang, Ming; Hong, Liang; Wang, Rui
Chiral phosphoric acid catalyzed enantioselective 1,3-dipolar cycloaddition reaction of azlactones.
Chemical communications (Cambridge, England), 2016, 52, 1377-1380
7118458 CIFC150 H116 Cl2 Cu3 La6 N12 O56P 63 2 213.008; 13.008; 50.2913
90; 90; 120
7369.6Fang, Wei-Hui; Zhang, Lei; Zhang, Jian; Yang, Guo-Yu
Halogen dependent symmetry change in two series of wheel cluster organic frameworks built from La18 tertiary building units.
Chemical communications (Cambridge, England), 2016, 52, 1455-1457
7118459 CIFC150 H101 Br3 Cu4 La6 N12 O39P -3 c 113.0109; 13.0109; 51.3152
90; 90; 120
7523Fang, Wei-Hui; Zhang, Lei; Zhang, Jian; Yang, Guo-Yu
Halogen dependent symmetry change in two series of wheel cluster organic frameworks built from La18 tertiary building units.
Chemical communications (Cambridge, England), 2016, 52, 1455-1457
7118460 CIFC150 H101 Cu4 I3 La6 N12 O39P -3 c 113.0142; 13.0142; 51.3233
90; 90; 120
7528Fang, Wei-Hui; Zhang, Lei; Zhang, Jian; Yang, Guo-Yu
Halogen dependent symmetry change in two series of wheel cluster organic frameworks built from La18 tertiary building units.
Chemical communications (Cambridge, England), 2016, 52, 1455-1457
7118461 CIFC77.5 H46 O10.5P 1 21/c 117.323; 22.428; 15.591
90; 95.051; 90
6033.9Suzuki, Akira; Kondo, Kei; Sei, Yoshihisa; Akita, Munetaka; Yoshizawa, Michito
A fluorescent molecular capsule with a flexible polyaromatic shell for the detection of monoterpene compounds in water.
Chemical communications (Cambridge, England), 2016, 52, 3151-3154
7118462 CIFC25 H31 N3 O4P b c a9.302; 15.8206; 32.7189
90; 90; 90
4815Diedrich, D.; Hamacher, A.; Gertzen, C. G. W.; Alves Avelar, L. A.; Reiss, G. J.; Kurz, T.; Gohlke, H.; Kassack, M. U.; Hansen, F. K.
Rational design and diversity-oriented synthesis of peptoid-based selective HDAC6 inhibitors.
Chemical communications (Cambridge, England), 2016, 52, 3219-3222
7118463 CIFC14 H20 F3 N O3P b c a7.7764; 15.755; 25.521
90; 90; 90
3126.8Yagafarov, Niyaz Z.; Kolesnikov, Pavel N.; Usanov, Dmitry L.; Novikov, Valentin V.; Nelyubina, Yulia V.; Chusov, Denis
The synthesis of sterically hindered amines by a direct reductive amination of ketones.
Chemical communications (Cambridge, England), 2016, 52, 1397-1400
7118464 CIFC90 H72 B2 N8 O6P -114.124; 15.235; 17.465
87.755; 69.97; 89.95
3527.8Copley, Graeme; Oh, Juwon; Yoshida, Kota; Shimizu, Daiki; Kim, Dongho; Osuka, Atsuhiro
Intramolecular electron transfer reactions in meso-(4-nitrophenyl)-substituted subporphyrins.
Chemical communications (Cambridge, England), 2016, 52, 1424-1427
7118465 CIFC104 H100 Cd2 N8 O13.63 V2P 2 2 2117.046; 24.0462; 28.8442
90; 90; 90
11823Bhunia, Asamanjoy; Dey, Subarna; Moreno, José María; Diaz, Urbano; Concepcion, Patricia; Van Hecke, Kristof; Janiak, Christoph; Van Der Voort, Pascal
A homochiral vanadium-salen based cadmium bpdc MOF with permanent porosity as an asymmetric catalyst in solvent-free cyanosilylation.
Chemical communications (Cambridge, England), 2016, 52, 1401-1404
7118466 CIFC27 H27 N3 O4 S2P -19.8347; 10.7763; 13.371
77.323; 76.332; 67.333
1257.5Chen, Yu-Ling; Sharma, Pankaj; Liu, Rai-Shung
Sulfonamide-directed gold-catalyzed [2+2+2]-cycloadditions of nitriles with two discrete ynamides to construct 2,4-diaminopyridine cores.
Chemical communications (Cambridge, England), 2016, 52, 3187-3190
7118478 CIFC60 H90 Li2 O12 ThR -3 :H14.8737; 14.8737; 24.3175
90; 90; 120
4658.9Elizabeth A. Pedrick; Peter Hrobarik; Lani A. Seaman; Guang Wu; Trevor W. Hayton
Synthesis, structure and bonding of hexaphenyl thorium(IV): observation of a non-octahedral structure
Chem.Commun., 2016, 52, 689
7118479 CIFC60 H78 Li2 O10 ThP 1 21/n 116.5641; 16.7043; 21.3854
90; 108.682; 90
5605.4Elizabeth A. Pedrick; Peter Hrobarik; Lani A. Seaman; Guang Wu; Trevor W. Hayton
Synthesis, structure and bonding of hexaphenyl thorium(IV): observation of a non-octahedral structure
Chem.Commun., 2016, 52, 689
7118480 CIFC36 H26 Br2 O4P 21 21 215.6288; 12.578; 41.669
90; 90; 90
2950.1Zhan-Yong Wang; Ya-Li Ding; Gang Wang; Ying Cheng
Chiral N-heterocyclic carbene/Lewis acid cooperative catalysis of the reaction of 2-aroylvinylcinnamaldehydes: a switch of the reaction pathway by Lewis acid activation
Chem.Commun., 2016, 52, 788
7118481 CIFC36 H28 O4P 21 21 219.263; 12.8186; 22.369
90; 90; 90
2656.1Zhan-Yong Wang; Ya-Li Ding; Gang Wang; Ying Cheng
Chiral N-heterocyclic carbene/Lewis acid cooperative catalysis of the reaction of 2-aroylvinylcinnamaldehydes: a switch of the reaction pathway by Lewis acid activation
Chem.Commun., 2016, 52, 788
7118482 CIFC36 H26 Br2 O4P 21 21 215.5911; 13.004; 40.623
90; 90; 90
2953.6Zhan-Yong Wang; Ya-Li Ding; Gang Wang; Ying Cheng
Chiral N-heterocyclic carbene/Lewis acid cooperative catalysis of the reaction of 2-aroylvinylcinnamaldehydes: a switch of the reaction pathway by Lewis acid activation
Chem.Commun., 2016, 52, 788
7118484 CIFC19 H21 N3C 1 2/c 121.0859; 8.8941; 8.6908
90; 110.448; 90
1527.18Hong, Seung Youn; Kwak, Jaesung; Chang, Sukbok
Rhodium-catalyzed selective CH functionalization of NNN tridentate chelating compounds via a rollover pathway.
Chemical communications (Cambridge, England), 2016, 52, 3159-3162
7118485 CIFC31 H39 N3C 1 2/c 130.5673; 9.9939; 8.7408
90; 106.271; 90
2563.2Hong, Seung Youn; Kwak, Jaesung; Chang, Sukbok
Rhodium-catalyzed selective CH functionalization of NNN tridentate chelating compounds via a rollover pathway.
Chemical communications (Cambridge, England), 2016, 52, 3159-3162
7118486 CIFC15 H15 Cl N2 OP 21 21 216.0936; 8.4244; 26.374
90; 90; 90
1353.9Feng, Qi; Li, Yuanyuan; Wang, Lili; Li, Chen; Wang, Jinmin; Liu, Yuanyuan; Li, Kai; Hou, Hongwei
Multiple-color aggregation-induced emission (AIE) molecules as chemodosimeters for pH sensing.
Chemical communications (Cambridge, England), 2016, 52, 3123-3126
7118487 CIFC16 H18 N2 O2P 1 21/c 114.9189; 5.968; 20.9971
90; 130.968; 90
1411.6Feng, Qi; Li, Yuanyuan; Wang, Lili; Li, Chen; Wang, Jinmin; Liu, Yuanyuan; Li, Kai; Hou, Hongwei
Multiple-color aggregation-induced emission (AIE) molecules as chemodosimeters for pH sensing.
Chemical communications (Cambridge, England), 2016, 52, 3123-3126
7118488 CIFC15 H16 N2 OP b c a11.278; 8.2043; 27.475
90; 90; 90
2542.2Feng, Qi; Li, Yuanyuan; Wang, Lili; Li, Chen; Wang, Jinmin; Liu, Yuanyuan; Li, Kai; Hou, Hongwei
Multiple-color aggregation-induced emission (AIE) molecules as chemodosimeters for pH sensing.
Chemical communications (Cambridge, England), 2016, 52, 3123-3126
7118489 CIFC78 H121 Cu6 N17 O54P 4/m n c26.956; 26.956; 39.145
90; 90; 90
28444Liu, Bing; Yao, Shuo; Shi, Chao; Li, Guanghua; Huo, Qisheng; Liu, Yunling
Significant enhancement of gas uptake capacity and selectivity via the judicious increase of open metal sites and Lewis basic sites within two polyhedron-based metal-organic frameworks.
Chemical communications (Cambridge, England), 2016, 52, 3223-3226
7118490 CIFC87 H126 Cu6 N20 O48P 4/m n c27.405; 27.405; 39.362
90; 90; 90
29562Liu, Bing; Yao, Shuo; Shi, Chao; Li, Guanghua; Huo, Qisheng; Liu, Yunling
Significant enhancement of gas uptake capacity and selectivity via the judicious increase of open metal sites and Lewis basic sites within two polyhedron-based metal-organic frameworks.
Chemical communications (Cambridge, England), 2016, 52, 3223-3226
7118491 CIFC3 H18 Bi2 I9 N3P 63/m m c8.5843; 8.5843; 21.69
90; 90; 120
1384.2Eckhardt, Kai; Bon, Volodymyr; Getzschmann, Jürgen; Grothe, Julia; Wisser, Florian M.; Kaskel, Stefan
Crystallographic insights into (CH3NH3)3(Bi2I9): a new lead-free hybrid organic-inorganic material as a potential absorber for photovoltaics.
Chemical communications (Cambridge, England), 2016, 52, 3058-3060
7118492 CIFC18 H12 O4C 1 2/c 121.876; 22.174; 15.3753
90; 130.23; 90
5694Reddy, Baddigam Kiran; Gadekar, Santosh C.; Anand, Venkataramanarao G.
The synthesis and characterization of the meso-meso linked antiaromatic tetraoxa isophlorin dimer.
Chemical communications (Cambridge, England), 2016, 52, 3007-3009
7118493 CIFC98 H14 F10 O4F d d 235.203; 55.389; 12.2274
90; 90; 90
23842Reddy, Baddigam Kiran; Gadekar, Santosh C.; Anand, Venkataramanarao G.
The synthesis and characterization of the meso-meso linked antiaromatic tetraoxa isophlorin dimer.
Chemical communications (Cambridge, England), 2016, 52, 3007-3009
7118494 CIFC84.86 H11.14 F8.57 O3.43F d -357.756; 57.756; 57.756
90; 90; 90
192660Reddy, Baddigam Kiran; Gadekar, Santosh C.; Anand, Venkataramanarao G.
The synthesis and characterization of the meso-meso linked antiaromatic tetraoxa isophlorin dimer.
Chemical communications (Cambridge, England), 2016, 52, 3007-3009
7118495 CIFC18 H19 N O3P 1 21/n 19.6614; 9.005; 18.1004
90; 91.9684; 90
1573.82Ramakrishna, Isai; Sahoo, Harekrishna; Baidya, Mahiuddin
Brønsted acid mediated N-O bond cleavage for α-amination of ketones through the aromatic nitroso aldol reaction.
Chemical communications (Cambridge, England), 2016, 52, 3215-3218
7118496 CIFC17 H16 N2 SP 1 21/c 19.0979; 9.836; 17.0069
90; 102.321; 90
1486.84Ramakrishna, Isai; Sahoo, Harekrishna; Baidya, Mahiuddin
Brønsted acid mediated N-O bond cleavage for α-amination of ketones through the aromatic nitroso aldol reaction.
Chemical communications (Cambridge, England), 2016, 52, 3215-3218
7118497 CIFC16 H16 Br N OP 1 21/n 112.4037; 9.4552; 13.0281
90; 100.594; 90
1501.88Ramakrishna, Isai; Sahoo, Harekrishna; Baidya, Mahiuddin
Brønsted acid mediated N-O bond cleavage for α-amination of ketones through the aromatic nitroso aldol reaction.
Chemical communications (Cambridge, England), 2016, 52, 3215-3218
7118498 CIFC15 H15 N OP 1 21/n 18.9551; 9.4163; 14.8711
90; 95.037; 90
1249.15Ramakrishna, Isai; Sahoo, Harekrishna; Baidya, Mahiuddin
Brønsted acid mediated N-O bond cleavage for α-amination of ketones through the aromatic nitroso aldol reaction.
Chemical communications (Cambridge, England), 2016, 52, 3215-3218
7118499 CIFC61 H52 B F8 N4 O10 Ru2 S2C 1 2/c 124.5419; 22.54; 25.4485
90; 111.767; 90
13073.7Gupta, Gajendra; Das, Abhishek; Ghate, Nikhil Baban; Kim, Takhyeon; Ryu, Ji Yeon; Lee, Junseong; Mandal, Nripendranath; Lee, Chang Yeon
Novel BODIPY-based Ru(ii) and Ir(iii) metalla-rectangles: cellular localization of compounds and their antiproliferative activities.
Chemical communications (Cambridge, England), 2016, 52, 4274-4277
7118500 CIFC126.67 B2 F8 N8 O12.67 Ru4 S2P -124.488; 24.507; 25.043
60.821; 61.007; 60.124
10782Gupta, Gajendra; Das, Abhishek; Ghate, Nikhil Baban; Kim, Takhyeon; Ryu, Ji Yeon; Lee, Junseong; Mandal, Nripendranath; Lee, Chang Yeon
Novel BODIPY-based Ru(ii) and Ir(iii) metalla-rectangles: cellular localization of compounds and their antiproliferative activities.
Chemical communications (Cambridge, England), 2016, 52, 4274-4277
7118501 CIFC67 H75 B F5 Ir2 N4 O9 SP 1 21/n 120.4184; 19.7746; 20.8298
90; 113.735; 90
7699Gupta, Gajendra; Das, Abhishek; Ghate, Nikhil Baban; Kim, Takhyeon; Ryu, Ji Yeon; Lee, Junseong; Mandal, Nripendranath; Lee, Chang Yeon
Novel BODIPY-based Ru(ii) and Ir(iii) metalla-rectangles: cellular localization of compounds and their antiproliferative activities.
Chemical communications (Cambridge, England), 2016, 52, 4274-4277
7118502 CIFC24 H17 Br O3P -19.703; 10.0809; 11.7856
68.569; 80.101; 67.458
990.43Wu, Jiaping; Wang, Dongxu; Wan, Yanjun; Ma, Cheng
Rhodium-catalyzed tunable oxidative cyclization toward the selective synthesis of α-pyrones and furans.
Chemical communications (Cambridge, England), 2016, 52, 1661-1664
7118503 CIFC22 H20 O5P 1 21/c 110.9313; 18.7544; 9.2937
90; 105.181; 90
1838.8Wu, Jiaping; Wang, Dongxu; Wan, Yanjun; Ma, Cheng
Rhodium-catalyzed tunable oxidative cyclization toward the selective synthesis of α-pyrones and furans.
Chemical communications (Cambridge, England), 2016, 52, 1661-1664
7118504 CIFC20 H20 O3 SP 21 21 219.2716; 11.6329; 17.2262
90; 90; 90
1857.94Wu, Jiaping; Wang, Dongxu; Wan, Yanjun; Ma, Cheng
Rhodium-catalyzed tunable oxidative cyclization toward the selective synthesis of α-pyrones and furans.
Chemical communications (Cambridge, England), 2016, 52, 1661-1664
7118505 CIFC1.33 H9.77 Al B5 N1.33 O10.88P 6321.4013; 21.4013; 7.1696
90; 90; 120
2843.8Cao, Gao-Juan; Wei, Qi; Cheng, Jian-Wen; Cheng, Lin; Yang, Guo-Yu
A zeolite CAN-type aluminoborate with gigantic 24-ring channels.
Chemical communications (Cambridge, England), 2016, 52, 1729-1732
7118506 CIFC38 H43 Cl3 O8C 1 2/c 128.118; 14.1732; 19.5603
90; 106.288; 90
7482.3Zhou, Jiong; Yang, Jie; Hua, Bin; Shao, Li; Zhang, Zhihua; Yu, Guocan
The synthesis, structure, and molecular recognition properties of a [2]calix[1]biphenyl-type hybrid[3]arene.
Chemical communications (Cambridge, England), 2016, 52, 1622-1624
7118507 CIFC34 H40 Cl2 F3 Ir2 N5 O3 SP 1 21/n 114.4786; 11.9118; 21.7475
90; 98.8187; 90
3706.37Valencia, Marta; Müller-Bunz, Helge; Gossage, Robert A.; Albrecht, Martin
Enhanced product selectivity promoted by remote metal coordination in acceptor-free alcohol dehydrogenation catalysis.
Chemical communications (Cambridge, England), 2016, 52, 3344-3347
7118508 CIFC25 H27 Cl F6 Ir N5 O6 S2P 1 21/n 114.4611; 8.8412; 24.209
90; 94.954; 90
3083.6Valencia, Marta; Müller-Bunz, Helge; Gossage, Robert A.; Albrecht, Martin
Enhanced product selectivity promoted by remote metal coordination in acceptor-free alcohol dehydrogenation catalysis.
Chemical communications (Cambridge, England), 2016, 52, 3344-3347
7118509 CIFC110 H78 N4 O56 S6 U8P 1 21/n 123.831; 20.716; 29.555
90; 90.75; 90
14590An, Shu-Wen; Mei, Lei; Hu, Kong-Qiu; Xia, Chuan-Qin; Chai, Zhi-Fang; Shi, Wei-Qun
The templated synthesis of a unique type of tetra-nuclear uranyl-mediated two-fold interpenetrating uranyl-organic framework.
Chemical communications (Cambridge, England), 2016, 52, 1641-1644
7118510 CIFC55 H29 N2 O28 S3 U4P -110.523; 11.866; 29.288
90.81; 92.91; 92.71
3647.8An, Shu-Wen; Mei, Lei; Hu, Kong-Qiu; Xia, Chuan-Qin; Chai, Zhi-Fang; Shi, Wei-Qun
The templated synthesis of a unique type of tetra-nuclear uranyl-mediated two-fold interpenetrating uranyl-organic framework.
Chemical communications (Cambridge, England), 2016, 52, 1641-1644
7118511 CIFC42 H37 Cl3 N2 PtP 1 21/c 113.9571; 14.1969; 18.5023
90; 102.735; 90
3576Juliá, Fabio; Bautista, Delia; González-Herrero, Pablo
Developing strongly luminescent platinum(iv) complexes: facile synthesis of bis-cyclometalated neutral emitters.
Chemical communications (Cambridge, England), 2016, 52, 1657-1660
7118512 CIFC25 H23 Cl N2 O2 PtP 1 21/n 110.0073; 21.4773; 11.0633
90; 109.939; 90
2235.3Juliá, Fabio; Bautista, Delia; González-Herrero, Pablo
Developing strongly luminescent platinum(iv) complexes: facile synthesis of bis-cyclometalated neutral emitters.
Chemical communications (Cambridge, England), 2016, 52, 1657-1660
7118513 CIFC23 H19 Cl N2 PtF d d 226.587; 40.68; 6.9773
90; 90; 90
7546.4Juliá, Fabio; Bautista, Delia; González-Herrero, Pablo
Developing strongly luminescent platinum(iv) complexes: facile synthesis of bis-cyclometalated neutral emitters.
Chemical communications (Cambridge, England), 2016, 52, 1657-1660
7118514 CIFC23 H15 Cl F4 N2 PtP -18.87; 10.7659; 12.1232
99.7042; 109.505; 104.886
1012.69Juliá, Fabio; Bautista, Delia; González-Herrero, Pablo
Developing strongly luminescent platinum(iv) complexes: facile synthesis of bis-cyclometalated neutral emitters.
Chemical communications (Cambridge, England), 2016, 52, 1657-1660
7118515 CIFC44 H32 F18 N9 P3 RuP -18.81; 14.662; 22.745
101.843; 100.698; 101.743
2734.9Gupta, Suraj K.; Choudhury, Joyanta
A remote coordination booster enhances the catalytic efficiency by accelerating the generation of an active catalyst.
Chemical communications (Cambridge, England), 2016, 52, 3384-3387
7118516 CIFC55 H46 F21 N14 O3 P3 Ru2 SP -18.7665; 12.4009; 37.66
81.692; 84.839; 78.866
3966.8Gupta, Suraj K.; Choudhury, Joyanta
A remote coordination booster enhances the catalytic efficiency by accelerating the generation of an active catalyst.
Chemical communications (Cambridge, England), 2016, 52, 3384-3387
7118517 CIFC21 H15 F2 N OP 1 21 15.498; 9.083; 16.538
90; 92.524; 90
825.1Wan, Wen; Ma, Guobin; Li, Jialiang; Chen, Yunrong; Hu, Qingyang; Li, Minjie; Jiang, Haizhen; Deng, Hongmei; Hao, Jian
Silver-catalyzed oxidative decarboxylation of difluoroacetates: efficient access to C-CF2 bond formation.
Chemical communications (Cambridge, England), 2016, 52, 1598-1601
7118518 CIFC34 H28 Cl2 N2 P2 ZnC 1 2/c 121.6754; 11.3153; 12.8588
90; 102.895; 90
3074.26Donovan, Elizabeth S.; Barry, Brian M.; Larsen, Christopher A.; Wirtz, Melissa N.; Geiger, William E.; Kemp, Richard A.
Facilitated carbon dioxide reduction using a Zn(ii) complex.
Chemical communications (Cambridge, England), 2016, 52, 1685-1688
7118519 CIFC36 H34 Cl4 N4 O P2 Zn2P 1 21/c 116.0669; 12.254; 19.5763
90; 98.966; 90
3807.2Donovan, Elizabeth S.; Barry, Brian M.; Larsen, Christopher A.; Wirtz, Melissa N.; Geiger, William E.; Kemp, Richard A.
Facilitated carbon dioxide reduction using a Zn(ii) complex.
Chemical communications (Cambridge, England), 2016, 52, 1685-1688
7118520 CIFC95 H124 B4 Ge2 N4 O5P -112.1574; 16.907; 23.516
110.972; 94.49; 95.764
4456.5Wu, Yile; Liu, Liu; Su, Jue; Yan, Kaili; Zhu, Jun; Zhao, Yufen
Synthesis of digermylene-stabilized linear tetraboronate and boroxine.
Chemical communications (Cambridge, England), 2016, 52, 1582-1585
7118521 CIFC67 H95 B3 Ge2 N4 O5P 1 21 113.192; 24.045; 13.298
90; 93.46; 90
4210Wu, Yile; Liu, Liu; Su, Jue; Yan, Kaili; Zhu, Jun; Zhao, Yufen
Synthesis of digermylene-stabilized linear tetraboronate and boroxine.
Chemical communications (Cambridge, England), 2016, 52, 1582-1585
7118522 CIFC41 H51 B Ge N2 O2P 1 21/c 113.605; 14.004; 19.843
90; 90.69; 90
3780Wu, Yile; Liu, Liu; Su, Jue; Yan, Kaili; Zhu, Jun; Zhao, Yufen
Synthesis of digermylene-stabilized linear tetraboronate and boroxine.
Chemical communications (Cambridge, England), 2016, 52, 1582-1585
7118523 CIFC69 H75 F24 N16 O2 P4 Pd2P 1 21/n 115.8294; 31.0399; 16.1007
90; 92.257; 90
7904.8Gazvoda, Martin; Virant, Miha; Pevec, Andrej; Urankar, Damijana; Bolje, Aljoša; Kočevar, Marijan; Košmrlj, Janez
A mesoionic bis(Py-tzNHC) palladium(ii) complex catalyses "green" Sonogashira reaction through an unprecedented mechanism.
Chemical communications (Cambridge, England), 2016, 52, 1571-1574
7118524 CIFC32 H31 B F4 N8 O2 PdI b c a16.4014; 19.0245; 41.5572
90; 90; 90
12967Gazvoda, Martin; Virant, Miha; Pevec, Andrej; Urankar, Damijana; Bolje, Aljoša; Kočevar, Marijan; Košmrlj, Janez
A mesoionic bis(Py-tzNHC) palladium(ii) complex catalyses "green" Sonogashira reaction through an unprecedented mechanism.
Chemical communications (Cambridge, England), 2016, 52, 1571-1574
7118525 CIFC23 H19 Cl N2 OP 1 21/c 111.925; 23.667; 7.039
90; 99.498; 90
1959.4Roy, Tony; Thangaraj, Manikandan; Gonnade, Rajesh G.; Biju, Akkattu T.
Synthesis of functionalized amino epoxides by a three-component coupling involving aziridines, arynes and aldehydes.
Chemical communications (Cambridge, England), 2016, 52, 9044-9047
7118526 CIFC23 H19 Cl N2 OP -19.859; 9.973; 11.943
103.759; 101.793; 114.317
976.9Roy, Tony; Thangaraj, Manikandan; Gonnade, Rajesh G.; Biju, Akkattu T.
Synthesis of functionalized amino epoxides by a three-component coupling involving aziridines, arynes and aldehydes.
Chemical communications (Cambridge, England), 2016, 52, 9044-9047
7118527 CIFC60 H95 B2 N6 O0.5 Si3P 1 21/n 113.12; 22.789; 21.2
90; 103.706; 90
6158.13Hadlington, Terrance J.; Abdalla, Joseph A. B.; Tirfoin, Rémi; Aldridge, Simon; Jones, Cameron
Stabilization of a two-coordinate, acyclic diaminosilylene (ADASi): completion of the series of isolable diaminotetrylenes, :E(NR2)2 (E = group 14 element).
Chemical communications (Cambridge, England), 2016, 52, 1717-1720
7118528 CIFC58 H90 B2 N6 Si2 SnC 1 2/c 126.444; 12.059; 18.181
90; 98.06; 90
5740Hadlington, Terrance J.; Abdalla, Joseph A. B.; Tirfoin, Rémi; Aldridge, Simon; Jones, Cameron
Stabilization of a two-coordinate, acyclic diaminosilylene (ADASi): completion of the series of isolable diaminotetrylenes, :E(NR2)2 (E = group 14 element).
Chemical communications (Cambridge, England), 2016, 52, 1717-1720
7118529 CIFC58 H90 B2 N6 Pb Si2C 1 2/c 126.6148; 12.0185; 18.1788
90; 97.896; 90
5759.7Hadlington, Terrance J.; Abdalla, Joseph A. B.; Tirfoin, Rémi; Aldridge, Simon; Jones, Cameron
Stabilization of a two-coordinate, acyclic diaminosilylene (ADASi): completion of the series of isolable diaminotetrylenes, :E(NR2)2 (E = group 14 element).
Chemical communications (Cambridge, England), 2016, 52, 1717-1720
7118530 CIFC32 H52 B Cl Ge N3 SiC 1 2/c 123.6484; 10.2456; 30.482
90; 108.41; 90
7007.56Hadlington, Terrance J.; Abdalla, Joseph A. B.; Tirfoin, Rémi; Aldridge, Simon; Jones, Cameron
Stabilization of a two-coordinate, acyclic diaminosilylene (ADASi): completion of the series of isolable diaminotetrylenes, :E(NR2)2 (E = group 14 element).
Chemical communications (Cambridge, England), 2016, 52, 1717-1720
7118531 CIFC58 H90 B2 N6 O2 Si3P 1 21/c 113.17; 20.129; 22.951
90; 104.647; 90
5886.56Hadlington, Terrance J.; Abdalla, Joseph A. B.; Tirfoin, Rémi; Aldridge, Simon; Jones, Cameron
Stabilization of a two-coordinate, acyclic diaminosilylene (ADASi): completion of the series of isolable diaminotetrylenes, :E(NR2)2 (E = group 14 element).
Chemical communications (Cambridge, England), 2016, 52, 1717-1720
7118532 CIFC29 H50 B N5 Si2P 1 21/c 110.0089; 16.8248; 19.7026
90; 104.172; 90
3216.9Hadlington, Terrance J.; Abdalla, Joseph A. B.; Tirfoin, Rémi; Aldridge, Simon; Jones, Cameron
Stabilization of a two-coordinate, acyclic diaminosilylene (ADASi): completion of the series of isolable diaminotetrylenes, :E(NR2)2 (E = group 14 element).
Chemical communications (Cambridge, England), 2016, 52, 1717-1720
7118533 CIFC29 H46 B Cl2 N3 Si2P 21 21 2110.162; 16.8562; 19.2329
90; 90; 90
3294.5Hadlington, Terrance J.; Abdalla, Joseph A. B.; Tirfoin, Rémi; Aldridge, Simon; Jones, Cameron
Stabilization of a two-coordinate, acyclic diaminosilylene (ADASi): completion of the series of isolable diaminotetrylenes, :E(NR2)2 (E = group 14 element).
Chemical communications (Cambridge, England), 2016, 52, 1717-1720
7118534 CIFC22 H18 N2 O6 ZnP n a 2118.972; 7.8309; 13.6741
90; 90; 90
2031.5Lama, Prem; Alimi, Lukman O.; Das, Raj Kumar; Barbour, Leonard J.
Hydration-dependent anomalous thermal expansion behaviour in a coordination polymer.
Chemical communications (Cambridge, England), 2016, 52, 3231-3234
7118535 CIFC22 H18 N2 O6 ZnP n a 2118.973; 7.8316; 13.6758
90; 90; 90
2032.1Lama, Prem; Alimi, Lukman O.; Das, Raj Kumar; Barbour, Leonard J.
Hydration-dependent anomalous thermal expansion behaviour in a coordination polymer.
Chemical communications (Cambridge, England), 2016, 52, 3231-3234
7118536 CIFC22 H20 N2 O7 ZnP n a 2119.1246; 7.804; 13.7839
90; 90; 90
2057.2Lama, Prem; Alimi, Lukman O.; Das, Raj Kumar; Barbour, Leonard J.
Hydration-dependent anomalous thermal expansion behaviour in a coordination polymer.
Chemical communications (Cambridge, England), 2016, 52, 3231-3234
7118537 CIFC22 H20 N2 O7 ZnP n a 2119.1221; 7.8119; 13.7812
90; 90; 90
2058.6Lama, Prem; Alimi, Lukman O.; Das, Raj Kumar; Barbour, Leonard J.
Hydration-dependent anomalous thermal expansion behaviour in a coordination polymer.
Chemical communications (Cambridge, England), 2016, 52, 3231-3234
7118538 CIFC22 H20 N2 O7 ZnP n a 2119.1203; 7.8191; 13.7785
90; 90; 90
2059.9Lama, Prem; Alimi, Lukman O.; Das, Raj Kumar; Barbour, Leonard J.
Hydration-dependent anomalous thermal expansion behaviour in a coordination polymer.
Chemical communications (Cambridge, England), 2016, 52, 3231-3234
7118539 CIFC22 H20 N2 O7 ZnP n a 2119.1211; 7.8289; 13.7769
90; 90; 90
2062.36Lama, Prem; Alimi, Lukman O.; Das, Raj Kumar; Barbour, Leonard J.
Hydration-dependent anomalous thermal expansion behaviour in a coordination polymer.
Chemical communications (Cambridge, England), 2016, 52, 3231-3234
7118540 CIFC22 H20 N2 O7 ZnP n a 2119.1196; 7.8379; 13.7729
90; 90; 90
2063.97Lama, Prem; Alimi, Lukman O.; Das, Raj Kumar; Barbour, Leonard J.
Hydration-dependent anomalous thermal expansion behaviour in a coordination polymer.
Chemical communications (Cambridge, England), 2016, 52, 3231-3234
7118541 CIFC22 H20 N2 O7 ZnP n a 2119.1195; 7.8491; 13.7716
90; 90; 90
2066.72Lama, Prem; Alimi, Lukman O.; Das, Raj Kumar; Barbour, Leonard J.
Hydration-dependent anomalous thermal expansion behaviour in a coordination polymer.
Chemical communications (Cambridge, England), 2016, 52, 3231-3234
7118542 CIFC22 H20 N2 O7 ZnP n a 2119.1176; 7.8572; 13.7712
90; 90; 90
2068.58Lama, Prem; Alimi, Lukman O.; Das, Raj Kumar; Barbour, Leonard J.
Hydration-dependent anomalous thermal expansion behaviour in a coordination polymer.
Chemical communications (Cambridge, England), 2016, 52, 3231-3234
7118543 CIFC22 H20 N2 O7 ZnP n a 2119.1136; 7.8642; 13.7696
90; 90; 90
2069.75Lama, Prem; Alimi, Lukman O.; Das, Raj Kumar; Barbour, Leonard J.
Hydration-dependent anomalous thermal expansion behaviour in a coordination polymer.
Chemical communications (Cambridge, England), 2016, 52, 3231-3234
7118544 CIFC22 H20 N2 O7 ZnP n a 2119.1062; 7.8702; 13.7665
90; 90; 90
2070.06Lama, Prem; Alimi, Lukman O.; Das, Raj Kumar; Barbour, Leonard J.
Hydration-dependent anomalous thermal expansion behaviour in a coordination polymer.
Chemical communications (Cambridge, England), 2016, 52, 3231-3234
7118545 CIFC22 H20 N2 O7 ZnP n a 2119.1073; 7.8706; 13.7668
90; 90; 90
2070.33Lama, Prem; Alimi, Lukman O.; Das, Raj Kumar; Barbour, Leonard J.
Hydration-dependent anomalous thermal expansion behaviour in a coordination polymer.
Chemical communications (Cambridge, England), 2016, 52, 3231-3234
7118546 CIFC22 H18 N2 O6 ZnP n a 2118.9732; 7.753; 13.6972
90; 90; 90
2014.8Lama, Prem; Alimi, Lukman O.; Das, Raj Kumar; Barbour, Leonard J.
Hydration-dependent anomalous thermal expansion behaviour in a coordination polymer.
Chemical communications (Cambridge, England), 2016, 52, 3231-3234
7118547 CIFC22 H18 N2 O6 ZnP n a 2118.9781; 7.766; 13.6963
90; 90; 90
2018.6Lama, Prem; Alimi, Lukman O.; Das, Raj Kumar; Barbour, Leonard J.
Hydration-dependent anomalous thermal expansion behaviour in a coordination polymer.
Chemical communications (Cambridge, England), 2016, 52, 3231-3234
7118548 CIFC22 H18 N2 O6 ZnP n a 2118.976; 7.7768; 13.692
90; 90; 90
2020.6Lama, Prem; Alimi, Lukman O.; Das, Raj Kumar; Barbour, Leonard J.
Hydration-dependent anomalous thermal expansion behaviour in a coordination polymer.
Chemical communications (Cambridge, England), 2016, 52, 3231-3234
7118549 CIFC22 H18 N2 O6 ZnP n a 2118.977; 7.7881; 13.689
90; 90; 90
2023.2Lama, Prem; Alimi, Lukman O.; Das, Raj Kumar; Barbour, Leonard J.
Hydration-dependent anomalous thermal expansion behaviour in a coordination polymer.
Chemical communications (Cambridge, England), 2016, 52, 3231-3234
7118550 CIFC22 H18 N2 O6 ZnP n a 2118.983; 7.8009; 13.6902
90; 90; 90
2027.3Lama, Prem; Alimi, Lukman O.; Das, Raj Kumar; Barbour, Leonard J.
Hydration-dependent anomalous thermal expansion behaviour in a coordination polymer.
Chemical communications (Cambridge, England), 2016, 52, 3231-3234
7118551 CIFC22 H18 N2 O6 ZnP n a 2118.9745; 7.808; 13.6816
90; 90; 90
2027Lama, Prem; Alimi, Lukman O.; Das, Raj Kumar; Barbour, Leonard J.
Hydration-dependent anomalous thermal expansion behaviour in a coordination polymer.
Chemical communications (Cambridge, England), 2016, 52, 3231-3234
7118552 CIFC22 H18 N2 O6 ZnP n a 2118.9725; 7.8178; 13.6767
90; 90; 90
2028.6Lama, Prem; Alimi, Lukman O.; Das, Raj Kumar; Barbour, Leonard J.
Hydration-dependent anomalous thermal expansion behaviour in a coordination polymer.
Chemical communications (Cambridge, England), 2016, 52, 3231-3234
7118553 CIFC144 H112 Co6 Gd6 N18 O44P 1 21/n 120.74; 22.507; 21.262
90; 113.972; 90
9068.9Alexandropoulos, Dimitris I.; Cunha-Silva, Luís; Lorusso, Giulia; Evangelisti, Marco; Tang, Jinkui; Stamatatos, Theocharis C.
Dodecanuclear 3d/4f-metal clusters with a 'Star of David' topology: single-molecule magnetism and magnetocaloric properties.
Chemical communications (Cambridge, England), 2016, 52, 1693-1696
7118554 CIFC144 H112 Gd6 N18 Ni6 O44C m c e35.3299; 22.8072; 22.7035
90; 90; 90
18293.9Alexandropoulos, Dimitris I.; Cunha-Silva, Luís; Lorusso, Giulia; Evangelisti, Marco; Tang, Jinkui; Stamatatos, Theocharis C.
Dodecanuclear 3d/4f-metal clusters with a 'Star of David' topology: single-molecule magnetism and magnetocaloric properties.
Chemical communications (Cambridge, England), 2016, 52, 1693-1696
7118555 CIFC132 H112 Gd6 N15 O48 Zn6C m c e35.809; 22.7395; 23.0503
90; 90; 90
18769Alexandropoulos, Dimitris I.; Cunha-Silva, Luís; Lorusso, Giulia; Evangelisti, Marco; Tang, Jinkui; Stamatatos, Theocharis C.
Dodecanuclear 3d/4f-metal clusters with a 'Star of David' topology: single-molecule magnetism and magnetocaloric properties.
Chemical communications (Cambridge, England), 2016, 52, 1693-1696
7118556 CIFC128 H104 Dy6 N10 O52 Zn6C m c e35.395; 22.7777; 22.9329
90; 90; 90
18489Alexandropoulos, Dimitris I.; Cunha-Silva, Luís; Lorusso, Giulia; Evangelisti, Marco; Tang, Jinkui; Stamatatos, Theocharis C.
Dodecanuclear 3d/4f-metal clusters with a 'Star of David' topology: single-molecule magnetism and magnetocaloric properties.
Chemical communications (Cambridge, England), 2016, 52, 1693-1696
7118557 CIFC128 H104 Dy6 N14 Ni6 O52C m c e35.887; 22.5851; 23.2338
90; 90; 90
18831Alexandropoulos, Dimitris I.; Cunha-Silva, Luís; Lorusso, Giulia; Evangelisti, Marco; Tang, Jinkui; Stamatatos, Theocharis C.
Dodecanuclear 3d/4f-metal clusters with a 'Star of David' topology: single-molecule magnetism and magnetocaloric properties.
Chemical communications (Cambridge, England), 2016, 52, 1693-1696
7118558 CIFC20 H12 Br N O5P 21 21 215.2566; 12.33003; 25.5995
90; 90; 90
1659.21Kaya, Uğur; Chauhan, Pankaj; Hack, Daniel; Deckers, Kristina; Puttreddy, Rakesh; Rissanen, Kari; Enders, Dieter
Enantioselective synthesis of 4H-pyranonaphthoquinones via sequential squaramide and silver catalysis.
Chemical communications (Cambridge, England), 2016, 52, 1669-1672
7118559 CIFC29 H21 B O7P 1 21/n 114.2762; 10.1806; 17.0287
90; 109.886; 90
2327.38Konishi, Akihito; Yasunaga, Ryosuke; Chiba, Kouji; Yasuda, Makoto
Synthesis, characterization, and properties of a benzofuran-based cage-shaped borate: photo activation of Lewis acid catalysts.
Chemical communications (Cambridge, England), 2016, 52, 3348-3351
7118560 CIFC36 H34 N4 O8P 1 21 17.9612; 24.5627; 16.5897
90; 90.823; 90
3243.76Wang, Yue-Ming; Zhang, Hong-Hao; Li, Can; Fan, Tao; Shi, Feng
Catalytic asymmetric chemoselective 1,3-dipolar cycloadditions of an azomethine ylide with isatin-derived imines: diastereo- and enantioselective construction of a spiro[imidazolidine-2,3'-oxindole] framework.
Chemical communications (Cambridge, England), 2016, 52, 1804-1807
7118561 CIFC29 H44 O6P 1 21 19.9607; 7.291; 18.5284
90; 95.286; 90
1339.9Wu, Jing-Jing; Shi, Yong; Tian, Wei-Sheng
Synthesis of the aglycon of aspafiliosides E and F based on cascade reactions.
Chemical communications (Cambridge, England), 2016, 52, 1942-1944
7118562 CIFC9 H10 Cl N O2P 1 21/c 15.5837; 8.5339; 19.865
90; 92.074; 90
945.96d'Agostino, Simone; Spinelli, Floriana; Boanini, Elisa; Braga, Dario; Grepioni, Fabrizia
Single crystal to single crystal [2+2] photoreactions in chloride and sulphate salts of 4-amino-cinnamic acid via solid-solution formation: a structural and kinetic study.
Chemical communications (Cambridge, England), 2016, 52, 1899-1902
7118563 CIFC9 H10 Cl N O2P 1 21/c 15.6063; 8.5811; 19.4662
90; 91.595; 90
936.12d'Agostino, Simone; Spinelli, Floriana; Boanini, Elisa; Braga, Dario; Grepioni, Fabrizia
Single crystal to single crystal [2+2] photoreactions in chloride and sulphate salts of 4-amino-cinnamic acid via solid-solution formation: a structural and kinetic study.
Chemical communications (Cambridge, England), 2016, 52, 1899-1902
7118564 CIFC9 H10 Cl N O2P 1 21/c 15.618; 8.5855; 19.373
90; 91.521; 90
934.1d'Agostino, Simone; Spinelli, Floriana; Boanini, Elisa; Braga, Dario; Grepioni, Fabrizia
Single crystal to single crystal [2+2] photoreactions in chloride and sulphate salts of 4-amino-cinnamic acid via solid-solution formation: a structural and kinetic study.
Chemical communications (Cambridge, England), 2016, 52, 1899-1902
7118565 CIFC9 H10 Cl N O2P 1 21/c 15.6294; 8.5824; 19.252
90; 91.427; 90
929.85d'Agostino, Simone; Spinelli, Floriana; Boanini, Elisa; Braga, Dario; Grepioni, Fabrizia
Single crystal to single crystal [2+2] photoreactions in chloride and sulphate salts of 4-amino-cinnamic acid via solid-solution formation: a structural and kinetic study.
Chemical communications (Cambridge, England), 2016, 52, 1899-1902
7118566 CIFC9 H10 Cl N O2P 1 21/c 15.6409; 8.5631; 19.131
90; 91.475; 90
923.79d'Agostino, Simone; Spinelli, Floriana; Boanini, Elisa; Braga, Dario; Grepioni, Fabrizia
Single crystal to single crystal [2+2] photoreactions in chloride and sulphate salts of 4-amino-cinnamic acid via solid-solution formation: a structural and kinetic study.
Chemical communications (Cambridge, England), 2016, 52, 1899-1902
7118567 CIFC9 H10 Cl N O2P 1 21/c 15.6523; 8.5616; 19.105
90; 91.471; 90
924.2d'Agostino, Simone; Spinelli, Floriana; Boanini, Elisa; Braga, Dario; Grepioni, Fabrizia
Single crystal to single crystal [2+2] photoreactions in chloride and sulphate salts of 4-amino-cinnamic acid via solid-solution formation: a structural and kinetic study.
Chemical communications (Cambridge, England), 2016, 52, 1899-1902
7118568 CIFC9 H10 Cl N O2P 1 21/c 15.6822; 8.5112; 18.888
90; 91.591; 90
913.1d'Agostino, Simone; Spinelli, Floriana; Boanini, Elisa; Braga, Dario; Grepioni, Fabrizia
Single crystal to single crystal [2+2] photoreactions in chloride and sulphate salts of 4-amino-cinnamic acid via solid-solution formation: a structural and kinetic study.
Chemical communications (Cambridge, England), 2016, 52, 1899-1902
7118569 CIFC9 H10 Cl N O2P 1 21/c 15.6907; 8.4732; 18.86
90; 91.741; 90
909d'Agostino, Simone; Spinelli, Floriana; Boanini, Elisa; Braga, Dario; Grepioni, Fabrizia
Single crystal to single crystal [2+2] photoreactions in chloride and sulphate salts of 4-amino-cinnamic acid via solid-solution formation: a structural and kinetic study.
Chemical communications (Cambridge, England), 2016, 52, 1899-1902
7118570 CIFC9 H10 Cl N O2P 1 21/c 15.7167; 8.417; 18.889
90; 91.904; 90
908.4d'Agostino, Simone; Spinelli, Floriana; Boanini, Elisa; Braga, Dario; Grepioni, Fabrizia
Single crystal to single crystal [2+2] photoreactions in chloride and sulphate salts of 4-amino-cinnamic acid via solid-solution formation: a structural and kinetic study.
Chemical communications (Cambridge, England), 2016, 52, 1899-1902
7118571 CIFC9 H10 Cl N O2P 1 21/c 15.7431; 8.221; 19.012
90; 92.47; 90
896.8d'Agostino, Simone; Spinelli, Floriana; Boanini, Elisa; Braga, Dario; Grepioni, Fabrizia
Single crystal to single crystal [2+2] photoreactions in chloride and sulphate salts of 4-amino-cinnamic acid via solid-solution formation: a structural and kinetic study.
Chemical communications (Cambridge, England), 2016, 52, 1899-1902
7118572 CIFC18 H22 N2 O9 SP 1 21/c 113.1014; 11.7129; 13.2735
90; 100.385; 90
2003.52d'Agostino, Simone; Spinelli, Floriana; Boanini, Elisa; Braga, Dario; Grepioni, Fabrizia
Single crystal to single crystal [2+2] photoreactions in chloride and sulphate salts of 4-amino-cinnamic acid via solid-solution formation: a structural and kinetic study.
Chemical communications (Cambridge, England), 2016, 52, 1899-1902
7118573 CIFC18 H22 N2 O9 SP -17.3374; 10.5566; 13.8798
103.793; 99.924; 102.838
988.8d'Agostino, Simone; Spinelli, Floriana; Boanini, Elisa; Braga, Dario; Grepioni, Fabrizia
Single crystal to single crystal [2+2] photoreactions in chloride and sulphate salts of 4-amino-cinnamic acid via solid-solution formation: a structural and kinetic study.
Chemical communications (Cambridge, England), 2016, 52, 1899-1902
7118574 CIFC18 H22 N O9 SP -17.3066; 10.5681; 13.8909
104.253; 99.577; 102.609
986.7d'Agostino, Simone; Spinelli, Floriana; Boanini, Elisa; Braga, Dario; Grepioni, Fabrizia
Single crystal to single crystal [2+2] photoreactions in chloride and sulphate salts of 4-amino-cinnamic acid via solid-solution formation: a structural and kinetic study.
Chemical communications (Cambridge, England), 2016, 52, 1899-1902
7118575 CIFC18 H22 N2 O9 SP -17.259; 10.5719; 13.8895
104.423; 98.792; 102.601
982.9d'Agostino, Simone; Spinelli, Floriana; Boanini, Elisa; Braga, Dario; Grepioni, Fabrizia
Single crystal to single crystal [2+2] photoreactions in chloride and sulphate salts of 4-amino-cinnamic acid via solid-solution formation: a structural and kinetic study.
Chemical communications (Cambridge, England), 2016, 52, 1899-1902
7118576 CIFC18 H22 N2 O9 SP -17.2497; 10.6164; 13.902
104.762; 98.258; 102.574
987.1d'Agostino, Simone; Spinelli, Floriana; Boanini, Elisa; Braga, Dario; Grepioni, Fabrizia
Single crystal to single crystal [2+2] photoreactions in chloride and sulphate salts of 4-amino-cinnamic acid via solid-solution formation: a structural and kinetic study.
Chemical communications (Cambridge, England), 2016, 52, 1899-1902
7118577 CIFC18 H22 N2 O9 SP -17.1238; 10.631; 13.925
106.01; 95.898; 102.081
976.7d'Agostino, Simone; Spinelli, Floriana; Boanini, Elisa; Braga, Dario; Grepioni, Fabrizia
Single crystal to single crystal [2+2] photoreactions in chloride and sulphate salts of 4-amino-cinnamic acid via solid-solution formation: a structural and kinetic study.
Chemical communications (Cambridge, England), 2016, 52, 1899-1902
7118578 CIFC18 H22 N2 O9 SP -17.096; 10.6518; 13.9338
106.307; 95.377; 101.948
975.91d'Agostino, Simone; Spinelli, Floriana; Boanini, Elisa; Braga, Dario; Grepioni, Fabrizia
Single crystal to single crystal [2+2] photoreactions in chloride and sulphate salts of 4-amino-cinnamic acid via solid-solution formation: a structural and kinetic study.
Chemical communications (Cambridge, England), 2016, 52, 1899-1902
7118579 CIFC18 H22 N2 O9 SP -17.0956; 10.6597; 13.943
106.348; 95.271; 101.923
977.4d'Agostino, Simone; Spinelli, Floriana; Boanini, Elisa; Braga, Dario; Grepioni, Fabrizia
Single crystal to single crystal [2+2] photoreactions in chloride and sulphate salts of 4-amino-cinnamic acid via solid-solution formation: a structural and kinetic study.
Chemical communications (Cambridge, England), 2016, 52, 1899-1902
7118580 CIFC9 H10 B F4 N O2I 1 2/a 17.262; 10.026; 30.424
90; 96.193; 90
2202.2d'Agostino, Simone; Spinelli, Floriana; Boanini, Elisa; Braga, Dario; Grepioni, Fabrizia
Single crystal to single crystal [2+2] photoreactions in chloride and sulphate salts of 4-amino-cinnamic acid via solid-solution formation: a structural and kinetic study.
Chemical communications (Cambridge, England), 2016, 52, 1899-1902
7118581 CIFC9 H10 B F4 N O2P -17.2802; 9.067; 9.7329
115.13; 100.802; 101.825
541.32d'Agostino, Simone; Spinelli, Floriana; Boanini, Elisa; Braga, Dario; Grepioni, Fabrizia
Single crystal to single crystal [2+2] photoreactions in chloride and sulphate salts of 4-amino-cinnamic acid via solid-solution formation: a structural and kinetic study.
Chemical communications (Cambridge, England), 2016, 52, 1899-1902
7118582 CIFC9 H10 N2 O5P 1 21/c 15.14519; 28.63202; 7.0164
90; 104.505; 90
1000.69d'Agostino, Simone; Spinelli, Floriana; Boanini, Elisa; Braga, Dario; Grepioni, Fabrizia
Single crystal to single crystal [2+2] photoreactions in chloride and sulphate salts of 4-amino-cinnamic acid via solid-solution formation: a structural and kinetic study.
Chemical communications (Cambridge, England), 2016, 52, 1899-1902
7118583 CIFC9 H10 F3 N O2 P0.5P -15.5647; 5.8519; 15.82
85.376; 86.255; 72.178
488.4d'Agostino, Simone; Spinelli, Floriana; Boanini, Elisa; Braga, Dario; Grepioni, Fabrizia
Single crystal to single crystal [2+2] photoreactions in chloride and sulphate salts of 4-amino-cinnamic acid via solid-solution formation: a structural and kinetic study.
Chemical communications (Cambridge, England), 2016, 52, 1899-1902
7118584 CIFC97 H85 N5 ZnP -113.8075; 20.3411; 27.8465
81.213; 86.01; 75.367
7474.5Diev, Vyacheslav V.; Femia, Denise; Zhong, Qiwen; Djurovich, Peter I.; Haiges, Ralf; Thompson, Mark E.
A quinoidal bis-phenalenyl-fused porphyrin with supramolecular organization and broad near-infrared absorption.
Chemical communications (Cambridge, England), 2016, 52, 1949-1952
7118585 CIFC13 H13 N O2P b c a13.273; 8.87; 18.749
90; 90; 90
2207.3Jha, Abadh Kishor; Jain, Nidhi
The microwave-assisted ortho-alkylation of azine N-oxides with N-tosylhydrazones catalyzed by copper(i) iodide.
Chemical communications (Cambridge, England), 2016, 52, 1831-1834
7118586 CIFC6 H6 N8 O5 Zn2P 1 21/c 117.576; 7.9026; 10.347
90; 100.213; 90
1414.4Banerjee, Aparna; Nandi, Shyamapada; Nasa, Parveen; Vaidhyanathan, Ramanathan
Enhancing the carbon capture capacities of a rigid ultra-microporous MOF through gate-opening at low CO2 pressures assisted by swiveling oxalate pillars.
Chemical communications (Cambridge, England), 2016, 52, 1851-1854
7118587 CIFC9 H14 N8 O5 Zn2P 1 21/n 19.1877; 13.6108; 12.5305
90; 104.629; 90
1516.16Banerjee, Aparna; Nandi, Shyamapada; Nasa, Parveen; Vaidhyanathan, Ramanathan
Enhancing the carbon capture capacities of a rigid ultra-microporous MOF through gate-opening at low CO2 pressures assisted by swiveling oxalate pillars.
Chemical communications (Cambridge, England), 2016, 52, 1851-1854
7118588 CIFC6 H6 N8 O4 Zn2P 1 21/c 117.576; 7.9026; 10.347
90; 100.213; 90
1414.4Banerjee, Aparna; Nandi, Shyamapada; Nasa, Parveen; Vaidhyanathan, Ramanathan
Enhancing the carbon capture capacities of a rigid ultra-microporous MOF through gate-opening at low CO2 pressures assisted by swiveling oxalate pillars.
Chemical communications (Cambridge, England), 2016, 52, 1851-1854
7118589 CIFC8 H11 N8 O5 Zn2P 1 21/n 18.9818; 13.8656; 12.4104
90; 105.36; 90
1490.4Banerjee, Aparna; Nandi, Shyamapada; Nasa, Parveen; Vaidhyanathan, Ramanathan
Enhancing the carbon capture capacities of a rigid ultra-microporous MOF through gate-opening at low CO2 pressures assisted by swiveling oxalate pillars.
Chemical communications (Cambridge, England), 2016, 52, 1851-1854
7118590 CIFC6 H5 N8 O4 Zn2P 1 21/n 18.9818; 13.8656; 12.4104
90; 105.36; 90
1490.4Banerjee, Aparna; Nandi, Shyamapada; Nasa, Parveen; Vaidhyanathan, Ramanathan
Enhancing the carbon capture capacities of a rigid ultra-microporous MOF through gate-opening at low CO2 pressures assisted by swiveling oxalate pillars.
Chemical communications (Cambridge, England), 2016, 52, 1851-1854
7118591 CIFC31 H23 Br Cl2 I N O5 S2P 1 21/c 111.1901; 36.49; 8.194
90; 96.076; 90
3327Zhu, Yi-Long; Jiang, Bo; Hao, Wen-Juan; Wang, Ai-Fang; Qiu, Jiang-Kai; Wei, Ping; Wang, De-Cai; Li, Guigen; Tu, Shu-Jiang
A new cascade halosulfonylation of 1,7-enynes toward 3,4-dihydroquinolin-2(1H)-ones via sulfonyl radical-triggered addition/6-exo-dig cyclization.
Chemical communications (Cambridge, England), 2016, 52, 1907-1910
7118592 CIFC69 H32 Co3 N5.75 O15P 1 21/n 115.6069; 26.4325; 16.6221
90; 90.155; 90
6857.1Wang, Xiuli; Gao, Wen-Yang; Luan, Jian; Wojtas, Lukasz; Ma, Shengqian
An effective strategy to boost the robustness of metal-organic frameworks via introduction of size-matching ligand braces.
Chemical communications (Cambridge, England), 2016, 52, 1971-1974
7118593 CIFC64 H24 Co3 N5 O18.75P -3 1 c15.3816; 15.3816; 16.8215
90; 90; 120
3446.66Wang, Xiuli; Gao, Wen-Yang; Luan, Jian; Wojtas, Lukasz; Ma, Shengqian
An effective strategy to boost the robustness of metal-organic frameworks via introduction of size-matching ligand braces.
Chemical communications (Cambridge, England), 2016, 52, 1971-1974
7118594 CIFC24 H20 N8 O2 Zn2P 43 2 211.6963; 11.6963; 47.2239
90; 90; 90
6460.39Xu, Zhong-Xuan; Ma, Yu-Lu; Zhang, Jian
Enantiopure anion templated synthesis of a zeolitic metal-organic framework.
Chemical communications (Cambridge, England), 2016, 52, 1923-1925
7118595 CIFC108 H48 In3 N12 O24F m -3 m43.645; 43.645; 43.645
90; 90; 90
83139Wang, Xuan; Lu, Weigang; Gu, Zhi-Yuan; Wei, Zhangwen; Zhou, Hong-Cai
Topology-guided design of an anionic bor-network for photocatalytic [Ru(bpy)3](2+) encapsulation.
Chemical communications (Cambridge, England), 2016, 52, 1926-1929
7118596 CIFC23 H19 N2P -16.2745; 10.4378; 13.5235
109.644; 97.81; 90.942
824.56Chen, Kai; Tang, Xiang-Ying; Shi, Min
Rh(ii)-Catalyzed formation of pyrrolo[2,3-b]quinolines from azide-methylenecyclopropanes and isonitriles.
Chemical communications (Cambridge, England), 2016, 52, 1967-1970
7118597 CIFC58 H66 N4 O4P -110.372; 12.1576; 21.0058
77.946; 84.483; 80.041
2546.41Chen, Kai; Tang, Xiang-Ying; Shi, Min
Rh(ii)-Catalyzed formation of pyrrolo[2,3-b]quinolines from azide-methylenecyclopropanes and isonitriles.
Chemical communications (Cambridge, England), 2016, 52, 1967-1970
7118598 CIFC26 H41 Br2 Fe N P2P 21 21 2112.014; 15.518; 15.75
90; 90; 90
2936.3Chakraborty, Subrata; Leitus, Gregory; Milstein, David
Selective hydrogenation of nitriles to primary amines catalyzed by a novel iron complex.
Chemical communications (Cambridge, England), 2016, 52, 1812-1815
7118599 CIFC21 H19 PP 15.6674; 8.267; 9.097
101.836; 101.813; 92.712
406.5Itazaki, Masumi; Katsube, Shinya; Kamitani, Masahiro; Nakazawa, Hiroshi
Synthesis of vinylphosphines and unsymmetric diphosphines: iron-catalyzed selective hydrophosphination reaction of alkynes and vinylphosphines with secondary phosphines.
Chemical communications (Cambridge, England), 2016, 52, 3163-3166
7118600 CIFC20 H18 N PP 1 21/n 116.561; 5.936; 17.511
90; 111.673; 90
1599.7Itazaki, Masumi; Katsube, Shinya; Kamitani, Masahiro; Nakazawa, Hiroshi
Synthesis of vinylphosphines and unsymmetric diphosphines: iron-catalyzed selective hydrophosphination reaction of alkynes and vinylphosphines with secondary phosphines.
Chemical communications (Cambridge, England), 2016, 52, 3163-3166
7118601 CIFC24 H21 Fe PP 21 21 219.5281; 11.4269; 17.881
90; 90; 90
1946.8Itazaki, Masumi; Katsube, Shinya; Kamitani, Masahiro; Nakazawa, Hiroshi
Synthesis of vinylphosphines and unsymmetric diphosphines: iron-catalyzed selective hydrophosphination reaction of alkynes and vinylphosphines with secondary phosphines.
Chemical communications (Cambridge, England), 2016, 52, 3163-3166
7118602 CIFC22 H22 N PP 1 21/n 113.7817; 5.8294; 22.8279
90; 97.672; 90
1817.6Itazaki, Masumi; Katsube, Shinya; Kamitani, Masahiro; Nakazawa, Hiroshi
Synthesis of vinylphosphines and unsymmetric diphosphines: iron-catalyzed selective hydrophosphination reaction of alkynes and vinylphosphines with secondary phosphines.
Chemical communications (Cambridge, England), 2016, 52, 3163-3166
7118603 CIFC34 H33 N P2P 1 21/c 118.2866; 6.0518; 25.5425
90; 94.9633; 90
2816.11Itazaki, Masumi; Katsube, Shinya; Kamitani, Masahiro; Nakazawa, Hiroshi
Synthesis of vinylphosphines and unsymmetric diphosphines: iron-catalyzed selective hydrophosphination reaction of alkynes and vinylphosphines with secondary phosphines.
Chemical communications (Cambridge, England), 2016, 52, 3163-3166
7118604 CIFC17 H23 Fe N OP 1 21/m 17.4495; 13.489; 8.484
90; 112.353; 90
788.5Itazaki, Masumi; Katsube, Shinya; Kamitani, Masahiro; Nakazawa, Hiroshi
Synthesis of vinylphosphines and unsymmetric diphosphines: iron-catalyzed selective hydrophosphination reaction of alkynes and vinylphosphines with secondary phosphines.
Chemical communications (Cambridge, England), 2016, 52, 3163-3166
7118605 CIFC31 H31 Fe O PP 1 21/c 113.439; 9.537; 20.11
90; 91.374; 90
2576.7Itazaki, Masumi; Katsube, Shinya; Kamitani, Masahiro; Nakazawa, Hiroshi
Synthesis of vinylphosphines and unsymmetric diphosphines: iron-catalyzed selective hydrophosphination reaction of alkynes and vinylphosphines with secondary phosphines.
Chemical communications (Cambridge, England), 2016, 52, 3163-3166
7118606 CIFC35 H36 Fe O P2P -110.8265; 11.9861; 13.0692
81.455; 88.558; 63.176
1494.98Itazaki, Masumi; Katsube, Shinya; Kamitani, Masahiro; Nakazawa, Hiroshi
Synthesis of vinylphosphines and unsymmetric diphosphines: iron-catalyzed selective hydrophosphination reaction of alkynes and vinylphosphines with secondary phosphines.
Chemical communications (Cambridge, England), 2016, 52, 3163-3166
7118607 CIFC24 H29 Fe O PP -18.282; 9.8286; 14.5509
74.635; 73.74; 75.57
1076.66Itazaki, Masumi; Katsube, Shinya; Kamitani, Masahiro; Nakazawa, Hiroshi
Synthesis of vinylphosphines and unsymmetric diphosphines: iron-catalyzed selective hydrophosphination reaction of alkynes and vinylphosphines with secondary phosphines.
Chemical communications (Cambridge, England), 2016, 52, 3163-3166
7118608 CIFC1401 H1152 B16 N125 O181 P32 Pt16 S32P c c n31.68; 38.34; 41.12
90; 90; 90
49945Kaloudi-Chantzea, Antonia; Martinou, Elisabeth; Seintis, Kostas; Karakostas, Nikolaos; Giastas, Petros; Pitterl, Florian; Oberacher, Herbert; Fakis, Mihalis; Pistolis, George
Formation of a highly-ordered rigid multichromophoric 3D supramolecular network by combining ionic and coordination-driven self-assembly.
Chemical communications (Cambridge, England), 2016, 52, 3388-3391
7118609 CIFC34 H37 Al N2 O7P -111.5013; 11.9173; 13.3035
102.745; 106.178; 112.038
1511.12Saikawa, Makoto; Daicho, Manami; Nakamura, Takashi; Uchida, Junji; Yamamura, Masaki; Nabeshima, Tatsuya
Synthesis of a new family of ionophores based on aluminum-dipyrrin complexes (ALDIPYs) and their strong recognition of alkaline earth ions.
Chemical communications (Cambridge, England), 2016, 52, 4014-4017
7118610 CIFC32 H27 B N2 O4P b c a17.1558; 11.8814; 24.8691
90; 90; 90
5069.2Saikawa, Makoto; Daicho, Manami; Nakamura, Takashi; Uchida, Junji; Yamamura, Masaki; Nabeshima, Tatsuya
Synthesis of a new family of ionophores based on aluminum-dipyrrin complexes (ALDIPYs) and their strong recognition of alkaline earth ions.
Chemical communications (Cambridge, England), 2016, 52, 4014-4017
7118611 CIFC64 H59 Al2 N4 Na O11C 1 2/c 124.6207; 7.271; 35.445
90; 111.987; 90
5884Saikawa, Makoto; Daicho, Manami; Nakamura, Takashi; Uchida, Junji; Yamamura, Masaki; Nabeshima, Tatsuya
Synthesis of a new family of ionophores based on aluminum-dipyrrin complexes (ALDIPYs) and their strong recognition of alkaline earth ions.
Chemical communications (Cambridge, England), 2016, 52, 4014-4017
7118612 CIFC60 H50 N4 O6C 1 2/c 123.498; 38.393; 23.36
90; 91.08; 90
21071Saikawa, Makoto; Daicho, Manami; Nakamura, Takashi; Uchida, Junji; Yamamura, Masaki; Nabeshima, Tatsuya
Synthesis of a new family of ionophores based on aluminum-dipyrrin complexes (ALDIPYs) and their strong recognition of alkaline earth ions.
Chemical communications (Cambridge, England), 2016, 52, 4014-4017
7118613 CIFC32 H30 N2 O4P 1 21/n 113.3625; 13.7619; 28.7802
90; 90.967; 90
5291.7Saikawa, Makoto; Daicho, Manami; Nakamura, Takashi; Uchida, Junji; Yamamura, Masaki; Nabeshima, Tatsuya
Synthesis of a new family of ionophores based on aluminum-dipyrrin complexes (ALDIPYs) and their strong recognition of alkaline earth ions.
Chemical communications (Cambridge, England), 2016, 52, 4014-4017
7118614 CIFC168 H118 N10 O31 Zn8P 1 21/a 115.4739; 57.1814; 24.7469
90; 94.602; 90
21825.9Bag, Partha Pratim; Wang, Dong; Chen, Zhuo; Cao, Rong
Outstanding drug loading capacity by water stable microporous MOF: a potential drug carrier.
Chemical communications (Cambridge, England), 2016, 52, 3669-3672
7118615 CIFC57 H62 Au Cl5 N2 O4 P2 RuP 1 21/n 114.385; 25.076; 17.318
90; 107.02; 90
5973Fernández-Gallardo, Jacob; Elie, Benelita T.; Sanaú, Mercedes; Contel, María
Versatile synthesis of cationic N-heterocyclic carbene-gold(i) complexes containing a second ancillary ligand. Design of heterobimetallic ruthenium-gold anticancer agents.
Chemical communications (Cambridge, England), 2016, 52, 3155-3158
7118616 CIFC62 H72 Au Cl3 N2 O4 P2 RuP 1 21/c 121.2; 14.09; 22.972
90; 93.02; 90
6852Fernández-Gallardo, Jacob; Elie, Benelita T.; Sanaú, Mercedes; Contel, María
Versatile synthesis of cationic N-heterocyclic carbene-gold(i) complexes containing a second ancillary ligand. Design of heterobimetallic ruthenium-gold anticancer agents.
Chemical communications (Cambridge, England), 2016, 52, 3155-3158
7118617 CIFC43 H45 B2 F15 N2 Ni O2 P2I 1 2/a 123.4136; 11.6676; 35.146
90; 102.822; 90
9361.8Ríos, Pablo; Curado, Natalia; López-Serrano, Joaquín; Rodríguez, Amor
Selective reduction of carbon dioxide to bis(silyl)acetal catalyzed by a PBP-supported nickel complex.
Chemical communications (Cambridge, England), 2016, 52, 2114-2117
7118618 CIFC72 H90 N7 O2 RhP -110.8323; 15.4988; 24.841
103.448; 97.059; 107.037
3795.4Kleinhans, George; Guisado-Barrios, Gregorio; Liles, David C.; Bertrand, Guy; Bezuidenhout, Daniela I.
A rhodium(i)-oxygen adduct as a selective catalyst for one-pot sequential alkyne dimerization-hydrothiolation tandem reactions.
Chemical communications (Cambridge, England), 2016, 52, 3504-3507
7118619 CIFC60 H69 Cl F6 N7 PP 1 21/c 116.2214; 24.0518; 15.2494
90; 108.856; 90
5630.3Kleinhans, George; Guisado-Barrios, Gregorio; Liles, David C.; Bertrand, Guy; Bezuidenhout, Daniela I.
A rhodium(i)-oxygen adduct as a selective catalyst for one-pot sequential alkyne dimerization-hydrothiolation tandem reactions.
Chemical communications (Cambridge, England), 2016, 52, 3504-3507
7118620 CIFC15 H20 F3 N4 O3 P S3P -18.3991; 10.1015; 13.5475
69.158; 78.162; 84.594
1051.08Henne, Florian D.; Watt, Fabian A.; Schwedtmann, Kai; Hennersdorf, Felix; Kokoschka, Malte; Weigand, Jan J.
Tetra-cationic imidazoliumyl-substituted phosphorus-sulfur heterocycles from a cationic organophosphorus sulfide.
Chemical communications (Cambridge, England), 2016, 52, 2023-2026
7118621 CIFC15 H20 F3 N4 O3 P S3P 1 21/m 16.5855; 12.5308; 12.4698
90; 91.568; 90
1028.64Henne, Florian D.; Watt, Fabian A.; Schwedtmann, Kai; Hennersdorf, Felix; Kokoschka, Malte; Weigand, Jan J.
Tetra-cationic imidazoliumyl-substituted phosphorus-sulfur heterocycles from a cationic organophosphorus sulfide.
Chemical communications (Cambridge, England), 2016, 52, 2023-2026
7118622 CIFC38 H57 F12 N11 O12 P4 S8P -19.1184; 13.9277; 25.5013
101.117; 91.826; 94.621
3163.8Henne, Florian D.; Watt, Fabian A.; Schwedtmann, Kai; Hennersdorf, Felix; Kokoschka, Malte; Weigand, Jan J.
Tetra-cationic imidazoliumyl-substituted phosphorus-sulfur heterocycles from a cationic organophosphorus sulfide.
Chemical communications (Cambridge, England), 2016, 52, 2023-2026
7118623 CIFC48 H80 F12 N8 O12 P4 S8I 417.5055; 17.5055; 13.3734
90; 90; 90
4098.2Henne, Florian D.; Watt, Fabian A.; Schwedtmann, Kai; Hennersdorf, Felix; Kokoschka, Malte; Weigand, Jan J.
Tetra-cationic imidazoliumyl-substituted phosphorus-sulfur heterocycles from a cationic organophosphorus sulfide.
Chemical communications (Cambridge, England), 2016, 52, 2023-2026
7118624 CIFC19 H33 N O5P 1 21/c 119.4474; 10.8872; 9.4942
90; 99.138; 90
1984.67Álvarez-Méndez, Sergio J; García, Celina; Martín, Víctor S
The Evans Aldol-Prins cyclization: a general and stereoselective method for the synthesis of 2,3,4,5,6-pentasubstituted tetrahydropyrans.
Chemical communications (Cambridge, England), 2016, 52, 3380-3383
7118625 CIFC13 H10 N2P 21 21 217.2543; 10.8861; 12.636
90; 90; 90
997.9Li, Yajun; Chao, Allen; Fleming, Fraser F.
Isonitrile alkylations: a rapid route to imidazo[1,5-a]pyridines.
Chemical communications (Cambridge, England), 2016, 52, 2111-2113
7118626 CIFC74 H54 N2 Na2 O10 ZnP 42/n b c30.871; 30.871; 10.6581
90; 90; 90
10157.4Chen, Dashu; Xing, Hongzhu; Su, Zhongmin; Wang, Chungang
Electrical conductivity and electroluminescence of a new anthracene-based metal-organic framework with π-conjugated zigzag chains.
Chemical communications (Cambridge, England), 2016, 52, 2019-2022
7118627 CIFC40 H26 Cu2 O10C c c m13.113; 29.058; 30.167
90; 90; 90
11495Chang, Ganggang; Li, Bin; Wang, Hailong; Hu, Tongliang; Bao, Zongbi; Chen, Banglin
Control of interpenetration in a microporous metal-organic framework for significantly enhanced C2H2/CO2 separation at room temperature.
Chemical communications (Cambridge, England), 2016, 52, 3494-3496
7118628 CIFC26 H25 B2 N2 PP 1 21/c 19.818; 18.2883; 13.7042
90; 97.628; 90
2438.9Liu, Tianlin; Qi, Xiujuan; Huang, Shi; Jiang, Linhai; Li, Jianling; Tang, Chenglong; Zhang, Qinghua
Exploiting hydrophobic borohydride-rich ionic liquids as faster-igniting rocket fuels.
Chemical communications (Cambridge, England), 2016, 52, 2031-2034
7118629 CIFH70 Na9 O71 Tb W10P -112.7251; 13.0624; 20.4974
82.857; 74.521; 88.927
3257.65Vonci, Michele; Giansiracusa, Marcus J.; Gable, Robert W.; Van den Heuvel, Willem; Latham, Kay; Moubaraki, Boujemaa; Murray, Keith S.; Yu, Dehong; Mole, Richard A.; Soncini, Alessandro; Boskovic, Colette
Ab initio calculations as a quantitative tool in the inelastic neutron scattering study of a single-molecule magnet analogue.
Chemical communications (Cambridge, England), 2016, 52, 2091-2094
7118630 CIFH72 Na9 O72 Tb W10P -112.8949; 13.1098; 20.9057
76.956; 83.954; 77.348
3353.5Vonci, Michele; Giansiracusa, Marcus J.; Gable, Robert W.; Van den Heuvel, Willem; Latham, Kay; Moubaraki, Boujemaa; Murray, Keith S.; Yu, Dehong; Mole, Richard A.; Soncini, Alessandro; Boskovic, Colette
Ab initio calculations as a quantitative tool in the inelastic neutron scattering study of a single-molecule magnet analogue.
Chemical communications (Cambridge, England), 2016, 52, 2091-2094
7118631 CIFH70 Na9 O71 W10 YP -112.7357; 13.0732; 20.4565
82.865; 74.492; 88.859
3256.2Vonci, Michele; Giansiracusa, Marcus J.; Gable, Robert W.; Van den Heuvel, Willem; Latham, Kay; Moubaraki, Boujemaa; Murray, Keith S.; Yu, Dehong; Mole, Richard A.; Soncini, Alessandro; Boskovic, Colette
Ab initio calculations as a quantitative tool in the inelastic neutron scattering study of a single-molecule magnet analogue.
Chemical communications (Cambridge, England), 2016, 52, 2091-2094
7118632 CIFC21 H15 F N O SP 21 21 217.7128; 8.5049; 26.8442
90; 90; 90
1760.89Suć, Josipa; Dokli, Irena; Gredičak, Matija
Chiral Brønsted acid-catalysed enantioselective synthesis of isoindolinone-derived N(acyl),S-acetals.
Chemical communications (Cambridge, England), 2016, 52, 2071-2074
7118633 CIFC40.5 H40.5 Cl1.5 N4 O2 S4P -112.8268; 13.2644; 24.5245
96.008; 95.267; 118.65
3593.1Llewellyn, Ben A.; Davies, E. Stephen; Pfeiffer, Constance R.; Cooper, Mick; Lewis, William; Champness, Neil R.
Thionated perylene diimides with intense absorbance in the near-IR.
Chemical communications (Cambridge, England), 2016, 52, 2099-2102
7118634 CIFC41 H41 Cl3 N4 O2 S4P -110.5929; 13.3915; 15.0416
93.393; 105.711; 107.519
1935.6Llewellyn, Ben A.; Davies, E. Stephen; Pfeiffer, Constance R.; Cooper, Mick; Lewis, William; Champness, Neil R.
Thionated perylene diimides with intense absorbance in the near-IR.
Chemical communications (Cambridge, England), 2016, 52, 2099-2102
7118635 CIFC40 H40 N4 O6P 1 21/c 112.7735; 8.3815; 32.1723
90; 111.684; 90
3200.66Llewellyn, Ben A.; Davies, E. Stephen; Pfeiffer, Constance R.; Cooper, Mick; Lewis, William; Champness, Neil R.
Thionated perylene diimides with intense absorbance in the near-IR.
Chemical communications (Cambridge, England), 2016, 52, 2099-2102
7118636 CIFC95.19 H158.44 Cl11.82 Mo3 O0.39 P4 Pd2 Ru2 S4P -113.8281; 17.5883; 23.8941
80.217; 75.331; 84.33
5530.7Reinholdt, Anders; Herbst, Konrad; Bendix, Jesper
Delivering carbide ligands to sulfide-rich clusters.
Chemical communications (Cambridge, England), 2016, 52, 2015-2018
7118637 CIFC65 H97 Cl11 Mo3 O3 P2 Pt Ru S5P 1 21/c 122.0554; 9.9627; 36.388
90; 93.738; 90
7978.6Reinholdt, Anders; Herbst, Konrad; Bendix, Jesper
Delivering carbide ligands to sulfide-rich clusters.
Chemical communications (Cambridge, England), 2016, 52, 2015-2018
7118638 CIFC94.65 H154.79 Cl12.35 O0.22 P4 Pd2 Ru2 S4 W3P -113.8702; 17.6143; 23.8397
80.295; 75.255; 83.949
5540Reinholdt, Anders; Herbst, Konrad; Bendix, Jesper
Delivering carbide ligands to sulfide-rich clusters.
Chemical communications (Cambridge, England), 2016, 52, 2015-2018
7118639 CIFC65 H97 Cl11 O3 P2 Pt Ru S5 W3P 1 21/c 122.1025; 9.9658; 36.424
90; 93.775; 90
8005.7Reinholdt, Anders; Herbst, Konrad; Bendix, Jesper
Delivering carbide ligands to sulfide-rich clusters.
Chemical communications (Cambridge, England), 2016, 52, 2015-2018
7118640 CIFC47 H86.5 B Cl5 Cu F4 O0.75 P2 Ru S3P -19.636; 17.256; 18.491
91.1; 97.986; 99.976
2995.9Reinholdt, Anders; Herbst, Konrad; Bendix, Jesper
Delivering carbide ligands to sulfide-rich clusters.
Chemical communications (Cambridge, England), 2016, 52, 2015-2018
7118641 CIFC46.92 H84.77 Ag Cl3.08 F3 O3.64 P2 Ru S4P 21 21 219.501; 22.3773; 27.2642
90; 90; 90
5796.6Reinholdt, Anders; Herbst, Konrad; Bendix, Jesper
Delivering carbide ligands to sulfide-rich clusters.
Chemical communications (Cambridge, England), 2016, 52, 2015-2018
7118642 CIFC84 H48 N6 Ni9 O41F m -3 m41.4694; 41.4694; 41.4694
90; 90; 90
71315.4Ren, Guo-Jian; Chang, Ze; Xu, Jian; Hu, Zhenpeng; Liu, Yan-Qing; Xu, Yue-Ling; Bu, Xian-He
Construction of a polyhedron decorated MOF with a unique network through the combination of two classic secondary building units.
Chemical communications (Cambridge, England), 2016, 52, 2079-2082
7118652 CIFC63.4 H56.57 N7.08 O15.08 Zn3P 1 21/c 119.6891; 13.7933; 26.276
90; 96.242; 90
7093.7Wang, Hao; Lashkari, Elham; Lim, Hyuna; Zheng, Chong; Emge, Thomas J.; Gong, Qihan; Yam, Kit; Li, Jing
The moisture-triggered controlled release of a natural food preservative from a microporous metal-organic framework.
Chemical communications (Cambridge, England), 2016, 52, 2129-2132
7118653 CIFC18 H21 N O7 SP 21 21 216.6015; 16.8605; 17.1484
90; 90; 90
1908.7Son, Se-Mi; Seo, Yeon Ji; Lee, Hyeon-Kyu
Stereoselective synthesis of 1,3-disubstituted isoindolines via Rh(iii)-catalyzed tandem oxidative olefination-cyclization of 4-aryl cyclic sulfamidates.
Chemical communications (Cambridge, England), 2016, 52, 4286-4289
7118654 CIFC17 H19 N O7 SP 21 21 216.2084; 13.742; 21.5303
90; 90; 90
1836.88Son, Se-Mi; Seo, Yeon Ji; Lee, Hyeon-Kyu
Stereoselective synthesis of 1,3-disubstituted isoindolines via Rh(iii)-catalyzed tandem oxidative olefination-cyclization of 4-aryl cyclic sulfamidates.
Chemical communications (Cambridge, England), 2016, 52, 4286-4289
7118655 CIFC11 H10 N2 O3 SP 1 21/c 18.1628; 8.1111; 17.0276
90; 90.533; 90
1127.34Son, Se-Mi; Seo, Yeon Ji; Lee, Hyeon-Kyu
Stereoselective synthesis of 1,3-disubstituted isoindolines via Rh(iii)-catalyzed tandem oxidative olefination-cyclization of 4-aryl cyclic sulfamidates.
Chemical communications (Cambridge, England), 2016, 52, 4286-4289
7118656 CIFC16 H17 N O7 SP 1 21 16.1638; 14.6526; 9.1812
90; 102.564; 90
809.35Son, Se-Mi; Seo, Yeon Ji; Lee, Hyeon-Kyu
Stereoselective synthesis of 1,3-disubstituted isoindolines via Rh(iii)-catalyzed tandem oxidative olefination-cyclization of 4-aryl cyclic sulfamidates.
Chemical communications (Cambridge, England), 2016, 52, 4286-4289
7118657 CIFC55 H88 O2P 21 21 217.3985; 19.856; 35.447
90; 90; 90
5207.3Wang, Jian-Rong; Yu, Qihui; Dai, Wenjuan; Mei, Xuefeng
Drug-drug co-crystallization presents a new opportunity for the development of stable vitamins.
Chemical communications (Cambridge, England), 2016, 52, 3572-3575
7118658 CIFC55 H88 O2P 1 21 120.6101; 7.2054; 35.408
90; 105.513; 90
5066.7Wang, Jian-Rong; Yu, Qihui; Dai, Wenjuan; Mei, Xuefeng
Drug-drug co-crystallization presents a new opportunity for the development of stable vitamins.
Chemical communications (Cambridge, England), 2016, 52, 3572-3575
7118659 CIFC49 H51 Br2 Cu N5P c a 2113.4817; 41.726; 31.034
90; 90; 90
17458Omori, Hiroto; Hiroto, Satoru; Shinokubo, Hiroshi
The synthesis of Ni(II) and Al(III) 10-azacorroles through coordination-induced cyclisation involving 1,2-migration.
Chemical communications (Cambridge, England), 2016, 52, 3540-3543
7118660 CIFC45 H39.5 Br1.5 Cl2 N5 NiP 1 21/c 116.489; 20.454; 12.894
90; 111.783; 90
4038.2Omori, Hiroto; Hiroto, Satoru; Shinokubo, Hiroshi
The synthesis of Ni(II) and Al(III) 10-azacorroles through coordination-induced cyclisation involving 1,2-migration.
Chemical communications (Cambridge, England), 2016, 52, 3540-3543
7118661 CIFC7 H8 Cl3 SbP -17.433; 11.831; 12.3401
75.797; 83.716; 89.257
1045.59Lo, Rabindranath; Švec, Petr; Růžičková, Zdeňka; Růžička, Aleš; Hobza, Pavel
On the nature of the stabilisation of the Eπ pnicogen bond in the SbCl3toluene complex.
Chemical communications (Cambridge, England), 2016, 52, 3500-3503
7118662 CIFC16 H14 O2C 1 2/c 113.8731; 8.1105; 23.2586
90; 111.782; 90
2430.2Sun, Denan; Li, Bijin; Lan, Jingbo; Huang, Quan; You, Jingsong
Chelation-assisted Pd-catalysed ortho-selective oxidative C-H/C-H cross-coupling of aromatic carboxylic acids with arenes and intramolecular Friedel-Crafts acylation: one-pot formation of fluorenones.
Chemical communications (Cambridge, England), 2016, 52, 3635-3638
7118663 CIFC14 H8 F2 O2P 1 21/n 17.2744; 11.9968; 12.4989
90; 99.099; 90
1077.05Sun, Denan; Li, Bijin; Lan, Jingbo; Huang, Quan; You, Jingsong
Chelation-assisted Pd-catalysed ortho-selective oxidative C-H/C-H cross-coupling of aromatic carboxylic acids with arenes and intramolecular Friedel-Crafts acylation: one-pot formation of fluorenones.
Chemical communications (Cambridge, England), 2016, 52, 3635-3638
7118664 CIFC30 H32 B2 Co2 N16 O11C 1 2/c 126.1535; 13.6168; 17.1807
90; 126.056; 90
4946.5Zhang, Hai-Xia; Liu, Min; Xu, Guilan; Liu, Liyang; Zhang, Jian
Selectivity of CO2via pore space partition in zeolitic boron imidazolate frameworks.
Chemical communications (Cambridge, England), 2016, 52, 3552-3555
7118665 CIFC21 H24 B Cd N9 O4P 1 21/n 19.003; 17.382; 17.057
90; 104.595; 90
2583Zhang, Hai-Xia; Liu, Min; Xu, Guilan; Liu, Liyang; Zhang, Jian
Selectivity of CO2via pore space partition in zeolitic boron imidazolate frameworks.
Chemical communications (Cambridge, England), 2016, 52, 3552-3555
7118666 CIFC111 H220 Cu18 N30 O42 S20 W5P 1 21/m 116.682; 21.662; 27.674
90; 96.49; 90
9936Zhang, Jinfang; Jia, Ding; Humphrey, Mark G.; Meng, Suci; Zaworotko, Michael J.; Cifuentes, Marie P.; Zhang, Chi
Ammonium-crown ether supramolecular cation-templated assembly of an unprecedented heterobicluster-metal coordination polymer with enhanced NLO properties.
Chemical communications (Cambridge, England), 2016, 52, 3797-3800
7118667 CIFC176 H266 Ag41 B0 F0 N7 O78 Si2 W22P -120.0748; 26.1979; 28.8126
104.876; 90.485; 92.908
14622.7Liu, Kuan-Guan; Liu, Xi-Yan; Guan, Zong-Jie; Shi, Kang; Lin, Yu-Mei; Wang, Quan-Ming
The transformation of polyoxometalates in the formation of intercluster compound [Ag41(α-SiW10O37)((t)BuC[triple bond, length as m-dash]C)27(CH3CN)3][β-SiW12O40].
Chemical communications (Cambridge, England), 2016, 52, 3801-3804
7118668 CIFC29 H21 N OP 21 21 219.002; 13.225; 17.293
90; 90; 90
2058.8Nagaraju Barsu; Malay Sen; J. Richard Premkumar; Basker Sundararaju
Cobalt(III) catalyzed C-8 selective C-H and C-O coupling of quinoline N-oxide with internal alkynes via C-H activation and oxygen atom transfer
Chem.Commun., 2016, 52, 1338
7118673 CIFC18 H44 Al B Cl4 N2 O6P n a 2112.7434; 13.7696; 16.4706
90; 90; 90
2890.12Less, Robert J.; García-Rodríguez, Raúl; Simmonds, Hayley R.; Allen, Lucy K.; Bond, Andrew D.; Wright, Dominic S.
Use of crown ethers to isolate intermediates in ammonia-borane dehydrocoupling reactions.
Chemical communications (Cambridge, England), 2016, 52, 3650-3652
7118674 CIFC16 H37 Al B Cl4 N O7P n a 2119.0847; 16.0369; 8.8244
90; 90; 90
2700.79Less, Robert J.; García-Rodríguez, Raúl; Simmonds, Hayley R.; Allen, Lucy K.; Bond, Andrew D.; Wright, Dominic S.
Use of crown ethers to isolate intermediates in ammonia-borane dehydrocoupling reactions.
Chemical communications (Cambridge, England), 2016, 52, 3650-3652
7118675 CIFC24 H56 Al B Cl4 N2 O12P 1 n 113.6132; 16.0212; 17.7762
90; 94.329; 90
3865.9Less, Robert J.; García-Rodríguez, Raúl; Simmonds, Hayley R.; Allen, Lucy K.; Bond, Andrew D.; Wright, Dominic S.
Use of crown ethers to isolate intermediates in ammonia-borane dehydrocoupling reactions.
Chemical communications (Cambridge, England), 2016, 52, 3650-3652
7118676 CIFC24 H26 N2P b c n11.9458; 12.6538; 25.2208
90; 90; 90
3812.4Hepburn, Hamish B.; Melchiorre, Paolo
Brønsted acid-catalysed conjugate addition of photochemically generated α-amino radicals to alkenylpyridines.
Chemical communications (Cambridge, England), 2016, 52, 3520-3523
7118677 CIFC13 H18 Cl3 N3 O4 SP 21 21 214.9957; 17.7935; 20.4746
90; 90; 90
1820.01Izgu, Enver Cagri; Oh, Seung Soo; Szostak, Jack W.
Synthesis of activated 3'-amino-3'-deoxy-2-thio-thymidine, a superior substrate for the nonenzymatic copying of nucleic acid templates.
Chemical communications (Cambridge, England), 2016, 52, 3684-3686
7118678 CIFC48 Cu16 Se31 Sn6P a -321.7015; 21.7015; 21.7015
90; 90; 90
10220.4Yang, Huajun; Wang, Le; Hu, Dandan; Lin, Jian; Luo, Li; Wang, Hongxiang; Wu, Tao
A novel copper-rich open-framework chalcogenide constructed from octahedral Cu4Se6 and icosahedral Cu8Se13 nanoclusters.
Chemical communications (Cambridge, England), 2016, 52, 4140-4143
7118679 CIFC15 H10 Cl2 N2 O6P -16.9802; 7.0738; 17.9149
88.122; 80.589; 67.293
804.58Ding, Ransheng; Wolf, Christian
Catalytic insertion of aldehydes into dihalonitroacetophenones via sequential bond scission-aldol reaction-acyl transfer.
Chemical communications (Cambridge, England), 2016, 52, 3576-3579
7118680 CIFC15 H10 Cl2 N2 O6P n a 217.0035; 37.401; 6.0429
90; 90; 90
1582.9Ding, Ransheng; Wolf, Christian
Catalytic insertion of aldehydes into dihalonitroacetophenones via sequential bond scission-aldol reaction-acyl transfer.
Chemical communications (Cambridge, England), 2016, 52, 3576-3579
7118681 CIFC39 H50 N3 P SiP -19.8573; 10.9843; 19.208
93.409; 98.295; 115.316
1843.2Khan, Shabana; Pal, Shiv; Kathewad, Neha; Purushothaman, Indu; De, Susmita; Parameswaran, Pattiyil
Stepwise isolation of an unprecedented silylene supported dinuclear gold(i) cation with aurophilic interaction.
Chemical communications (Cambridge, England), 2016, 52, 3880-3882
7118682 CIFC40 H52 Au Cl3 N3 P SiP -111.933; 12.334; 17.499
81.27; 82.82; 65.87
2318Khan, Shabana; Pal, Shiv; Kathewad, Neha; Purushothaman, Indu; De, Susmita; Parameswaran, Pattiyil
Stepwise isolation of an unprecedented silylene supported dinuclear gold(i) cation with aurophilic interaction.
Chemical communications (Cambridge, England), 2016, 52, 3880-3882
7118683 CIFC80 H104 Au2 Cl4 F12 N6 P2 Sb2 Si2P -112.058; 14.762; 15.001
116.997; 104.713; 95.716
2229Khan, Shabana; Pal, Shiv; Kathewad, Neha; Purushothaman, Indu; De, Susmita; Parameswaran, Pattiyil
Stepwise isolation of an unprecedented silylene supported dinuclear gold(i) cation with aurophilic interaction.
Chemical communications (Cambridge, England), 2016, 52, 3880-3882
7118684 CIFC31 H44 P2 Pd SiP b c a17.0258; 18.6108; 19.0877
90; 90; 90
6048.2Comanescu, Cezar C.; Iluc, Vlad M.
E-H (E = B, Si, Ge) bond activation of pinacolborane, silanes, and germanes by nucleophilic palladium carbene complexes.
Chemical communications (Cambridge, England), 2016, 52, 9048-9051
7118685 CIFC37 H48 P2 Pd SiP 1 21/n 19.402; 19.186; 19.053
90; 93.284; 90
3431.3Comanescu, Cezar C.; Iluc, Vlad M.
E-H (E = B, Si, Ge) bond activation of pinacolborane, silanes, and germanes by nucleophilic palladium carbene complexes.
Chemical communications (Cambridge, England), 2016, 52, 9048-9051
7118686 CIFC43 H52 P2 Pd SiP -19.5894; 10.6642; 19.5486
78.851; 76.192; 76.697
1868.9Comanescu, Cezar C.; Iluc, Vlad M.
E-H (E = B, Si, Ge) bond activation of pinacolborane, silanes, and germanes by nucleophilic palladium carbene complexes.
Chemical communications (Cambridge, England), 2016, 52, 9048-9051
7118687 CIFC48 H64 P2 Pd SiP 1 21/c 111.401; 12.592; 30.423
90; 97.666; 90
4328.5Comanescu, Cezar C.; Iluc, Vlad M.
E-H (E = B, Si, Ge) bond activation of pinacolborane, silanes, and germanes by nucleophilic palladium carbene complexes.
Chemical communications (Cambridge, England), 2016, 52, 9048-9051
7118688 CIFC31 H49 B O2 P2 PdP 1 21/c 117.3966; 10.0819; 19.8141
90; 115.896; 90
3126.3Comanescu, Cezar C.; Iluc, Vlad M.
E-H (E = B, Si, Ge) bond activation of pinacolborane, silanes, and germanes by nucleophilic palladium carbene complexes.
Chemical communications (Cambridge, England), 2016, 52, 9048-9051
7118689 CIFC31 H44 Ge P2 PdP -18.3636; 10.0092; 18.4078
94.2185; 93.3363; 100.776
1505.62Comanescu, Cezar C.; Iluc, Vlad M.
E-H (E = B, Si, Ge) bond activation of pinacolborane, silanes, and germanes by nucleophilic palladium carbene complexes.
Chemical communications (Cambridge, England), 2016, 52, 9048-9051
7118690 CIFC37 H48 Ge P2 PdI 1 2/a 122.9918; 12.0605; 25.6249
90; 105.728; 90
6839.6Comanescu, Cezar C.; Iluc, Vlad M.
E-H (E = B, Si, Ge) bond activation of pinacolborane, silanes, and germanes by nucleophilic palladium carbene complexes.
Chemical communications (Cambridge, England), 2016, 52, 9048-9051
7118691 CIFC43 H52 Ge P2 PdP 1 21/c 111.6399; 19.396; 17.6306
90; 105.713; 90
3831.7Comanescu, Cezar C.; Iluc, Vlad M.
E-H (E = B, Si, Ge) bond activation of pinacolborane, silanes, and germanes by nucleophilic palladium carbene complexes.
Chemical communications (Cambridge, England), 2016, 52, 9048-9051
7118692 CIFC85 H114 Ge2 P6 Pd2P 1 21/c 19.543; 20.387; 21.3674
90; 99.3602; 90
4101.7Comanescu, Cezar C.; Iluc, Vlad M.
E-H (E = B, Si, Ge) bond activation of pinacolborane, silanes, and germanes by nucleophilic palladium carbene complexes.
Chemical communications (Cambridge, England), 2016, 52, 9048-9051
7118693 CIFC22 H23 Br N2 O4 SP 1 21 110.3517; 17.5995; 13.2555
90; 103.504; 90
2348.2Cheng, Ping; Guo, Wengang; Chen, Ping; Liu, Yan; Du, Xin; Li, Can
The enantioselective construction of chiral spirooxindole-based 4-thiazolidinone via asymmetric catalytic formal [3+2] annulation using a bifunctional catalyst.
Chemical communications (Cambridge, England), 2016, 52, 3418-3421
7118694 CIFC22 H21 Br N2 O5 SP 21 21 219.0059; 12.9439; 18.305
90; 90; 90
2133.8Cheng, Ping; Guo, Wengang; Chen, Ping; Liu, Yan; Du, Xin; Li, Can
The enantioselective construction of chiral spirooxindole-based 4-thiazolidinone via asymmetric catalytic formal [3+2] annulation using a bifunctional catalyst.
Chemical communications (Cambridge, England), 2016, 52, 3418-3421
7118695 CIFC79 H114 Co2 N4P 1 21/c 117.663; 18.6473; 23.0752
90; 107.032; 90
7266.9Andjaba, John M.; Tye, Jesse W.; Yu, Pony; Pappas, Iraklis; Bradley, Christopher A.
Cp*Co(IPr): synthesis and reactivity of an unsaturated Co(i) complex.
Chemical communications (Cambridge, England), 2016, 52, 2469-2472
7118696 CIFC38 H51 Co N2 OA e a 223.5831; 17.9998; 16.1483
90; 90; 90
6854.8Andjaba, John M.; Tye, Jesse W.; Yu, Pony; Pappas, Iraklis; Bradley, Christopher A.
Cp*Co(IPr): synthesis and reactivity of an unsaturated Co(i) complex.
Chemical communications (Cambridge, England), 2016, 52, 2469-2472
7118697 CIFC49 H32 Cl2 N4R -3 :H30.549; 30.549; 11.026
90; 90; 120
8911.33Feng, Cunfang; Wang, Kai; Xu, Yuanxiang; Liu, Liqun; Zou, Bo; Lu, Ping
Unique piezochromic fluorescence behavior of organic crystal of carbazole-substituted CNDSB.
Chemical communications (Cambridge, England), 2016, 52, 3836-3839
7118698 CIFC28 H22 Br2 N4C 1 2/c 126.108; 8.7687; 21.6124
90; 112.199; 90
4581.1Xiong, Ruisheng; Arkhypchuk, Anna I.; Kovacs, Daniel; Orthaber, Andreas; Eszter Borbas, K.
Directly linked hydroporphyrin dimers.
Chemical communications (Cambridge, England), 2016, 52, 9056-9058
7118699 CIFC29 H35 Cl Ir N O2P -18.5776; 11.6804; 14.133
98.609; 98.743; 101.874
1345.4Mukhopadhyay, Sujay; Singh, Roop Shikha; Biswas, Arnab; Pandey, Daya Shankar
Photochemical water oxidation by cyclometalated iridium(iii) complexes: a mechanistic insight.
Chemical communications (Cambridge, England), 2016, 52, 3840-3843
7118700 CIFC28 H32 Cl Ir N2P -18.4227; 11.622; 13.821
100.173; 98.473; 99.561
1291.2Mukhopadhyay, Sujay; Singh, Roop Shikha; Biswas, Arnab; Pandey, Daya Shankar
Photochemical water oxidation by cyclometalated iridium(iii) complexes: a mechanistic insight.
Chemical communications (Cambridge, England), 2016, 52, 3840-3843
7118701 CIFC8 H6 I2 S4P 1 21/n 16.2612; 15.4368; 6.6118
90; 96.285; 90
635.21Jeannin, Olivier; Canadell, Enric; Auban-Senzier, Pascale; Fourmigué, Marc
Correlating conduction properties with the molecular symmetry: segregation of Z and E isomers in the charge-assisted, halogen-bonded cocrystal [(Z,E)-Me2I2TTF]2Br.
Chemical communications (Cambridge, England), 2016, 52, 308-311
7118702 CIFC18 H15 Br I4 N S8P 1 21/n 17.888; 27.12; 14.215
90; 95.259; 90
3028.1Jeannin, Olivier; Canadell, Enric; Auban-Senzier, Pascale; Fourmigué, Marc
Correlating conduction properties with the molecular symmetry: segregation of Z and E isomers in the charge-assisted, halogen-bonded cocrystal [(Z,E)-Me2I2TTF]2Br.
Chemical communications (Cambridge, England), 2016, 52, 308-311
7118703 CIFC26 H32 N2 O5 SP 1 21/n 19.814; 10.84; 23.074
90; 95.566; 90
2443.1Yang, Jin-Ming; Li, Peng-Hua; Wei, Yin; Tang, Xiang-Ying; Shi, Min
Gold(i)-catalyzed highly stereoselective synthesis of polycyclic indolines: the construction of four contiguous stereocenters.
Chemical communications (Cambridge, England), 2016, 52, 346-349
7118704 CIFC23 H24 N2 O4 SP 1 21/c 19.5226; 36.221; 24.769
90; 99.375; 90
8429.2Yang, Jin-Ming; Li, Peng-Hua; Wei, Yin; Tang, Xiang-Ying; Shi, Min
Gold(i)-catalyzed highly stereoselective synthesis of polycyclic indolines: the construction of four contiguous stereocenters.
Chemical communications (Cambridge, England), 2016, 52, 346-349
7118705 CIFC288 H288 Cu12 O108 Pd12I 4/m28.98; 28.98; 40.961
90; 90; 90
34401Teo, Jesse M.; Coghlan, Campbell J.; Evans, Jack D.; Tsivion, Ehud; Head-Gordon, Martin; Sumby, Christopher J.; Doonan, Christian J.
Hetero-bimetallic metal-organic polyhedra.
Chemical communications (Cambridge, England), 2016, 52, 276-279
7118706 CIFC288 H288 Ni12 O108 Pd12I 4/m29.174; 29.174; 41.296
90; 90; 90
35148Teo, Jesse M.; Coghlan, Campbell J.; Evans, Jack D.; Tsivion, Ehud; Head-Gordon, Martin; Sumby, Christopher J.; Doonan, Christian J.
Hetero-bimetallic metal-organic polyhedra.
Chemical communications (Cambridge, England), 2016, 52, 276-279
7118707 CIFC288 H288 O108 Pd12 Zn12I 4/m28.935; 28.935; 41.164
90; 90; 90
34464Teo, Jesse M.; Coghlan, Campbell J.; Evans, Jack D.; Tsivion, Ehud; Head-Gordon, Martin; Sumby, Christopher J.; Doonan, Christian J.
Hetero-bimetallic metal-organic polyhedra.
Chemical communications (Cambridge, England), 2016, 52, 276-279
7118708 CIFC65.5 H54 N3 O7.75 TbP 1 2/c 126.8876; 16.8644; 25.0129
90; 95.248; 90
11294.4Zhang, Zhao; He, Ya-Ni; Liu, Lin; Lü, Xing-Qiang; Zhu, Xun-Jin; Wong, Wai-Kwok; Pan, Mei; Su, Cheng-Yong
Pure white-light and colour-tuning of Eu(3+)-Gd(3+)-containing metallopolymer.
Chemical communications (Cambridge, England), 2016, 52, 3713-3716
7118718 CIFC18 H21 Br N2 O2 SiP -16.623; 8.437; 17.92
88.636; 88.061; 85.928
998Zhao, Yu-Lei; Cao, Zhong-Yan; Zeng, Xing-Ping; Shi, Jia-Meng; Yu, Yi-Hua; Zhou, Jian
Asymmetric sequential Au(i)/chiral tertiary amine catalysis: an enone-formation/cyanosilylation sequence to synthesize optically active 3-alkenyloxindoles from diazooxindoles.
Chemical communications (Cambridge, England), 2016, 52, 3943-3946
7118719 CIFC105 H109.5 N21 O21 S0.5P 1 21/c 134.596; 23.529; 32.903
90; 113.63; 90
24538Chandramouli, Nagula; Ferrand, Yann; Kauffmann, Brice; Huc, Ivan
Citric acid encapsulation by a double helical foldamer in competitive solvents.
Chemical communications (Cambridge, England), 2016, 52, 3939-3942
7118720 CIFC428 H413 N84 O92P -128.125; 30.271; 35.821
69.22; 80.81; 88.35
28134Chandramouli, Nagula; Ferrand, Yann; Kauffmann, Brice; Huc, Ivan
Citric acid encapsulation by a double helical foldamer in competitive solvents.
Chemical communications (Cambridge, England), 2016, 52, 3939-3942
7118721 CIFC35 H46 Cu F6 N4 PP 1 21/c 18.96; 24.2; 17.53
90; 104.8; 90
3675Cheung, Pui Man; Berger, Robert F.; Zakharov, Lev N.; Gilbertson, John D.
Square planar Cu(i) stabilized by a pyridinediimine ligand.
Chemical communications (Cambridge, England), 2016, 52, 4156-4159
7118722 CIFC33 H43 Cl Cu F6 N3 PP 1 21 18.6259; 11.8633; 16.6506
90; 100.785; 90
1673.8Cheung, Pui Man; Berger, Robert F.; Zakharov, Lev N.; Gilbertson, John D.
Square planar Cu(i) stabilized by a pyridinediimine ligand.
Chemical communications (Cambridge, England), 2016, 52, 4156-4159
7118723 CIFC34 H43 Cu F6 N3 O PP 1 21 18.8683; 12.1402; 16.1427
90; 100.426; 90
1709.3Cheung, Pui Man; Berger, Robert F.; Zakharov, Lev N.; Gilbertson, John D.
Square planar Cu(i) stabilized by a pyridinediimine ligand.
Chemical communications (Cambridge, England), 2016, 52, 4156-4159
7118724 CIFC39 H54 Cu F6 N4 O PP 112.4078; 13.287; 14.052
96.92; 105.67; 107.141
2080.5Cheung, Pui Man; Berger, Robert F.; Zakharov, Lev N.; Gilbertson, John D.
Square planar Cu(i) stabilized by a pyridinediimine ligand.
Chemical communications (Cambridge, England), 2016, 52, 4156-4159
7118725 CIFC42 H38 Cu F6 N6 PP 1 21/n 114.8812; 17.179; 15.5446
90; 95.597; 90
3954.9Cheung, Pui Man; Berger, Robert F.; Zakharov, Lev N.; Gilbertson, John D.
Square planar Cu(i) stabilized by a pyridinediimine ligand.
Chemical communications (Cambridge, England), 2016, 52, 4156-4159
7118726 CIFC22 N9 Na O5P 1 21/n 132.313; 19.769; 3.7343
90; 98.59; 90
2358.7Lee, Gil Ryeong; Ohtsu, Hiroyoshi; Koo, Jinyoung; Yakiyama, Yumi; Park, Moon Jeong; Inoue, Daishi; Hashizume, Daisuke; Kawano, Masaki
Crystallinity-dependence of ionic conductivity in the ion pairs of a multi-interactive anion.
Chemical communications (Cambridge, England), 2016, 52, 3962-3965
7118727 CIFC27 H32 N9 Na O5P b c n13.908; 20.33; 10.298
90; 90; 90
2912Lee, Gil Ryeong; Ohtsu, Hiroyoshi; Koo, Jinyoung; Yakiyama, Yumi; Park, Moon Jeong; Inoue, Daishi; Hashizume, Daisuke; Kawano, Masaki
Crystallinity-dependence of ionic conductivity in the ion pairs of a multi-interactive anion.
Chemical communications (Cambridge, England), 2016, 52, 3962-3965
7118728 CIFC22 H16 N10 O3.75C 1 2/c 139.9667; 3.761; 35.3988
90; 122.88; 90
4468.59Lee, Gil Ryeong; Ohtsu, Hiroyoshi; Koo, Jinyoung; Yakiyama, Yumi; Park, Moon Jeong; Inoue, Daishi; Hashizume, Daisuke; Kawano, Masaki
Crystallinity-dependence of ionic conductivity in the ion pairs of a multi-interactive anion.
Chemical communications (Cambridge, England), 2016, 52, 3962-3965
7118729 CIFC22.88 H19 N10 O0.87P 42/n21.6792; 21.6792; 9.235
90; 90; 90
4340.34Lee, Gil Ryeong; Ohtsu, Hiroyoshi; Koo, Jinyoung; Yakiyama, Yumi; Park, Moon Jeong; Inoue, Daishi; Hashizume, Daisuke; Kawano, Masaki
Crystallinity-dependence of ionic conductivity in the ion pairs of a multi-interactive anion.
Chemical communications (Cambridge, England), 2016, 52, 3962-3965
7118730 CIFC17 H22 I2 N2 O3P 21 21 219.1833; 10.6603; 20.8558
90; 90; 90
2041.7Huang, Hai; Tang, Luning; Han, Xiaobo; He, Guangke; Xi, Yang; Zhu, Hongjun
Regioselective iodoamination of terminal ynamides for the synthesis of α-amino-β,β-diiodo-enamides.
Chemical communications (Cambridge, England), 2016, 52, 4321-4324
7118731 CIFC15 H13 N O3 S2P 1 21/n 114.7831; 5.6288; 18.2621
90; 98.364; 90
1503.4Swapna, Battini; Suresh, Kuthuru; Nangia, Ashwini
Color polymorphs of aldose reductase inhibitor epalrestat: configurational, conformational and synthon differences.
Chemical communications (Cambridge, England), 2016, 52, 4037-4040
7118732 CIFC15 H13 N O3 S2C 1 2/c 113.7384; 9.1063; 24.1429
90; 100.747; 90
2967.44Swapna, Battini; Suresh, Kuthuru; Nangia, Ashwini
Color polymorphs of aldose reductase inhibitor epalrestat: configurational, conformational and synthon differences.
Chemical communications (Cambridge, England), 2016, 52, 4037-4040
7118733 CIFC15 H13 N O3 S2P -18.1399; 11.5584; 16.1506
96.721; 93.818; 104.724
1452.2Swapna, Battini; Suresh, Kuthuru; Nangia, Ashwini
Color polymorphs of aldose reductase inhibitor epalrestat: configurational, conformational and synthon differences.
Chemical communications (Cambridge, England), 2016, 52, 4037-4040
7118734 CIFC15 H13 N O3 S2P 1 21/c 111.4252; 6.9479; 19.4673
90; 102.898; 90
1506.35Swapna, Battini; Suresh, Kuthuru; Nangia, Ashwini
Color polymorphs of aldose reductase inhibitor epalrestat: configurational, conformational and synthon differences.
Chemical communications (Cambridge, England), 2016, 52, 4037-4040
7118735 CIFC66 H102 Cl4 Li N4 O4 W2C 1 2/c 123.7527; 12.0648; 25.9809
90; 113.065; 90
6850.2Ventura, K.; Prat, J. R.; Aguirre Quintana, L. M.; Goos, A.; Villagran, D.
Unprecedented W2(0) quadruply bonded complex supported by π-donor ligands.
Chemical communications (Cambridge, England), 2016, 52, 3974-3976
7118736 CIFC58 H88 K2 N4 O2 W2P -110.879; 13.364; 23.272
96.119; 99.34; 105.7
3173.4Ventura, K.; Prat, J. R.; Aguirre Quintana, L. M.; Goos, A.; Villagran, D.
Unprecedented W2(0) quadruply bonded complex supported by π-donor ligands.
Chemical communications (Cambridge, England), 2016, 52, 3974-3976
7118737 CIFC24 H44 Br F10 P2 Pd S2P -110.6334; 12.3442; 12.6391
102.884; 91.323; 90.704
1616.56Berg, Claudia; Braun, Thomas; Laubenstein, Reik; Braun, Beatrice
Palladium-mediated borylation of pentafluorosulfanyl functionalized compounds: the crucial role of metal fluorido complexes.
Chemical communications (Cambridge, England), 2016, 52, 3931-3934
7118738 CIFC24 H46 F5 I P2 Pd SP 1 21/n 114.4952; 12.5053; 18.0453
90; 112.244; 90
3027.59Berg, Claudia; Braun, Thomas; Laubenstein, Reik; Braun, Beatrice
Palladium-mediated borylation of pentafluorosulfanyl functionalized compounds: the crucial role of metal fluorido complexes.
Chemical communications (Cambridge, England), 2016, 52, 3931-3934
7118739 CIFC24 H46 Br F5 P2 Pd SP 1 21/c 19.3877; 12.7766; 26.0735
90; 108.762; 90
2961.2Berg, Claudia; Braun, Thomas; Laubenstein, Reik; Braun, Beatrice
Palladium-mediated borylation of pentafluorosulfanyl functionalized compounds: the crucial role of metal fluorido complexes.
Chemical communications (Cambridge, England), 2016, 52, 3931-3934
7118740 CIFC12 H8 F10 S2P 1 21/n 112.1389; 8.7547; 13.5608
90; 100.44; 90
1417.3Berg, Claudia; Braun, Thomas; Laubenstein, Reik; Braun, Beatrice
Palladium-mediated borylation of pentafluorosulfanyl functionalized compounds: the crucial role of metal fluorido complexes.
Chemical communications (Cambridge, England), 2016, 52, 3931-3934
7118741 CIFC24 H45 F11 P2 Pd S2P -110.779; 12.164; 12.241
80.079; 89.555; 88.284
1580.3Berg, Claudia; Braun, Thomas; Laubenstein, Reik; Braun, Beatrice
Palladium-mediated borylation of pentafluorosulfanyl functionalized compounds: the crucial role of metal fluorido complexes.
Chemical communications (Cambridge, England), 2016, 52, 3931-3934
7118742 CIFC18 H18 B F20 O2 S4P -19.9552; 11.159; 13.6383
73.775; 71.961; 76.711
1366.1Berg, Claudia; Braun, Thomas; Laubenstein, Reik; Braun, Beatrice
Palladium-mediated borylation of pentafluorosulfanyl functionalized compounds: the crucial role of metal fluorido complexes.
Chemical communications (Cambridge, England), 2016, 52, 3931-3934
7118743 CIFC136 H191 Na6 O20P -117.7793; 18.0796; 22.8488
83.835; 84.664; 61.434
6405.9Ryan, Jason D.; Gagnon, Kevin J.; Teat, Simon J.; McIntosh, Ruaraidh D.
Flexible macrocycles as versatile supports for catalytically active metal clusters.
Chemical communications (Cambridge, England), 2016, 52, 9071-9073
7118744 CIFC200 H254 O24 Ti8C 1 2/c 142.023; 18.0435; 30.746
90; 95.407; 90
23209Ryan, Jason D.; Gagnon, Kevin J.; Teat, Simon J.; McIntosh, Ruaraidh D.
Flexible macrocycles as versatile supports for catalytically active metal clusters.
Chemical communications (Cambridge, England), 2016, 52, 9071-9073
7118745 CIFC140 H216 O23 Ti4P -114.496; 16.122; 17.367
77.94; 70.572; 63.959
3429.6Ryan, Jason D.; Gagnon, Kevin J.; Teat, Simon J.; McIntosh, Ruaraidh D.
Flexible macrocycles as versatile supports for catalytically active metal clusters.
Chemical communications (Cambridge, England), 2016, 52, 9071-9073
7118746 CIFC14 H14 F5 N OP -18.4914; 10.2896; 15.2108
89.626; 85.989; 89.673
1325.7Katayev, D.; Václavík, J; Brüning, F; Commare, B.; Togni, A.
Synthesis of quaternary α-perfluoroalkyl lactams via electrophilic perfluoroalkylation.
Chemical communications (Cambridge, England), 2016, 52, 4049-4052
7118747 CIFC10 H17 Br O2P 1 21 16.2235; 9.799; 9.2211
90; 97.094; 90
558.04Verma, Ajay; Jana, Sadhan; Durga Prasad, Ch; Yadav, Abhimanyu; Kumar, Sangit
Organoselenium and DMAP co-catalysis: regioselective synthesis of medium-sized halolactones and bromooxepanes from unactivated alkenes.
Chemical communications (Cambridge, England), 2016, 52, 4179-4182
7118748 CIFC7 H11 Br O2P b c a13.176; 7.6455; 15.656
90; 90; 90
1577.1Verma, Ajay; Jana, Sadhan; Durga Prasad, Ch; Yadav, Abhimanyu; Kumar, Sangit
Organoselenium and DMAP co-catalysis: regioselective synthesis of medium-sized halolactones and bromooxepanes from unactivated alkenes.
Chemical communications (Cambridge, England), 2016, 52, 4179-4182
7118749 CIFC14 H14 O2 SeP 1 21/n 16.1527; 26.213; 8.0982
90; 95.797; 90
1299.4Verma, Ajay; Jana, Sadhan; Durga Prasad, Ch; Yadav, Abhimanyu; Kumar, Sangit
Organoselenium and DMAP co-catalysis: regioselective synthesis of medium-sized halolactones and bromooxepanes from unactivated alkenes.
Chemical communications (Cambridge, England), 2016, 52, 4179-4182
7118750 CIFC14 H14 Br2 O2 SeP -17.8195; 8.6185; 11.8731
84.638; 85.762; 75.567
770.45Verma, Ajay; Jana, Sadhan; Durga Prasad, Ch; Yadav, Abhimanyu; Kumar, Sangit
Organoselenium and DMAP co-catalysis: regioselective synthesis of medium-sized halolactones and bromooxepanes from unactivated alkenes.
Chemical communications (Cambridge, England), 2016, 52, 4179-4182
7118751 CIFC11 H11 Br O4P 1 21/c 110.6207; 8.4724; 12.7806
90; 104.935; 90
1111.18Verma, Ajay; Jana, Sadhan; Durga Prasad, Ch; Yadav, Abhimanyu; Kumar, Sangit
Organoselenium and DMAP co-catalysis: regioselective synthesis of medium-sized halolactones and bromooxepanes from unactivated alkenes.
Chemical communications (Cambridge, England), 2016, 52, 4179-4182
7118752 CIFC11 H12 Br N O4P 1 21/n 15.4464; 8.716; 25.2572
90; 91.713; 90
1198.44Santra, Sourav Kumar; Banerjee, Arghya; Rajamanickam, Suresh; Khatun, Nilufa; Patel, Bhisma K.
Pd(II)/CuBr2 catalysed keto α-Csp3-H benzoxylation of N,N-dialkylamides directed by o-hydroxy groups.
Chemical communications (Cambridge, England), 2016, 52, 4501-4504
7118753 CIFC13 H16 Cl2 N4 O3P 1 21/n 16.9732; 15.0872; 14.2862
90; 95.411; 90
1496.3Sashuk, Volodymyr; Butkiewicz, Helena; Fiałkowski, Marcin; Danylyuk, Oksana
Triggering autocatalytic reaction by host-guest interactions.
Chemical communications (Cambridge, England), 2016, 52, 4191-4194
7118754 CIFC49 H49 Cl N28 O29P 1 c 112.6037; 18.505; 14.088
90; 97.74; 90
3255.83Sashuk, Volodymyr; Butkiewicz, Helena; Fiałkowski, Marcin; Danylyuk, Oksana
Triggering autocatalytic reaction by host-guest interactions.
Chemical communications (Cambridge, England), 2016, 52, 4191-4194
7118755 CIFC13 H15 Cl N4 O2P 1 21/a 17.4885; 10.5846; 17.5033
90; 98.615; 90
1371.71Sashuk, Volodymyr; Butkiewicz, Helena; Fiałkowski, Marcin; Danylyuk, Oksana
Triggering autocatalytic reaction by host-guest interactions.
Chemical communications (Cambridge, England), 2016, 52, 4191-4194
7118756 CIFC42 H42 N24 O21.5P 1 21 112.6407; 15.8596; 12.6429
90; 102.853; 90
2471.1Sashuk, Volodymyr; Butkiewicz, Helena; Fiałkowski, Marcin; Danylyuk, Oksana
Triggering autocatalytic reaction by host-guest interactions.
Chemical communications (Cambridge, England), 2016, 52, 4191-4194
7118757 CIFC38 H41 N O2P 1 21 19.5705; 20.6075; 15.8172
90; 90.295; 90
3119.49Deng, Yu-Hua; Zhang, Xiang-Zhi; Yu, Ke-Yin; Yan, Xu; Du, Ji-Yuan; Huang, Hanmin; Fan, Chun-An
Bifunctional tertiary amine-squaramide catalyzed asymmetric catalytic 1,6-conjugate addition/aromatization of para-quinone methides with oxindoles.
Chemical communications (Cambridge, England), 2016, 52, 4183-4186
7118758 CIFC160 H112 Cu6 F18 Ge3 N32P m -321.2111; 21.2111; 21.2111
90; 90; 90
9543.1Lusi, Matteo; Fechine, Pierre B. A.; Chen, Kai-Jie; Perry, John J.; Zaworotko, Michael J.
A rare cationic building block that generates a new type of polyhedral network with "cross-linked" pto topology.
Chemical communications (Cambridge, England), 2016, 52, 4160-4162
7118759 CIFC160 H112 Cu6 F18 N32 Si3P m -321.1882; 21.1882; 21.1882
90; 90; 90
9512.2Lusi, Matteo; Fechine, Pierre B. A.; Chen, Kai-Jie; Perry, John J.; Zaworotko, Michael J.
A rare cationic building block that generates a new type of polyhedral network with "cross-linked" pto topology.
Chemical communications (Cambridge, England), 2016, 52, 4160-4162
7118760 CIFC160 H112 Cu6 F18 N32 Sn3P m -321.2379; 21.2379; 21.2379
90; 90; 90
9579.3Lusi, Matteo; Fechine, Pierre B. A.; Chen, Kai-Jie; Perry, John J.; Zaworotko, Michael J.
A rare cationic building block that generates a new type of polyhedral network with "cross-linked" pto topology.
Chemical communications (Cambridge, England), 2016, 52, 4160-4162
7118761 CIFC160 H112 Cu6 F18 N32 Ti3P m -321.2174; 21.2174; 21.2174
90; 90; 90
9551.6Lusi, Matteo; Fechine, Pierre B. A.; Chen, Kai-Jie; Perry, John J.; Zaworotko, Michael J.
A rare cationic building block that generates a new type of polyhedral network with "cross-linked" pto topology.
Chemical communications (Cambridge, England), 2016, 52, 4160-4162
7118762 CIFC160 H112 Cu6 F18 N32 Zr3P m -321.165; 21.165; 21.165
90; 90; 90
9481Lusi, Matteo; Fechine, Pierre B. A.; Chen, Kai-Jie; Perry, John J.; Zaworotko, Michael J.
A rare cationic building block that generates a new type of polyhedral network with "cross-linked" pto topology.
Chemical communications (Cambridge, England), 2016, 52, 4160-4162
7118763 CIFC75 H81 Cl9 N6 O8 S2P -112.1788; 13.6793; 24.891
89.173; 85.674; 65.484
3761.5Huang, Guobao; Valkonen, Arto; Rissanen, Kari; Jiang, Wei
endo-Functionalized molecular tubes: selective encapsulation of neutral molecules in non-polar media.
Chemical communications (Cambridge, England), 2016, 52, 9078-9081
7118764 CIFC9 H24 B10 N2 O SC 1 2 126.2252; 6.7734; 11.5919
90; 115.831; 90
1853.37de Bruin, Gerjan; Mock, Elliot D.; Hoogendoorn, Sascha; van den Nieuwendijk, Adrianus M. C. H.; Mazurek, Jaroslaw; van der Marel, Gijsbert A.; Florea, Bogdan I.; Overkleeft, Herman S.
Enantioselective synthesis of adamantylalanine and carboranylalanine and their incorporation into the proteasome inhibitor bortezomib.
Chemical communications (Cambridge, England), 2016, 52, 4064-4067
7118765 CIFC9 H26 B10 N2 O2 SP 21 21 216.7451; 11.1419; 26.4844
90; 90; 90
1990.39de Bruin, Gerjan; Mock, Elliot D.; Hoogendoorn, Sascha; van den Nieuwendijk, Adrianus M. C. H.; Mazurek, Jaroslaw; van der Marel, Gijsbert A.; Florea, Bogdan I.; Overkleeft, Herman S.
Enantioselective synthesis of adamantylalanine and carboranylalanine and their incorporation into the proteasome inhibitor bortezomib.
Chemical communications (Cambridge, England), 2016, 52, 4064-4067
7118766 CIFC28 H47 N3 O6P 1 21 111.5615; 10.114; 12.3397
90; 100.223; 90
1420.01Zalewski, A. N.; Nathanael, J. G.; White, J. M.; Wille, U.
Oxidation of cholesterol and O-protected derivatives by the environmental pollutant NO2˙.
Chemical communications (Cambridge, England), 2016, 52, 4060-4063
7118767 CIFC28 H23 Cl N O P Pd SP 21 21 218.3737; 12.3461; 23.8575
90; 90; 90
2466.45Yang, Xiang-Yuan; Tay, Wee Shan; Li, Yongxin; Pullarkat, Sumod A.; Leung, Pak-Hing
The synthesis and efficient one-pot catalytic "self-breeding" of asymmetrical NC(sp(3))E-hybridised pincer complexes.
Chemical communications (Cambridge, England), 2016, 52, 4211-4214
7118768 CIFC28 H23 Cl N O2 P PdP 1 21 18.4079; 12.0255; 23.7756
90; 90.682; 90
2403.8Yang, Xiang-Yuan; Tay, Wee Shan; Li, Yongxin; Pullarkat, Sumod A.; Leung, Pak-Hing
The synthesis and efficient one-pot catalytic "self-breeding" of asymmetrical NC(sp(3))E-hybridised pincer complexes.
Chemical communications (Cambridge, England), 2016, 52, 4211-4214
7118769 CIFC27 H43 N3 O5P 1 21/c 111.0838; 50.0332; 10.6703
90; 107.01; 90
5658.4Angelici, G.; Bhattacharjee, N.; Roy, O.; Faure, S.; Didierjean, C.; Jouffret, L.; Jolibois, F.; Perrin, L.; Taillefumier, C.
Weak backbone CHO[double bond, length as m-dash]C and side chain tButBu London interactions help promote helix folding of achiral NtBu peptoids.
Chemical communications (Cambridge, England), 2016, 52, 4573-4576
7118770 CIFC37 H64 N5 O6P 1 21 111.149; 17.2409; 11.1991
90; 116.772; 90
1921.9Angelici, G.; Bhattacharjee, N.; Roy, O.; Faure, S.; Didierjean, C.; Jouffret, L.; Jolibois, F.; Perrin, L.; Taillefumier, C.
Weak backbone CHO[double bond, length as m-dash]C and side chain tButBu London interactions help promote helix folding of achiral NtBu peptoids.
Chemical communications (Cambridge, England), 2016, 52, 4573-4576
7118771 CIFC23 H26 N2 O3P 1 21/n 15.1957; 24.5851; 16.0276
90; 93.625; 90
2043.22Smith, Joshua J.; Best, Daniel; Lam, Hon Wai
Copper-catalyzed borylative coupling of vinylazaarenes and N-Boc imines.
Chemical communications (Cambridge, England), 2016, 52, 3770-3772
7118772 CIFC21 H24 N2 O3 SP 1 21/c 15.28349; 9.9736; 36.4673
90; 92.3374; 90
1920.06Smith, Joshua J.; Best, Daniel; Lam, Hon Wai
Copper-catalyzed borylative coupling of vinylazaarenes and N-Boc imines.
Chemical communications (Cambridge, England), 2016, 52, 3770-3772
7118773 CIFC28 H19 B NP -111.899; 13.11; 18.036
73.51; 89.05; 64.38
2414.2Huang, Huanan; Pan, Zexiong; Cui, Chunming
The synthesis of BN-embedded tetraphenes and their photophysical properties.
Chemical communications (Cambridge, England), 2016, 52, 4227-4230
7118774 CIFC36 H24 B NP -19.942; 16.9; 18.738
105.481; 92.118; 92.215
3028.2Huang, Huanan; Pan, Zexiong; Cui, Chunming
The synthesis of BN-embedded tetraphenes and their photophysical properties.
Chemical communications (Cambridge, England), 2016, 52, 4227-4230
7118775 CIFC8 H7 Au O2 SP b c a37.4027; 7.01569; 6.36593
90; 90; 90
1670.46Lavenn, Christophe; Guillou, Nathalie; Monge, Miguel; Podbevšek, Darjan; Ledoux, Gilles; Fateeva, Alexandra; Demessence, Aude
Shedding light on an ultra-bright photoluminescent lamellar gold thiolate coordination polymer [Au(p-SPhCO2Me)]n.
Chemical communications (Cambridge, England), 2016, 52, 9063-9066
7118776 CIFC16 H14 O4 S2P -15.9165; 7.6653; 17.819
79.997; 85.946; 75.915
771.57Lavenn, Christophe; Guillou, Nathalie; Monge, Miguel; Podbevšek, Darjan; Ledoux, Gilles; Fateeva, Alexandra; Demessence, Aude
Shedding light on an ultra-bright photoluminescent lamellar gold thiolate coordination polymer [Au(p-SPhCO2Me)]n.
Chemical communications (Cambridge, England), 2016, 52, 9063-9066
7118777 CIFC22 H34 N2 O7P 1 21 16.582; 10.854; 15.521
90; 94.787; 90
1105Wang, Siyuan; Taniguchi, Tohru; Monde, Kenji; Kawahata, Masatoshi; Yamaguchi, Kentaro; Otani, Yuko; Ohwada, Tomohiko
Hydrogen bonding to carbonyl oxygen of nitrogen-pyramidalized amide - detection of pyramidalization direction preference by vibrational circular dichroism spectroscopy.
Chemical communications (Cambridge, England), 2016, 52, 4018-4021
7118778 CIFC63 H66 B N2 O3 P2 RuP -112.4687; 15.731; 17.5343
67.02; 80.866; 70.636
2985.5Janes, Trevor; Osten, Kimberly M.; Pantaleo, Adam; Yan, Ellen; Yang, Yanxin; Song, Datong
Insertion of CO2 into the carbon-boron bond of a boronic ester ligand.
Chemical communications (Cambridge, England), 2016, 52, 4148-4151
7118779 CIFC55 H49 B N2 O5 P2 RuP 4110.4711; 10.4711; 44.073
90; 90; 90
4832.3Janes, Trevor; Osten, Kimberly M.; Pantaleo, Adam; Yan, Ellen; Yang, Yanxin; Song, Datong
Insertion of CO2 into the carbon-boron bond of a boronic ester ligand.
Chemical communications (Cambridge, England), 2016, 52, 4148-4151
7118780 CIFC40 H47 B N4 O2 ZnP -114.4273; 14.5211; 21.5927
100.551; 91.968; 102.418
4330.3Janes, Trevor; Osten, Kimberly M.; Pantaleo, Adam; Yan, Ellen; Yang, Yanxin; Song, Datong
Insertion of CO2 into the carbon-boron bond of a boronic ester ligand.
Chemical communications (Cambridge, England), 2016, 52, 4148-4151
7118781 CIFC41 H47 B N4 O4 ZnP b c a15.0418; 21.3952; 28.2235
90; 90; 90
9083Janes, Trevor; Osten, Kimberly M.; Pantaleo, Adam; Yan, Ellen; Yang, Yanxin; Song, Datong
Insertion of CO2 into the carbon-boron bond of a boronic ester ligand.
Chemical communications (Cambridge, England), 2016, 52, 4148-4151
7118782 CIFC34 H36 N4 ZnC 1 2/c 121.309; 10.0652; 29.168
90; 108.052; 90
5948Janes, Trevor; Osten, Kimberly M.; Pantaleo, Adam; Yan, Ellen; Yang, Yanxin; Song, Datong
Insertion of CO2 into the carbon-boron bond of a boronic ester ligand.
Chemical communications (Cambridge, England), 2016, 52, 4148-4151
7118783 CIFC30 H50 O4 Rh2 S2C 1 c 113.97; 25.545; 8.975
90; 97.362; 90
3176Nakai, Hidetaka; Matsuba, Kengo; Akimoto, Masataka; Nozaki, Tomonori; Matsumoto, Takahiro; Isobe, Kiyoshi; Irie, Masahiro; Ogo, Seiji
Photoinduced bending of rod-like millimetre-size crystals of a rhodium dithionite complex with n-pentyl moieties.
Chemical communications (Cambridge, England), 2016, 52, 4349-4352
7118784 CIFC9 H11 N O2 S2P 1 21/c 113.333; 5.705; 13.908
90; 91.316; 90
1057.6Javorskis, Tomas; Bagdžiūnas, Gintautas; Orentas, Edvinas
N-Tosyl-1,5,2,6-dithiadiazocane: a waste-free electrophilic sulfur reagent for the efficient synthesis of medium-ring S,N-heterocycles.
Chemical communications (Cambridge, England), 2016, 52, 4325-4328
7118785 CIFC19 H17 N O2 S2P 1 21/n 19.92; 17.616; 10.628
90; 111.511; 90
1728Javorskis, Tomas; Bagdžiūnas, Gintautas; Orentas, Edvinas
N-Tosyl-1,5,2,6-dithiadiazocane: a waste-free electrophilic sulfur reagent for the efficient synthesis of medium-ring S,N-heterocycles.
Chemical communications (Cambridge, England), 2016, 52, 4325-4328
7118786 CIFC279 H156 Co18 N124 O83 W12P -119.1433; 20.6439; 27.4002
77.864; 80.791; 66.5
9673.2Chorazy, Szymon; Rams, Michał; Hoczek, Anna; Czarnecki, Bernard; Sieklucka, Barbara; Ohkoshi, Shin-Ichi; Podgajny, Robert
Structural anisotropy of cyanido-bridged {CoW} single-molecule magnets induced by bidentate ligands: towards the rational enhancement of an energy barrier.
Chemical communications (Cambridge, England), 2016, 52, 4772-4775
7118787 CIFC68 H86 N12 O17 Ti4P -4 21 c17.367; 17.367; 13.73
90; 90; 90
4141.1Su, Hu-Chao; Wu, Yin-Yin; Hou, Jin-Le; Zhang, Guang-Ling; Zhu, Qin-Yu; Dai, Jie
Dye molecule bonded titanium alkoxide: a possible new type of dye for sensitized solar cells.
Chemical communications (Cambridge, England), 2016, 52, 4072-4075
7118788 CIFC28 H35 F24 N13 P4C 1 2/c 123.2328; 9.5152; 20.7638
90; 112.516; 90
4240.2Altmann, Philipp J.; Pöthig, Alexander
Capsoplexes: encapsulating complexes via guest recognition.
Chemical communications (Cambridge, England), 2016, 52, 9089-9092
7118789 CIFC28 H29 F12 N13 Ni2 P2P 1 21/c 115.613; 13.757; 16.854
90; 96.309; 90
3598.1Altmann, Philipp J.; Pöthig, Alexander
Capsoplexes: encapsulating complexes via guest recognition.
Chemical communications (Cambridge, England), 2016, 52, 9089-9092
7118790 CIFC60 H64 Br F18 N28 Ni4 P3C 1 2/c 115.985; 30.833; 15.2616
90; 93.494; 90
7507.9Altmann, Philipp J.; Pöthig, Alexander
Capsoplexes: encapsulating complexes via guest recognition.
Chemical communications (Cambridge, England), 2016, 52, 9089-9092
7118791 CIFC64 H80 Cl F18 N28 Ni4 O4 P3C 1 2/c 116.233; 31.342; 15.432
90; 95.632; 90
7814Altmann, Philipp J.; Pöthig, Alexander
Capsoplexes: encapsulating complexes via guest recognition.
Chemical communications (Cambridge, England), 2016, 52, 9089-9092
7118792 CIFC336 H312 N48 O38 Pd6I 4/m33.231; 33.231; 28.78
90; 90; 90
31782Roy, Bijan; Zangrando, Ennio; Mukherjee, Partha Sarathi
Self-assembly of a redox active water soluble Pd6L8 'molecular dice'.
Chemical communications (Cambridge, England), 2016, 52, 4489-4492
7118793 CIFC33 H26.5 Cu4 I4 N9 O3P 1 21/c 119.4538; 32.5779; 22.6155
90; 103.876; 90
13914.6Zhao, Chao-Wei; Ma, Jian-Ping; Liu, Qi-Kui; Wang, Xue-Ru; Liu, Yi; Yang, Jing; Yang, Jia-Shi; Dong, Yu-Bin
An in situ self-assembled Cu4I4-MOF-based mixed matrix membrane: a highly sensitive and selective naked-eye sensor for gaseous HCl.
Chemical communications (Cambridge, England), 2016, 52, 5238-5241
7118794 CIFC54 H54 B2 F4 N8 O5P 1 21/c 113.3756; 14.865; 24.544
90; 91.671; 90
4878Doulain, Pierre-Emmanuel; Goze, Christine; Bodio, Ewen; Richard, Philippe; Decréau, Richard A
BODIPY atropisomer interconversion, face discrimination, and superstructure appending.
Chemical communications (Cambridge, England), 2016, 52, 4474-4477
7118795 CIFC123 H116 B4 F16 Ir2 N22 O7 Zn3P 1 21/c 129.0096; 19.0252; 24.8069
90; 111.599; 90
12729.9Li, Xuezhao; Wu, Jinguo; He, Cheng; Zhang, Rong; Duan, Chunying
Multicomponent self-assembly of a pentanuclear Ir-Zn heterometal-organic polyhedron for carbon dioxide fixation and sulfite sequestration.
Chemical communications (Cambridge, England), 2016, 52, 5104-5107
7118796 CIFC116 H98 B4 F17 Ir2 N25 O3 Zn3P 1 21/c 129.505; 19.1096; 24.976
90; 112.295; 90
13029.4Li, Xuezhao; Wu, Jinguo; He, Cheng; Zhang, Rong; Duan, Chunying
Multicomponent self-assembly of a pentanuclear Ir-Zn heterometal-organic polyhedron for carbon dioxide fixation and sulfite sequestration.
Chemical communications (Cambridge, England), 2016, 52, 5104-5107
7118797 CIFC118 H104 B4 F16 Ir2 N24 O6 S Zn3P 1 21/c 129.347; 18.8722; 25.16
90; 112.374; 90
12886Li, Xuezhao; Wu, Jinguo; He, Cheng; Zhang, Rong; Duan, Chunying
Multicomponent self-assembly of a pentanuclear Ir-Zn heterometal-organic polyhedron for carbon dioxide fixation and sulfite sequestration.
Chemical communications (Cambridge, England), 2016, 52, 5104-5107
7118798 CIFC45 H48 Au3 F18 N12 O P3P -111.7938; 13.6822; 20.7195
76.314; 74.412; 83.443
3124.4Xiao, Xin-Shan; Zou, Chao; Guan, Xiangguo; Yang, Chen; Lu, Wei; Che, Chi-Ming
Homoleptic gold(i) N-heterocyclic allenylidene complexes: excited-state properties and lyotropic chromonics.
Chemical communications (Cambridge, England), 2016, 52, 4983-4986
7118799 CIFC16 H20 Au F6 N2 O2 PP 21 21 217.3239; 13.6625; 21.1998
90; 90; 90
2121.31Xiao, Xin-Shan; Zou, Chao; Guan, Xiangguo; Yang, Chen; Lu, Wei; Che, Chi-Ming
Homoleptic gold(i) N-heterocyclic allenylidene complexes: excited-state properties and lyotropic chromonics.
Chemical communications (Cambridge, England), 2016, 52, 4983-4986
7118800 CIFC20 H21 Au F6 N3 PP n m a15.7075; 6.8525; 20.3447
90; 90; 90
2189.81Xiao, Xin-Shan; Zou, Chao; Guan, Xiangguo; Yang, Chen; Lu, Wei; Che, Chi-Ming
Homoleptic gold(i) N-heterocyclic allenylidene complexes: excited-state properties and lyotropic chromonics.
Chemical communications (Cambridge, England), 2016, 52, 4983-4986
7118801 CIFC45 H44 Cl Ir N4 O S2P 1 21/c 118.999; 13.938; 18.33
90; 100.52; 90
4772.3Tian, Cheng; Gong, Lei; Meggers, Eric
Chiral-at-metal iridium complex for efficient enantioselective transfer hydrogenation of ketones.
Chemical communications (Cambridge, England), 2016, 52, 4207-4210
7118802 CIFC20 H14 O3P 1 21/n 110.307; 6.9664; 20.194
90; 92.558; 90
1448.5Sezukuri, Kyohei; Suzuki, Mitsuharu; Hayashi, Hironobu; Kuzuhara, Daiki; Aratani, Naoki; Yamada, Hiroko
A laterally π-expanded fluorone dye as an efficient near infrared fluorophore.
Chemical communications (Cambridge, England), 2016, 52, 4872-4875
7118803 CIFC19 H13 Br O3P n n a6.4553; 15.35; 15.588
90; 90; 90
1544.6Sezukuri, Kyohei; Suzuki, Mitsuharu; Hayashi, Hironobu; Kuzuhara, Daiki; Aratani, Naoki; Yamada, Hiroko
A laterally π-expanded fluorone dye as an efficient near infrared fluorophore.
Chemical communications (Cambridge, England), 2016, 52, 4872-4875
7118804 CIFC29 H18 Cl2 F2 O3C 1 2/c 122.6443; 6.8474; 30.763
90; 100.073; 90
4696.4Sezukuri, Kyohei; Suzuki, Mitsuharu; Hayashi, Hironobu; Kuzuhara, Daiki; Aratani, Naoki; Yamada, Hiroko
A laterally π-expanded fluorone dye as an efficient near infrared fluorophore.
Chemical communications (Cambridge, England), 2016, 52, 4872-4875
7118805 CIFC12 H12 N2 O3P 1 21/n 113.0764; 6.7268; 26.5912
90; 99.083; 90
2309.69Roy, Saikat; Goud, N. Rajesh; Matzger, Adam J.
Polymorphism in phenobarbital: discovery of a new polymorph and crystal structure of elusive form V.
Chemical communications (Cambridge, England), 2016, 52, 4389-4392
7118806 CIFC12 H12 N2 O3P 1 21/n 114.5744; 6.88; 22.9964
90; 93.987; 90
2300.31Roy, Saikat; Goud, N. Rajesh; Matzger, Adam J.
Polymorphism in phenobarbital: discovery of a new polymorph and crystal structure of elusive form V.
Chemical communications (Cambridge, England), 2016, 52, 4389-4392
7118807 CIFC30 H34 N2 O9P 21 21 219.09127; 10.54359; 30.6974
90; 90; 90
2942.49Yu, Kuan; Gao, Beiling; Liu, Zhaobo; Ding, Hanfeng
Enantioselective total synthesis and structural reassignment of (+)-alsmaphorazine E via a traceless chirality transfer strategy.
Chemical communications (Cambridge, England), 2016, 52, 4485-4488
7118808 CIFC21 H26 N2 O6P 1 n 17.323; 9.703; 13.3813
90; 93.357; 90
949.18Yu, Kuan; Gao, Beiling; Liu, Zhaobo; Ding, Hanfeng
Enantioselective total synthesis and structural reassignment of (+)-alsmaphorazine E via a traceless chirality transfer strategy.
Chemical communications (Cambridge, England), 2016, 52, 4485-4488
7118809 CIFC36 H40 Br2 Cl6 Fe N2 P2P 1 21/n 110.6315; 25.473; 14.959
90; 90.028; 90
4051.1Ghosh, Chandrani; Groy, Thomas L.; Bowman, Amanda C.; Trovitch, Ryan J.
Two-step C-H, C-P bond activation at an α-diimine iron dinitrogen complex.
Chemical communications (Cambridge, England), 2016, 52, 4553-4556
7118810 CIFC34 H38 Fe N4 P2P -19.2948; 12.9539; 13.7381
79.3091; 77.1334; 72.6186
1526.31Ghosh, Chandrani; Groy, Thomas L.; Bowman, Amanda C.; Trovitch, Ryan J.
Two-step C-H, C-P bond activation at an α-diimine iron dinitrogen complex.
Chemical communications (Cambridge, England), 2016, 52, 4553-4556
7118811 CIFC61.84 H70.97 Fe2 N4 P4P -113.1669; 21.8049; 22.842
109.42; 104.575; 105.963
5504.3Ghosh, Chandrani; Groy, Thomas L.; Bowman, Amanda C.; Trovitch, Ryan J.
Two-step C-H, C-P bond activation at an α-diimine iron dinitrogen complex.
Chemical communications (Cambridge, England), 2016, 52, 4553-4556
7118812 CIFC16 H19 BrC 1 2/c 118.281; 7.3569; 19.925
90; 104.092; 90
2599.1Su, Xiang; Sun, Yihua; Yao, Jiannian; Chen, Hui; Chen, Chao
Acid-promoted bicyclization of arylacetylenes to benzobicyclo[3.2.1]octanes through cationic rearrangements.
Chemical communications (Cambridge, England), 2016, 52, 4537-4540
7118813 CIFC26 H42 Fe N P3P 1 21/c 117.283; 19.422; 15.933
90; 92.103; 90
5344.6Lindley, Brian M.; Jacobs, Brian P.; MacMillan, Samantha N.; Wolczanski, Peter T.
Neutral Fe(iv) alkylidenes, including some that bind dinitrogen.
Chemical communications (Cambridge, England), 2016, 52, 3891-3894
7118814 CIFC30 H41 Fe N3 P2P 1 21/n 110.6131; 14.2296; 19.7148
90; 97.83; 90
2949.6Lindley, Brian M.; Jacobs, Brian P.; MacMillan, Samantha N.; Wolczanski, Peter T.
Neutral Fe(iv) alkylidenes, including some that bind dinitrogen.
Chemical communications (Cambridge, England), 2016, 52, 3891-3894
7118815 CIFC60 H54 Cl2 Cu4 N12 O35 W10C 1 2/m 120.0634; 17.3159; 15.642
90; 124.211; 90
4494Shi, Dongying; He, Cheng; Sun, Wenlong; Ming, Zheng; Meng, Changgong; Duan, Chunying
A photosensitizing decatungstate-based MOF as heterogeneous photocatalyst for the selective C-H alkylation of aliphatic nitriles.
Chemical communications (Cambridge, England), 2016, 52, 4714-4717
7118816 CIFC63 H53 Cl2 Cu4 N13 O33 W10C 1 2/m 120.0299; 17.2261; 15.8221
90; 125.919; 90
4421.1Shi, Dongying; He, Cheng; Sun, Wenlong; Ming, Zheng; Meng, Changgong; Duan, Chunying
A photosensitizing decatungstate-based MOF as heterogeneous photocatalyst for the selective C-H alkylation of aliphatic nitriles.
Chemical communications (Cambridge, England), 2016, 52, 4714-4717
7118817 CIFC21 H26 Cl3 N2 RhP n m a22.5211; 12.1599; 7.8427
90; 90; 90
2147.76Pitman, C. L.; Finster, O. N. L.; Miller, A. J. M.
Cyclopentadiene-mediated hydride transfer from rhodium complexes.
Chemical communications (Cambridge, England), 2016, 52, 9105-9108
7118818 CIFC18 H16 N2 O2I 41/a24.392; 24.392; 4.8236
90; 90; 90
2869.9Grzybowski, Marek; Deperasińska, Irena; Chotkowski, Maciej; Banasiewicz, Marzena; Makarewicz, Artur; Kozankiewicz, Bolesław; Gryko, Daniel T.
Dipyrrolonaphthyridinediones - structurally unique cross-conjugated dyes.
Chemical communications (Cambridge, England), 2016, 52, 5108-5111
7118819 CIFC25 H41 Fe N2 O4 P Si3P 1 21/n 111.1641; 16.6308; 17.5587
90; 94.787; 90
3248.72Breit, Nora C.; Eisenhut, Carsten; Inoue, Shigeyoshi
Phosphinosilylenes as a novel ligand system for heterobimetallic complexes.
Chemical communications (Cambridge, England), 2016, 52, 5523-5526
7118820 CIFC53 H62 Fe2 N4 O18 P2 Si2 W2C 1 2/c 125.6547; 10.4018; 24.8836
90; 91.797; 90
6637.05Breit, Nora C.; Eisenhut, Carsten; Inoue, Shigeyoshi
Phosphinosilylenes as a novel ligand system for heterobimetallic complexes.
Chemical communications (Cambridge, England), 2016, 52, 5523-5526
7118821 CIFC19 H25 Fe N2 O4 P SiP 21 21 2112.5723; 13.3184; 13.6939
90; 90; 90
2292.95Breit, Nora C.; Eisenhut, Carsten; Inoue, Shigeyoshi
Phosphinosilylenes as a novel ligand system for heterobimetallic complexes.
Chemical communications (Cambridge, England), 2016, 52, 5523-5526
7118822 CIFC28.8 H30.2 Fe N3 O7.3P 1 21/c 116.0853; 28.696; 7.0062
90; 96.758; 90
3211.5Breit, Nora C.; Eisenhut, Carsten; Inoue, Shigeyoshi
Phosphinosilylenes as a novel ligand system for heterobimetallic complexes.
Chemical communications (Cambridge, England), 2016, 52, 5523-5526
7118823 CIFC26 H44 N5 O7P 21 21 2111.936; 16.0501; 16.5597
90; 90; 90
3172.4Metrano, A. J.; Abascal, N. C.; Mercado, B. Q.; Paulson, E. K.; Miller, S. J.
Structural studies of β-turn-containing peptide catalysts for atroposelective quinazolinone bromination.
Chemical communications (Cambridge, England), 2016, 52, 4816-4819
7118824 CIFC27 H48 N6 O6P 21 21 2111.7899; 15.9908; 16.3363
90; 90; 90
3079.9Metrano, A. J.; Abascal, N. C.; Mercado, B. Q.; Paulson, E. K.; Miller, S. J.
Structural studies of β-turn-containing peptide catalysts for atroposelective quinazolinone bromination.
Chemical communications (Cambridge, England), 2016, 52, 4816-4819
7118825 CIFC29 H30 N2 O4P 1 21/c 115.268; 11.6042; 15.6622
90; 115.596; 90
2502.6Li, Zhenghua; Sharma, Nandini; Sharma, Upendra K.; Jacobs, Jeroen; Van Meervelt, Luc; Van der Eycken, Erik V.
Ligand-controlled product selectivity in palladium-catalyzed domino post-Ugi construction of (spiro)polyheterocycles.
Chemical communications (Cambridge, England), 2016, 52, 5516-5519
7118826 CIFC31 H32 F N3 O3P 1 21/c 19.0977; 16.6165; 17.6
90; 96.066; 90
2645.7Li, Zhenghua; Sharma, Nandini; Sharma, Upendra K.; Jacobs, Jeroen; Van Meervelt, Luc; Van der Eycken, Erik V.
Ligand-controlled product selectivity in palladium-catalyzed domino post-Ugi construction of (spiro)polyheterocycles.
Chemical communications (Cambridge, England), 2016, 52, 5516-5519
7118827 CIFC31 H32 F N3 O3P 1 21/c 19.0851; 16.648; 17.522
90; 98.553; 90
2620.71Li, Zhenghua; Sharma, Nandini; Sharma, Upendra K.; Jacobs, Jeroen; Van Meervelt, Luc; Van der Eycken, Erik V.
Ligand-controlled product selectivity in palladium-catalyzed domino post-Ugi construction of (spiro)polyheterocycles.
Chemical communications (Cambridge, England), 2016, 52, 5516-5519
7118828 CIFC18 H18P 1 21/n 110.23; 4.7903; 14.674
90; 108.855; 90
680.5Lungerich, Dominik; Nizovtsev, Alexey V.; Heinemann, Frank W.; Hampel, Frank; Meyer, Karsten; Majetich, George; Schleyer, Paul V. R.; Jux, Norbert
[18]Annulene put into a new perspective.
Chemical communications (Cambridge, England), 2016, 52, 4710-4713
7118829 CIFC24 H12I 41/a c d21.6492; 21.6492; 14.6312
90; 90; 90
6857.47Lungerich, Dominik; Nizovtsev, Alexey V.; Heinemann, Frank W.; Hampel, Frank; Meyer, Karsten; Majetich, George; Schleyer, Paul V. R.; Jux, Norbert
[18]Annulene put into a new perspective.
Chemical communications (Cambridge, England), 2016, 52, 4710-4713
7118830 CIFC192 H240 B6.25 F25 Fe4 N38P 6340.6845; 40.6845; 34.133
90; 90; 120
48929Zhang, Feng-Li; Chen, Jia-Qian; Qin, Long-Fang; Tian, Lei; Li, Zaijun; Ren, Xuehong; Gu, Zhi-Guo
Metal-center exchange of tetrahedral cages: single crystal to single crystal and spin-crossover properties.
Chemical communications (Cambridge, England), 2016, 52, 4796-4799
7118831 CIFC192 H240 B4 F16 N36 Ni4I 2 323.2474; 23.2474; 23.2474
90; 90; 90
12563.9Zhang, Feng-Li; Chen, Jia-Qian; Qin, Long-Fang; Tian, Lei; Li, Zaijun; Ren, Xuehong; Gu, Zhi-Guo
Metal-center exchange of tetrahedral cages: single crystal to single crystal and spin-crossover properties.
Chemical communications (Cambridge, England), 2016, 52, 4796-4799
7118832 CIFC192 H240 B4 F16 Fe0.8 N36 Ni3.2I 2 323.2506; 23.2506; 23.2506
90; 90; 90
12569.1Zhang, Feng-Li; Chen, Jia-Qian; Qin, Long-Fang; Tian, Lei; Li, Zaijun; Ren, Xuehong; Gu, Zhi-Guo
Metal-center exchange of tetrahedral cages: single crystal to single crystal and spin-crossover properties.
Chemical communications (Cambridge, England), 2016, 52, 4796-4799
7118833 CIFC26 H25 N O5 S2P 1 21/c 113.9256; 10.3322; 17.0868
90; 94.647; 90
2450.4Undeela, Sridhar; Ravikumar, Gurram; Nanubolu, Jagadeesh Babu; Singarapu, Kiran Kumar; Menon, Rajeev S.
The facile synthesis of 1-benzoazepine derivatives via gold-catalyzed regioselective cycloisomerization reactions of N-(o-alkynylaryl)-N-vinyl sulfonamides.
Chemical communications (Cambridge, England), 2016, 52, 4824-4827
7118834 CIFC26 H24 Cl N O5 S2P -19.7246; 11.0418; 12.8181
70.832; 71.93; 88.331
1231.88Undeela, Sridhar; Ravikumar, Gurram; Nanubolu, Jagadeesh Babu; Singarapu, Kiran Kumar; Menon, Rajeev S.
The facile synthesis of 1-benzoazepine derivatives via gold-catalyzed regioselective cycloisomerization reactions of N-(o-alkynylaryl)-N-vinyl sulfonamides.
Chemical communications (Cambridge, England), 2016, 52, 4824-4827
7118835 CIFC36 H20 SP 1 21/c 123.8009; 3.8485; 26.3591
90; 113.997; 90
2205.75Oniwa, Kazuaki; Kikuchi, Hiromasa; Shimotani, Hidekazu; Ikeda, Susumu; Asao, Naoki; Yamamoto, Yoshinori; Tanigaki, Katsumi; Jin, Tienan
2-Positional pyrene end-capped oligothiophenes for high performance organic field effect transistors.
Chemical communications (Cambridge, England), 2016, 52, 4800-4803
7118836 CIFC40 H22 S2P 1 21/c 122.725; 3.8289; 15.667
90; 109.481; 90
1285.2Oniwa, Kazuaki; Kikuchi, Hiromasa; Shimotani, Hidekazu; Ikeda, Susumu; Asao, Naoki; Yamamoto, Yoshinori; Tanigaki, Katsumi; Jin, Tienan
2-Positional pyrene end-capped oligothiophenes for high performance organic field effect transistors.
Chemical communications (Cambridge, England), 2016, 52, 4800-4803
7118837 CIFC15 H9 Dy N2 O6.5C 1 2/c 113.666; 15.154; 15.228
90; 101.24; 90
3093.1Liu, Cai-Ming; Zhang, De-Qing; Zhu, Dao-Ben
A 3D MOF constructed from dysprosium(iii) oxalate and capping ligands: ferromagnetic coupling and field-induced two-step magnetic relaxation.
Chemical communications (Cambridge, England), 2016, 52, 4804-4807
7118838 CIFC38 H12 F10 N4P -16.799; 8.219; 13.376
82.308; 75.542; 83.754
715.1Gadekar, Santosh C.; Reddy, Baddigam K.; Panchal, Santosh P.; Anand, Venkataramanarao G.
Metal assisted cyclomerization of benzodipyrrins into expanded norroles, aza-heptalene and acyclic dimers.
Chemical communications (Cambridge, England), 2016, 52, 4565-4568
7118839 CIFC41 H22 F10 N4 OP -19.9304; 12.231; 14.545
75.314; 82.512; 80.77
1679.3Gadekar, Santosh C.; Reddy, Baddigam K.; Panchal, Santosh P.; Anand, Venkataramanarao G.
Metal assisted cyclomerization of benzodipyrrins into expanded norroles, aza-heptalene and acyclic dimers.
Chemical communications (Cambridge, England), 2016, 52, 4565-4568
7118840 CIFC46 H18 F10 N4P 1 21/n 110.144; 12.998; 25.579
90; 96.312; 90
3352.2Gadekar, Santosh C.; Reddy, Baddigam K.; Panchal, Santosh P.; Anand, Venkataramanarao G.
Metal assisted cyclomerization of benzodipyrrins into expanded norroles, aza-heptalene and acyclic dimers.
Chemical communications (Cambridge, England), 2016, 52, 4565-4568
7118841 CIFC57 H36 N6 O4P -112.261; 13.38; 14.218
77.74; 81.518; 89.721
2253.5Gadekar, Santosh C.; Reddy, Baddigam K.; Panchal, Santosh P.; Anand, Venkataramanarao G.
Metal assisted cyclomerization of benzodipyrrins into expanded norroles, aza-heptalene and acyclic dimers.
Chemical communications (Cambridge, England), 2016, 52, 4565-4568
7118842 CIFC62 H21 F15 N6 O3P 1 21/c 18.6387; 14.094; 42.764
90; 91.418; 90
5205Gadekar, Santosh C.; Reddy, Baddigam K.; Panchal, Santosh P.; Anand, Venkataramanarao G.
Metal assisted cyclomerization of benzodipyrrins into expanded norroles, aza-heptalene and acyclic dimers.
Chemical communications (Cambridge, England), 2016, 52, 4565-4568
7118843 CIFC86 H132 N16 O16P 1 21 114.1965; 21.9607; 16.3804
90; 111.904; 90
4738.2Bandyopadhyay, Anupam; Misra, Rajkumar; Gopi, Hosahudya N.
Structural features and molecular aggregations of designed triple-stranded β-sheets in single crystals.
Chemical communications (Cambridge, England), 2016, 52, 4938-4941
7118844 CIFC79 H134 N16 O16P 112.367; 13.818; 16.091
105.224; 97.197; 113.827
2342.2Bandyopadhyay, Anupam; Misra, Rajkumar; Gopi, Hosahudya N.
Structural features and molecular aggregations of designed triple-stranded β-sheets in single crystals.
Chemical communications (Cambridge, England), 2016, 52, 4938-4941
7118845 CIFC20 H26 B2 F2P 1 21/n 19.024; 15.783; 12.907
90; 96.65; 90
1825.9Arnold, Nicole; Braunschweig, Holger; Damme, Alexander; Dewhurst, Rian D.; Pentecost, Leanne; Radacki, Krzysztof; Stellwag-Konertz, Sascha; Thiess, Torsten; Trumpp, Alexandra; Vargas, Alfredo
New outcomes of Lewis base addition to diboranes(4): electronic effects override strong steric disincentives.
Chemical communications (Cambridge, England), 2016, 52, 4898-4901
7118846 CIFC21 H31 B2 F2 PP b c a8.463; 14.865; 32.625
90; 90; 90
4104.3Arnold, Nicole; Braunschweig, Holger; Damme, Alexander; Dewhurst, Rian D.; Pentecost, Leanne; Radacki, Krzysztof; Stellwag-Konertz, Sascha; Thiess, Torsten; Trumpp, Alexandra; Vargas, Alfredo
New outcomes of Lewis base addition to diboranes(4): electronic effects override strong steric disincentives.
Chemical communications (Cambridge, England), 2016, 52, 4898-4901
7118847 CIFC21 H31 B2 F2 O3 PP 1 21/c 110.3; 14.375; 15.204
90; 104.85; 90
2176Arnold, Nicole; Braunschweig, Holger; Damme, Alexander; Dewhurst, Rian D.; Pentecost, Leanne; Radacki, Krzysztof; Stellwag-Konertz, Sascha; Thiess, Torsten; Trumpp, Alexandra; Vargas, Alfredo
New outcomes of Lewis base addition to diboranes(4): electronic effects override strong steric disincentives.
Chemical communications (Cambridge, England), 2016, 52, 4898-4901
7118848 CIFC33 H44 B2 Cl2 F2 N4P -111.043; 11.083; 14.473
92.267; 92.359; 113.535
1619.6Arnold, Nicole; Braunschweig, Holger; Damme, Alexander; Dewhurst, Rian D.; Pentecost, Leanne; Radacki, Krzysztof; Stellwag-Konertz, Sascha; Thiess, Torsten; Trumpp, Alexandra; Vargas, Alfredo
New outcomes of Lewis base addition to diboranes(4): electronic effects override strong steric disincentives.
Chemical communications (Cambridge, England), 2016, 52, 4898-4901
7118849 CIFC32 H14 B2 Cl2 F15 N O2P -111.253; 11.41; 14.135
69.313; 74.449; 84.848
1635.7Zheng, Junhao; Fan, Xiaoting; Zhou, Benyu; Li, Zhen Hua; Wang, Huadong
Tautomerization of 2,6-lutidines in the presence of B(C6F5)3 using catecholborane as a precatalyst.
Chemical communications (Cambridge, England), 2016, 52, 4655-4658
7118850 CIFC25 H9 B F15 NP 1 21/c 17.69; 18.994; 15.963
90; 92.675; 90
2329Zheng, Junhao; Fan, Xiaoting; Zhou, Benyu; Li, Zhen Hua; Wang, Huadong
Tautomerization of 2,6-lutidines in the presence of B(C6F5)3 using catecholborane as a precatalyst.
Chemical communications (Cambridge, England), 2016, 52, 4655-4658
7118851 CIFC26 H27 Cl F N O8 SP 1 21/c 111.3397; 20.295; 13.45
90; 114.44; 90
2818Yang, Jieru; Zhou, Xiaofan; Zeng, Yu; Huang, Chaoqian; Xiao, Yuanjing; Zhang, Junliang
Synthesis of 2-fluoro-2-pyrrolines via tandem reaction of α-trifluoromethyl-α,β-unsaturated carbonyl compounds with N-tosylated 2-aminomalonates.
Chemical communications (Cambridge, England), 2016, 52, 4922-4925
7118852 CIFC15 H10 N2 O2C 1 2/c 119.7366; 11.0069; 14.8933
90; 130.433; 90
2462.7Fan, Liwen; Wang, Tao; Tian, Ying; Xiong, Fei; Wu, Simei; Liang, Qingjin; Zhao, Junfeng
Copper-catalyzed oxidative coupling between quinazoline 3-oxides and unactivated aldehydes: an efficient approach to functionalized quinazolines.
Chemical communications (Cambridge, England), 2016, 52, 5375-5378
7118853 CIFC15 H10 N2 O3P 1 21/n 16.8611; 18.3584; 9.5657
90; 90.0894; 90
1204.88Fan, Liwen; Wang, Tao; Tian, Ying; Xiong, Fei; Wu, Simei; Liang, Qingjin; Zhao, Junfeng
Copper-catalyzed oxidative coupling between quinazoline 3-oxides and unactivated aldehydes: an efficient approach to functionalized quinazolines.
Chemical communications (Cambridge, England), 2016, 52, 5375-5378
7118854 CIFC19 H17 N O4P -18.9379; 10.7203; 11.0337
118.687; 110.073; 93.964
835.3Tiwari, Dipak Kumar; Phanindrudu, Mandalaparthi; Aravilli, Vinod Kumar; Sridhar, B.; Likhar, Pravin R.; Tiwari, Dharmendra Kumar
Magnetically recoverable Cu(0)/Fe3O4 catalyzed highly regioselective synthesis of 2,3,4-trisubstituted pyrroles from unactivated terminal alkynes and isocyanides.
Chemical communications (Cambridge, England), 2016, 52, 4675-4678
7118855 CIFC23 H21 K N5 O10 YbC 1 2/c 119.9224; 14.1721; 10.3924
90; 111.833; 90
2723.75Chen, Wanmin; Tang, Xiaoliang; Dou, Wei; Ju, Zhenghua; Xu, Benhua; Xu, Wenxuan; Liu, Weisheng
K(+)-Induced in situ self-assembly of near-infrared luminescent membrane material armored with bigger Yb(iii) complex crystallites.
Chemical communications (Cambridge, England), 2016, 52, 5124-5127
7118856 CIFC25 H29 Li N5 O12 YbP 1 21/c 110.5784; 17.3413; 16.6413
90; 104.996; 90
2948.8Chen, Wanmin; Tang, Xiaoliang; Dou, Wei; Ju, Zhenghua; Xu, Benhua; Xu, Wenxuan; Liu, Weisheng
K(+)-Induced in situ self-assembly of near-infrared luminescent membrane material armored with bigger Yb(iii) complex crystallites.
Chemical communications (Cambridge, England), 2016, 52, 5124-5127
7118857 CIFC25 H29 N5 Na O12 YbP 1 21/c 110.5784; 17.3413; 16.6413
90; 104.996; 90
2948.8Chen, Wanmin; Tang, Xiaoliang; Dou, Wei; Ju, Zhenghua; Xu, Benhua; Xu, Wenxuan; Liu, Weisheng
K(+)-Induced in situ self-assembly of near-infrared luminescent membrane material armored with bigger Yb(iii) complex crystallites.
Chemical communications (Cambridge, England), 2016, 52, 5124-5127
7118858 CIFC92 H84 N20 O40 Rb4 Yb4P -112.2689; 13.8207; 16.0314
89.063; 84.408; 88.521
2704.3Chen, Wanmin; Tang, Xiaoliang; Dou, Wei; Ju, Zhenghua; Xu, Benhua; Xu, Wenxuan; Liu, Weisheng
K(+)-Induced in situ self-assembly of near-infrared luminescent membrane material armored with bigger Yb(iii) complex crystallites.
Chemical communications (Cambridge, England), 2016, 52, 5124-5127
7118859 CIFC46 H42 N9 O17 Rb Yb2C 1 2/c 118.668; 17.357; 16.785
90; 102.458; 90
5311Chen, Wanmin; Tang, Xiaoliang; Dou, Wei; Ju, Zhenghua; Xu, Benhua; Xu, Wenxuan; Liu, Weisheng
K(+)-Induced in situ self-assembly of near-infrared luminescent membrane material armored with bigger Yb(iii) complex crystallites.
Chemical communications (Cambridge, England), 2016, 52, 5124-5127
7118860 CIFC232.5 H275.5 Cl8 Cu32 N67.5 O57R -3 :H23.108; 23.108; 56.327
90; 90; 120
26048Feng, Sisi; Jia, Fei; Lu, Liping; Li, Zhongping; Zhang, Shuo
An unusual 32-membered copper(ii) metallomacrocube based on a Cu4O3X cubic core: photocatalytic, electrocatalytic, and magnetic properties.
Chemical communications (Cambridge, England), 2016, 52, 4294-4297
7118861 CIFC50 H73 Br N3 Na O10P 21 21 2114.7059; 18.0236; 19.3772
90; 90; 90
5135.99Shi, Qiuyan; Li, Yu; Bo, Shaowei; Li, Xiaofei; Zhao, Peng; Liu, Qi; Yang, Zhigang; Cong, Hengjiang; Deng, Hexiang; Chen, Mingnan; Chen, Shizhen; Zhou, Xin; Ding, Hong; Jiang, Zhong-Xing
Discovery of a (19)F MRI sensitive salinomycin derivative with high cytotoxicity towards cancer cells.
Chemical communications (Cambridge, England), 2016, 52, 5136-5139
7118862 CIFC50 H75 Br K N3 O11P 41 21 213.5526; 13.5526; 57.9362
90; 90; 90
10641.3Shi, Qiuyan; Li, Yu; Bo, Shaowei; Li, Xiaofei; Zhao, Peng; Liu, Qi; Yang, Zhigang; Cong, Hengjiang; Deng, Hexiang; Chen, Mingnan; Chen, Shizhen; Zhou, Xin; Ding, Hong; Jiang, Zhong-Xing
Discovery of a (19)F MRI sensitive salinomycin derivative with high cytotoxicity towards cancer cells.
Chemical communications (Cambridge, England), 2016, 52, 5136-5139
7118863 CIFC67 H58 Cl2 N2 P4 RuP -110.5042; 12.4115; 22.3482
75.394; 77.732; 86.444
2754.9Sugimoto, Kaho; Tanaka, Yuya; Fujii, Shintaro; Tada, Tomofumi; Kiguchi, Manabu; Akita, Munetaka
Organometallic molecular wires as versatile modules for energy-level alignment of the metal-molecule-metal junction.
Chemical communications (Cambridge, England), 2016, 52, 5796-5799
7118864 CIFC21 H30 Bi2 Br13 N3C 1 2/c 111.91371; 15.9042; 21.6218
90; 91.0689; 90
4096.14Adonin, Sergey A.; Gorokh, Igor D.; Samsonenko, Denis G.; Sokolov, Maxim N.; Fedin, Vladimir P.
Bi(iii) polybromides: a new chapter in coordination chemistry of bismuth.
Chemical communications (Cambridge, England), 2016, 52, 5061-5063
7118865 CIFC18 H24 Bi2 Br11 N3P 1 21/c 19.5341; 21.4727; 35.055
90; 97.093; 90
7121.6Adonin, Sergey A.; Gorokh, Igor D.; Samsonenko, Denis G.; Sokolov, Maxim N.; Fedin, Vladimir P.
Bi(iii) polybromides: a new chapter in coordination chemistry of bismuth.
Chemical communications (Cambridge, England), 2016, 52, 5061-5063
7118866 CIFC12 H14 Bi Br7 N2C m c m14.1671; 19.7299; 7.74397
90; 90; 90
2164.56Adonin, Sergey A.; Gorokh, Igor D.; Samsonenko, Denis G.; Sokolov, Maxim N.; Fedin, Vladimir P.
Bi(iii) polybromides: a new chapter in coordination chemistry of bismuth.
Chemical communications (Cambridge, England), 2016, 52, 5061-5063
7118867 CIFC28 H36 Bi Br13 N4P n m a16.0606; 13.9864; 19.4745
90; 90; 90
4374.56Adonin, Sergey A.; Gorokh, Igor D.; Samsonenko, Denis G.; Sokolov, Maxim N.; Fedin, Vladimir P.
Bi(iii) polybromides: a new chapter in coordination chemistry of bismuth.
Chemical communications (Cambridge, England), 2016, 52, 5061-5063
7118868 CIFC92 H28 Cl8 F40 N8 O2P 1 21/n 117.2568; 14.4839; 18.3034
90; 96.454; 90
4545.9Zhang, Kai; Savage, Mathew; Li, Xin; Jiang, Yu; Ishida, Masatoshi; Mitsuno, Koki; Karasawa, Satoru; Kato, Tatsuhisa; Zhu, Weihua; Yang, Sihai; Furuta, Hiroyuki; Xie, Yongshu
Rational syntheses of helical π-conjugated oligopyrrins with a bipyrrole linkage: geometry control of bis-copper(ii) coordination.
Chemical communications (Cambridge, England), 2016, 52, 5148-5151
7118869 CIFC70 H24 Cu2 F30 N6 O4 S2P 1 21/n 111.1752; 16.3892; 37.51
90; 93.375; 90
6858.1Zhang, Kai; Savage, Mathew; Li, Xin; Jiang, Yu; Ishida, Masatoshi; Mitsuno, Koki; Karasawa, Satoru; Kato, Tatsuhisa; Zhu, Weihua; Yang, Sihai; Furuta, Hiroyuki; Xie, Yongshu
Rational syntheses of helical π-conjugated oligopyrrins with a bipyrrole linkage: geometry control of bis-copper(ii) coordination.
Chemical communications (Cambridge, England), 2016, 52, 5148-5151
7118870 CIFC83 H23 Cu2 F35 N10 O2P 1 21/c 115.2047; 23.71; 25.959
90; 103.577; 90
9096.8Zhang, Kai; Savage, Mathew; Li, Xin; Jiang, Yu; Ishida, Masatoshi; Mitsuno, Koki; Karasawa, Satoru; Kato, Tatsuhisa; Zhu, Weihua; Yang, Sihai; Furuta, Hiroyuki; Xie, Yongshu
Rational syntheses of helical π-conjugated oligopyrrins with a bipyrrole linkage: geometry control of bis-copper(ii) coordination.
Chemical communications (Cambridge, England), 2016, 52, 5148-5151
7118871 CIFC92 H24 Cl8 Cu2 F40 N8 O2P 1 21/c 117.0506; 14.6158; 23.435
90; 129.005; 90
4538.4Zhang, Kai; Savage, Mathew; Li, Xin; Jiang, Yu; Ishida, Masatoshi; Mitsuno, Koki; Karasawa, Satoru; Kato, Tatsuhisa; Zhu, Weihua; Yang, Sihai; Furuta, Hiroyuki; Xie, Yongshu
Rational syntheses of helical π-conjugated oligopyrrins with a bipyrrole linkage: geometry control of bis-copper(ii) coordination.
Chemical communications (Cambridge, England), 2016, 52, 5148-5151
7118872 CIFC94 H29 F40 N11 O2 Zn2P -113.133; 16.1932; 20.7009
81.317; 86.431; 83.348
4318.1Zhang, Kai; Savage, Mathew; Li, Xin; Jiang, Yu; Ishida, Masatoshi; Mitsuno, Koki; Karasawa, Satoru; Kato, Tatsuhisa; Zhu, Weihua; Yang, Sihai; Furuta, Hiroyuki; Xie, Yongshu
Rational syntheses of helical π-conjugated oligopyrrins with a bipyrrole linkage: geometry control of bis-copper(ii) coordination.
Chemical communications (Cambridge, England), 2016, 52, 5148-5151
7118873 CIFC140 H266 Ag19.4 Au5.6 N S18P -117.0545; 29.3289; 35.668
85.911; 89.317; 86.562
17762.8Li, Qi; Wang, Shuxin; Kirschbaum, Kristin; Lambright, Kelly J.; Das, Anindita; Jin, Rongchao
Heavily doped Au25-xAgx(SC6H11)18(-) nanoclusters: silver goes from the core to the surface.
Chemical communications (Cambridge, England), 2016, 52, 5194-5197
7118874 CIFC76 H66 B F24 Ir N O PP 1 21 113.5677; 13.0684; 20.6626
90; 105.603; 90
3528.6Yu, Yan-Bo; Cheng, Lei; Li, Yi-Pan; Fu, Yue; Zhu, Shou-Fei; Zhou, Qi-Lin
Enantioselective iridium-catalyzed hydrogenation of β,β-disubstituted nitroalkenes.
Chemical communications (Cambridge, England), 2016, 52, 4812-4815
7118875 CIFC30 H24 Au2 Cl2 P2C 1 2/c 117.4201; 13.4798; 12.0817
90; 102.537; 90
2769.37O'Connor, Alice E; Mirzadeh, Nedaossadat; Bhargava, Suresh K.; Easun, Timothy L.; Schröder, Martin; Blake, Alexander J.
Aurophilicity under pressure: a combined crystallographic and in situ spectroscopic study.
Chemical communications (Cambridge, England), 2016, 52, 6769-6772
7118876 CIFC30 H24 Au2 Cl2 P2C 1 2/c 117.4151; 13.4808; 12.079
90; 102.508; 90
2768.48O'Connor, Alice E; Mirzadeh, Nedaossadat; Bhargava, Suresh K.; Easun, Timothy L.; Schröder, Martin; Blake, Alexander J.
Aurophilicity under pressure: a combined crystallographic and in situ spectroscopic study.
Chemical communications (Cambridge, England), 2016, 52, 6769-6772
7118877 CIFC30 H24 Au2 Cl2 P2C 1 2/c 117.2129; 13.3158; 11.79
90; 102.848; 90
2634.65O'Connor, Alice E; Mirzadeh, Nedaossadat; Bhargava, Suresh K.; Easun, Timothy L.; Schröder, Martin; Blake, Alexander J.
Aurophilicity under pressure: a combined crystallographic and in situ spectroscopic study.
Chemical communications (Cambridge, England), 2016, 52, 6769-6772
7118878 CIFC30 H24 Au2 Cl2 P2C 1 2/c 117.0509; 13.1824; 11.579
90; 103.183; 90
2534.04O'Connor, Alice E; Mirzadeh, Nedaossadat; Bhargava, Suresh K.; Easun, Timothy L.; Schröder, Martin; Blake, Alexander J.
Aurophilicity under pressure: a combined crystallographic and in situ spectroscopic study.
Chemical communications (Cambridge, England), 2016, 52, 6769-6772
7118879 CIFC30 H24 Au2 Cl2 P2C 1 2/c 116.8213; 13.0052; 11.2967
90; 103.502; 90
2403O'Connor, Alice E; Mirzadeh, Nedaossadat; Bhargava, Suresh K.; Easun, Timothy L.; Schröder, Martin; Blake, Alexander J.
Aurophilicity under pressure: a combined crystallographic and in situ spectroscopic study.
Chemical communications (Cambridge, England), 2016, 52, 6769-6772
7118880 CIFC30 H24 Au2 Cl2 P2C 1 2/c 116.6333; 12.8767; 11.1124
90; 103.804; 90
2311.3O'Connor, Alice E; Mirzadeh, Nedaossadat; Bhargava, Suresh K.; Easun, Timothy L.; Schröder, Martin; Blake, Alexander J.
Aurophilicity under pressure: a combined crystallographic and in situ spectroscopic study.
Chemical communications (Cambridge, England), 2016, 52, 6769-6772
7118881 CIFC30 H24 Au2 Cl2 P2C 1 2/c 116.5181; 12.7957; 10.9986
90; 103.959; 90
2256.02O'Connor, Alice E; Mirzadeh, Nedaossadat; Bhargava, Suresh K.; Easun, Timothy L.; Schröder, Martin; Blake, Alexander J.
Aurophilicity under pressure: a combined crystallographic and in situ spectroscopic study.
Chemical communications (Cambridge, England), 2016, 52, 6769-6772
7118882 CIFC30 H24 Au2 Cl2 P2C 1 2/c 116.3552; 12.6807; 10.8457
90; 104.192; 90
2180.7O'Connor, Alice E; Mirzadeh, Nedaossadat; Bhargava, Suresh K.; Easun, Timothy L.; Schröder, Martin; Blake, Alexander J.
Aurophilicity under pressure: a combined crystallographic and in situ spectroscopic study.
Chemical communications (Cambridge, England), 2016, 52, 6769-6772
7118883 CIFC30 H24 Au2 Cl2 P2C 1 2/c 116.1848; 12.5654; 10.6996
90; 104.452; 90
2107.11O'Connor, Alice E; Mirzadeh, Nedaossadat; Bhargava, Suresh K.; Easun, Timothy L.; Schröder, Martin; Blake, Alexander J.
Aurophilicity under pressure: a combined crystallographic and in situ spectroscopic study.
Chemical communications (Cambridge, England), 2016, 52, 6769-6772
7118884 CIFC30 H24 Au2 Cl2 P2C 1 2/c 116.1185; 12.5191; 10.6485
90; 104.564; 90
2079.71O'Connor, Alice E; Mirzadeh, Nedaossadat; Bhargava, Suresh K.; Easun, Timothy L.; Schröder, Martin; Blake, Alexander J.
Aurophilicity under pressure: a combined crystallographic and in situ spectroscopic study.
Chemical communications (Cambridge, England), 2016, 52, 6769-6772
7118885 CIFC30 H24 Au2 Cl2 P2C 1 2/c 115.9507; 12.4062; 10.5188
90; 104.813; 90
2012.4O'Connor, Alice E; Mirzadeh, Nedaossadat; Bhargava, Suresh K.; Easun, Timothy L.; Schröder, Martin; Blake, Alexander J.
Aurophilicity under pressure: a combined crystallographic and in situ spectroscopic study.
Chemical communications (Cambridge, England), 2016, 52, 6769-6772
7118886 CIFC30 H24 Au2 Cl2 P2C 1 2/c 115.9198; 12.3906; 10.5027
90; 104.853; 90
2002.5O'Connor, Alice E; Mirzadeh, Nedaossadat; Bhargava, Suresh K.; Easun, Timothy L.; Schröder, Martin; Blake, Alexander J.
Aurophilicity under pressure: a combined crystallographic and in situ spectroscopic study.
Chemical communications (Cambridge, England), 2016, 52, 6769-6772
7118887 CIFC30 H24 Au2 Cl2 P2C 1 2/c 115.8861; 12.3656; 10.4819
90; 104.901; 90
1989.83O'Connor, Alice E; Mirzadeh, Nedaossadat; Bhargava, Suresh K.; Easun, Timothy L.; Schröder, Martin; Blake, Alexander J.
Aurophilicity under pressure: a combined crystallographic and in situ spectroscopic study.
Chemical communications (Cambridge, England), 2016, 52, 6769-6772
7118888 CIFC30 H24 Au2 Cl2 P2C 1 2/c 115.8107; 12.3314; 10.4704
90; 104.924; 90
1972.5O'Connor, Alice E; Mirzadeh, Nedaossadat; Bhargava, Suresh K.; Easun, Timothy L.; Schröder, Martin; Blake, Alexander J.
Aurophilicity under pressure: a combined crystallographic and in situ spectroscopic study.
Chemical communications (Cambridge, England), 2016, 52, 6769-6772
7118889 CIFC5 H6 F4P 1 21/c 110.115; 4.5875; 11.876
90; 90.026; 90
551.1Fang, Zeguo; Al-Maharik, Nawaf; Slawin, Alexandra M. Z.; Bühl, Michael; O'Hagan, David
Polar alicyclic rings: synthesis and structure of all cis-1,2,3,4-tetrafluorocyclopentane.
Chemical communications (Cambridge, England), 2016, 52, 5116-5119
7118890 CIFC18 H19 N O2P b c a9.5809; 13.6588; 22.8484
90; 90; 90
2990Nandi, Raj Kumar; Ratsch, Friederike; Beaud, Rodolphe; Guillot, Régis; Kouklovsky, Cyrille; Vincent, Guillaume
Intermolecular dearomative C2-arylation of N-Ac indoles activated by FeCl3.
Chemical communications (Cambridge, England), 2016, 52, 5328-5331
7118891 CIFC28 H25 N O3P 1 21/n 17.7189; 9.7482; 29.5931
90; 94.235; 90
2220.66Nandi, Raj Kumar; Ratsch, Friederike; Beaud, Rodolphe; Guillot, Régis; Kouklovsky, Cyrille; Vincent, Guillaume
Intermolecular dearomative C2-arylation of N-Ac indoles activated by FeCl3.
Chemical communications (Cambridge, England), 2016, 52, 5328-5331
7118892 CIFC18 H16 Br N OP -17.9573; 9.6303; 10.5963
68.147; 75.128; 69.312
697.7Nandi, Raj Kumar; Ratsch, Friederike; Beaud, Rodolphe; Guillot, Régis; Kouklovsky, Cyrille; Vincent, Guillaume
Intermolecular dearomative C2-arylation of N-Ac indoles activated by FeCl3.
Chemical communications (Cambridge, England), 2016, 52, 5328-5331
7118893 CIFC33 H75 Cl N4 Pu Si3P 1 21/n 113.0136; 15.5458; 20.433
90; 90.546; 90
4133.5Brown, Jessie L.; Gaunt, Andrew J.; King, David M.; Liddle, Stephen T.; Reilly, Sean D.; Scott, Brian L.; Wooles, Ashley J.
Neptunium and plutonium complexes with a sterically encumbered triamidoamine (TREN) scaffold.
Chemical communications (Cambridge, England), 2016, 52, 5428-5431
7118894 CIFC33 H75 Cl N4 Np Si3P 1 21/n 112.9845; 15.6008; 20.4035
90; 90.648; 90
4132.8Brown, Jessie L.; Gaunt, Andrew J.; King, David M.; Liddle, Stephen T.; Reilly, Sean D.; Scott, Brian L.; Wooles, Ashley J.
Neptunium and plutonium complexes with a sterically encumbered triamidoamine (TREN) scaffold.
Chemical communications (Cambridge, England), 2016, 52, 5428-5431
7118897 CIFC61 H95 N8 O12P 21 21 222.4; 29.9961; 9.5945
90; 90; 90
6446.7Yoon, Eunyoung; Gong, Jintaek; Jung, Yoonchul; Lee, Wonchul; Driver, Russell W.; Lee, Hee-Seung
Unambiguous characterization of anisotropic foldamer packing in a foldecture with an elongated hexagonal plate shape.
Chemical communications (Cambridge, England), 2016, 52, 5250-5253
7118898 CIFC12 H96 K3 Mo16 N O74 S16C 1 2/m 120.6782; 11.2433; 23.3822
90; 108.634; 90
5151.2Zang, Hongying; Surman, Andrew; Long, Deliang; Cronin, Leroy; Miras, Haralampos N.
Exploiting the equilibrium dynamics in the self-assembly of inorganic macrocycles based upon polyoxothiometalate building blocks.
Chemical communications (Cambridge, England), 2016, 52, 9109-9112
7118899 CIFC12 H90 Mo12 N2 O52 S12C 1 2/c 138.31; 17.3787; 12.5611
90; 91.431; 90
8360.3Zang, Hongying; Surman, Andrew; Long, Deliang; Cronin, Leroy; Miras, Haralampos N.
Exploiting the equilibrium dynamics in the self-assembly of inorganic macrocycles based upon polyoxothiometalate building blocks.
Chemical communications (Cambridge, England), 2016, 52, 9109-9112
7118900 CIFC14 H22 Cl2 I6 N4 PtP -19.1654; 9.1839; 10.0995
113.841; 100.43; 108.001
692.27Ivanov, Daniil M.; Novikov, Alexander S.; Ananyev, Ivan V.; Kirina, Yulia V.; Kukushkin, Vadim Yu
Halogen bonding between metal centers and halocarbons.
Chemical communications (Cambridge, England), 2016, 52, 5565-5568
7118901 CIFC14 H22 Cl2 I6 N4 PtP -19.1564; 9.1703; 10.0589
113.561; 100.692; 107.883
689.26Ivanov, Daniil M.; Novikov, Alexander S.; Ananyev, Ivan V.; Kirina, Yulia V.; Kukushkin, Vadim Yu
Halogen bonding between metal centers and halocarbons.
Chemical communications (Cambridge, England), 2016, 52, 5565-5568
7118902 CIFC14 H22 Cl2 I6 N4 PtP -19.1806; 9.3566; 10.3153
114.93; 99.18; 108.364
717.25Ivanov, Daniil M.; Novikov, Alexander S.; Ananyev, Ivan V.; Kirina, Yulia V.; Kukushkin, Vadim Yu
Halogen bonding between metal centers and halocarbons.
Chemical communications (Cambridge, England), 2016, 52, 5565-5568
7118903 CIFC8 H14 Cl2 I6 N4 PtP -19.2555; 9.6136; 15.3533
81.5317; 75.7689; 65.7138
1205.36Ivanov, Daniil M.; Novikov, Alexander S.; Ananyev, Ivan V.; Kirina, Yulia V.; Kukushkin, Vadim Yu
Halogen bonding between metal centers and halocarbons.
Chemical communications (Cambridge, England), 2016, 52, 5565-5568
7118904 CIFC16 H28 Cl7 I9 N8 Pt2P -19.2558; 9.3667; 15.2697
75.799; 81.826; 65.21
1163.95Ivanov, Daniil M.; Novikov, Alexander S.; Ananyev, Ivan V.; Kirina, Yulia V.; Kukushkin, Vadim Yu
Halogen bonding between metal centers and halocarbons.
Chemical communications (Cambridge, England), 2016, 52, 5565-5568
7118905 CIFC6 H12 Br2 N4 PtP 1 21/c 15.7573; 11.8165; 9.2197
90; 108.047; 90
596.37Ivanov, Daniil M.; Novikov, Alexander S.; Ananyev, Ivan V.; Kirina, Yulia V.; Kukushkin, Vadim Yu
Halogen bonding between metal centers and halocarbons.
Chemical communications (Cambridge, England), 2016, 52, 5565-5568
7118906 CIFC8 H14 Br2 I6 N4 PtP -19.28; 9.8201; 15.7209
81.037; 75.8368; 65.7179
1263.74Ivanov, Daniil M.; Novikov, Alexander S.; Ananyev, Ivan V.; Kirina, Yulia V.; Kukushkin, Vadim Yu
Halogen bonding between metal centers and halocarbons.
Chemical communications (Cambridge, England), 2016, 52, 5565-5568
7118907 CIFC12 H22 Cl2 I6 N4 PtP -18.2473; 8.7723; 11.3779
104.013; 98.93; 116.223
683.18Ivanov, Daniil M.; Novikov, Alexander S.; Ananyev, Ivan V.; Kirina, Yulia V.; Kukushkin, Vadim Yu
Halogen bonding between metal centers and halocarbons.
Chemical communications (Cambridge, England), 2016, 52, 5565-5568
7118908 CIFC12 H18 Cl2 I6 N4 PtP 1 21/c 19.9496; 9.35436; 14.6232
90; 103.295; 90
1324.54Ivanov, Daniil M.; Novikov, Alexander S.; Ananyev, Ivan V.; Kirina, Yulia V.; Kukushkin, Vadim Yu
Halogen bonding between metal centers and halocarbons.
Chemical communications (Cambridge, England), 2016, 52, 5565-5568
7118909 CIFC14 H22 Cl2 I6 N4 PtP -19.129; 9.1612; 10.0487
100.776; 113.593; 107.793
685.71Ivanov, Daniil M.; Novikov, Alexander S.; Ananyev, Ivan V.; Kirina, Yulia V.; Kukushkin, Vadim Yu
Halogen bonding between metal centers and halocarbons.
Chemical communications (Cambridge, England), 2016, 52, 5565-5568
7118910 CIFC14 H22 Cl2 I6 N4 PtP -19.1465; 9.1681; 10.068
113.589; 100.676; 107.808
689.34Ivanov, Daniil M.; Novikov, Alexander S.; Ananyev, Ivan V.; Kirina, Yulia V.; Kukushkin, Vadim Yu
Halogen bonding between metal centers and halocarbons.
Chemical communications (Cambridge, England), 2016, 52, 5565-5568
7118911 CIFC14 H22 Cl2 I6 N4 PtP -19.168; 9.1918; 10.109
113.897; 100.373; 107.948
693.9Ivanov, Daniil M.; Novikov, Alexander S.; Ananyev, Ivan V.; Kirina, Yulia V.; Kukushkin, Vadim Yu
Halogen bonding between metal centers and halocarbons.
Chemical communications (Cambridge, England), 2016, 52, 5565-5568
7118912 CIFC14 H22 Cl2 I6 N4 PtP -19.1724; 9.2419; 10.1625
114.172; 100.036; 108.096
700.48Ivanov, Daniil M.; Novikov, Alexander S.; Ananyev, Ivan V.; Kirina, Yulia V.; Kukushkin, Vadim Yu
Halogen bonding between metal centers and halocarbons.
Chemical communications (Cambridge, England), 2016, 52, 5565-5568
7118913 CIFC14 H22 Cl2 I6 N4 PtP -19.1743; 9.2939; 10.2287
114.48; 99.652; 108.236
707.88Ivanov, Daniil M.; Novikov, Alexander S.; Ananyev, Ivan V.; Kirina, Yulia V.; Kukushkin, Vadim Yu
Halogen bonding between metal centers and halocarbons.
Chemical communications (Cambridge, England), 2016, 52, 5565-5568
7118914 CIFC14 H22 Cl2 I6 N4 PtP -19.158; 9.3355; 10.2955
114.801; 99.221; 108.383
713.2Ivanov, Daniil M.; Novikov, Alexander S.; Ananyev, Ivan V.; Kirina, Yulia V.; Kukushkin, Vadim Yu
Halogen bonding between metal centers and halocarbons.
Chemical communications (Cambridge, England), 2016, 52, 5565-5568
7118915 CIFC145 H161 Co24 N9 O101P -4 21 m27.646; 27.646; 17.306
90; 90; 90
13227Liang, Guang-Ming; Ni, Qing-Ling; Zou, Hua-Hong; Gui, Liu-Cheng; Wang, Xiu-Jian
Rare double spin canting antiferromagnetic behaviours in a [Co24] cluster.
Chemical communications (Cambridge, England), 2016, 52, 5293-5296
7118916 CIFC38 H36 Cu2 P2P -110.0317; 12.1017; 13.3609
97.647; 94.311; 95.342
1594.3Molteni, Roberto; Bertermann, Rüdiger; Edkins, Katharina; Steffen, Andreas
An unexpected transmetalation intermediate: isolation and structural characterization of a solely CH3 bridged di-copper(i) complex.
Chemical communications (Cambridge, England), 2016, 52, 5019-5022
7118917 CIFC16 H13 F3 N2 OP -15.4475; 12.1951; 12.2971
114.682; 98.556; 98.672
713.13Tomakinian, Terry; Guillot, Régis; Kouklovsky, Cyrille; Vincent, Guillaume
Synthesis of benzofuro[3,2-b]indoline amines via deamination-interrupted Fischer indolization and their unexpected reactivity towards nucleophiles.
Chemical communications (Cambridge, England), 2016, 52, 5443-5446
7118918 CIFC17 H18 N2 O5 S2P -19.2208; 9.2881; 11.3189
92.755; 107.193; 106.506
878.64Tomakinian, Terry; Guillot, Régis; Kouklovsky, Cyrille; Vincent, Guillaume
Synthesis of benzofuro[3,2-b]indoline amines via deamination-interrupted Fischer indolization and their unexpected reactivity towards nucleophiles.
Chemical communications (Cambridge, England), 2016, 52, 5443-5446
7118919 CIFC18 H16 B F2 N OP b c a13.5204; 12.9163; 17.273
90; 90; 90
3016.4Tomakinian, Terry; Guillot, Régis; Kouklovsky, Cyrille; Vincent, Guillaume
Synthesis of benzofuro[3,2-b]indoline amines via deamination-interrupted Fischer indolization and their unexpected reactivity towards nucleophiles.
Chemical communications (Cambridge, England), 2016, 52, 5443-5446
7118920 CIFC17.09 H116.4 Br N O38P m m a21.0329; 12.5972; 12.0333
90; 90; 90
3188.3Muromachi, Sanehiro; Udachin, Konstantin A.; Alavi, Saman; Ohmura, Ryo; Ripmeester, John A.
Selective occupancy of methane by cage symmetry in TBAB ionic clathrate hydrate.
Chemical communications (Cambridge, England), 2016, 52, 5621-5624
7118921 CIFC22 H16 O3P n a 2111.353; 16.909; 8.235
90; 90; 90
1580.9Mao, Wenbin; Zhu, Chen
Synthesis of highly substituted γ-hydroxybutenolides through the annulation of keto acids with alkynes and subsequent hydroxyl transposition.
Chemical communications (Cambridge, England), 2016, 52, 5269-5272
7118922 CIFC34.5 H25 Cl N2 O2C 1 2/c 115.3088; 17.993; 19.4932
90; 92.57; 90
5364Wang, Huan; Zhang, Zhiyun; Zhou, Haitao; Wang, Tonghai; Su, Jianhua; Tong, Xiaofeng; Tian, He
Cu-catalyzed C-H amination/Ullmann N-arylation domino reaction: a straightforward synthesis of 9,14-diaryl-9,14-dihydrodibenzo[a,c]phenazine.
Chemical communications (Cambridge, England), 2016, 52, 5459-5462
7118923 CIFC36 H24 N2C 1 2/c 114.0547; 19.251; 18.41
90; 90.832; 90
4980.6Wang, Huan; Zhang, Zhiyun; Zhou, Haitao; Wang, Tonghai; Su, Jianhua; Tong, Xiaofeng; Tian, He
Cu-catalyzed C-H amination/Ullmann N-arylation domino reaction: a straightforward synthesis of 9,14-diaryl-9,14-dihydrodibenzo[a,c]phenazine.
Chemical communications (Cambridge, England), 2016, 52, 5459-5462
7118924 CIFC42 H26 N2P 1 21/n 111.4684; 18.005; 13.845
90; 92.989; 90
2854.9Wang, Huan; Zhang, Zhiyun; Zhou, Haitao; Wang, Tonghai; Su, Jianhua; Tong, Xiaofeng; Tian, He
Cu-catalyzed C-H amination/Ullmann N-arylation domino reaction: a straightforward synthesis of 9,14-diaryl-9,14-dihydrodibenzo[a,c]phenazine.
Chemical communications (Cambridge, England), 2016, 52, 5459-5462
7118925 CIFC33 H24 N2P 1 21/n 113.67; 10.7087; 16.477
90; 98.766; 90
2383.9Wang, Huan; Zhang, Zhiyun; Zhou, Haitao; Wang, Tonghai; Su, Jianhua; Tong, Xiaofeng; Tian, He
Cu-catalyzed C-H amination/Ullmann N-arylation domino reaction: a straightforward synthesis of 9,14-diaryl-9,14-dihydrodibenzo[a,c]phenazine.
Chemical communications (Cambridge, England), 2016, 52, 5459-5462
7118926 CIFC20 H19 N O3 SP -17.326; 10.134; 12.489
80.774; 82.54; 77.77
890Huang, Hai; Tang, Luning; Liu, Qi; Xi, Yang; He, Guangke; Zhu, Hongjun
Formation of α-chalcogenyl acrylamides through unprecedented chalcogen-mediated metal-free oxyfunctionalization of ynamides with DMSO as an oxidant.
Chemical communications (Cambridge, England), 2016, 52, 5605-5608
7118927 CIFC23 H25 N O3 SP 1 21 113.598; 5.7831; 14.8716
90; 111.469; 90
1088.34Huang, Hai; Tang, Luning; Liu, Qi; Xi, Yang; He, Guangke; Zhu, Hongjun
Formation of α-chalcogenyl acrylamides through unprecedented chalcogen-mediated metal-free oxyfunctionalization of ynamides with DMSO as an oxidant.
Chemical communications (Cambridge, England), 2016, 52, 5605-5608
7118928 CIFC27 H29 N O3 S2P 1 21/c 112.8698; 13.262; 15.0271
90; 92.583; 90
2562.2Huang, Hai; Tang, Luning; Liu, Qi; Xi, Yang; He, Guangke; Zhu, Hongjun
Formation of α-chalcogenyl acrylamides through unprecedented chalcogen-mediated metal-free oxyfunctionalization of ynamides with DMSO as an oxidant.
Chemical communications (Cambridge, England), 2016, 52, 5605-5608
7118929 CIFC4 H6 N8 O0 ZnI -4 3 m17.1168; 17.1168; 17.1168
90; 90; 90
5014.96Tang, Yu-Huan; Wang, Fei; Liu, Jin-Xiu; Zhang, Jian
Diverse tetrahedral tetrazolate frameworks with N-rich surface.
Chemical communications (Cambridge, England), 2016, 52, 5625-5628
7118930 CIFC4 H6 N8 O0 ZnI -4 3 m17.0293; 17.0293; 17.0293
90; 90; 90
4938.4Tang, Yu-Huan; Wang, Fei; Liu, Jin-Xiu; Zhang, Jian
Diverse tetrahedral tetrazolate frameworks with N-rich surface.
Chemical communications (Cambridge, England), 2016, 52, 5625-5628
7118931 CIFC18 H45 N15 O8 S2 Zn2P 21 21 2115.7886; 15.9425; 16.3286
90; 90; 90
4110.1Tang, Yu-Huan; Wang, Fei; Liu, Jin-Xiu; Zhang, Jian
Diverse tetrahedral tetrazolate frameworks with N-rich surface.
Chemical communications (Cambridge, England), 2016, 52, 5625-5628
7118932 CIFC24 H52 B3 F12 N48 O8 Zn7I -4 3 d22.3819; 22.3819; 22.3819
90; 90; 90
11212.2Tang, Yu-Huan; Wang, Fei; Liu, Jin-Xiu; Zhang, Jian
Diverse tetrahedral tetrazolate frameworks with N-rich surface.
Chemical communications (Cambridge, England), 2016, 52, 5625-5628
7118933 CIFC11 H15 N4 O2P 1 21/c 16.211; 40.769; 9.646
90; 96.104; 90
2428.7Wang, Jian; Li, Jia-Nan; Zhang, Shao-Liang; Zhao, Xin-Hua; Shao, Dong; Wang, Xin-Yi
Syntheses and magnetic properties of a pyrimidyl-substituted nitronyl nitroxide radical and its cobalt(ii) complexes.
Chemical communications (Cambridge, England), 2016, 52, 5033-5036
7118934 CIFC21 H19 Co F12 N4 O6P -114.967; 15.106; 15.938
69.812; 62.763; 66.38
2877.1Wang, Jian; Li, Jia-Nan; Zhang, Shao-Liang; Zhao, Xin-Hua; Shao, Dong; Wang, Xin-Yi
Syntheses and magnetic properties of a pyrimidyl-substituted nitronyl nitroxide radical and its cobalt(ii) complexes.
Chemical communications (Cambridge, England), 2016, 52, 5033-5036
7118935 CIFC31 H23 Co2 F24 N4 O10P 1 21/n 112.6019; 20.7451; 17.6713
90; 104.665; 90
4469.3Wang, Jian; Li, Jia-Nan; Zhang, Shao-Liang; Zhao, Xin-Hua; Shao, Dong; Wang, Xin-Yi
Syntheses and magnetic properties of a pyrimidyl-substituted nitronyl nitroxide radical and its cobalt(ii) complexes.
Chemical communications (Cambridge, England), 2016, 52, 5033-5036
7118936 CIFC36 H40 B N O2P -19.7416; 10.1024; 16.6
92.408; 106.474; 105.593
1496.5Jiang, Han-Chun; Tang, Xiang-Ying; Shi, Min
Copper-catalyzed regio- and enantioselective aminoboration of alkylidenecyclopropanes: the synthesis of cyclopropane-containing β-aminoalkylboranes.
Chemical communications (Cambridge, England), 2016, 52, 5273-5276
7118937 CIFC30 H36 B N O2P -110.5305; 11.491; 13.29
68.577; 71.096; 63.363
1313.1Jiang, Han-Chun; Tang, Xiang-Ying; Shi, Min
Copper-catalyzed regio- and enantioselective aminoboration of alkylidenecyclopropanes: the synthesis of cyclopropane-containing β-aminoalkylboranes.
Chemical communications (Cambridge, England), 2016, 52, 5273-5276
7118938 CIFC18 H48 Li3 N6 P7P -311.3403; 11.3403; 15.1182
90; 90; 120
1683.76Bhattacharyya, Koyel X.; Dreyfuss, Sébastien; Saffon-Merceron, Nathalie; Mézailles, Nicolas
P4 functionalization by hydrides: direct synthesis of P-H bonds.
Chemical communications (Cambridge, England), 2016, 52, 5179-5182
7118939 CIFC50 H32 O2P 1 21/c 18.8161; 13.0764; 29.5577
90; 94.937; 90
3394.9Pozo, Iago; Cobas, Agustín; Peña, Diego; Guitián, Enrique; Pérez, Dolores
1,7-Naphthodiyne: a new platform for the synthesis of novel, sterically congested PAHs.
Chemical communications (Cambridge, England), 2016, 52, 5534-5537
7118940 CIFC39 H25 Cl3P 1 21/c 114.0105; 13.0164; 16.1008
90; 102.591; 90
2865.63Pozo, Iago; Cobas, Agustín; Peña, Diego; Guitián, Enrique; Pérez, Dolores
1,7-Naphthodiyne: a new platform for the synthesis of novel, sterically congested PAHs.
Chemical communications (Cambridge, England), 2016, 52, 5534-5537
7118941 CIFC27 H43 Li N4P 1 21/c 116.526; 9.874; 18.038
90; 115.24; 90
2662.4Finkelmeier, Nils; Visscher, Arne; Wandtke, Sebastian; Herbst-Irmer, Regine; Stalke, Dietmar
CH3-deprotonation of 9-methylanthracene under mild conditions.
Chemical communications (Cambridge, England), 2016, 52, 5440-5442
7118942 CIFC69 H98 Li2 N8P 1 21/n 19.486; 34.841; 19.391
90; 93.77; 90
6394.9Finkelmeier, Nils; Visscher, Arne; Wandtke, Sebastian; Herbst-Irmer, Regine; Stalke, Dietmar
CH3-deprotonation of 9-methylanthracene under mild conditions.
Chemical communications (Cambridge, England), 2016, 52, 5440-5442
7118943 CIFC16 H14 N2 OP 21 21 216.4272; 11.7684; 18.3674
90; 90; 90
1389.27Laugeois, Maxime; Ponra, Sudipta; Ratovelomanana-Vidal, Virginie; Michelet, Véronique; Vitale, Maxime R.
Asymmetric preparation of polysubstituted cyclopentanes by synergistic Pd(0)/amine catalyzed formal [3+2] cycloadditions of vinyl cyclopropanes with enals.
Chemical communications (Cambridge, England), 2016, 52, 5332-5335
7118944 CIFC16 H14 N2 OP 1 21 19.0535; 7.4148; 10.4203
90; 104.406; 90
677.52Laugeois, Maxime; Ponra, Sudipta; Ratovelomanana-Vidal, Virginie; Michelet, Véronique; Vitale, Maxime R.
Asymmetric preparation of polysubstituted cyclopentanes by synergistic Pd(0)/amine catalyzed formal [3+2] cycloadditions of vinyl cyclopropanes with enals.
Chemical communications (Cambridge, England), 2016, 52, 5332-5335
7118945 CIFC16 H16 N2 OP 1 21 16.9841; 12.5978; 15.735
90; 97.885; 90
1371.3Laugeois, Maxime; Ponra, Sudipta; Ratovelomanana-Vidal, Virginie; Michelet, Véronique; Vitale, Maxime R.
Asymmetric preparation of polysubstituted cyclopentanes by synergistic Pd(0)/amine catalyzed formal [3+2] cycloadditions of vinyl cyclopropanes with enals.
Chemical communications (Cambridge, England), 2016, 52, 5332-5335
7118946 CIFC20 H15 N O3P 1 21/c 116.698; 5.9368; 15.65
90; 97.783; 90
1537.1Rathore, Kuldeep Singh; Lad, Bapurao Sudam; Chennamsetti, Haribabu; Katukojvala, Sreenivas
An unprecedented benzannulation of oxindoles with enalcarbenoids: a regioselective approach to functionalized carbazoles.
Chemical communications (Cambridge, England), 2016, 52, 5812-5815
7118947 CIFC20 H14 Cl N O3P -16.977; 8.8337; 14.5708
93.367; 102.682; 108.417
823.26Rathore, Kuldeep Singh; Lad, Bapurao Sudam; Chennamsetti, Haribabu; Katukojvala, Sreenivas
An unprecedented benzannulation of oxindoles with enalcarbenoids: a regioselective approach to functionalized carbazoles.
Chemical communications (Cambridge, England), 2016, 52, 5812-5815
7118948 CIFC19 H12 Cl N O2P 1 21/c 116.024; 15.055; 6.3189
90; 101.11; 90
1495.8Rathore, Kuldeep Singh; Lad, Bapurao Sudam; Chennamsetti, Haribabu; Katukojvala, Sreenivas
An unprecedented benzannulation of oxindoles with enalcarbenoids: a regioselective approach to functionalized carbazoles.
Chemical communications (Cambridge, England), 2016, 52, 5812-5815
7118949 CIFC113 H38 N2 O2 S2C 1 2/c 121.845; 16.43; 20.014
90; 107.937; 90
6834.2Li, Shu-Hui; Li, Zong-Jun; Nakagawa, Takafumi; Jeon, Il; Ju, Zheng; Matsuo, Yutaka; Gao, Xiang
Multifunctionalization of C70 at the two polar regions with a high regioselectivity via oxazolination and benzylation reactions.
Chemical communications (Cambridge, England), 2016, 52, 5710-5713
7118957 CIFC76 H68 Cl8 Fe2 N4 O4 P4 PtC 1 2/c 129.1376; 15.0037; 18.0317
90; 109.95; 90
7409.9Masaki Ito; Masato Iseki; Masumi Itazaki; Hiroshi Nakazawa
Tetrahedral cage complex with planar vertices: selective synthesis of Pt4L6 cage complexes involving hydrogen bonds driven by halide binding
Chem.Commun., 2016, 52, 7205
7118958 CIFC224 H188 Cl32 Fe6 N12 O12 P12 Pt4P -121.3085; 22.6838; 31.6313
90.2849; 90.4102; 117.182
13599.8Masaki Ito; Masato Iseki; Masumi Itazaki; Hiroshi Nakazawa
Tetrahedral cage complex with planar vertices: selective synthesis of Pt4L6 cage complexes involving hydrogen bonds driven by halide binding
Chem.Commun., 2016, 52, 7205
7118959 CIFC237 H201 Br8 Cl63 Fe6 N12 O12 P12 Pt4P -121.4683; 23.594; 32.9537
88.034; 89.129; 65.458
15174.9Masaki Ito; Masato Iseki; Masumi Itazaki; Hiroshi Nakazawa
Tetrahedral cage complex with planar vertices: selective synthesis of Pt4L6 cage complexes involving hydrogen bonds driven by halide binding
Chem.Commun., 2016, 52, 7205
7118960 CIFC61 H58 Cl2 N3 O4 P3 PtP -111.7999; 12.6886; 19.4168
83.953; 73.888; 87.375
2777.02Masaki Ito; Masato Iseki; Masumi Itazaki; Hiroshi Nakazawa
Tetrahedral cage complex with planar vertices: selective synthesis of Pt4L6 cage complexes involving hydrogen bonds driven by halide binding
Chem.Commun., 2016, 52, 7205
7118961 CIFC36 H30 Fe N2 O2 P2P 1 21/c 113.7346; 11.888; 9.9583
90; 104.743; 90
1572.4Masaki Ito; Masato Iseki; Masumi Itazaki; Hiroshi Nakazawa
Tetrahedral cage complex with planar vertices: selective synthesis of Pt4L6 cage complexes involving hydrogen bonds driven by halide binding
Chem.Commun., 2016, 52, 7205
7118962 CIFC7 H3 Cl F2 OP 1 21/n 13.8289; 14.522; 12.2527
90; 95.836; 90
677.76Dhananjay Dey; Subhrajyoti Bhandary; Abhishek Sirohiwal; Venkatesha R. Hathwar; Deepak Chopra
'Conformational lock' via unusual intramolecular C-F^...^O[double bond, length as m-dash]C and C-H^...^Cl-C parallel dipoles observed in in situ cryocrystallized liquids
Chem.Commun., 2016, 52, 7225
7118963 CIFC7 H3 Cl F2 OP -17.4814; 8.5648; 10.7372
100.231; 95.404; 91.365
673.48Dhananjay Dey; Subhrajyoti Bhandary; Abhishek Sirohiwal; Venkatesha R. Hathwar; Deepak Chopra
'Conformational lock' via unusual intramolecular C-F^...^O[double bond, length as m-dash]C and C-H^...^Cl-C parallel dipoles observed in in situ cryocrystallized liquids
Chem.Commun., 2016, 52, 7225
7118964 CIFC7 H3 Cl F2 OP 1 21/c 17.4388; 15.7661; 11.8282
90; 93.597; 90
1384.49Dhananjay Dey; Subhrajyoti Bhandary; Abhishek Sirohiwal; Venkatesha R. Hathwar; Deepak Chopra
'Conformational lock' via unusual intramolecular C-F^...^O[double bond, length as m-dash]C and C-H^...^Cl-C parallel dipoles observed in in situ cryocrystallized liquids
Chem.Commun., 2016, 52, 7225
7118965 CIFC7 H4 Cl F OP n a 2113.8205; 12.5452; 3.8197
90; 90; 90
662.26Dhananjay Dey; Subhrajyoti Bhandary; Abhishek Sirohiwal; Venkatesha R. Hathwar; Deepak Chopra
'Conformational lock' via unusual intramolecular C-F^...^O[double bond, length as m-dash]C and C-H^...^Cl-C parallel dipoles observed in in situ cryocrystallized liquids
Chem.Commun., 2016, 52, 7225
7118966 CIFC7 H5 Cl OP 1 21/n 17.4704; 3.9581; 22.3439
90; 93.566; 90
659.4Dhananjay Dey; Subhrajyoti Bhandary; Abhishek Sirohiwal; Venkatesha R. Hathwar; Deepak Chopra
'Conformational lock' via unusual intramolecular C-F^...^O[double bond, length as m-dash]C and C-H^...^Cl-C parallel dipoles observed in in situ cryocrystallized liquids
Chem.Commun., 2016, 52, 7225
7118967 CIFC7 H3 Cl F2 OP -16.859; 7.2006; 8.0365
94.613; 104.275; 115.906
337.85Dhananjay Dey; Subhrajyoti Bhandary; Abhishek Sirohiwal; Venkatesha R. Hathwar; Deepak Chopra
'Conformational lock' via unusual intramolecular C-F^...^O[double bond, length as m-dash]C and C-H^...^Cl-C parallel dipoles observed in in situ cryocrystallized liquids
Chem.Commun., 2016, 52, 7225
7118968 CIFC20 H37 Gd Mn2 N8 O44 P4P 1 21/c 112.3; 19.75; 24.63
90; 95.3; 90
5958Javier Arinez-Soriano; Jorge Albalad; Christian Vila-Parrondo; Javier Perez-Carvajal; Sabina Rodriguez-Hermida; Aurelio Cabeza; Jordi Juanhuix; Inhar Imaz; Daniel Maspoch
Single-crystal and humidity-controlled powder diffraction study of the breathing effect in a metal-organic framework upon water adsorption/desorption
Chem.Commun., 2016, 52, 7229
7118969 CIFC20 H37 Gd Mn2 N8 O28 P4C 1 2/c 126.09; 14.51; 12.2
90; 110.19; 90
4335Javier Arinez-Soriano; Jorge Albalad; Christian Vila-Parrondo; Javier Perez-Carvajal; Sabina Rodriguez-Hermida; Aurelio Cabeza; Jordi Juanhuix; Inhar Imaz; Daniel Maspoch
Single-crystal and humidity-controlled powder diffraction study of the breathing effect in a metal-organic framework upon water adsorption/desorption
Chem.Commun., 2016, 52, 7229
7118970 CIFC30 H40 O4 SP 1 21 113.5064; 5.8689; 17.8643
90; 102.617; 90
1381.87Congde Huo; Yajun Wang; Yong Yuan; Fengjuan Chen; Jing Tang
Auto-oxidative hydroxysulfenylation of alkenes
Chem.Commun., 2016, 52, 7233
7118971 CIFC12 H9 F5 N2 O2 SP 1 21/c 111.8093; 10.6449; 10.6262
90; 91.185; 90
1335.52V. V. Khutorianskyi; M. Sonawane; M. Posta; B. Klepetarova; P. Beier
Oxidative nucleophilic aromatic amination of nitrobenzenes
Chem.Commun., 2016, 52, 7237
7118972 CIFC51 H23 Cu6 N3 O33C 1 2/c 132.27; 18.631; 23.512
90; 117.225; 90
12570Mingxing Zhang; Bin Li; Yunzhi Li; Qian Wang; Wenwei Zhang; Banglin Chen; Shuhua Li; Yi Pan; Xiaozeng You; Junfeng Bai
Finely tuning MOFs towards high performance in C2H2 storage: synthesis and properties of a new MOF-505 analogue with an inserted amide functional group
Chem.Commun., 2016, 52, 7241
7118973 CIFC26 H28 N2 O6 SP n a 2119.8378; 9.3737; 13.4463
90; 90; 90
2500.4Peng-Long Zhu; Xiang-Ying Tang; Min Shi
Intramolecular cyclizations of cyclopropenes with indole
Chem.Commun., 2016, 52, 7245
7118974 CIFC26 H27 F3 N2 O4 SP -19.9556; 14.589; 18.274
81.682; 76.959; 88.485
2558.4Peng-Long Zhu; Xiang-Ying Tang; Min Shi
Intramolecular cyclizations of cyclopropenes with indole
Chem.Commun., 2016, 52, 7245
7118975 CIFC28 H26 N2 O4 SP n a 2112.3454; 8.661; 22.8626
90; 90; 90
2444.5Peng-Long Zhu; Xiang-Ying Tang; Min Shi
Intramolecular cyclizations of cyclopropenes with indole
Chem.Commun., 2016, 52, 7245
7118976 CIFC30 H27 N3 O8 SP 1 21/n 114.3817; 10.8082; 19.0025
90; 109.283; 90
2788Peng-Long Zhu; Xiang-Ying Tang; Min Shi
Intramolecular cyclizations of cyclopropenes with indole
Chem.Commun., 2016, 52, 7245
7118977 CIFC26 H25 N3 O5 SP -19.3636; 10.8898; 12.521
99.75; 95.533; 107.818
1182.9Peng-Long Zhu; Xiang-Ying Tang; Min Shi
Intramolecular cyclizations of cyclopropenes with indole
Chem.Commun., 2016, 52, 7245
7118980 CIFC19 H36 B10 Cl2 N PP 1 21/c 19.8778; 19.2098; 16.2304
90; 101.765; 90
3015Tek Long Chan; Zuowei Xie
The synthesis, structure and reactivity of an imine-stabilized carboranylphosphorus(I) compound
Chem.Commun., 2016, 52, 7280
7118981 CIFC19 H36 B10 N PP n m a17.159; 13.438; 11.014
90; 90; 90
2539.6Tek Long Chan; Zuowei Xie
The synthesis, structure and reactivity of an imine-stabilized carboranylphosphorus(I) compound
Chem.Commun., 2016, 52, 7280
7118982 CIFC23 H42 B10 N O4 PP -110.3092; 10.9189; 16.0645
80.327; 73.798; 74.727
1666.41Tek Long Chan; Zuowei Xie
The synthesis, structure and reactivity of an imine-stabilized carboranylphosphorus(I) compound
Chem.Commun., 2016, 52, 7280
7118983 CIFC38 H72 B20 N2 P2 SP -110.177; 10.4214; 25.2588
101.476; 99.642; 90.279
2586.2Tek Long Chan; Zuowei Xie
The synthesis, structure and reactivity of an imine-stabilized carboranylphosphorus(I) compound
Chem.Commun., 2016, 52, 7280
7118984 CIFC38 H72 B20 N2 P2 SeP -110.2136; 10.4144; 25.274
101.61; 99.7572; 90.6407
2592.4Tek Long Chan; Zuowei Xie
The synthesis, structure and reactivity of an imine-stabilized carboranylphosphorus(I) compound
Chem.Commun., 2016, 52, 7280
7118985 CIFC27 H56 B10 N3 P Si2P b c a18.683; 13.262; 31.5134
90; 90; 90
7808.2Tek Long Chan; Zuowei Xie
The synthesis, structure and reactivity of an imine-stabilized carboranylphosphorus(I) compound
Chem.Commun., 2016, 52, 7280
7118986 CIFC19 H37 B10 Cl N PP n m a17.4405; 13.6893; 10.8979
90; 90; 90
2601.85Tek Long Chan; Zuowei Xie
The synthesis, structure and reactivity of an imine-stabilized carboranylphosphorus(I) compound
Chem.Commun., 2016, 52, 7280
7118987 CIFC25 H55 B10 N2 P Si2P 1 21/c 117.4404; 12.4044; 18.5294
90; 115.893; 90
3606.2Tek Long Chan; Zuowei Xie
The synthesis, structure and reactivity of an imine-stabilized carboranylphosphorus(I) compound
Chem.Commun., 2016, 52, 7280
7118988 CIFC31 H24 Au Cl2 O PP b c a13.4335; 9.7044; 42.1106
90; 90; 90
5489.71Eric Omar Asomoza-Solis; Jonathan Rojas-Ocampo; Ruben Alfredo Toscano; Susana Porcel
Arenediazonium salts as electrophiles for the oxidative addition of gold(I)
Chem.Commun., 2016, 52, 7295
7118989 CIFC24 H19 Au Cl2 N O2 PP 1 21/n 19.36; 16.371; 16.662
90; 95.597; 90
2541Eric Omar Asomoza-Solis; Jonathan Rojas-Ocampo; Ruben Alfredo Toscano; Susana Porcel
Arenediazonium salts as electrophiles for the oxidative addition of gold(I)
Chem.Commun., 2016, 52, 7295
7118990 CIFC105 H143 K2 N12 O37 PP -116.775; 19.152; 20.418
93.782; 113.688; 106.847
5623.4Liguo Ji; Zaiwen Yang; Yanxia Zhao; Meng Sun; Liping Cao; Xiao-Juan Yang; Yao-Yu Wang; Biao Wu
Sandwich phosphate complexes of macrocyclic tris(urea) ligands and their rotation around the anion
Chem.Commun., 2016, 52, 7310
7118991 CIFC98 H128 K N16 O28 PP -114.99; 16.27; 25.088
99.668; 100.824; 105.587
5632Liguo Ji; Zaiwen Yang; Yanxia Zhao; Meng Sun; Liping Cao; Xiao-Juan Yang; Yao-Yu Wang; Biao Wu
Sandwich phosphate complexes of macrocyclic tris(urea) ligands and their rotation around the anion
Chem.Commun., 2016, 52, 7310
7118992 CIFC116 H174 N17 O27 PP -114.782; 19.415; 21.552
85.538; 85.989; 89.867
6151.4Liguo Ji; Zaiwen Yang; Yanxia Zhao; Meng Sun; Liping Cao; Xiao-Juan Yang; Yao-Yu Wang; Biao Wu
Sandwich phosphate complexes of macrocyclic tris(urea) ligands and their rotation around the anion
Chem.Commun., 2016, 52, 7310
7118993 CIFC360 H490 K8 N48 O133 S4P 1 21/c 116.6867; 19.4; 32.767
90; 112.755; 90
9781.8Liguo Ji; Zaiwen Yang; Yanxia Zhao; Meng Sun; Liping Cao; Xiao-Juan Yang; Yao-Yu Wang; Biao Wu
Sandwich phosphate complexes of macrocyclic tris(urea) ligands and their rotation around the anion
Chem.Commun., 2016, 52, 7310
7118994 CIFC97 H132 K2 N13 O35 SP 1 21/c 118.0761; 21.11; 32.803
90; 122.13; 90
10600.1Liguo Ji; Zaiwen Yang; Yanxia Zhao; Meng Sun; Liping Cao; Xiao-Juan Yang; Yao-Yu Wang; Biao Wu
Sandwich phosphate complexes of macrocyclic tris(urea) ligands and their rotation around the anion
Chem.Commun., 2016, 52, 7310
7118995 CIFC50 H75 Cl N10 O14C 1 c 120.611; 31.842; 8.872
90; 104.307; 90
5642Liguo Ji; Zaiwen Yang; Yanxia Zhao; Meng Sun; Liping Cao; Xiao-Juan Yang; Yao-Yu Wang; Biao Wu
Sandwich phosphate complexes of macrocyclic tris(urea) ligands and their rotation around the anion
Chem.Commun., 2016, 52, 7310
7118996 CIFC51 H78 Cl N9 O14P 1 21/c 118.572; 34.162; 8.774
90; 94.732; 90
5548Liguo Ji; Zaiwen Yang; Yanxia Zhao; Meng Sun; Liping Cao; Xiao-Juan Yang; Yao-Yu Wang; Biao Wu
Sandwich phosphate complexes of macrocyclic tris(urea) ligands and their rotation around the anion
Chem.Commun., 2016, 52, 7310
7118997 CIFC51 H68 I2 N10 O10P -112.275; 13.0629; 19.863
71.072; 78.86; 70.582
2828.3Liguo Ji; Zaiwen Yang; Yanxia Zhao; Meng Sun; Liping Cao; Xiao-Juan Yang; Yao-Yu Wang; Biao Wu
Sandwich phosphate complexes of macrocyclic tris(urea) ligands and their rotation around the anion
Chem.Commun., 2016, 52, 7310
7118998 CIFC29 H21 P SeP -19.4639; 10.1522; 14.1214
77.6074; 86.1247; 71.6074
1257.47Massimo Rigo; Manuela Weber; Christian Muller
Expanding the phosphorus-carbon analogy: formation of an unprecedented 5-phosphasemibullvalene derivative
Chem.Commun., 2016, 52, 7090
7118999 CIFC18 H9 B O3C 1 2/c 117.055; 10.409; 7.301
90; 111.071; 90
1209.4Yuichi Kitamoto; Takatsugu Suzuki; Yasuo Miyata; Hiroshi Kita; Kenji Funaki; Shuichi Oi
The first synthesis and X-ray crystallographic analysis of an oxygen-bridged planarized triphenylborane
Chem.Commun., 2016, 52, 7098
7119000 CIFC37 H33 N5 NiP 1 21/a 17.0843; 25.1223; 8.2327
90; 103.844; 90
1422.65Ryo Nozawa; Keitaro Yamamoto; Ichiro Hisaki; Ji-Young Shin; Hiroshi Shinokubo
Ni^II^ tetrahydronorcorroles: antiaromatic porphyrinoids with saturated pyrrole units
Chem.Commun., 2016, 52, 7106
7119001 CIFC14 H15 N O3P 1 21/c 114.579; 9.8759; 9.0753
90; 102.459; 90
1275.9Nicole S. Y. Loy; Subin Choi; Sunggak Kim; Cheol-Min Park
The synthesis of pyrroles and oxazoles based on gold alpha-imino carbene complexes
Chem.Commun., 2016, 52, 7336
7119002 CIFC14 H15 N3 O5I 1 2/a 130.509; 14.5498; 33.049
90; 91.858; 90
14663Nicole S. Y. Loy; Subin Choi; Sunggak Kim; Cheol-Min Park
The synthesis of pyrroles and oxazoles based on gold alpha-imino carbene complexes
Chem.Commun., 2016, 52, 7336
7119003 CIFC44 H65 B Br Cl9 F N2 PP 1 21/c 124.7264; 9.6603; 23.4725
90; 109.127; 90
5297.2Shubhanchi Nigam; Benjamin P. Burke; Laura H. Davies; Juozas Domarkas; Jennifer F. Wallis; Paul G. Waddell; Jennifer S. Waby; David M. Benoit; Anne-Marie Seymour; Christopher Cawthorne; Lee J. Higham; Stephen J. Archibald
Structurally optimised BODIPY derivatives for imaging of mitochondrial dysfunction in cancer and heart cells
Chem.Commun., 2016, 52, 7114
7119004 CIFC25 H28 Br N3 O3P 1 21 110.064; 8.502; 13.718
90; 100.284; 90
1154.9Jakob Blom; Tore Kiilerich Johansen; Frank Jensen; Karl Anker Jorgensen
Dynamic resolution of 2-cyclohexylidene acetaldehydes through organocatalytic dienamine [4+2] cycloaddition
Chem.Commun., 2016, 52, 7153
7119005 CIFC30 H27 N3 O4P 1 21 112.983; 10.976; 16.961
90; 99.955; 90
2380.6Jakob Blom; Tore Kiilerich Johansen; Frank Jensen; Karl Anker Jorgensen
Dynamic resolution of 2-cyclohexylidene acetaldehydes through organocatalytic dienamine [4+2] cycloaddition
Chem.Commun., 2016, 52, 7153
7119006 CIFC26 H24 N2 O6P 1 21/c 115.361; 4.955; 14.843
90; 98.245; 90
1118.1Kazuto Nakamura; Nobuhiro Yasuda; Hiromitsu Maeda
Dimension-controlled assemblies of modified bipyrroles stabilized by electron-withdrawing moieties
Chem.Commun., 2016, 52, 7157
7119007 CIFC30 H32 N2 O9P -17.9706; 10.519; 17.44
87.803; 86.847; 78.375
1429.5Kazuto Nakamura; Nobuhiro Yasuda; Hiromitsu Maeda
Dimension-controlled assemblies of modified bipyrroles stabilized by electron-withdrawing moieties
Chem.Commun., 2016, 52, 7157
7119008 CIFC40 H112 I3 N8 Nd O10 P4P -113.7969; 14.7646; 20.728
92.826; 108.606; 114.956
3544Sandeep K. Gupta; Thayalan Rajeshkumar; Gopalan Rajaraman; Ramaswamy Murugavel
An unprecedented zero field neodymium(III) single-ion magnet based on a phosphonic diamide
Chem.Commun., 2016, 52, 7168
7119009 CIFC54 H38 Cd N8 O4P -18.8932; 11.8369; 15.1942
72.926; 88.754; 88.696
1528.4Jian-Cheng Wang; Jian-Ping Ma; Qi-Kui Liu; Yu-Hong Hu; Yu-Bin Dong
Cd(II)-MOF-IM: post-synthesis functionalization of a Cd(II)-MOF as a triphase transfer catalyst
Chem.Commun., 2016, 52, 6989
7119010 CIFC22 H24 Co N4 O7 SP 1 21 111.479; 8.356; 12.079
90; 104.039; 90
1124Jian-Shen Feng; Min Ren; Zhong-Sheng Cai; Kun Fan; Song-Song Bao; Li-Min Zheng
Enantiopure phosphonic acids as chiral inducers: homochiral crystallization of cobalt coordination polymers showing field-induced slow magnetization relaxation
Chem.Commun., 2016, 52, 6877
7119011 CIFC22 H24 Co N4 O7 SP 1 21 111.495; 8.412; 12.098
90; 103.45; 90
1137.7Jian-Shen Feng; Min Ren; Zhong-Sheng Cai; Kun Fan; Song-Song Bao; Li-Min Zheng
Enantiopure phosphonic acids as chiral inducers: homochiral crystallization of cobalt coordination polymers showing field-induced slow magnetization relaxation
Chem.Commun., 2016, 52, 6877
7119012 CIFC55 H31 N3C c m 2113.9705; 34.3796; 8.1479
90; 90; 90
3913.4Helena Isla; Monika Srebro-Hooper; Marion Jean; Nicolas Vanthuyne; Thierry Roisnel; Jamie L. Lunkley; Gilles Muller; J. A. Gareth Williams; Jochen Autschbach; Jeanne Crassous
Conformational changes and chiroptical switching of enantiopure bis-helicenic terpyridine upon Zn^2+^ binding
Chem.Commun., 2016, 52, 5932
7119013 CIFC61 H41 Cl4 N3 O4 ZnP 1 21/n 115.3452; 16.8828; 18.9071
90; 94.356; 90
4884.1Helena Isla; Monika Srebro-Hooper; Marion Jean; Nicolas Vanthuyne; Thierry Roisnel; Jamie L. Lunkley; Gilles Muller; J. A. Gareth Williams; Jochen Autschbach; Jeanne Crassous
Conformational changes and chiroptical switching of enantiopure bis-helicenic terpyridine upon Zn^2+^ binding
Chem.Commun., 2016, 52, 5932
7119014 CIFC55 H31 N3P 21 2 218.9558; 11.4826; 21.7545
90; 90; 90
2237.1Helena Isla; Monika Srebro-Hooper; Marion Jean; Nicolas Vanthuyne; Thierry Roisnel; Jamie L. Lunkley; Gilles Muller; J. A. Gareth Williams; Jochen Autschbach; Jeanne Crassous
Conformational changes and chiroptical switching of enantiopure bis-helicenic terpyridine upon Zn^2+^ binding
Chem.Commun., 2016, 52, 5932
7119015 CIFC27 H18 Ag7 F15 N6 O10P -18.7316; 15.311; 16.873
72.77; 82.43; 86.08
2134.7Xin He; Hai-Xia Liu; Liang Zhao
Integration of acetylenic carbon clusters and silver clusters: template synthesis and stability enhancement
Chem.Commun., 2016, 52, 5682
7119016 CIFC82 H96 Ag22 F48 O48.5 S16P 1 21/n 120.7; 23.694; 31.929
90; 92.38; 90
15647Xin He; Hai-Xia Liu; Liang Zhao
Integration of acetylenic carbon clusters and silver clusters: template synthesis and stability enhancement
Chem.Commun., 2016, 52, 5682
7119017 CIFC128 H150 Ag34 F72 O74 S24P 1 21/c 126.341; 13.125; 36.552
90; 105.85; 90
12157Xin He; Hai-Xia Liu; Liang Zhao
Integration of acetylenic carbon clusters and silver clusters: template synthesis and stability enhancement
Chem.Commun., 2016, 52, 5682
7119018 CIFC15 H7 N4 O7 Zn2C m c m10.267; 32.086; 6.955
90; 90; 90
2291Yingli Hu; Meili Ding; Xiao-Qin Liu; Lin-Bing Sun; Hai-Long Jiang
Rational synthesis of an exceptionally stable Zn(II) metal-organic framework for the highly selective and sensitive detection of picric acid
Chem.Commun., 2016, 52, 5734
7119019 CIFC62 H89 Cl N4 O2 P2P 1 21/n 112.974; 31.717; 15.286
90; 95.96; 90
6256Yuzhong Wang; Hunter P. Hickox; Yaoming Xie; Pingrong Wei; Dongtao Cui; Melody R. Walter; Henry F. Schaefer III; Gregory H. Robinson
Protonation of carbene-stabilized diphosphorus: complexation of HP2+
Chem.Commun., 2016, 52, 5746
7119020 CIFC76 H76 O8P -111.4425; 11.4934; 13.0446
74.006; 71.922; 78.818
1556.65Bo Gao; Li-Li Tan; Nan Song; Ke Li; Ying-Wei Yang
A high-yield synthesis of [m]biphenyl-extended pillar[n]arenes for an efficient selective inclusion of toluene and m-xylene in the solid state
Chem.Commun., 2016, 52, 5804
7119021 CIFC78 H80 O8P -111.3535; 11.5292; 13.4501
70.421; 73.067; 78.916
1578.1Bo Gao; Li-Li Tan; Nan Song; Ke Li; Ying-Wei Yang
A high-yield synthesis of [m]biphenyl-extended pillar[n]arenes for an efficient selective inclusion of toluene and m-xylene in the solid state
Chem.Commun., 2016, 52, 5804
7119022 CIFC4 H6 N4 O3 S2P 1 21/n 14.7306; 21.6655; 8.1069
90; 103.803; 90
806.89Sounak Sarkar; Mysore S. Pavan; Suryanarayan Cherukuvada; Tayur N. Guru Row
Acetazolamide polymorphism: a case of hybridization induced polymorphism?
Chem.Commun., 2016, 52, 5820
7119023 CIFC28 H27 N O6P 1 21/c 112.3361; 16.8521; 12.0571
90; 112.1; 90
2322.38Ying Xie; Xun Chen; Xin Liu; Shi-Jian Su; Jianzhang Li; Wei Zeng
Rh(III)-catalyzed relay carbenoid functionalization of aromatic C-H bonds: access to pi-conjugated fused heteroarenes
Chem.Commun., 2016, 52, 5856
7119024 CIFC61.4 H43.6 Cl4 N2 O6.2P 6329.44; 29.44; 11.679
90; 90; 120
8766Midori Nagamoto; Daisuke Yamauchi; Takahiro Nishimura
Iridium-catalyzed asymmetric [3+2] annulation of aromatic ketimines with alkynes via C-H activation: unexpected inversion of the enantioselectivity induced by protic acids
Chem.Commun., 2016, 52, 5876
7119025 CIFC11 H10 N2 S2P -19.2746; 10.8353; 11.1364
91.652; 103.923; 90.151
1085.75M. S. C. Pedras; Q. H. To
Unveiling the first indole-fused thiazepine: structure, synthesis and biosynthesis of cyclonasturlexin, a remarkable cruciferous phytoalexin
Chem.Commun., 2016, 52, 5880
7119031 CIFC34.5 H23 Au2 Cl N2P 21 21 2113.3962; 19.3637; 22.587
90; 90; 90
5859.1Jin, Mingoo; Seki, Tomohiro; Ito, Hajime
Luminescent mechanochromism of a chiral complex: distinct crystal structures and color changes of racemic and homochiral gold( <scp>i</scp> ) isocyanide complexes with a binaphthyl moiety
Chem. Commun., 2016, 52, 8083-8086
7119032 CIFC34.25 H22.5 Au2 Cl0.5 N2P b c n13.0435; 18.7272; 23.6159
90; 90; 90
5768.6Jin, Mingoo; Seki, Tomohiro; Ito, Hajime
Luminescent mechanochromism of a chiral complex: distinct crystal structures and color changes of racemic and homochiral gold( <scp>i</scp> ) isocyanide complexes with a binaphthyl moiety
Chem. Commun., 2016, 52, 8083-8086
7119034 CIFC20 H57 B2 Li N2 P2 SnC m c m18.985; 10.8911; 14.8749
90; 90; 90
3075.6Maria Fernandez-Millan; Lucy K. Allen; Raul Garcia-Rodriguez; Andrew D. Bond; Marta E. G. Mosquera; Dominic S. Wright
Formation of a unique 'unsupported' hydridic stannate(II)
Chem.Commun., 2016, 52, 5993
7119035 CIFC216 H228 F96 N72 Sb16 Zn8P a -340.8424; 40.8424; 40.8424
90; 90; 90
68129Jing Yang; Xiao-Yong Chang; Kiu-Chor Sham; Shek-Man Yiu; Hoi-Lun Kwong; Chi-Ming Che
M8L12 cubic cages with all facial delta or facial lamda configuration: effects of surface anions on the occupancy of the cage and anion exchange
Chem.Commun., 2016, 52, 5981
7119036 CIFC232 H240 Cd8 F48 N72 O48 S16P a -341.313; 41.313; 41.313
90; 90; 90
70512Jing Yang; Xiao-Yong Chang; Kiu-Chor Sham; Shek-Man Yiu; Hoi-Lun Kwong; Chi-Ming Che
M8L12 cubic cages with all facial delta or facial lamda configuration: effects of surface anions on the occupancy of the cage and anion exchange
Chem.Commun., 2016, 52, 5981
7119037 CIFC240 H240 F39 Mn8 N84 P6.5P n -3 n :226.6801; 26.6801; 26.6801
90; 90; 90
18991.6Jing Yang; Xiao-Yong Chang; Kiu-Chor Sham; Shek-Man Yiu; Hoi-Lun Kwong; Chi-Ming Che
M8L12 cubic cages with all facial delta or facial lamda configuration: effects of surface anions on the occupancy of the cage and anion exchange
Chem.Commun., 2016, 52, 5981
7119038 CIFC20 H35 N3 O6P 21 21 219.1953; 15.9688; 16.377
90; 90; 90
2404.8Mihye Lee; Jihyun Shim; Philjae Kang; Moon-Gun Choi; Soo Hyuk Choi
Stabilization of 11/9-helical alpha/beta-peptide foldamers in protic solvents
Chem.Commun., 2016, 52, 5950
7119039 CIFC29 H49 N5 O8P 21 21 219.7107; 17.8054; 18.6925
90; 90; 90
3232Mihye Lee; Jihyun Shim; Philjae Kang; Moon-Gun Choi; Soo Hyuk Choi
Stabilization of 11/9-helical alpha/beta-peptide foldamers in protic solvents
Chem.Commun., 2016, 52, 5950
7119040 CIFC31 H52 Cl3 N5 O8P 21 21 219.5052; 17.583; 23.471
90; 90; 90
3922.7Mihye Lee; Jihyun Shim; Philjae Kang; Moon-Gun Choi; Soo Hyuk Choi
Stabilization of 11/9-helical alpha/beta-peptide foldamers in protic solvents
Chem.Commun., 2016, 52, 5950
7119041 CIFC26 H25 N O SP -18.28; 11.804; 12.324
64.811; 88.065; 80.753
1075Jia-Jia Zhao; Man Tang; Hong-Hao Zhang; Meng-Meng Xu; Feng Shi
Bronsted acid-catalyzed chemodivergent reactions of ortho-mercaptobenzyl alcohols with 3-alkyl-2-vinylindoles and styrenes: [5+2] cyclization versus hydroxysulfenylation
Chem.Commun., 2016, 52, 5953
7119042 CIFC35 H42 O4 S3C 1 c 18.5603; 22.813; 17.3998
90; 94.2688; 90
3388.5Jia-Jia Zhao; Man Tang; Hong-Hao Zhang; Meng-Meng Xu; Feng Shi
Bronsted acid-catalyzed chemodivergent reactions of ortho-mercaptobenzyl alcohols with 3-alkyl-2-vinylindoles and styrenes: [5+2] cyclization versus hydroxysulfenylation
Chem.Commun., 2016, 52, 5953
7119043 CIFC20 H14 F4 N2 O2P -111.228; 12.46; 12.943
77.35; 89.67; 86.39
1763.2Yingle Liu; Ke Zhang; Yangen Huang; Shen Pan; Xiao-Qiang Liu; Yi Yang; Yan Jiang; Xiu-Hua Xu
Synthesis of 3-fluoroalkenyl-3-trifluoromethyl-2-oxindoles by the reaction of indoline-2,3-diones with difluoromethylene phosphabetaine
Chem.Commun., 2016, 52, 5969
7119044 CIFC14 H8 Fe N6 O2 PtC 1 2/c 115.667; 15.136; 7.3104
90; 110.57; 90
1623Tomoyuki Haraguchi; Kazuya Otsubo; Osami Sakata; Shogo Kawaguchi; Akihiko Fujiwara; Hiroshi Kitagawa
A three-dimensional accordion-like metal∓organic framework: synthesis and unconventional oriented growth on a surface
Chem.Commun., 2016, 52, 6017
7119045 CIFC23 H17 N O4 SP 1 21 18.33; 12.431; 9.528
90; 93.09; 90
985.2Zhuang Song; Yizhou Wu; Tao Xin; Chao Jin; Xiaoan Wen; Hongbin Sun; Qing-Long Xu
The Rh(II)-catalyzed formal N-S bond insertion reaction of aryldiazoacetates into N-phenyl-sulfenyl phthalimide
Chem.Commun., 2016, 52, 6079
7119046 CIFC467 Ag120 B4 Cl4 F64 N10 O45 S24 Si8C 1 2/m 143.889; 31.033; 26.186
90; 123.512; 90
29737Zi-Yi Chen; Dennis Y. S. Tam; Thomas C. W. Mak
Ethynide-stabilized high-nuclearity silver(I) sulfido molecular clusters assembled using organic sulfide precursors
Chem.Commun., 2016, 52, 6119
7119047 CIFC198 Ag46 B2 F8 N2 O14 S6P 1 21/n 119.8433; 28.203; 23.1207
90; 97.808; 90
12819.3Zi-Yi Chen; Dennis Y. S. Tam; Thomas C. W. Mak
Ethynide-stabilized high-nuclearity silver(I) sulfido molecular clusters assembled using organic sulfide precursors
Chem.Commun., 2016, 52, 6119
7119048 CIFC62.5 H75 Cl3 F5 N5 O WP 1 21/c 111.2444; 26.1267; 20.6154
90; 94.991; 90
6033.4Dominik A. Imbrich; Wolfgang Frey; Stefan Naumann; Michael R. Buchmeiser
Application of imidazolinium salts and N-heterocyclic olefins for the synthesis of anionic and neutral tungsten imido alkylidene complexes
Chem.Commun., 2016, 52, 6099
7119049 CIFC40.5 H58 Cl F6 N5 O6 S2 WP -111.7112; 20.3641; 21.9201
103.305; 97.459; 100.855
4913.7Dominik A. Imbrich; Wolfgang Frey; Stefan Naumann; Michael R. Buchmeiser
Application of imidazolinium salts and N-heterocyclic olefins for the synthesis of anionic and neutral tungsten imido alkylidene complexes
Chem.Commun., 2016, 52, 6099
7119050 CIFC55 H76 Cl2 N4 WP -110.5591; 13.627; 21.2326
86.879; 81.476; 88.576
3016.47Dominik A. Imbrich; Wolfgang Frey; Stefan Naumann; Michael R. Buchmeiser
Application of imidazolinium salts and N-heterocyclic olefins for the synthesis of anionic and neutral tungsten imido alkylidene complexes
Chem.Commun., 2016, 52, 6099
7119051 CIFC58.5 H79 Cl8 N5 WP 1 21/c 121.6865; 18.8737; 16.1005
90; 106.667; 90
6313.1Dominik A. Imbrich; Wolfgang Frey; Stefan Naumann; Michael R. Buchmeiser
Application of imidazolinium salts and N-heterocyclic olefins for the synthesis of anionic and neutral tungsten imido alkylidene complexes
Chem.Commun., 2016, 52, 6099
7119052 CIFC124 H90 F40 N12P -116.634; 18.391; 18.849
88.309; 76.986; 82.645
5571.9Won-Young Cha; Takanori Soya; Takayuki Tanaka; Hirotaka Mori; Yongseok Hong; Sangsu Lee; Kyu Hyung Park; Atsuhiro Osuka; Dongho Kim
Multifaceted [36]octaphyrin(1.1.1.1.1.1.1.1): deprotonation-induced switching among nonaromatic, Mobius aromatic, and Huckel antiaromatic species
Chem.Commun., 2016, 52, 6076
7119053 CIFC182 H256 N2 O16 P8 Ru4P 1 21/c 116.1117; 26.6027; 21.6003
90; 100.029; 90
9116.7Daniel Fink; Bernhard Weibert; Rainer F. Winter
Redox-active tetraruthenium metallacycles: reversible release of up to eight electrons resulting in strong electrochromism
Chem.Commun., 2016, 52, 6103
7119054 CIFC148 H234 Cl16 N2 O16 P8 Ru4P -111.6168; 16.816; 23.594
94.41; 99.289; 107.587
4297.1Daniel Fink; Bernhard Weibert; Rainer F. Winter
Redox-active tetraruthenium metallacycles: reversible release of up to eight electrons resulting in strong electrochromism
Chem.Commun., 2016, 52, 6103
7119055 CIFC72 H64 Cl4 N2 P2 Ru2P 110.3736; 13.2432; 13.7718
99.178; 107.636; 97.263
1748.99Demyan E. Prokopchuk; Alan J. Lough; Rafael E. Rodriguez-Lugo; Robert H. Morris; Hansjorg Grutzmacher
Insights into metal-ligand hydrogen transfer: a square-planar ruthenate complex supported by a tetradentate amino-amido-diolefin ligand
Chem.Commun., 2016, 52, 6138
7119056 CIFC40 H42 N2 O RuP 1 21/c 19.121; 15.475; 21.72
90; 92.615; 90
3062.5Demyan E. Prokopchuk; Alan J. Lough; Rafael E. Rodriguez-Lugo; Robert H. Morris; Hansjorg Grutzmacher
Insights into metal-ligand hydrogen transfer: a square-planar ruthenate complex supported by a tetradentate amino-amido-diolefin ligand
Chem.Commun., 2016, 52, 6138
7119057 CIFC56 H73 K N2 O8 RuP 1 21/c 111.8733; 24.8708; 17.2324
90; 95.965; 90
5061.1Demyan E. Prokopchuk; Alan J. Lough; Rafael E. Rodriguez-Lugo; Robert H. Morris; Hansjorg Grutzmacher
Insights into metal-ligand hydrogen transfer: a square-planar ruthenate complex supported by a tetradentate amino-amido-diolefin ligand
Chem.Commun., 2016, 52, 6138
7119058 CIFC35 H39 Br N2 O9P 21 21 2112.919; 15.875; 17.332
90; 90; 90
3554.6Bo-Liang Zhao; Da-Ming Du
Organocatalytic cascade Michael/Michael reaction for the asymmetric synthesis of spirooxindoles containing five contiguous stereocenters
Chem.Commun., 2016, 52, 6162
7119059 CIFC30 H27.5 F6 N2.5 O6 S2P 1 21 111.6454; 12.5993; 21.7275
90; 104.608; 90
3084.9Jaroslav Sebestik; Filip Teply; Ivana Cisarova; Jan Vavra; Dusan Koval; Petr Bour
Intense chirality induction in nitrile solvents by a helquat dye monitored by near resonance Raman scattering
Chem.Commun., 2016, 52, 6257
7119060 CIFC28 H29 I2 N3 O2P 21 21 217.9386; 17.6476; 19.6814
90; 90; 90
2757.31Jaroslav Sebestik; Filip Teply; Ivana Cisarova; Jan Vavra; Dusan Koval; Petr Bour
Intense chirality induction in nitrile solvents by a helquat dye monitored by near resonance Raman scattering
Chem.Commun., 2016, 52, 6257
7119061 CIFC41 H38 Dy F9 N14 O9 S3P b c a20.8179; 19.5864; 24.4923
90; 90; 90
9986.7Zhong-Xia Jiang; Jun-Liang Liu; Yan-Cong Chen; Jiang Liu; Jian-Hua Jia; Ming-Liang Tong
Lanthanoid single-ion magnets with the LnN10 coordination geometry
Chem.Commun., 2016, 52, 6261
7119062 CIFC41 H38 Er F9 N14 O9 S3P b c a20.69; 19.5456; 24.427
90; 90; 90
9878.2Zhong-Xia Jiang; Jun-Liang Liu; Yan-Cong Chen; Jiang Liu; Jian-Hua Jia; Ming-Liang Tong
Lanthanoid single-ion magnets with the LnN10 coordination geometry
Chem.Commun., 2016, 52, 6261
7119064 CIFC40 H40 Cl4 Cu4 N2 P2P 1 21/c 111.1272; 13.525; 13.4866
90; 104.147; 90
1968.11Xu-Lin Chen; Rongmin Yu; Xiao-Yuan Wu; Dong Liang; Ji-Hui Jia; Can-Zhong Lu
A strongly greenish-blue-emitting Cu4Cl4 cluster with an efficient spin-orbit coupling (SOC): fast phosphorescence versus thermally activated delayed fluorescence
Chem.Commun., 2016, 52, 6288
7119065 CIFC22 H18 N2 O3 SP 1 21/n 19.4353; 17.316; 11.6428
90; 92.321; 90
1900.7Ming Chen; Ning Sun; Haoyi Chen; Yuanhong Liu
Dioxazoles, a new mild nitrene transfer reagent in gold catalysis: highly efficient synthesis of functionalized oxazoles
Chem.Commun., 2016, 52, 6324
7119066 CIFC23 H18 N2 O3 S2P 1 21/c 118.929; 12.43; 8.472
90; 91.235; 90
1992.9Ming Chen; Ning Sun; Haoyi Chen; Yuanhong Liu
Dioxazoles, a new mild nitrene transfer reagent in gold catalysis: highly efficient synthesis of functionalized oxazoles
Chem.Commun., 2016, 52, 6324
7119067 CIFC29 H36 Au F6 N3 O4 S2P 32 2 111.4418; 11.4418; 23.88
90; 90; 120
2707.4Ming Chen; Ning Sun; Haoyi Chen; Yuanhong Liu
Dioxazoles, a new mild nitrene transfer reagent in gold catalysis: highly efficient synthesis of functionalized oxazoles
Chem.Commun., 2016, 52, 6324
7119068 CIFC94.45 H106.45 N6 P2P -112.2213; 16.2437; 22.0973
97.7; 93.029; 106.714
4144.2Alexander Hinz; Axel Schulz; Alexander Villinger
On the behaviour of biradicaloid [P(mu-NTer)]2 towards Lewis acids and bases
Chem.Commun., 2016, 52, 6328
7119069 CIFC56.95 H58.95 Au Cl N2 P2P -110.94; 11.9932; 21.421
87.907; 76.158; 65.57
2478.4Alexander Hinz; Axel Schulz; Alexander Villinger
On the behaviour of biradicaloid [P(mu-NTer)]2 towards Lewis acids and bases
Chem.Commun., 2016, 52, 6328
7119070 CIFC51 H53 Au1.33 Cl1.33 N2 P2P -111.168; 12.029; 18.686
94.538; 94.411; 114.833
2254.1Alexander Hinz; Axel Schulz; Alexander Villinger
On the behaviour of biradicaloid [P(mu-NTer)]2 towards Lewis acids and bases
Chem.Commun., 2016, 52, 6328
7119071 CIFC51 H53 Au1.44 Cl1.44 N2 P2P -111.243; 12.0524; 18.7795
94.113; 94.288; 114.879
2287.1Alexander Hinz; Axel Schulz; Alexander Villinger
On the behaviour of biradicaloid [P(mu-NTer)]2 towards Lewis acids and bases
Chem.Commun., 2016, 52, 6328
7119072 CIFC25 H14 F N O4P 1 21/c 19.7639; 19.413; 10.4751
90; 105.633; 90
1912.1Rong-Guo Shi; Xiao-Hua Wang; Ruzhang Liu; Chao-Guo Yan
Two-carbon ring expansion of isatin: a convenient construction of a dibenzo[b,d]azepinone scaffold
Chem.Commun., 2016, 52, 6280
7119073 CIFC26 H17 N O5P 21 21 2111.2312; 16.239; 22.524
90; 90; 90
4108Rong-Guo Shi; Xiao-Hua Wang; Ruzhang Liu; Chao-Guo Yan
Two-carbon ring expansion of isatin: a convenient construction of a dibenzo[b,d]azepinone scaffold
Chem.Commun., 2016, 52, 6280
7119074 CIFC25 H13 F2 N O4P 1 21/c 110.033; 19.091; 10.544
90; 107.453; 90
1926.6Rong-Guo Shi; Xiao-Hua Wang; Ruzhang Liu; Chao-Guo Yan
Two-carbon ring expansion of isatin: a convenient construction of a dibenzo[b,d]azepinone scaffold
Chem.Commun., 2016, 52, 6280
7119075 CIFC25 H13 Cl F N O4P -19.9815; 10.7217; 10.8522
66.536; 86.529; 76.874
1036.9Rong-Guo Shi; Xiao-Hua Wang; Ruzhang Liu; Chao-Guo Yan
Two-carbon ring expansion of isatin: a convenient construction of a dibenzo[b,d]azepinone scaffold
Chem.Commun., 2016, 52, 6280
7119076 CIFC20 H12 F N O5P -111.727; 12.81; 12.935
103.837; 115.433; 91.903
1683.3Rong-Guo Shi; Xiao-Hua Wang; Ruzhang Liu; Chao-Guo Yan
Two-carbon ring expansion of isatin: a convenient construction of a dibenzo[b,d]azepinone scaffold
Chem.Commun., 2016, 52, 6280
7119077 CIFC21 H14 Cl N O5C 1 2/c 122.142; 15.2704; 12.2599
90; 115.973; 90
3726.6Rong-Guo Shi; Xiao-Hua Wang; Ruzhang Liu; Chao-Guo Yan
Two-carbon ring expansion of isatin: a convenient construction of a dibenzo[b,d]azepinone scaffold
Chem.Commun., 2016, 52, 6280
7119078 CIFC30 H21 N3 O5P 1 21/c 112.8577; 14.7678; 16.2529
90; 112.154; 90
2858.3Rong-Guo Shi; Xiao-Hua Wang; Ruzhang Liu; Chao-Guo Yan
Two-carbon ring expansion of isatin: a convenient construction of a dibenzo[b,d]azepinone scaffold
Chem.Commun., 2016, 52, 6280
7119079 CIFC25 H17 Cl N2 O5P 1 21/n 111.783; 13.245; 15.8627
90; 94.265; 90
2468.8Rong-Guo Shi; Xiao-Hua Wang; Ruzhang Liu; Chao-Guo Yan
Two-carbon ring expansion of isatin: a convenient construction of a dibenzo[b,d]azepinone scaffold
Chem.Commun., 2016, 52, 6280
7119080 CIFC27 H39 Cl Cu NP 1 21/c 115.9209; 19.4144; 16.2447
90; 103.631; 90
4879.72Alexander S. Romanov; Dawei Di; Le Yang; Julio Fernandez-Cestau; Ciaran R. Becker; Charlotte E. James; Bonan Zhu; Mikko Linnolahti; Dan Credgington; Manfred Bochmann
Highly photoluminescent copper carbene complexes based on prompt rather than delayed fluorescence
Chem.Commun., 2016, 52, 6379
7119081 CIFC27.5 H40 Cl Cu I NP -111.1918; 11.9685; 20.7901
101.52; 94.798; 94.419
2706.59Alexander S. Romanov; Dawei Di; Le Yang; Julio Fernandez-Cestau; Ciaran R. Becker; Charlotte E. James; Bonan Zhu; Mikko Linnolahti; Dan Credgington; Manfred Bochmann
Highly photoluminescent copper carbene complexes based on prompt rather than delayed fluorescence
Chem.Commun., 2016, 52, 6379
7119082 CIFC27 H39 Br Cu NP 1 21/c 116.0878; 19.4137; 16.2912
90; 103.54; 90
4946.71Alexander S. Romanov; Dawei Di; Le Yang; Julio Fernandez-Cestau; Ciaran R. Becker; Charlotte E. James; Bonan Zhu; Mikko Linnolahti; Dan Credgington; Manfred Bochmann
Highly photoluminescent copper carbene complexes based on prompt rather than delayed fluorescence
Chem.Commun., 2016, 52, 6379
7119083 CIFC18 H14 FeP 1 21/c 113.4447; 19.4178; 9.8391
90; 91.496; 90
2567.8Antonio Urbano; Gloria Hernandez-Torres; Ana M. del Hoyo; Alicia Martinez-Carrion; M. Carmen Carreno
Mild access to planar-chiral ortho-condensed aromatic ferrocenes via gold(I)-catalyzed cycloisomerization of ortho-alkynylaryl ferrocenes
Chem.Commun., 2016, 52, 6419
7119084 CIFC19 H16 Fe OP 41 21 27.8273; 7.8273; 47.227
90; 90; 90
2893.4Antonio Urbano; Gloria Hernandez-Torres; Ana M. del Hoyo; Alicia Martinez-Carrion; M. Carmen Carreno
Mild access to planar-chiral ortho-condensed aromatic ferrocenes via gold(I)-catalyzed cycloisomerization of ortho-alkynylaryl ferrocenes
Chem.Commun., 2016, 52, 6419
7119085 CIFC122 H74 B2 F48 Pd4P -113.2706; 15.2693; 16.3133
101.437; 110.526; 102.271
2887.5Kohei Masai; Katsunori Shirato; Koji Yamamoto; Yuki Kurashige; Tetsuro Murahashi
A mechanistic insight into metal-cluster pi-envelopment: a dual binding mode involving bent and planar ligand-conformers
Chem.Commun., 2016, 52, 6427
7119086 CIFC128 H78 B2 Cl2 F48 Pd4P -114.2381; 15.6226; 28.2509
81.3277; 79.8346; 77.6849
6001.1Kohei Masai; Katsunori Shirato; Koji Yamamoto; Yuki Kurashige; Tetsuro Murahashi
A mechanistic insight into metal-cluster pi-envelopment: a dual binding mode involving bent and planar ligand-conformers
Chem.Commun., 2016, 52, 6427
7119087 CIFC153 H106 B2 Cl2 F48 Pd4P 1 21 118.5114; 21.0181; 19.5326
90; 111.452; 90
7073.2Kohei Masai; Katsunori Shirato; Koji Yamamoto; Yuki Kurashige; Tetsuro Murahashi
A mechanistic insight into metal-cluster pi-envelopment: a dual binding mode involving bent and planar ligand-conformers
Chem.Commun., 2016, 52, 6427
7119088 CIFC27 H21 Au B Cl F4 N PP 1 21/c 110.394; 16.6422; 15.389
90; 108.771; 90
2520.39Long Huang; Frank Rominger; Matthias Rudolph; A. Stephen K. Hashmi
A general access to organogold(III) complexes by oxidative addition of diazonium salts
Chem.Commun., 2016, 52, 6435
7119089 CIFC27 H20 Au B Cl2 F4 N PP -19.3558; 11.4552; 13.9422
86.4666; 70.5144; 67.9291
1301.94Long Huang; Frank Rominger; Matthias Rudolph; A. Stephen K. Hashmi
A general access to organogold(III) complexes by oxidative addition of diazonium salts
Chem.Commun., 2016, 52, 6435
7119090 CIFC26.5 H38.5 Au Cl6.5 F3 PP 1 21/c 112.1272; 14.5748; 18.6371
90; 96.632; 90
3272.09Long Huang; Frank Rominger; Matthias Rudolph; A. Stephen K. Hashmi
A general access to organogold(III) complexes by oxidative addition of diazonium salts
Chem.Commun., 2016, 52, 6435
7119091 CIFC12 H28.5 B10 Br N2.5P 1 21/c 17.6257; 25.7293; 10.2076
90; 92.279; 90
2001.19Jordan Holmes; Christopher M. Pask; Mark A. Fox; Charlotte E. Willans
Tethered N-heterocyclic carbene-carboranes: unique ligands that exhibit unprecedented and versatile coordination modes at rhodium
Chem.Commun., 2016, 52, 6443
7119092 CIFC11 H27 B9 N2P 1 21/c 115.6541; 13.7503; 18.375
90; 115.101; 90
3581.7Jordan Holmes; Christopher M. Pask; Mark A. Fox; Charlotte E. Willans
Tethered N-heterocyclic carbene-carboranes: unique ligands that exhibit unprecedented and versatile coordination modes at rhodium
Chem.Commun., 2016, 52, 6443
7119093 CIFC31 H55 B9 N4 Rh2P b c a11.9249; 23.7834; 25.2349
90; 90; 90
7157Jordan Holmes; Christopher M. Pask; Mark A. Fox; Charlotte E. Willans
Tethered N-heterocyclic carbene-carboranes: unique ligands that exhibit unprecedented and versatile coordination modes at rhodium
Chem.Commun., 2016, 52, 6443
7119094 CIFC32 H58 B9 N3 O Rh2P -111.1781; 12.5631; 14.8258
111.322; 92.917; 105.326
1845.32Jordan Holmes; Christopher M. Pask; Mark A. Fox; Charlotte E. Willans
Tethered N-heterocyclic carbene-carboranes: unique ligands that exhibit unprecedented and versatile coordination modes at rhodium
Chem.Commun., 2016, 52, 6443
7119095 CIFC29 H54 B9 N2 O0.5 Rh2P -110.7898; 11.4212; 14.8764
71.73; 83.274; 69.415
1629.6Jordan Holmes; Christopher M. Pask; Mark A. Fox; Charlotte E. Willans
Tethered N-heterocyclic carbene-carboranes: unique ligands that exhibit unprecedented and versatile coordination modes at rhodium
Chem.Commun., 2016, 52, 6443
7119096 CIFC19 H38 B10 Cl N2 RhP 1 21/c 112.3894; 15.3629; 13.6908
90; 93.441; 90
2601.17Jordan Holmes; Christopher M. Pask; Mark A. Fox; Charlotte E. Willans
Tethered N-heterocyclic carbene-carboranes: unique ligands that exhibit unprecedented and versatile coordination modes at rhodium
Chem.Commun., 2016, 52, 6443
7119097 CIFC19 H37 B10 N2 RhP 1 21/c 117.2832; 10.5283; 14.1775
90; 113.02; 90
2374.34Jordan Holmes; Christopher M. Pask; Mark A. Fox; Charlotte E. Willans
Tethered N-heterocyclic carbene-carboranes: unique ligands that exhibit unprecedented and versatile coordination modes at rhodium
Chem.Commun., 2016, 52, 6443
7119098 CIFC27 H38 O3P 1 21 15.8458; 12.3784; 16.7657
90; 98.058; 90
1201.22Qiqiao Lin; Yuanzhen Li; Deb Kumar Das; Guoxiang Zhang; Zhifei Zhao; Shuang Yang; Xinqiang Fang
N-Heterocyclic carbene-catalyzed desymmetrization of functionalized 1,4-dienes via Stetter Reaction
Chem.Commun., 2016, 52, 6459
7119099 CIFC384 H288 Cu4.8 N288 Zn43.2I a -3 d34.4885; 34.4885; 34.4885
90; 90; 90
41022.6Xiao-Wei Zhu; Xiao-Ping Zhou; Dan Li
Exceptionally water stable heterometallic gyroidal MOFs: tuning the porosity and hydrophobicity by doping metal ions
Chem.Commun., 2016, 52, 6513
7119102 CIFC47 H82 O5 Si4P -111.8267; 13.4665; 18.3608
106.876; 92.299; 109.501
2607.2Jian Zhang; Hong Kang; Jacob Martin; Shouhai Zhang; Sylvie Thomas; Tim C. Merkel; Jianyong Jin
The enhancement of chain rigidity and gas transport performance of polymers of intrinsic microporosity via intramolecular locking of the spiro-carbon
Chem.Commun., 2016, 52, 6553
7119103 CIFC16 H28 O3P 21 21 216.67202; 12.80551; 18.3291
90; 90; 90
1566.01Yajun Ren; Marc Presset; Jeremy Godemert; Nicolas Vanthuyne; Jean-Valere Naubron; Michel Giorgi; Jean Rodriguez; Yoann Coquerel
A switchable dual organocatalytic system and the enantioselective total synthesis of the quadrane sesquiterpene suberosanone
Chem.Commun., 2016, 52, 6565
7119114 CIFC17 H16 F3 N O4 SP -19.3925; 9.5682; 10.9216
73.528; 66.26; 85.458
860.9Zhi-Wei Yang; Qi Zhang; Yuan-Ye Jiang; Lei Li; Bin Xiao; Yao Fu
Palladium-catalyzed directing group-assisted C8-triflation of naphthalenes
Chem.Commun., 2016, 52, 6709
7119115 CIFC45 H68 O3 S Sm2P 1 21/c 110.7989; 23.324; 18.592
90; 106.381; 90
4492.7Christoph Schoo; Svetlana V. Klementyeva; Michael T. Gamer; Sergey N. Konchenko; Peter W. Roesky
Samarocene oxide: from an undesired decomposition product to a new reagent
Chem.Commun., 2016, 52, 6654
7119116 CIFC45 H68 O2 S2 Sm2P 1 21/n 118.588; 23.602; 21.654
90; 107.26; 90
9072Christoph Schoo; Svetlana V. Klementyeva; Michael T. Gamer; Sergey N. Konchenko; Peter W. Roesky
Samarocene oxide: from an undesired decomposition product to a new reagent
Chem.Commun., 2016, 52, 6654
7119117 CIFC44 H68 O4 S Sm2P 1 21/c 117.824; 16.299; 16.056
90; 108.56; 90
4421.9Christoph Schoo; Svetlana V. Klementyeva; Michael T. Gamer; Sergey N. Konchenko; Peter W. Roesky
Samarocene oxide: from an undesired decomposition product to a new reagent
Chem.Commun., 2016, 52, 6654
7119118 CIFC50 H70 N2 O4 S Sm2P 1 21/n 116.952; 13.879; 20.819
90; 90.81; 90
4897.7Christoph Schoo; Svetlana V. Klementyeva; Michael T. Gamer; Sergey N. Konchenko; Peter W. Roesky
Samarocene oxide: from an undesired decomposition product to a new reagent
Chem.Commun., 2016, 52, 6654
7119119 CIFC68 H86 O4 Sm2P -110.561; 10.7; 15.035
110.25; 97.77; 98.73
1542.9Christoph Schoo; Svetlana V. Klementyeva; Michael T. Gamer; Sergey N. Konchenko; Peter W. Roesky
Samarocene oxide: from an undesired decomposition product to a new reagent
Chem.Commun., 2016, 52, 6654
7119120 CIFC44 H66 N2 O8 Re2 Sm2P b c a16.207; 14; 21.465
90; 90; 90
4870.4Christoph Schoo; Svetlana V. Klementyeva; Michael T. Gamer; Sergey N. Konchenko; Peter W. Roesky
Samarocene oxide: from an undesired decomposition product to a new reagent
Chem.Commun., 2016, 52, 6654
7119121 CIFC34 H25 B OP -19.7747; 11.2285; 12.079
86.4386; 70.8147; 85.0255
1246.59Sam Yruegas; Dayna C. Patterson; Caleb D. Martin
Oxygen insertion into boroles as a route to 1,2-oxaborines
Chem.Commun., 2016, 52, 6658
7119122 CIFC40 H29 B OP -110.5923; 11.7946; 12.5909
91.8608; 94.7506; 113.478
1434.13Sam Yruegas; Dayna C. Patterson; Caleb D. Martin
Oxygen insertion into boroles as a route to 1,2-oxaborines
Chem.Commun., 2016, 52, 6658
7119123 CIFC12 H11 Cl N2 O5 SP -19.5347; 10.4694; 15.6057
92.938; 107.085; 116.622
1300.34Cory M. Widdifield; Harry Robson; Paul Hodgkinson
Furosemide's one little hydrogen atom: NMR crystallography structure verification of powdered molecular organics
Chem.Commun., 2016, 52, 6685
7119124 CIFC31 H20 N2 OP 1 21/n 115.6295; 11.7772; 23.646
90; 100.375; 90
4281.4Katsuya Mutoh; Yoichi Kobayashi; Yasukazu Hirao; Takashi Kubo; Jiro Abe
Stealth fast photoswitching of negative photochromic naphthalene-bridged phenoxyl-imidazolyl radical complexes
Chem.Commun., 2016, 52, 6797
7119125 CIFC35 H22 N2 OP 1 21 110.417; 7.846; 15.614
90; 109.024; 90
1206.5Katsuya Mutoh; Yoichi Kobayashi; Yasukazu Hirao; Takashi Kubo; Jiro Abe
Stealth fast photoswitching of negative photochromic naphthalene-bridged phenoxyl-imidazolyl radical complexes
Chem.Commun., 2016, 52, 6797
7119126 CIFC31 H20 N2 O3P 1 21/n 110.4123; 10.6141; 22.372
90; 101.14; 90
2425.9Katsuya Mutoh; Yoichi Kobayashi; Yasukazu Hirao; Takashi Kubo; Jiro Abe
Stealth fast photoswitching of negative photochromic naphthalene-bridged phenoxyl-imidazolyl radical complexes
Chem.Commun., 2016, 52, 6797
7119127 CIFC31 H19.46 Cl0.08 N2 OP 1 21/n 115.6018; 11.8059; 23.666
90; 100.492; 90
4286.2Katsuya Mutoh; Yoichi Kobayashi; Yasukazu Hirao; Takashi Kubo; Jiro Abe
Stealth fast photoswitching of negative photochromic naphthalene-bridged phenoxyl-imidazolyl radical complexes
Chem.Commun., 2016, 52, 6797
7119128 CIFC24 H21 N O4 SP 1 21/c 110.284; 26.1213; 15.8601
90; 102.69; 90
4156.4Hongxu Liu; Yanyan Yang; Jie Wu; Xiao-Na Wang; Junbiao Chang
Regioselective synthesis of 3,4-disubstituted isocoumarins through the Pd-catalyzed annulation of 2-iodoaromatic acids with ynamides
Chem.Commun., 2016, 52, 6801
7119129 CIFC30 H25 N O4 SP -112.2963; 13.8393; 16.8203
71.704; 82.18; 66.12
2484.87Hongxu Liu; Yanyan Yang; Jie Wu; Xiao-Na Wang; Junbiao Chang
Regioselective synthesis of 3,4-disubstituted isocoumarins through the Pd-catalyzed annulation of 2-iodoaromatic acids with ynamides
Chem.Commun., 2016, 52, 6801
7119130 CIFC40 H32 Cl4 P2 PdP 1 21/c 19.8924; 19.0871; 19.8273
90; 100.618; 90
3679.63Avassaya Vanitcha; Cecilia Damelincourt; Geoffrey Gontard; Nicolas Vanthuyne; Virginie Mouries-Mansuy; Louis Fensterbank
Bis-phosphine allene ligand: coordination chemistry and preliminary applications in catalysis
Chem.Commun., 2016, 52, 6785
7119131 CIFC41 H32 Cl8 P2 PtP 1 21 19.9582; 21.3845; 10.1108
90; 103.135; 90
2096.78Avassaya Vanitcha; Cecilia Damelincourt; Geoffrey Gontard; Nicolas Vanthuyne; Virginie Mouries-Mansuy; Louis Fensterbank
Bis-phosphine allene ligand: coordination chemistry and preliminary applications in catalysis
Chem.Commun., 2016, 52, 6785
7119132 CIFC82 H68 Au2 Cl4 O P4P -112.7889; 16.392; 19.0982
93.515; 96.512; 112.335
3655.6Avassaya Vanitcha; Cecilia Damelincourt; Geoffrey Gontard; Nicolas Vanthuyne; Virginie Mouries-Mansuy; Louis Fensterbank
Bis-phosphine allene ligand: coordination chemistry and preliminary applications in catalysis
Chem.Commun., 2016, 52, 6785
7119133 CIFC40 H32 Au2 Cl4 P2P 1 21/n 112.6409; 16.973; 18.0808
90; 104.661; 90
3753Avassaya Vanitcha; Cecilia Damelincourt; Geoffrey Gontard; Nicolas Vanthuyne; Virginie Mouries-Mansuy; Louis Fensterbank
Bis-phosphine allene ligand: coordination chemistry and preliminary applications in catalysis
Chem.Commun., 2016, 52, 6785
7119134 CIFC39.5 H31 Au2 Cl3 P2C 1 2 134.8; 9.8414; 10.8355
90; 96.507; 90
3687Avassaya Vanitcha; Cecilia Damelincourt; Geoffrey Gontard; Nicolas Vanthuyne; Virginie Mouries-Mansuy; Louis Fensterbank
Bis-phosphine allene ligand: coordination chemistry and preliminary applications in catalysis
Chem.Commun., 2016, 52, 6785
7119135 CIFC39.5 H31 Au2 Cl3 P2C 1 2 134.8079; 9.8397; 10.8227
90; 96.441; 90
3683.4Avassaya Vanitcha; Cecilia Damelincourt; Geoffrey Gontard; Nicolas Vanthuyne; Virginie Mouries-Mansuy; Louis Fensterbank
Bis-phosphine allene ligand: coordination chemistry and preliminary applications in catalysis
Chem.Commun., 2016, 52, 6785
7119136 CIFC38 H62 Li4 N2 O4P -18.7871; 9.5833; 13.1959
104.353; 93.696; 116.282
945.63Quentin Dufrois; Laure Vendier; Michel Etienne
alpha-CC agostic structures and aggregation diversity in cyclopropyllithium derivatives
Chem.Commun., 2016, 52, 6781
7119137 CIFC33 H49 Li2 O3P -18.5802; 9.438; 20.2265
80.998; 82.494; 70.198
1516.79Quentin Dufrois; Laure Vendier; Michel Etienne
alpha-CC agostic structures and aggregation diversity in cyclopropyllithium derivatives
Chem.Commun., 2016, 52, 6781
7119138 CIFC39 H32 B2 F12 N2 S2P 1 2/c 117.8505; 8.3333; 13.1813
90; 104.671; 90
1896.84Kazuki Takase; Kengo Hyodo; Masakazu Morimoto; Yuko Kojima; Hiroyuki Mayama; Satoshi Yokojima; Shinichiro Nakamura; Kingo Uchida
Photoinduced reversible formation of a superhydrophilic surface by crystal growth of diarylethene
Chem.Commun., 2016, 52, 6885
7119139 CIFC39 H34 B2 F12 N2 O S2P 1 21/c 19.7143; 32.9243; 11.9342
90; 96.4166; 90
3793.08Kazuki Takase; Kengo Hyodo; Masakazu Morimoto; Yuko Kojima; Hiroyuki Mayama; Satoshi Yokojima; Shinichiro Nakamura; Kingo Uchida
Photoinduced reversible formation of a superhydrophilic surface by crystal growth of diarylethene
Chem.Commun., 2016, 52, 6885
7119140 CIFC20 H23 N O3P 21 21 218.6053; 11.6403; 17.468
90; 90; 90
1749.7Yuan-Ming Sun; Peng Gu; Yu-Ning Gao; Qin Xu; Min Shi
Gold(I) catalyzed tandem cyclization of propargylic esters to 4-acyloxy-1,2-dihydroquinolines
Chem.Commun., 2016, 52, 6942
7119141 CIFC21 H29 F6 Ir N O PP 21 21 217.0929; 15.6774; 20.8647
90; 90; 90
2320.12Ross A. Arthurs; Peter N. Horton; Simon J. Coles; Christopher J. Richards
Metallocene to metallocene conversion. Synthesis of an oxazoline-substituted pentamethyliridocenium cation from a ferrocenyloxazoline
Chem.Commun., 2016, 52, 7024
7119142 CIFC14 H8 F2 N4P 1 21/c 14.375; 20.1126; 13.1678
90; 98.317; 90
1146.48Erchang Shang; Junzhi Zhang; Jinyi Bai; Zhan Wang; Xiang Li; Bing Zhu; Xiaoguang Lei
Syntheses of [1,2,4]triazolo[1,5-a]benzazoles enabled by the transition-metal-free oxidative N-N bond formation
Chem.Commun., 2016, 52, 7028
7119143 CIFC14 H9 N3 OP c a 2121.401; 4.7059; 10.6453
90; 90; 90
1072.1Erchang Shang; Junzhi Zhang; Jinyi Bai; Zhan Wang; Xiang Li; Bing Zhu; Xiaoguang Lei
Syntheses of [1,2,4]triazolo[1,5-a]benzazoles enabled by the transition-metal-free oxidative N-N bond formation
Chem.Commun., 2016, 52, 7028
7119144 CIFC16 H14 N4P 1 21/n 15.9753; 15.9285; 13.447
90; 90.062; 90
1279.9Erchang Shang; Junzhi Zhang; Jinyi Bai; Zhan Wang; Xiang Li; Bing Zhu; Xiaoguang Lei
Syntheses of [1,2,4]triazolo[1,5-a]benzazoles enabled by the transition-metal-free oxidative N-N bond formation
Chem.Commun., 2016, 52, 7028
7119145 CIFC38 H42 F10 P2 Pt ZnP 1 21/n 110.9506; 19.9969; 17.6775
90; 96.054; 90
3849.4Allegra L. Liberman-Martin; Daniel S. Levine; Micah S. Ziegler; Robert G. Bergman; T. Don Tilley
Lewis acid-base interactions between platinum(II) diaryl complexes and bis(perfluorophenyl)zinc: strongly accelerated reductive elimination induced by a Z-type ligand
Chem.Commun., 2016, 52, 7039
7119146 CIFC51 H42 F10 N2 Pt ZnP 1 21/c 112.995; 16.7483; 21.185
90; 106.136; 90
4429.1Allegra L. Liberman-Martin; Daniel S. Levine; Micah S. Ziegler; Robert G. Bergman; T. Don Tilley
Lewis acid-base interactions between platinum(II) diaryl complexes and bis(perfluorophenyl)zinc: strongly accelerated reductive elimination induced by a Z-type ligand
Chem.Commun., 2016, 52, 7039
7119147 CIFC56 H40 BP 1 21/c 114.436; 9.801; 28.668
90; 100.42; 90
3989Holger Braunschweig; Ivo Krummenacher; Lisa Mailander; Leanne Pentecost; Alfredo Vargas
Formation of a stable radical by oxidation of a tetraorganoborate
Chem.Commun., 2016, 52, 7005
7119148 CIFC40.17 H62.43 Na2 O28P 1 21 16.6058; 24.886; 14.6272
90; 102.224; 90
2350.08Guo-Hong Ning; Kazuki Matsumura; Yasuhide Inokuma; Makoto Fujita
A saccharide-based crystalline sponge for hydrophilic guests
Chem.Commun., 2016, 52, 7013
7119149 CIFC21 H34 Na O13.5P 1 21 16.6503; 24.44; 14.717
90; 101.39; 90
2344.9Guo-Hong Ning; Kazuki Matsumura; Yasuhide Inokuma; Makoto Fujita
A saccharide-based crystalline sponge for hydrophilic guests
Chem.Commun., 2016, 52, 7013
7119150 CIFC20.45 H30.90 Na O14.46P 1 21 16.6481; 24.625; 14.756
90; 102.798; 90
2355.7Guo-Hong Ning; Kazuki Matsumura; Yasuhide Inokuma; Makoto Fujita
A saccharide-based crystalline sponge for hydrophilic guests
Chem.Commun., 2016, 52, 7013
7119151 CIFC20.29 H30.59 Na O14P 1 21 16.6239; 24.772; 14.6783
90; 102.43; 90
2352.1Guo-Hong Ning; Kazuki Matsumura; Yasuhide Inokuma; Makoto Fujita
A saccharide-based crystalline sponge for hydrophilic guests
Chem.Commun., 2016, 52, 7013
7119152 CIFC2 H6 CdP 42/m n m7.195; 7.195; 4.118
90; 90; 90
213.2Hanke, Felix; Hindley, Sarah; Jones, Anthony C.; Steiner, Alexander
The solid state structures of the high and low temperature phases of dimethylcadmium
Chemical Communications, 2016, 52, 10144
7119153 CIFC2 H6 CdP 1 21/n 17.483; 7.711; 7.734
90; 115.85; 90
401.6Hanke, Felix; Hindley, Sarah; Jones, Anthony C.; Steiner, Alexander
The solid state structures of the high and low temperature phases of dimethylcadmium
Chemical Communications, 2016, 52, 10144
7119160 CIFC13 H16 N2 O7P 1 21/c 112.554; 8.8499; 12.6253
90; 103.988; 90
1361.1Lynne H. Thomas; Craig Wales; Chick C. Wilson
Selective preparation of elusive and alternative single component polymorphic solid forms through multi-component crystallisation routes
Chem.Commun., 2016, 52, 7372
7119161 CIFC7 H8 O6P 1 21/n 13.6803; 27.724; 9.3579
90; 94.397; 90
952Lynne H. Thomas; Craig Wales; Chick C. Wilson
Selective preparation of elusive and alternative single component polymorphic solid forms through multi-component crystallisation routes
Chem.Commun., 2016, 52, 7372
7119162 CIFC15 H13 N3 O4 SP -17.8557; 10.1043; 10.4713
80.602; 68.952; 69.742
727.01Lynne H. Thomas; Craig Wales; Chick C. Wilson
Selective preparation of elusive and alternative single component polymorphic solid forms through multi-component crystallisation routes
Chem.Commun., 2016, 52, 7372
7119163 CIFC15 H13 N3 O4 SP -112.6899; 14.6928; 20.5097
84.866; 74.669; 84.683
3663.7Lynne H. Thomas; Craig Wales; Chick C. Wilson
Selective preparation of elusive and alternative single component polymorphic solid forms through multi-component crystallisation routes
Chem.Commun., 2016, 52, 7372
7119164 CIFC46 H43 N9 O13 S3P -17.0374; 12.917; 25.467
84.077; 89.174; 83.327
2287Lynne H. Thomas; Craig Wales; Chick C. Wilson
Selective preparation of elusive and alternative single component polymorphic solid forms through multi-component crystallisation routes
Chem.Commun., 2016, 52, 7372
7119165 CIFC16 H15 N OP b c a9.0171; 11.0071; 23.9483
90; 90; 90
2376.9Vijay K. Srirambhatla; Rui Guo; Sarah L. Price; Alastair J. Florence
Isomorphous template induced crystallisation: a robust method for the targeted crystallisation of computationally predicted metastable polymorphs
Chem.Commun., 2016, 52, 7384
7119166 CIFC26 H16 S2P 1 21/n 115.113; 7.708; 16.178
90; 94; 90
1880Haichao Liu; Liang Yao; Bao Li; Xiankai Chen; Yu Gao; Shitong Zhang; Weijun Li; Ping Lu; Bing Yang; Yuguang Ma
Excimer-induced high-efficiency fluorescence due to pairwise anthracene stacking in a crystal with long lifetime
Chem.Commun., 2016, 52, 7356
7119167 CIFC26 H16 S2C 1 2/c 117.08; 11.919; 19.8
90; 104.04; 90
3910.4Haichao Liu; Liang Yao; Bao Li; Xiankai Chen; Yu Gao; Shitong Zhang; Weijun Li; Ping Lu; Bing Yang; Yuguang Ma
Excimer-induced high-efficiency fluorescence due to pairwise anthracene stacking in a crystal with long lifetime
Chem.Commun., 2016, 52, 7356
7119168 CIFC22 H23 N3 O4P 1 21/n 110.9129; 7.8194; 22.428
90; 97.304; 90
1898.3Haiyan Yu; Wang Ren; Hongguang Lu; Yanan Liang; Qiusheng Wang
Synthesis and piezochromic luminescence study of a coumarin hydrozone compound
Chem.Commun., 2016, 52, 7387
7119169 CIFC21 H11 F26 N O2P -112.37; 12.834; 18.49
98.783; 91.487; 104.872
2797.3Yohei Haketa; Ryota Takasago; Hiromitsu Maeda
beta-Perfluoroalkyl-substituted pyrrole as an anion-responsive pi-electronic system through a single NH moiety
Chem.Commun., 2016, 52, 7364
7119170 CIFC132 H108 Cd4 N20 O12C 1 2/c 131.093; 34.507; 24.271
90; 128.646; 90
20339Thirumurugan Prakasam; Rana A. Bilbeisi; Matteo Lusi; John-Carl Olsen; Carlos Platas-Iglesias; Ali Trabolsi
Post-synthetic modifications of cadmium-based knots and links
Chem.Commun., 2016, 52, 7398
7119171 CIFC70 H56 B Cd2 F4 N10 O8I b a m12.5188; 15.3848; 42.5644
90; 90; 90
8197.9Thirumurugan Prakasam; Rana A. Bilbeisi; Matteo Lusi; John-Carl Olsen; Carlos Platas-Iglesias; Ali Trabolsi
Post-synthetic modifications of cadmium-based knots and links
Chem.Commun., 2016, 52, 7398
7119172 CIFC105 H69 Cd3 F9 N15 O24 Re3R 3 c :H18.6042; 18.6042; 51.5285
90; 90; 120
15445.4Thirumurugan Prakasam; Rana A. Bilbeisi; Matteo Lusi; John-Carl Olsen; Carlos Platas-Iglesias; Ali Trabolsi
Post-synthetic modifications of cadmium-based knots and links
Chem.Commun., 2016, 52, 7398
7119173 CIFC64 H60 F3 N12 O52 P W12 Zn2P 4/n :219.5965; 19.5965; 16.078
90; 90; 90
6174.32Jian-Zhen Liao; Chen Wu; Xiao-Yuan Wu; Shui-Quan Deng; Can-Zhong Lu
Exceptional photosensitivity of a polyoxometalate-based charge-transfer hybrid material
Chem.Commun., 2016, 52, 7394
7119174 CIFC18 H16 O4P 1 21/c 111.891; 16.2219; 15.2941
90; 93.262; 90
2945.4Rajkumar Lalji Sahani; Rai-Shung Liu
Gold-catalyzed [4+3] and [4+4]-annulation reactions of t-butyl propiolate derivatives with epoxides and oxetanes for the construction of 1,4-dioxepane and 1,5-dioxocane cores
Chem.Commun., 2016, 52, 7482
7119175 CIFC19 H18 O4P 1 21/n 15.7294; 16.4971; 16.9275
90; 96.391; 90
1590Rajkumar Lalji Sahani; Rai-Shung Liu
Gold-catalyzed [4+3] and [4+4]-annulation reactions of t-butyl propiolate derivatives with epoxides and oxetanes for the construction of 1,4-dioxepane and 1,5-dioxocane cores
Chem.Commun., 2016, 52, 7482
7119176 CIFMn1.5 N O13 V4P 1 2/m 18.2011; 3.5207; 9.9129
90; 110.987; 90
267.234Martin K. Dufficy; Lan Luo; Peter S. Fedkiw; Paul A. Maggard
Vacancy-induced manganese vanadates and their potential application to Li-ion batteries
Chem.Commun., 2016, 52, 7509
7119177 CIFC12 H8 Co3 K O20I -4 2 d13.0691; 13.0691; 30.157
90; 90; 90
5150.9Jack Binns; Konstantin V. Kamenev; Katie E. R. Marriott; Garry J. McIntyre; Stephen A. Moggach; Mark Murrie; Simon Parsons
A non-topological mechanism for negative linear compressibility
Chem.Commun., 2016, 52, 7486
7119178 CIFC12 H8 Co3 K O18I -4 2 d13.0005; 13.0005; 30.2002
90; 90; 90
5104.2Jack Binns; Konstantin V. Kamenev; Katie E. R. Marriott; Garry J. McIntyre; Stephen A. Moggach; Mark Murrie; Simon Parsons
A non-topological mechanism for negative linear compressibility
Chem.Commun., 2016, 52, 7486
7119179 CIFC12 H8 Co3 K O18I -4 2 d12.8201; 12.8201; 30.2685
90; 90; 90
4974.8Jack Binns; Konstantin V. Kamenev; Katie E. R. Marriott; Garry J. McIntyre; Stephen A. Moggach; Mark Murrie; Simon Parsons
A non-topological mechanism for negative linear compressibility
Chem.Commun., 2016, 52, 7486
7119180 CIFC12 H8 Co3 K O18I -4 2 d12.6111; 12.6111; 30.2999
90; 90; 90
4818.9Jack Binns; Konstantin V. Kamenev; Katie E. R. Marriott; Garry J. McIntyre; Stephen A. Moggach; Mark Murrie; Simon Parsons
A non-topological mechanism for negative linear compressibility
Chem.Commun., 2016, 52, 7486
7119181 CIFC21 H20 O4P 21 21 215.9638; 7.4011; 40.7678
90; 90; 90
1799.44Wei Zhou; Peng Chen; Mengna Tao; Xiao Su; Qingjie Zhao; Junliang Zhang
Enantioselective intermolecular cross Rauhut-Currier reactions of activated alkenes with acrolein
Chem.Commun., 2016, 52, 7612
7119182 CIFC39 H38 N O P SP 21 21 218.966; 10.6824; 34.6972
90; 90; 90
3323.2Wei Zhou; Peng Chen; Mengna Tao; Xiao Su; Qingjie Zhao; Junliang Zhang
Enantioselective intermolecular cross Rauhut-Currier reactions of activated alkenes with acrolein
Chem.Commun., 2016, 52, 7612
7119183 CIFC16 H21 B Fe O2P 1 21/n 112.7414; 7.5452; 15.8499
90; 104.524; 90
1475.06Anis Tlili; Arnaud Voituriez; Angela Marinetti; Pierre Thuery; Thibault Cantat
Synergistic effects in ambiphilic phosphino-borane catalysts for the hydroboration of CO2
Chem.Commun., 2016, 52, 7553
7119350 CIFC6 Cl8 N10 O8P 1 21/c 16.1067; 13.7465; 12.4167
90; 96.024; 90
1036.57Srinivas, Dharavath; Mitchell, Lauren A.; Parrish, Damon A.; Shreeve, Jean'ne M.
From FOX-7 to H-FOX to insensitive energetic materials with hypergolic properties
Chemical Communications, 2016, 52, 7668-7671
7119351 CIFC4 H2 Cl2 N10 O8P 1 21/c 110.3037; 9.6323; 14.3934
90; 107.927; 90
1359.17Srinivas, Dharavath; Mitchell, Lauren A.; Parrish, Damon A.; Shreeve, Jean'ne M.
From FOX-7 to H-FOX to insensitive energetic materials with hypergolic properties
Chemical Communications, 2016, 52, 7668-7671
7119352 CIFC47 H43 Ag3 F6 N12 O7 S2P -112.88; 13.13; 15.88
99.38; 90.29; 101.76
2592Hui; Guo; Xin; He; Chong-Qing; Wan; Liang; Zhao
A stepwise bulk-to-cluster-to-particle transformation toward the efficient synthesis of alkynyl-protected silver nanoclusters
Chem.Commun., 2016, 52, 7723
7119353 CIFC24 H27 Br O5P 1 21 111.882; 6.1817; 15.84
90; 108.485; 90
1103.4Liangliang; Song; Lei; Gong; Eric; Meggers
Asymmetric dual catalysis via fragmentation of a single rhodium precursor complex
Chem.Commun., 2016, 52, 7699
7119354 CIFC43 H44 N3 O5 RhP 21 21 2112.6831; 13.3648; 25.5629
90; 90; 90
4333.1Liangliang; Song; Lei; Gong; Eric; Meggers
Asymmetric dual catalysis via fragmentation of a single rhodium precursor complex
Chem.Commun., 2016, 52, 7699
7119355 CIFC24 H27 Br O5P 21 21 216.202; 12.159; 30.276
90; 90; 90
2283.12Liangliang; Song; Lei; Gong; Eric; Meggers
Asymmetric dual catalysis via fragmentation of a single rhodium precursor complex
Chem.Commun., 2016, 52, 7699
7119356 CIFC12 H8 I2 N O3C 1 2/c 117.6; 4.372; 34.3
90; 97.444; 90
2617Subhankar; Saha; Gautam; R.; Desiraju
Using structural modularity in cocrystals to engineer properties: elasticity
Chem.Commun., 2016, 52, 7676
7119357 CIFC24 H16 Cl4 N2 O6P -13.795; 14.7; 21.4
80.7; 89.35; 89.09
1178Subhankar; Saha; Gautam; R.; Desiraju
Using structural modularity in cocrystals to engineer properties: elasticity
Chem.Commun., 2016, 52, 7676
7119358 CIFC11 H8 Br2 N OP -14.183; 8.769; 15.366
94.1; 95.78; 99.68
550.5Subhankar; Saha; Gautam; R.; Desiraju
Using structural modularity in cocrystals to engineer properties: elasticity
Chem.Commun., 2016, 52, 7676
7119359 CIFC9 H6 Cl2 N O3P -13.777; 10.382; 13.45
68.43; 85.15; 80.26
483.3Subhankar; Saha; Gautam; R.; Desiraju
Using structural modularity in cocrystals to engineer properties: elasticity
Chem.Commun., 2016, 52, 7676
7119360 CIFC9 H6 I2 N O3C 1 2/c 127.78; 4.706; 17.566
90; 96.051; 90
2284Subhankar; Saha; Gautam; R.; Desiraju
Using structural modularity in cocrystals to engineer properties: elasticity
Chem.Commun., 2016, 52, 7676
7119361 CIFC91.75 H99.7 Cl12.48 N14.43 O4.45 Pd6 S0.48P 1 21/c 119.6264; 52.3974; 14.3627
90; 90.6803; 90
14769.2Shohei; Tashiro; Hirotaka; Yonezawa; Ryou; Kubota; Tsutomu; Umeki; Mitsuhiko; Shionoya
Non-covalent immobilisation of p-toluenesulfonic acid in a porous molecular crystal for size-specific acid-catalysed reactions
Chem.Commun., 2016, 52, 7657
7119362 CIFC43 H52 Cl8 N6 O4 Pd3P 1 21/c 119.5796; 52.142; 14.2469
90; 91.162; 90
14541.9Shohei; Tashiro; Hirotaka; Yonezawa; Ryou; Kubota; Tsutomu; Umeki; Mitsuhiko; Shionoya
Non-covalent immobilisation of p-toluenesulfonic acid in a porous molecular crystal for size-specific acid-catalysed reactions
Chem.Commun., 2016, 52, 7657
7119363 CIFC94.65 H105.36 Cl12 N16.29 O3.82 Pd6 S0.41P 1 21/c 119.5493; 51.784; 14.2759
90; 90.7569; 90
14450.8Shohei; Tashiro; Hirotaka; Yonezawa; Ryou; Kubota; Tsutomu; Umeki; Mitsuhiko; Shionoya
Non-covalent immobilisation of p-toluenesulfonic acid in a porous molecular crystal for size-specific acid-catalysed reactions
Chem.Commun., 2016, 52, 7657
7119373 CIFC13 H17 N3 O3 S2P b c a10.4816; 12.7531; 22.3603
90; 90; 90
2989Celia; Ruiz-Palomero; Stuart; R.; Kennedy; M.; Laura; Soriano; Christopher; D.; Jones; Miguel; Valcarcel; Jonathan; W.; Steed
Pharmaceutical crystallization with nanocellulose organogels
Chem.Commun., 2016, 52, 7782
7119374 CIFC32 H62 N4 O5 S3P -15.7565; 10.7037; 31.057
87.126; 85.544; 86.192
1901.7Celia; Ruiz-Palomero; Stuart; R.; Kennedy; M.; Laura; Soriano; Christopher; D.; Jones; Miguel; Valcarcel; Jonathan; W.; Steed
Pharmaceutical crystallization with nanocellulose organogels
Chem.Commun., 2016, 52, 7782
7119375 CIFC20 H15 N O3P 21 21 215.5517; 11.006; 24.121
90; 90; 90
1473.8Chun-Wei; Kuo; Ashok; Konala; Lyu; Lin; Ting-Ta; Chiang; Chia-Yu; Huang; Tang-Hao; Yang; Veerababurao; Kavala; Ching-Fa; Yao
Synthesis of benzo[a]carbazole derivatives from 3-ethylindoles by exploiting the dual character of benzoquinone as an oxidizing agent and dienophile
Chem.Commun., 2016, 52, 7870
7119376 CIFC25 H19 N O2C 1 2/c 137.27; 7.992; 12.774
90; 91.797; 90
3803Chun-Wei; Kuo; Ashok; Konala; Lyu; Lin; Ting-Ta; Chiang; Chia-Yu; Huang; Tang-Hao; Yang; Veerababurao; Kavala; Ching-Fa; Yao
Synthesis of benzo[a]carbazole derivatives from 3-ethylindoles by exploiting the dual character of benzoquinone as an oxidizing agent and dienophile
Chem.Commun., 2016, 52, 7870
7119377 CIFC20 H15 Cl N2 O2P 21 21 217.174; 14.3271; 17.4194
90; 90; 90
1790.4Zhu, Gongming; Yang, Junxian; Bao, Guangjun; Zhang, Ming; Li, Jing; Li, Yiping; Sun, Wangsheng; Hong, Liang; Wang, Rui
Catalyst-controlled switch of regioselectivity in the asymmetric allylic alkylation of oxazolones with MBHCs
Chemical Communications, 2016, 52, 7882-7885
7119378 CIFC21 H18 Cl N O4P 21 21 217.1668; 12.4455; 21.2096
90; 90; 90
1891.78Zhu, Gongming; Yang, Junxian; Bao, Guangjun; Zhang, Ming; Li, Jing; Li, Yiping; Sun, Wangsheng; Hong, Liang; Wang, Rui
Catalyst-controlled switch of regioselectivity in the asymmetric allylic alkylation of oxazolones with MBHCs
Chemical Communications, 2016, 52, 7882-7885
7119379 CIFC62 H58 Gd2 N8 O20 Zn2P 1 21/c 113.8176; 14.3073; 16.9982
90; 95.502; 90
3344.9Griffiths, Kieran; Kumar, Prashant; Akien, Geoffrey R.; Chilton, Nicholas F.; Abdul-Sada, Alaa; Tizzard, Graham J.; Coles, Simon J.; Kostakis, George E.
Tetranuclear Zn/4f coordination clusters as highly efficient catalysts for Friedel-Crafts alkylation
Chemical Communications, 2016, 52, 7866-7869
7119380 CIFC62 H58 Dy2 N8 O20 Zn2P 1 21/c 113.75033; 14.3147; 16.9418
90; 95.2801; 90
3320.54Griffiths, Kieran; Kumar, Prashant; Akien, Geoffrey R.; Chilton, Nicholas F.; Abdul-Sada, Alaa; Tizzard, Graham J.; Coles, Simon J.; Kostakis, George E.
Tetranuclear Zn/4f coordination clusters as highly efficient catalysts for Friedel-Crafts alkylation
Chemical Communications, 2016, 52, 7866-7869
7119381 CIFC62 H58 N8 O20 Y2 Zn2P 1 21/c 113.7448; 14.3133; 16.9268
90; 95.068; 90
3317Griffiths, Kieran; Kumar, Prashant; Akien, Geoffrey R.; Chilton, Nicholas F.; Abdul-Sada, Alaa; Tizzard, Graham J.; Coles, Simon J.; Kostakis, George E.
Tetranuclear Zn/4f coordination clusters as highly efficient catalysts for Friedel-Crafts alkylation
Chemical Communications, 2016, 52, 7866-7869
7119382 CIFC62 H58 Eu2 N8 O20 Zn2P 1 21/c 113.8125; 14.3087; 16.9783
90; 95.498; 90
3340.14Griffiths, Kieran; Kumar, Prashant; Akien, Geoffrey R.; Chilton, Nicholas F.; Abdul-Sada, Alaa; Tizzard, Graham J.; Coles, Simon J.; Kostakis, George E.
Tetranuclear Zn/4f coordination clusters as highly efficient catalysts for Friedel-Crafts alkylation
Chemical Communications, 2016, 52, 7866-7869
7119383 CIFC23 H18 N2P 1 21/c 110.0681; 9.7551; 17.5082
90; 94.291; 90
1714.8Griffiths, Kieran; Kumar, Prashant; Akien, Geoffrey R.; Chilton, Nicholas F.; Abdul-Sada, Alaa; Tizzard, Graham J.; Coles, Simon J.; Kostakis, George E.
Tetranuclear Zn/4f coordination clusters as highly efficient catalysts for Friedel-Crafts alkylation
Chemical Communications, 2016, 52, 7866-7869
7119384 CIFC29 H24 N2 O2P -19.9468; 10.285; 11.5735
75.327; 82.383; 81.347
1126.82Griffiths, Kieran; Kumar, Prashant; Akien, Geoffrey R.; Chilton, Nicholas F.; Abdul-Sada, Alaa; Tizzard, Graham J.; Coles, Simon J.; Kostakis, George E.
Tetranuclear Zn/4f coordination clusters as highly efficient catalysts for Friedel-Crafts alkylation
Chemical Communications, 2016, 52, 7866-7869
7119385 CIFC23 H20 N2 O3P 1 21/n 18.8491; 10.6531; 20.9154
90; 96.794; 90
1957.9Griffiths, Kieran; Kumar, Prashant; Akien, Geoffrey R.; Chilton, Nicholas F.; Abdul-Sada, Alaa; Tizzard, Graham J.; Coles, Simon J.; Kostakis, George E.
Tetranuclear Zn/4f coordination clusters as highly efficient catalysts for Friedel-Crafts alkylation
Chemical Communications, 2016, 52, 7866-7869
7119386 CIFC25 H22 N2I 1 2/a 118.3322; 10.0821; 20.0451
90; 90.573; 90
3704.7Griffiths, Kieran; Kumar, Prashant; Akien, Geoffrey R.; Chilton, Nicholas F.; Abdul-Sada, Alaa; Tizzard, Graham J.; Coles, Simon J.; Kostakis, George E.
Tetranuclear Zn/4f coordination clusters as highly efficient catalysts for Friedel-Crafts alkylation
Chemical Communications, 2016, 52, 7866-7869
7119387 CIFC96 H92 N12 O32 Zr6F m -3 m29.983; 29.983; 29.983
90; 90; 90
26954Naeem, Ayesha; Ting, Valeska P.; Hintermair, Ulrich; Tian, Mi; Telford, Richard; Halim, Saaiba; Nowell, Harriott; Hołyńska, Małgorzata; Teat, Simon J.; Scowen, Ian J.; Nayak, Sanjit
Mixed-linker approach in designing porous zirconium-based metal‒organic frameworks with high hydrogen storage capacity
Chemical Communications, 2016, 52, 7826-7829
7119388 CIFC96 H80 O32 Zr6F m -3 m29.941; 29.941; 29.941
90; 90; 90
26841Naeem, Ayesha; Ting, Valeska P.; Hintermair, Ulrich; Tian, Mi; Telford, Richard; Halim, Saaiba; Nowell, Harriott; Hołyńska, Małgorzata; Teat, Simon J.; Scowen, Ian J.; Nayak, Sanjit
Mixed-linker approach in designing porous zirconium-based metal‒organic frameworks with high hydrogen storage capacity
Chemical Communications, 2016, 52, 7826-7829
7119389 CIFC36 H36 Cl6 Ge3 N4P 1 21/c 19.4771; 16.9192; 25.2949
90; 92.298; 90
4052.6Swamy, V. S. V. S. N.; Yadav, Sandeep; Pal, Shiv; Das, Tamal; Vanka, Kumar; Sen, Sakya S.
Facile access to a Ge(II) dication stabilized by isocyanides
Chemical Communications, 2016, 52, 7890-7892
7119440 CIFC29 H36 Br F3 N O3 PP 1 21/n 19.477; 15.308; 21.114
90; 102.525; 90
2990Ryosuke; Saijo; Hidemitsu; Uno; Shigeki; Mori; Masami; Kawase
Synthesis and structures of stable phosphorus zwitterions derived from mesoionic 4_trifluoroacetyl-1,3-oxazolium-5-olates
Chem.Commun., 2016, 52, 8006
7119441 CIFC39 H31 N O3 SP 4/n c c25.9455; 25.9455; 24.2457
90; 90; 90
16321.5Tetsuya; Hasegawa; Kei; Ohkubo; Ichiro; Hisaki; Mikiji; Miyata; Norimitsu; Tohnai; Shunichi; Fukuzumi
Photoinduced electron transfer in porous organic salt crystals impregnated with fullerenes
Chem.Commun., 2016, 52, 7928
7119442 CIFC60 H45 N O3 SP 4/n c c26.7747; 26.7747; 24.0725
90; 90; 90
17257.2Tetsuya; Hasegawa; Kei; Ohkubo; Ichiro; Hisaki; Mikiji; Miyata; Norimitsu; Tohnai; Shunichi; Fukuzumi
Photoinduced electron transfer in porous organic salt crystals impregnated with fullerenes
Chem.Commun., 2016, 52, 7928
7119443 CIFC62.5 H45 N O3 SP 4/n c c27.3864; 27.3864; 24.2386
90; 90; 90
18179.3Tetsuya; Hasegawa; Kei; Ohkubo; Ichiro; Hisaki; Mikiji; Miyata; Norimitsu; Tohnai; Shunichi; Fukuzumi
Photoinduced electron transfer in porous organic salt crystals impregnated with fullerenes
Chem.Commun., 2016, 52, 7928
7119446 CIFC26 H28 F12 N6 P2 RuC 1 2/c 120.6432; 12.1018; 12.8802
90; 110.019; 90
3023.3Yanay; Popowski; Israel; Goldberg; Moshe; Kol
The stereoselectivity of bipyrrolidine-based sequential polydentate ligands around Ru(II)
Chem.Commun., 2016, 52, 7932
7119447 CIFC30 H32 F12 N6 P2 RuC 1 2 125.132; 9.8199; 17.2577
90; 131.012; 90
3213.8Yanay; Popowski; Israel; Goldberg; Moshe; Kol
The stereoselectivity of bipyrrolidine-based sequential polydentate ligands around Ru(II)
Chem.Commun., 2016, 52, 7932
7119448 CIFC24 H32 F12 N6 P2 RuP 31 2 110.2422; 10.2422; 24.9887
90; 90; 120
2270.18Yanay; Popowski; Israel; Goldberg; Moshe; Kol
The stereoselectivity of bipyrrolidine-based sequential polydentate ligands around Ru(II)
Chem.Commun., 2016, 52, 7932
7119449 CIFC25 H29 Cl F12 Fe N5 P2P 1 21 110.1753; 16.8389; 9.2498
90; 112.218; 90
1467.2Yanay; Popowski; Israel; Goldberg; Moshe; Kol
The stereoselectivity of bipyrrolidine-based sequential polydentate ligands around Ru(II)
Chem.Commun., 2016, 52, 7932
7119450 CIFC60 H74 B2 F8 N10 O20 Ru3P 1 21/n 114.515; 14.999; 15.692
90; 96.15; 90
3397Yuta; Tsubonouchi; Shu; Lin; Alexander; R.; Parent; Gary; W.; Brudvig; Ken; Sakai
Light-induced water oxidation catalyzed by an oxido-bridged triruthenium complex with a Ru-O-Ru-O-Ru motif
Chem.Commun., 2016, 52, 8018
7119451 CIFC60 H82 B F4 N10 O32 Ru3 S2P -115.229; 17.001; 17.204
65.62; 84.91; 71.63
3845.9Yuta; Tsubonouchi; Shu; Lin; Alexander; R.; Parent; Gary; W.; Brudvig; Ken; Sakai
Light-induced water oxidation catalyzed by an oxido-bridged triruthenium complex with a Ru-O-Ru-O-Ru motif
Chem.Commun., 2016, 52, 8018
7119454 CIFC36 H26 Cd N2 O4P 41 21 214.5436; 14.5436; 29.1864
90; 90; 90
6173.4Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119455 CIFC36 H25 Cd N2 O4P 43 21 214.573; 14.573; 28.941
90; 90; 90
6146Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119456 CIFC36 H26 Cd N2 O4P 43 21 214.523; 14.523; 29.1177
90; 90; 90
6141.4Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119457 CIFC36 H24 Cd N2 O4P 43 21 214.3555; 14.3555; 29.4087
90; 90; 90
6060.6Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119458 CIFC36 H26 Cd N2 O4P 41 21 214.5029; 14.5029; 29.2053
90; 90; 90
6142.9Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119459 CIFC36 H24 Cd N2 O4P 41 21 214.3664; 14.3664; 29.399
90; 90; 90
6067.8Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119460 CIFC36 H26 Cd N2 O4P 43 21 214.5318; 14.5318; 29.1429
90; 90; 90
6154.2Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119461 CIFC36 H26 Cd N2 O4P 41 21 214.5128; 14.5128; 29.194
90; 90; 90
6148.9Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119462 CIFC36 H26 Cd N2 O4P 43 21 214.4791; 14.4791; 29.069
90; 90; 90
6094.2Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119463 CIFC36 H26 Cd N2 O4P 43 21 214.4739; 14.4739; 29.0695
90; 90; 90
6089.9Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119464 CIFC36 H26 Cd N2 O4P 43 21 214.4958; 14.4958; 29.0361
90; 90; 90
6101.3Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119465 CIFC36 H26 Cd N2 O4P 43 21 214.5294; 14.5294; 29.1842
90; 90; 90
6160.9Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119466 CIFC36 H26 Cd N2 O4P 41 21 214.4838; 14.4838; 29.2182
90; 90; 90
6129.4Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119467 CIFC36 H26 Cd N2 O4P 41 21 214.4458; 14.4458; 29.3447
90; 90; 90
6123.7Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119468 CIFC36 H26 Cd N2 O4P 41 21 214.4171; 14.4171; 29.1929
90; 90; 90
6067.8Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119469 CIFC36 H26 Cd N2 O4P 41 21 214.5097; 14.5097; 28.8452
90; 90; 90
6072.8Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119470 CIFC36 H26 Cd N2 O4P 41 21 214.5222; 14.5222; 29.245
90; 90; 90
6167.6Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119471 CIFC36 H26 Cd N2 O4P 41 21 214.5387; 14.5387; 29.246
90; 90; 90
6181.8Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119472 CIFC36 H26 Cd N2 O4P 43 21 214.5486; 14.5486; 29.1966
90; 90; 90
6179.8Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119473 CIFC36 H26 Cd N2 O4P 43 21 214.486; 14.486; 28.911
90; 90; 90
6066.8Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119474 CIFC36 H26 Cd N2 O4P 41 21 214.4896; 14.4896; 29.1167
90; 90; 90
6113Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119475 CIFC36 H26 Cd N2 O4P 43 21 214.4789; 14.4789; 29.007
90; 90; 90
6081Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119476 CIFC36 H26 Cd N2 O4P 41 21 214.5067; 14.5067; 28.888
90; 90; 90
6079.3Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119477 CIFC36 H26 Cd N2 O4P 41 21 214.4975; 14.4975; 29.1189
90; 90; 90
6120.1Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119478 CIFC36 H26 Cd N2 O4P 43 21 214.5803; 14.5803; 29.181
90; 90; 90
6203.4Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119479 CIFC36 H26 Cd N2 O4P 41 21 214.5474; 14.5474; 29.2215
90; 90; 90
6184.1Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119480 CIFC36 H26 Cd N2 O4P 43 21 214.5616; 14.5616; 29.153
90; 90; 90
6181.6Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119481 CIFC36 H25 Cd N2 O4P 41 21 214.4906; 14.4906; 29.1148
90; 90; 90
6113.5Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119482 CIFC72 H40 In2 O16R -3 :H44.874; 44.874; 42.074
90; 90; 120
73373Panpan; Yu; Qipeng; Li; Yue; Hu; Nannan; Liu; Lijie; Zhang; Kongzhao; Su; Jinjie; Qian; Shaoming; Huang; Maochun; Hong
Cuboctahedron-based indium-organic frameworks for gas sorption and selective cation exchange
Chem.Commun., 2016, 52, 7978
7119483 CIFC25 H16 O3C 1 2/c 125.507; 8.1552; 16.661
90; 92.869; 90
3461.4Hikaru; Yanai; Nobuyuki; Ishii; Takashi; Matsumoto
Synthesis of 1,2,3,4-tetrasubstituted naphthalenes through a cascade reaction triggered by silyl acetal activation
Chem.Commun., 2016, 52, 7974
7119484 CIFC27 H22 O4P -19.173; 10.382; 12.748
104.062; 94.66; 116.023
1033.4Hikaru; Yanai; Nobuyuki; Ishii; Takashi; Matsumoto
Synthesis of 1,2,3,4-tetrasubstituted naphthalenes through a cascade reaction triggered by silyl acetal activation
Chem.Commun., 2016, 52, 7974

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