Crystallography Open Database

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7125042 CIFC52 H42 B F2 Fe2 N3 O4P -112.567; 13.2195; 14.1831
114.172; 93.299; 97.933
2112Didukh, Natalia O.; Zatsikha, Yuriy V.; Rohde, Gregory T.; Blesener, Tanner S.; Yakubovskyi, Viktor P.; Kovtun, Yuriy P.; Nemykin, Victor N.
NIR absorbing diferrocene-containing meso-cyano-BODIPY with a UV-Vis-NIR spectrum remarkably close to that of magnesium tetracyanotetraferrocenyltetraazaporphyrin.
Chemical communications (Cambridge, England), 2016, 52, 11563-11566
7125043 CIFC29 H21 Br Cl3 F3 N2 O3P 21 21 2112.0262; 13.8263; 17.009
90; 90; 90
2828.2Wang, Zhen-Hua; Wu, Zhi-Jun; Yue, Deng-Feng; Hu, Wen-Fei; Zhang, Xiao-Mei; Xu, Xiao-Ying; Yuan, Wei-Cheng
Organocatalytic asymmetric [3+2] cycloaddition of N-2,2,2-trifluoroethylisatin ketimines with 3-alkenyl-5-arylfuran-2(3H)-ones.
Chemical communications (Cambridge, England), 2016, 52, 11708-11711
7125044 CIFC31 H30 Bi F6 Mn N3 O12 S2P -19.6023; 12.8674; 15.9332
96.095; 105.256; 104.605
1806.25Pearson, Tyler J.; Fataftah, Majed S.; Freedman, Danna E.
Enhancement of magnetic anisotropy in a Mn-Bi heterobimetallic complex.
Chemical communications (Cambridge, England), 2016, 52, 11394-11397
7125045 CIFC23 H31 BrC 1 2/c 122.7174; 6.5055; 25.667
90; 94.802; 90
3780Christopher Braddock, D.; Mahtey, Areeb; Rzepa, Henry S.; White, Andrew J. P.
Stable bromoallene oxides.
Chemical communications (Cambridge, England), 2016, 52, 11219-11222
7125046 CIFC17 H25 Br OP 1 21/n 110.8427; 6.8117; 21.255
90; 94.932; 90
1564.02Christopher Braddock, D.; Mahtey, Areeb; Rzepa, Henry S.; White, Andrew J. P.
Stable bromoallene oxides.
Chemical communications (Cambridge, England), 2016, 52, 11219-11222
7125047 CIFC19 H24 N2 O5P 1 21/c 112.59; 8.3056; 17.163
90; 97.211; 90
1780.5Cheng, Jian; Xu, Pan; Li, Weipeng; Cheng, Yixiang; Zhu, Chengjian
The functionalization of a cascade of C(sp(2))-H/C(sp(3))-H bonds: synthesis of fused dihydropyrazoles via visible-light photoredox catalysis.
Chemical communications (Cambridge, England), 2016, 52, 11901-11904
7125048 CIFC48 H64 B4 N4 O8P 1 21/n 16.4277; 10.233; 18.9139
90; 94.954; 90
1239.41Barbero, Héctor; Ferrero, Sergio; Álvarez-Miguel, Lucía; Gómez-Iglesias, Patricia; Miguel, Daniel; Álvarez, Celedonio M
Affinity modulation of photoresponsive hosts for fullerenes: light-gated corannulene tweezers.
Chemical communications (Cambridge, England), 2016, 52, 12964-12967
7125049 CIFC40 H26 N2P -13.9995; 9.9251; 17.4542
106.27; 91.672; 92.388
663.92Barbero, Héctor; Ferrero, Sergio; Álvarez-Miguel, Lucía; Gómez-Iglesias, Patricia; Miguel, Daniel; Álvarez, Celedonio M
Affinity modulation of photoresponsive hosts for fullerenes: light-gated corannulene tweezers.
Chemical communications (Cambridge, England), 2016, 52, 12964-12967
7125050 CIFC40 H26 N2P 1 21/c 111.0512; 14.4682; 8.5519
90; 91.007; 90
1367.2Barbero, Héctor; Ferrero, Sergio; Álvarez-Miguel, Lucía; Gómez-Iglesias, Patricia; Miguel, Daniel; Álvarez, Celedonio M
Affinity modulation of photoresponsive hosts for fullerenes: light-gated corannulene tweezers.
Chemical communications (Cambridge, England), 2016, 52, 12964-12967
7125051 CIFC52 H26 N2P 1 21/c 19.1494; 8.9306; 20.285
90; 92.501; 90
1655.9Barbero, Héctor; Ferrero, Sergio; Álvarez-Miguel, Lucía; Gómez-Iglesias, Patricia; Miguel, Daniel; Álvarez, Celedonio M
Affinity modulation of photoresponsive hosts for fullerenes: light-gated corannulene tweezers.
Chemical communications (Cambridge, England), 2016, 52, 12964-12967
7125052 CIFC18 H19 Br O3P 21 21 218.7409; 12.0555; 16.4217
90; 90; 90
1730.45Liu, Yangbin; Hu, Haipeng; Lin, Lili; Hao, Xiaoyu; Liu, Xiaohua; Feng, Xiaoming
Enantioselective construction of branched 1,3-dienyl substituted quaternary carbon stereocenters by asymmetric allenyl Claisen rearrangement.
Chemical communications (Cambridge, England), 2016, 52, 11963-11966
7125053 CIFC16 H13 Br I O3P 21 21 217.5432; 12.7924; 17.2791
90; 90; 90
1667.36Liu, Yangbin; Hu, Haipeng; Lin, Lili; Hao, Xiaoyu; Liu, Xiaohua; Feng, Xiaoming
Enantioselective construction of branched 1,3-dienyl substituted quaternary carbon stereocenters by asymmetric allenyl Claisen rearrangement.
Chemical communications (Cambridge, England), 2016, 52, 11963-11966
7125054 CIFC46 H29.41 Ba3.99 Br0 N2 O20 P6C 1 2/c 143.611; 8.549; 34.589
90; 103.59; 90
12535Fard, Z. H.; Kalinovskyy, Y.; Spasyuk, D. M.; Blight, B. A.; Shimizu, G. K. H.
Alkaline-earth phosphonate MOFs with reversible hydration-dependent fluorescence.
Chemical communications (Cambridge, England), 2016, 52, 12865-12868
7125055 CIFC52 H41 N3C 1 2/c 127.2441; 12.2005; 23.5008
90; 103.574; 90
7593.3Norouzi-Arasi, Hassan; Pal, Amlan K.; Nag, Samik; Chartrand, Daniel; Hanan, Garry S.
Synthesis and photophysical properties of C<sub>3</sub>-symmetric tris(pyridyl)truxene scaffolds of Ru(ii) and Re(i).
Chemical communications (Cambridge, England), 2016, 52, 12159-12162
7125056 CIFC68 H53 Cl60 F6 N3 O3 P ReR -3 :H13.4468; 13.4468; 53.0891
90; 90; 120
8313.3Norouzi-Arasi, Hassan; Pal, Amlan K.; Nag, Samik; Chartrand, Daniel; Hanan, Garry S.
Synthesis and photophysical properties of C<sub>3</sub>-symmetric tris(pyridyl)truxene scaffolds of Ru(ii) and Re(i).
Chemical communications (Cambridge, England), 2016, 52, 12159-12162
7125057 CIFC176 H532 N135 O209 Pd20P -125.125; 25.841; 36.446
71.625; 74.386; 67.204
20408Wang, Shitao; Sawada, Tomohisa; Fujita, Makoto
Capsule-bowl conversion triggered by a guest reaction.
Chemical communications (Cambridge, England), 2016, 52, 11653-11656
7125058 CIFC204 H351 N130 O191 Pd20C 1 2/c 148.457; 27.761; 37.941
90; 108.713; 90
48341Wang, Shitao; Sawada, Tomohisa; Fujita, Makoto
Capsule-bowl conversion triggered by a guest reaction.
Chemical communications (Cambridge, England), 2016, 52, 11653-11656
7125059 CIFC196 H357 N118.5 O119.5 Pd20 Si3P 1 21/c 146.603; 25.734; 37.303
90; 113.398; 90
41058Wang, Shitao; Sawada, Tomohisa; Fujita, Makoto
Capsule-bowl conversion triggered by a guest reaction.
Chemical communications (Cambridge, England), 2016, 52, 11653-11656
7125060 CIFC108 H166 N55 O59.5 Pd8 Si4P 1 21/n 124.8071; 18.2127; 40.556
90; 96.472; 90
18207Wang, Shitao; Sawada, Tomohisa; Fujita, Makoto
Capsule-bowl conversion triggered by a guest reaction.
Chemical communications (Cambridge, England), 2016, 52, 11653-11656
7125061 CIFC20 H16 F2 N6 O4P -15.502; 8.865; 10.409
107.757; 97.878; 93.199
476.4Duncan, Andrew J. E.; Dudovitz, Roxanne L.; Dudovitz, Shawna J.; Stojaković, Jelena; Mariappan, S. V. Santhana; MacGillivray, Leonard R.
Quantitative and regiocontrolled cross-photocycloaddition of the anticancer drug 5-fluorouracil achieved in a cocrystal.
Chemical communications (Cambridge, England), 2016, 52, 13109-13111
7125062 CIFC16 H13 F N4 O2P -17.8358; 12.4452; 15.629
98.513; 102.02; 101.749
1430.3Duncan, Andrew J. E.; Dudovitz, Roxanne L.; Dudovitz, Shawna J.; Stojaković, Jelena; Mariappan, S. V. Santhana; MacGillivray, Leonard R.
Quantitative and regiocontrolled cross-photocycloaddition of the anticancer drug 5-fluorouracil achieved in a cocrystal.
Chemical communications (Cambridge, England), 2016, 52, 13109-13111
7125063 CIFC102 H88 Cl0 Cu4 F12 N2 P10P 1 21/n 113.802; 20.7715; 18.8547
90; 100.48; 90
5315.3El Sayed Moussa, M.; Evariste, S.; Wong, H.-L.; Le Bras, L.; Roiland, C.; Le Polles, L.; Le Guennic, B.; Costuas, K.; Yam, V. W.-W.; Lescop, C.
A solid state highly emissive Cu(i) metallacycle: promotion of cuprophilic interactions at the excited states.
Chemical communications (Cambridge, England), 2016, 52, 11370-11373
7125064 CIFC102 H88 Cl0 Cu4 F12 N2 P10P 1 21/n 113.869; 20.739; 18.963
90; 100.223; 90
5368El Sayed Moussa, M.; Evariste, S.; Wong, H.-L.; Le Bras, L.; Roiland, C.; Le Polles, L.; Le Guennic, B.; Costuas, K.; Yam, V. W.-W.; Lescop, C.
A solid state highly emissive Cu(i) metallacycle: promotion of cuprophilic interactions at the excited states.
Chemical communications (Cambridge, England), 2016, 52, 11370-11373
7125065 CIFC102 H88 Cl0 Cu4 F12 N2 P10P 1 21/n 113.935; 20.745; 19.086
90; 100.55; 90
5424El Sayed Moussa, M.; Evariste, S.; Wong, H.-L.; Le Bras, L.; Roiland, C.; Le Polles, L.; Le Guennic, B.; Costuas, K.; Yam, V. W.-W.; Lescop, C.
A solid state highly emissive Cu(i) metallacycle: promotion of cuprophilic interactions at the excited states.
Chemical communications (Cambridge, England), 2016, 52, 11370-11373
7125066 CIFC102 H88 Cl0 Cu4 F12 N2 P10P 1 21/n 114.023; 20.778; 19.191
90; 100.733; 90
5494El Sayed Moussa, M.; Evariste, S.; Wong, H.-L.; Le Bras, L.; Roiland, C.; Le Polles, L.; Le Guennic, B.; Costuas, K.; Yam, V. W.-W.; Lescop, C.
A solid state highly emissive Cu(i) metallacycle: promotion of cuprophilic interactions at the excited states.
Chemical communications (Cambridge, England), 2016, 52, 11370-11373
7125067 CIFC4 H4 N2 O2.5 S0.5P 1 21/c 18.533; 13.0141; 9.6918
90; 92.131; 90
1075.5Shemchuk, O.; Braga, D.; Grepioni, F.
Alloying barbituric and thiobarbituric acids: from solid solutions to a highly stable keto co-crystal form.
Chemical communications (Cambridge, England), 2016, 52, 11815-11818
7125068 CIFC8 H8 N4 O5.4 S0.6P 1 21/c 18.4569; 12.94; 9.5593
90; 92.626; 90
1045Shemchuk, O.; Braga, D.; Grepioni, F.
Alloying barbituric and thiobarbituric acids: from solid solutions to a highly stable keto co-crystal form.
Chemical communications (Cambridge, England), 2016, 52, 11815-11818
7125069 CIFC8 H8 N4 O5.2 S0.8P 1 21/c 18.4662; 12.9681; 9.6819
90; 92.49; 90
1062Shemchuk, O.; Braga, D.; Grepioni, F.
Alloying barbituric and thiobarbituric acids: from solid solutions to a highly stable keto co-crystal form.
Chemical communications (Cambridge, England), 2016, 52, 11815-11818
7125070 CIFC5 H12 O P2P n m a18.159; 7.4484; 6.3101
90; 90; 90
853.5Jost, Maximilian; Finger, Lars H.; Sundermeyer, Jörg; von Hänisch, Carsten
Simple access to ionic liquids and organic salts containing the phosphaethynolate (PCO(-)) and Zintl (Sb11(3-)) anions.
Chemical communications (Cambridge, England), 2016, 52, 11646-11648
7125071 CIFC18 H39 N7 O2 P2P 1 21/c 111.8762; 15.7545; 13.6079
90; 94.012; 90
2539.8Jost, Maximilian; Finger, Lars H.; Sundermeyer, Jörg; von Hänisch, Carsten
Simple access to ionic liquids and organic salts containing the phosphaethynolate (PCO(-)) and Zintl (Sb11(3-)) anions.
Chemical communications (Cambridge, England), 2016, 52, 11646-11648
7125072 CIFC5 H12 N O PP 1 21/m 15.941; 7.4092; 8.8324
90; 99.184; 90
383.8Jost, Maximilian; Finger, Lars H.; Sundermeyer, Jörg; von Hänisch, Carsten
Simple access to ionic liquids and organic salts containing the phosphaethynolate (PCO(-)) and Zintl (Sb11(3-)) anions.
Chemical communications (Cambridge, England), 2016, 52, 11646-11648
7125073 CIFC39 H90 P3 Sb11C 1 c 131.443; 11.2133; 21.6617
90; 123.21; 90
6390Jost, Maximilian; Finger, Lars H.; Sundermeyer, Jörg; von Hänisch, Carsten
Simple access to ionic liquids and organic salts containing the phosphaethynolate (PCO(-)) and Zintl (Sb11(3-)) anions.
Chemical communications (Cambridge, England), 2016, 52, 11646-11648
7125074 CIFC26 H19 Cl O4P -18.8081; 9.9881; 12.6194
79.9048; 82.4837; 80.2931
1071.49Gao, Wen-Chao; Hu, Fei; Tian, Jun; Li, Xing; Wei, Wen-Long; Chang, Hong-Hong
Hypoiodite-catalysed oxidative cyclisation of Michael adducts of chalcones with 1,3-dicarbonyl compounds: a facile and versatile approach to substituted furans and cyclopropanes.
Chemical communications (Cambridge, England), 2016, 52, 13097-13100
7125075 CIFC26 H22 O4P 1 21/n 18.5852; 15.905; 15.6721
90; 95.176; 90
2131.3Gao, Wen-Chao; Hu, Fei; Tian, Jun; Li, Xing; Wei, Wen-Long; Chang, Hong-Hong
Hypoiodite-catalysed oxidative cyclisation of Michael adducts of chalcones with 1,3-dicarbonyl compounds: a facile and versatile approach to substituted furans and cyclopropanes.
Chemical communications (Cambridge, England), 2016, 52, 13097-13100
7125076 CIFC27 H30 F2 N4 O6P -19.423; 12.742; 12.89
62.717; 70.16; 76.407
1288Gunnam, Anilkumar; Suresh, Kuthuru; Ganduri, Ramesh; Nangia, Ashwini
Crystal engineering of a zwitterionic drug to neutral cocrystals: a general solution for floxacins.
Chemical communications (Cambridge, England), 2016, 52, 12610-12613
7125077 CIFC29 H34 F2 N4 O6P -17.9588; 10.3333; 17.8484
80.749; 87.489; 72.019
1377.99Gunnam, Anilkumar; Suresh, Kuthuru; Ganduri, Ramesh; Nangia, Ashwini
Crystal engineering of a zwitterionic drug to neutral cocrystals: a general solution for floxacins.
Chemical communications (Cambridge, England), 2016, 52, 12610-12613
7125078 CIFC28 H32 F2 N4 O6P -19.5457; 12.8769; 13.338
62.8916; 71.3599; 77.1301
1377.05Gunnam, Anilkumar; Suresh, Kuthuru; Ganduri, Ramesh; Nangia, Ashwini
Crystal engineering of a zwitterionic drug to neutral cocrystals: a general solution for floxacins.
Chemical communications (Cambridge, England), 2016, 52, 12610-12613
7125079 CIFC30 H36 F2 N4 O6P -19.5693; 9.7134; 17.7964
74.767; 76.025; 69.597
1475.24Gunnam, Anilkumar; Suresh, Kuthuru; Ganduri, Ramesh; Nangia, Ashwini
Crystal engineering of a zwitterionic drug to neutral cocrystals: a general solution for floxacins.
Chemical communications (Cambridge, England), 2016, 52, 12610-12613
7125080 CIFC27 H28 Cl2 N6 Ni O8P 1 21/c 19.5286; 17.004; 17.9431
90; 96.744; 90
2887.1Kankanamalage, Pavithra H. A.; Mazumder, Shivnath; Tiwari, Vishwas; Kpogo, Kenneth K.; Bernhard Schlegel, H.; Verani, Cláudio N
Efficient electro/photocatalytic water reduction using a [Ni<sup>II</sup>(N<sub>2</sub>Py<sub>3</sub>)]<sup>2+</sup> complex.
Chemical communications (Cambridge, England), 2016, 52, 13357-13360
7125081 CIFC22 H28 O3P -17.8366; 8.8547; 14.3134
84.725; 88.103; 87.621
987.73Tharra, Prabhakararao; Baire, Beeraiah
The Z-enoate assisted, Meyer-Schuster rearrangement cascade: unconventional synthesis of α-arylenone esters.
Chemical communications (Cambridge, England), 2016, 52, 12147-12150
7125082 CIFC144 H126 Br12 Mn18 N24 Na6 O66R -3 c :H44.3099; 44.3099; 21.2242
90; 90; 120
36088Manoli, Maria; Inglis, Ross; Piligkos, Stergios; Yanhua, Lan; Wernsdorfer, Wolfgang; Brechin, Euan K.; Tasiopoulos, Anastasios J.
A hexameric [MnNa<sub>6</sub>] wheel based on [MnO]<sup>7+</sup> sub-units.
Chemical communications (Cambridge, England), 2016, 52, 12829-12832
7125083 CIFC20 H20 As F6 S12P -16.6588; 8.4075; 15.219
83.79; 77.405; 67.799
769.6Pop, Flavia; Auban-Senzier, Pascale; Canadell, Enric; Avarvari, Narcis
Anion size control of the packing in the metallic versus semiconducting chiral radical cation salts (DM-EDT-TTF)<sub>2</sub>XF<sub>6</sub> (X = P, As, Sb).
Chemical communications (Cambridge, England), 2016, 52, 12438-12441
7125084 CIFC20 H20 As F6 S12P 16.6849; 8.3964; 15.203
86.78; 77.306; 68.018
771.63Pop, Flavia; Auban-Senzier, Pascale; Canadell, Enric; Avarvari, Narcis
Anion size control of the packing in the metallic versus semiconducting chiral radical cation salts (DM-EDT-TTF)<sub>2</sub>XF<sub>6</sub> (X = P, As, Sb).
Chemical communications (Cambridge, England), 2016, 52, 12438-12441
7125085 CIFC20 H20 F6 S12 SbP -16.6221; 8.485; 15.3114
87.078; 77.556; 68.221
779.75Pop, Flavia; Auban-Senzier, Pascale; Canadell, Enric; Avarvari, Narcis
Anion size control of the packing in the metallic versus semiconducting chiral radical cation salts (DM-EDT-TTF)<sub>2</sub>XF<sub>6</sub> (X = P, As, Sb).
Chemical communications (Cambridge, England), 2016, 52, 12438-12441
7125086 CIFC20 H20 F6 S12 SbP 16.6529; 8.4663; 15.2766
87.151; 77.495; 68.478
781.06Pop, Flavia; Auban-Senzier, Pascale; Canadell, Enric; Avarvari, Narcis
Anion size control of the packing in the metallic versus semiconducting chiral radical cation salts (DM-EDT-TTF)<sub>2</sub>XF<sub>6</sub> (X = P, As, Sb).
Chemical communications (Cambridge, England), 2016, 52, 12438-12441
7125087 CIFC20 H20 As2 F12 S12P 1 21 18.0663; 16.177; 14.023
90; 100.231; 90
1800.7Pop, Flavia; Auban-Senzier, Pascale; Canadell, Enric; Avarvari, Narcis
Anion size control of the packing in the metallic versus semiconducting chiral radical cation salts (DM-EDT-TTF)<sub>2</sub>XF<sub>6</sub> (X = P, As, Sb).
Chemical communications (Cambridge, England), 2016, 52, 12438-12441
7125088 CIFC20 H20 As2 F12 S12P 1 21 18.0746; 16.1837; 14.0446
90; 100.159; 90
1806.53Pop, Flavia; Auban-Senzier, Pascale; Canadell, Enric; Avarvari, Narcis
Anion size control of the packing in the metallic versus semiconducting chiral radical cation salts (DM-EDT-TTF)<sub>2</sub>XF<sub>6</sub> (X = P, As, Sb).
Chemical communications (Cambridge, England), 2016, 52, 12438-12441
7125089 CIFC26 H16 N2 O8 Zn2P -110.887; 10.896; 14.07
91.252; 92.588; 104.43
1613.8Bhatt, Prashant M.; Batisai, Eustina; Smith, Vincent J.; Barbour, Leonard J.
Creation of new guest accessible space under gas pressure in a flexible MOF: multidimensional insight through combination of in situ techniques.
Chemical communications (Cambridge, England), 2016, 52, 11374-11377
7125090 CIFC13 H8 N O4 ZnP -17.9917; 9.4227; 10.5835
65.314; 86.464; 76.513
703.6Bhatt, Prashant M.; Batisai, Eustina; Smith, Vincent J.; Barbour, Leonard J.
Creation of new guest accessible space under gas pressure in a flexible MOF: multidimensional insight through combination of in situ techniques.
Chemical communications (Cambridge, England), 2016, 52, 11374-11377
7125091 CIFC26.87 H16 N2 O9.73 Zn2P 1 21/c 114.099; 10.997; 21.865
90; 93.971; 90
3382Bhatt, Prashant M.; Batisai, Eustina; Smith, Vincent J.; Barbour, Leonard J.
Creation of new guest accessible space under gas pressure in a flexible MOF: multidimensional insight through combination of in situ techniques.
Chemical communications (Cambridge, England), 2016, 52, 11374-11377
7125092 CIFC13 H8 N O4 ZnP -17.871; 9.34; 10.629
65.253; 86.362; 77.446
692.3Bhatt, Prashant M.; Batisai, Eustina; Smith, Vincent J.; Barbour, Leonard J.
Creation of new guest accessible space under gas pressure in a flexible MOF: multidimensional insight through combination of in situ techniques.
Chemical communications (Cambridge, England), 2016, 52, 11374-11377
7125093 CIFC26 H16 N2 O8 Zn2P 1 21/c 114.065; 10.949; 21.771
90; 94.319; 90
3343Bhatt, Prashant M.; Batisai, Eustina; Smith, Vincent J.; Barbour, Leonard J.
Creation of new guest accessible space under gas pressure in a flexible MOF: multidimensional insight through combination of in situ techniques.
Chemical communications (Cambridge, England), 2016, 52, 11374-11377
7125094 CIFC30 Cu2 N2 O12F m -3 m46.542; 46.542; 46.542
90; 90; 90
100817Zheng, Baishu; Wang, Hang; Wang, Zhaoxu; Ozaki, Noriaki; Hang, Cheng; Luo, Xin; Huang, Lu; Zeng, Wenjiang; Yang, Ming; Duan, Jingui
A highly porous rht-type acylamide-functionalized metal-organic framework exhibiting large CO<sub>2</sub> uptake capabilities.
Chemical communications (Cambridge, England), 2016, 52, 12988-12991
7125095 CIFC20 H26 N O4P 1 21/n 16.1031; 11.4651; 26.396
90; 95.114; 90
1839.6Zhang, Hang; Wang, Bo; Yi, Heng; Sun, Tong; Zhang, Yan; Wang, Jianbo
Transition-metal-free three-component reaction of cyclopropenes, aldehydes and amines.
Chemical communications (Cambridge, England), 2016, 52, 13285-13287
7125096 CIFC144 H232 Sn10P -114.287; 15.4; 16.699
102.618; 97.963; 99.865
3472.7Wiederkehr, J.; Wölper, C; Schulz, S.
Synthesis and solid state structure of a metalloid tin cluster [Sn<sub>10</sub>(trip<sub>8</sub>)].
Chemical communications (Cambridge, England), 2016, 52, 12282-12285
7125097 CIFC44 H64 Mg N2P 21 21 219.0942; 20.5821; 21.2116
90; 90; 90
3970.3Wiederkehr, J.; Wölper, C; Schulz, S.
Synthesis and solid state structure of a metalloid tin cluster [Sn<sub>10</sub>(trip<sub>8</sub>)].
Chemical communications (Cambridge, England), 2016, 52, 12282-12285
7125098 CIFC38 H52 Mg N2P 21 21 2111.2579; 16.4458; 18.2926
90; 90; 90
3386.79Wiederkehr, J.; Wölper, C; Schulz, S.
Synthesis and solid state structure of a metalloid tin cluster [Sn<sub>10</sub>(trip<sub>8</sub>)].
Chemical communications (Cambridge, England), 2016, 52, 12282-12285
7125099 CIFC15 H24 O3P 1 21 19.9792; 6.6848; 10.2099
90; 96.735; 90
676.39Li, Fu-Zhuo; Li, Shuang; Zhang, Peng-Peng; Huang, Zhi-Hui; Zhang, Wei-Bin; Gong, Jianxian; Yang, Zhen
A chiral pool approach for asymmetric syntheses of (-)-antrocin, (+)-asperolide C, and (-)-trans-ozic acid.
Chemical communications (Cambridge, England), 2016, 52, 12426-12429
7125100 CIFC54 H64 B2 Mg O8P 1 21/n 111.3567; 12.2346; 18.4353
90; 108.188; 90
2433.5Mukherjee, Debabrata; Shirase, Satoru; Spaniol, Thomas P.; Mashima, Kazushi; Okuda, Jun
Magnesium hydridotriphenylborate [Mg(thf)<sub>6</sub>][HBPh<sub>3</sub>]<sub>2</sub>: a versatile hydroboration catalyst.
Chemical communications (Cambridge, England), 2016, 52, 13155-13158
7125101 CIFC15 H25 N O3P 1 21/n 111.3879; 10.6012; 12.1055
90; 98.506; 90
1445.37Ho, Guo-Ming; Li, Yu-Jang
Stereoselective synthesis of 2,3,4-highly substituted oxetanes by intramolecular C-C bond forming Michael addition.
Chemical communications (Cambridge, England), 2016, 52, 12108-12111
7125102 CIFC13 H39 N24 O13P -111.1811; 11.6175; 14.5096
70.505; 78.122; 74.189
1695.7Zhang, Cheng; Chang, Sailan; Qiu, Lihua; Xu, Xinfang
Chemodivergent synthesis of multi-substituted/fused pyrroles via copper-catalyzed carbene cascade reaction of propargyl α-iminodiazoacetates.
Chemical communications (Cambridge, England), 2016, 52, 12470-12473
7125103 CIFC19 H13 N O4P 1 21/n 110.7549; 7.0492; 19.1664
90; 102.5; 90
1418.63Zhang, Cheng; Chang, Sailan; Qiu, Lihua; Xu, Xinfang
Chemodivergent synthesis of multi-substituted/fused pyrroles via copper-catalyzed carbene cascade reaction of propargyl α-iminodiazoacetates.
Chemical communications (Cambridge, England), 2016, 52, 12470-12473
7125104 CIFC23 H21 N O3P -18.6755; 10.6916; 11.439
69.968; 73.363; 72.428
930.3Zhang, Cheng; Chang, Sailan; Qiu, Lihua; Xu, Xinfang
Chemodivergent synthesis of multi-substituted/fused pyrroles via copper-catalyzed carbene cascade reaction of propargyl α-iminodiazoacetates.
Chemical communications (Cambridge, England), 2016, 52, 12470-12473
7125105 CIFC20 H16 Br N O3P 1 21/c 14.288; 27.2739; 14.6976
90; 90.213; 90
1718.9Zhang, Cheng; Chang, Sailan; Qiu, Lihua; Xu, Xinfang
Chemodivergent synthesis of multi-substituted/fused pyrroles via copper-catalyzed carbene cascade reaction of propargyl α-iminodiazoacetates.
Chemical communications (Cambridge, England), 2016, 52, 12470-12473
7125106 CIFC31 H55 Co Fe P5 SiP -110.1595; 12.5137; 15.7867
100.375; 100.066; 108.045
1819.16Mädl, Eric; Peresypkina, Eugenia; Timoshkin, Alexey Y.; Scheer, Manfred
Triple-decker sandwich complexes with a bent cyclo-P<sub>5</sub> middle-deck.
Chemical communications (Cambridge, England), 2016, 52, 12298-12301
7125107 CIFC29 H50 Co Fe N P5P 1 21/n 112.73; 15.579; 17.3044
90; 108.258; 90
3259.05Mädl, Eric; Peresypkina, Eugenia; Timoshkin, Alexey Y.; Scheer, Manfred
Triple-decker sandwich complexes with a bent cyclo-P<sub>5</sub> middle-deck.
Chemical communications (Cambridge, England), 2016, 52, 12298-12301
7125108 CIFC29 H50 Fe N Ni P5P 1 21/n 112.7483; 15.4746; 17.3699
90; 107.71; 90
3264.25Mädl, Eric; Peresypkina, Eugenia; Timoshkin, Alexey Y.; Scheer, Manfred
Triple-decker sandwich complexes with a bent cyclo-P<sub>5</sub> middle-deck.
Chemical communications (Cambridge, England), 2016, 52, 12298-12301
7125109 CIFC29 H50 Fe2 N P5P 1 21/c 117.2557; 12.4359; 16.6796
90; 114.972; 90
3244.67Mädl, Eric; Peresypkina, Eugenia; Timoshkin, Alexey Y.; Scheer, Manfred
Triple-decker sandwich complexes with a bent cyclo-P<sub>5</sub> middle-deck.
Chemical communications (Cambridge, England), 2016, 52, 12298-12301
7125110 CIFC31 H55 Cr Fe P5 SiP 1 21/c 119.9256; 11.6275; 16.4157
90; 106.491; 90
3646.82Mädl, Eric; Peresypkina, Eugenia; Timoshkin, Alexey Y.; Scheer, Manfred
Triple-decker sandwich complexes with a bent cyclo-P<sub>5</sub> middle-deck.
Chemical communications (Cambridge, England), 2016, 52, 12298-12301
7125111 CIFC31 H55 Co F6 Fe P6 SiP 1 21/n 114.9545; 16.8539; 15.7381
90; 98.016; 90
3927.9Mädl, Eric; Peresypkina, Eugenia; Timoshkin, Alexey Y.; Scheer, Manfred
Triple-decker sandwich complexes with a bent cyclo-P<sub>5</sub> middle-deck.
Chemical communications (Cambridge, England), 2016, 52, 12298-12301
7125112 CIFC50 H60 B2 N2P b c n12.89; 9.6595; 16.653
90; 90; 90
2073.5Yuan, Ningning; Wang, Wenqing; Wu, Ziye; Chen, Sheng; Tan, Gengwen; Sui, Yunxia; Wang, Xinping; Jiang, Jun; Power, Philip P.
A boron-centered radical: a potassium-crown ether stabilized boryl radical anion.
Chemical communications (Cambridge, England), 2016, 52, 12714-12716
7125113 CIFC41 H62 B K N O7P 1 21 18.243; 20.22; 12.5726
90; 101.097; 90
2056.3Yuan, Ningning; Wang, Wenqing; Wu, Ziye; Chen, Sheng; Tan, Gengwen; Sui, Yunxia; Wang, Xinping; Jiang, Jun; Power, Philip P.
A boron-centered radical: a potassium-crown ether stabilized boryl radical anion.
Chemical communications (Cambridge, England), 2016, 52, 12714-12716
7125114 CIFC60 H93 Cd3 Ce I6 N6 O11 P2P 1 21/c 126.1665; 15.2608; 23.2073
90; 114.863; 90
8408.3Li, Quan-Wen; Wan, Rui-Chen; Chen, Yan-Cong; Liu, Jun-Liang; Wang, Long-Fei; Jia, Jian-Hua; Chilton, Nicholas F.; Tong, Ming-Liang
Unprecedented hexagonal bipyramidal single-ion magnets based on metallacrowns.
Chemical communications (Cambridge, England), 2016, 52, 13365-13368
7125115 CIFC60 H93 Cd3 I6 N6 Nd O11 P2P 1 21/c 126.2751; 15.2788; 23.1448
90; 114.769; 90
8436.7Li, Quan-Wen; Wan, Rui-Chen; Chen, Yan-Cong; Liu, Jun-Liang; Wang, Long-Fei; Jia, Jian-Hua; Chilton, Nicholas F.; Tong, Ming-Liang
Unprecedented hexagonal bipyramidal single-ion magnets based on metallacrowns.
Chemical communications (Cambridge, England), 2016, 52, 13365-13368
7125116 CIFC12 H8 F2 O SP -16.924; 8.665; 8.772
108.778; 94.634; 90.55
496.3Tsao, Fu An; Waked, Alexander E.; Cao, Levy; Hofmann, Jordan; Liu, Lei; Grimme, Stefan; Stephan, Douglas W.
S(vi) Lewis acids: fluorosulfoxonium cations.
Chemical communications (Cambridge, England), 2016, 52, 12418-12421
7125117 CIFC37 H12 B F21 O SP n a 2114.6347; 9.785; 23.547
90; 90; 90
3371.9Tsao, Fu An; Waked, Alexander E.; Cao, Levy; Hofmann, Jordan; Liu, Lei; Grimme, Stefan; Stephan, Douglas W.
S(vi) Lewis acids: fluorosulfoxonium cations.
Chemical communications (Cambridge, England), 2016, 52, 12418-12421
7125118 CIFC36 H10 B F21 O SP b c a15.099; 18.8792; 23.143
90; 90; 90
6597.1Tsao, Fu An; Waked, Alexander E.; Cao, Levy; Hofmann, Jordan; Liu, Lei; Grimme, Stefan; Stephan, Douglas W.
S(vi) Lewis acids: fluorosulfoxonium cations.
Chemical communications (Cambridge, England), 2016, 52, 12418-12421
7125119 CIFC24 H8 B0.5 F11 O SC 1 2/c 125.433; 8.7969; 18.856
90; 97.15; 90
4185.9Tsao, Fu An; Waked, Alexander E.; Cao, Levy; Hofmann, Jordan; Liu, Lei; Grimme, Stefan; Stephan, Douglas W.
S(vi) Lewis acids: fluorosulfoxonium cations.
Chemical communications (Cambridge, England), 2016, 52, 12418-12421
7125120 CIFC12 H8 B F5 O SP 1 21/n 16.9113; 10.7857; 16.5078
90; 99.049; 90
1215.2Tsao, Fu An; Waked, Alexander E.; Cao, Levy; Hofmann, Jordan; Liu, Lei; Grimme, Stefan; Stephan, Douglas W.
S(vi) Lewis acids: fluorosulfoxonium cations.
Chemical communications (Cambridge, England), 2016, 52, 12418-12421
7125121 CIFC30 H55 Au3 Co2 N6 O18 S6 ZnI 2 2 210.307; 18.544; 27.144
90; 90; 90
5188Surinwong, Sireenart; Yoshinari, Nobuto; Kojima, Tatsuhiro; Konno, Takumi
A drastic change in the superhydrophilic crystal porosities of metallosupramolecular structures via a slight change in pH.
Chemical communications (Cambridge, England), 2016, 52, 12893-12896
7125122 CIFC94 H168 Au9 Co6 N18 Na2 O50 S18 ZnP 61 2 244.2485; 44.2485; 28.4446
90; 90; 120
48231.1Surinwong, Sireenart; Yoshinari, Nobuto; Kojima, Tatsuhiro; Konno, Takumi
A drastic change in the superhydrophilic crystal porosities of metallosupramolecular structures via a slight change in pH.
Chemical communications (Cambridge, England), 2016, 52, 12893-12896
7125123 CIFC29 H80 B20 Cl2 N4 O P2P -111.8867; 12.3732; 16.807
92.305; 91.809; 98.884
2438.5Wong, Yuen Onn; Smith, Mark D.; Peryshkov, Dmitry V.
Reversible water activation driven by contraction and expansion of a 12-vertex-closo-12-vertex-nido biscarborane cluster.
Chemical communications (Cambridge, England), 2016, 52, 12710-12713
7125124 CIFC30 H81 B20 N5 O P2P n a 2144.006; 9.8902; 22.5051
90; 90; 90
9794.9Wong, Yuen Onn; Smith, Mark D.; Peryshkov, Dmitry V.
Reversible water activation driven by contraction and expansion of a 12-vertex-closo-12-vertex-nido biscarborane cluster.
Chemical communications (Cambridge, England), 2016, 52, 12710-12713
7125125 CIFC62 H80 O2 Sn2P 1 21/n 113.542; 13.931; 14.562
90; 97.201; 90
2725.5Erickson, Jeremy D.; Lai, Ting Yi; Liptrot, David J.; Olmstead, Marilyn M.; Power, Philip P.
Catalytic dehydrocoupling of amines and boranes by an incipient tin(ii) hydride.
Chemical communications (Cambridge, England), 2016, 52, 13656-13659
7125126 CIFC59 H69 N Sn2C 1 2/c 125.5341; 22.081; 21.1566
90; 122.336; 90
10078.7Erickson, Jeremy D.; Lai, Ting Yi; Liptrot, David J.; Olmstead, Marilyn M.; Power, Philip P.
Catalytic dehydrocoupling of amines and boranes by an incipient tin(ii) hydride.
Chemical communications (Cambridge, England), 2016, 52, 13656-13659
7125127 CIFC40 H40 B P3 PdP 1 21/c 110.6783; 18.823; 17.516
90; 97.699; 90
3488.9Schuhknecht, Danny; Ritter, Florian; Tauchert, Michael E.
Isolation and properties of a palladium PBP pincer complex featuring an ambiphilic boryl site.
Chemical communications (Cambridge, England), 2016, 52, 11823-11826
7125128 CIFC32 H30 Cl2 I2 N P PdP -19.0882; 10.5044; 16.7224
82.47; 80.174; 86.84
1558.56Schuhknecht, Danny; Ritter, Florian; Tauchert, Michael E.
Isolation and properties of a palladium PBP pincer complex featuring an ambiphilic boryl site.
Chemical communications (Cambridge, England), 2016, 52, 11823-11826
7125129 CIFC46 H45 B I N P2 PdP 1 21/c 18.8638; 22.432; 19.469
90; 94.012; 90
3861.6Schuhknecht, Danny; Ritter, Florian; Tauchert, Michael E.
Isolation and properties of a palladium PBP pincer complex featuring an ambiphilic boryl site.
Chemical communications (Cambridge, England), 2016, 52, 11823-11826
7125130 CIFC36 H28 B I P2 PdF d d 218.47; 31.893; 10.3482
90; 90; 90
6095.7Schuhknecht, Danny; Ritter, Florian; Tauchert, Michael E.
Isolation and properties of a palladium PBP pincer complex featuring an ambiphilic boryl site.
Chemical communications (Cambridge, England), 2016, 52, 11823-11826
7125131 CIFC66 H55 B I N O2 P2 PdP 1 21/c 115.188; 20.733; 18.38
90; 109.077; 90
5469.9Schuhknecht, Danny; Ritter, Florian; Tauchert, Michael E.
Isolation and properties of a palladium PBP pincer complex featuring an ambiphilic boryl site.
Chemical communications (Cambridge, England), 2016, 52, 11823-11826
7125132 CIFC24 H42 B O6 P Si2 WC 1 2/c 119.042; 9.093; 35.451
90; 94.657; 90
6118Kyri, A. W.; Kunzmann, R.; Schnakenburg, G.; Qu, Z.-W.; Grimme, S.; Streubel, R.
Synthesis of a monomolecular anionic FLP complex.
Chemical communications (Cambridge, England), 2016, 52, 13361-13364
7125133 CIFC14 H23 O6 P Si2 WP 21 21 219.7786; 9.9521; 21.9977
90; 90; 90
2140.76Kyri, A. W.; Kunzmann, R.; Schnakenburg, G.; Qu, Z.-W.; Grimme, S.; Streubel, R.
Synthesis of a monomolecular anionic FLP complex.
Chemical communications (Cambridge, England), 2016, 52, 13361-13364
7125134 CIFC22 H24 B10P -19.52; 13.825; 17.646
88.713; 88.594; 79.932
2285.6Tu, Deshuang; Leong, Pakkin; Li, Zhihong; Hu, Rongrong; Shi, Chao; Zhang, Kenneth Yin; Yan, Hong; Zhao, Qiang
A carborane-triggered metastable charge transfer state leading to spontaneous recovery of mechanochromic luminescence.
Chemical communications (Cambridge, England), 2016, 52, 12494-12497
7125135 CIFC23 H26 B10P 1 21/n 17.684; 23.434; 12.637
90; 94.433; 90
2268.7Tu, Deshuang; Leong, Pakkin; Li, Zhihong; Hu, Rongrong; Shi, Chao; Zhang, Kenneth Yin; Yan, Hong; Zhao, Qiang
A carborane-triggered metastable charge transfer state leading to spontaneous recovery of mechanochromic luminescence.
Chemical communications (Cambridge, England), 2016, 52, 12494-12497
7125136 CIFC H BP 1 21/c 115.683; 13.493; 11.675
90; 108.429; 90
2343.9Tu, Deshuang; Leong, Pakkin; Li, Zhihong; Hu, Rongrong; Shi, Chao; Zhang, Kenneth Yin; Yan, Hong; Zhao, Qiang
A carborane-triggered metastable charge transfer state leading to spontaneous recovery of mechanochromic luminescence.
Chemical communications (Cambridge, England), 2016, 52, 12494-12497
7125137 CIFC25 H15 Cl O4P 21 21 216.3385; 15.072; 20.735
90; 90; 90
1980.9Liu, Yang; Li, Jiangtao; Ye, Xinyi; Zhao, Xiaowei; Jiang, Zhiyong
Organocatalytic asymmetric formal arylation of benzofuran-2(3H)-ones with cooperative visible light photocatalysis.
Chemical communications (Cambridge, England), 2016, 52, 13955-13958
7125138 CIFC26 H18 O5P 1 21 19.903; 6.3446; 16.4435
90; 94.703; 90
1029.68Liu, Yang; Li, Jiangtao; Ye, Xinyi; Zhao, Xiaowei; Jiang, Zhiyong
Organocatalytic asymmetric formal arylation of benzofuran-2(3H)-ones with cooperative visible light photocatalysis.
Chemical communications (Cambridge, England), 2016, 52, 13955-13958
7125139 CIFC31 H20 O4P 1 21 111.1942; 6.6554; 16.7572
90; 108.366; 90
1184.85Liu, Yang; Li, Jiangtao; Ye, Xinyi; Zhao, Xiaowei; Jiang, Zhiyong
Organocatalytic asymmetric formal arylation of benzofuran-2(3H)-ones with cooperative visible light photocatalysis.
Chemical communications (Cambridge, England), 2016, 52, 13955-13958
7125140 CIFC84 H114 Cl3 Ir3 N12 Si3P 1 21/c 120.9974; 14.9781; 31.1032
90; 94.152; 90
9756.3Olaru, Alexandra M.; Burt, Alister; Rayner, Peter J.; Hart, Sam J.; Whitwood, Adrian C.; Green, Gary G. R.; Duckett, Simon B.
Using signal amplification by reversible exchange (SABRE) to hyperpolarise <sup>119</sup>Sn and <sup>29</sup>Si NMR nuclei.
Chemical communications (Cambridge, England), 2016, 52, 14482-14485
7125141 CIFC89.42 H141.68 Cl3 Ir3 N12 O5.42 Si3P a -327.98535; 27.98535; 27.98535
90; 90; 90
21917.6Olaru, Alexandra M.; Burt, Alister; Rayner, Peter J.; Hart, Sam J.; Whitwood, Adrian C.; Green, Gary G. R.; Duckett, Simon B.
Using signal amplification by reversible exchange (SABRE) to hyperpolarise <sup>119</sup>Sn and <sup>29</sup>Si NMR nuclei.
Chemical communications (Cambridge, England), 2016, 52, 14482-14485

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