Crystallography Open Database

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7124742 CIFC93 H55 Cl6 N O13P -112.0893; 17.1939; 24.6711
104.88; 90.051; 98.347		4899.8Hisaki, Ichiro; Nakagawa, Shoichi; Sato, Hiroyasu; Tohnai, Norimitsu
Alignment of paired molecules of C60 within a hexagonal platform networked through hydrogen-bonds.
Chemical communications (Cambridge, England), 2016, 52, 9781-9784
7124743 CIFC18 H23 Cl2 N O2 RuP 1 21/n 113.7506; 7.06591; 19.8176
90; 109.476; 90		1815.31Ma, Lili; Ma, Rong; Wang, Zhigang; Yiu, Shek-Man; Zhu, Guangyu
Heterodinuclear Pt(iv)-Ru(ii) anticancer prodrugs to combat both drug resistance and tumor metastasis.
Chemical communications (Cambridge, England), 2016, 52, 10735-10738
7124744 CIFC9.5 H20 Cl3 N3 O4 Pt S0.5P -18.8701; 12.497; 17.2431
92.445; 103.722; 104.921		1783.24Ma, Lili; Ma, Rong; Wang, Zhigang; Yiu, Shek-Man; Zhu, Guangyu
Heterodinuclear Pt(iv)-Ru(ii) anticancer prodrugs to combat both drug resistance and tumor metastasis.
Chemical communications (Cambridge, England), 2016, 52, 10735-10738
7124745 CIFC28 H46 Ir O2 P3P 1 21/c 112.8054; 12.7662; 20.774
90; 104.821; 90		3283.1Paul, Ursula S. D.; Braunschweig, Holger; Radius, Udo
Iridium-catalysed dehydrocoupling of aryl phosphine-borane adducts: synthesis and characterisation of high molecular weight poly(phosphinoboranes).
Chemical communications (Cambridge, England), 2016, 52, 8573-8576
7124746 CIFC29 H48 Ir O2 P3P -110.2215; 11.864; 16.0253
103.712; 100.633; 93.622		1843.9Paul, Ursula S. D.; Braunschweig, Holger; Radius, Udo
Iridium-catalysed dehydrocoupling of aryl phosphine-borane adducts: synthesis and characterisation of high molecular weight poly(phosphinoboranes).
Chemical communications (Cambridge, England), 2016, 52, 8573-8576
7124747 CIFC31 H52 Ir O2 P3C 1 2/c 110.5197; 20.993; 30.334
90; 99.463; 90		6607.8Paul, Ursula S. D.; Braunschweig, Holger; Radius, Udo
Iridium-catalysed dehydrocoupling of aryl phosphine-borane adducts: synthesis and characterisation of high molecular weight poly(phosphinoboranes).
Chemical communications (Cambridge, England), 2016, 52, 8573-8576
7124748 CIFC28 H48 Ir O2 P3P 1 21/c 112.8121; 12.7747; 20.771
90; 104.573; 90		3290.2Paul, Ursula S. D.; Braunschweig, Holger; Radius, Udo
Iridium-catalysed dehydrocoupling of aryl phosphine-borane adducts: synthesis and characterisation of high molecular weight poly(phosphinoboranes).
Chemical communications (Cambridge, England), 2016, 52, 8573-8576
7124749 CIFC29 H50 Ir O2 P3P -110.23; 11.9105; 15.9818
103.735; 100.957; 93.714		1844.8Paul, Ursula S. D.; Braunschweig, Holger; Radius, Udo
Iridium-catalysed dehydrocoupling of aryl phosphine-borane adducts: synthesis and characterisation of high molecular weight poly(phosphinoboranes).
Chemical communications (Cambridge, England), 2016, 52, 8573-8576
7124750 CIFC36 H66 Ir O2 P3P -110.901; 12.686; 15.2272
78.184; 72.973; 73.418		1912.8Paul, Ursula S. D.; Braunschweig, Holger; Radius, Udo
Iridium-catalysed dehydrocoupling of aryl phosphine-borane adducts: synthesis and characterisation of high molecular weight poly(phosphinoboranes).
Chemical communications (Cambridge, England), 2016, 52, 8573-8576
7124751 CIFC40 H30 N2 O2P -17.2874; 14.4206; 15.0229
64.011; 79.684; 83.373		1394.93Das, Amrita; Ghosh, Indrajit; König, Burkhard
Synthesis of pyrrolo[1,2-a]quinolines and ullazines by visible light mediated one- and twofold annulation of N-arylpyrroles with arylalkynes.
Chemical communications (Cambridge, England), 2016, 52, 8695-8698
7124752 CIFC20 H14 Cl N OP 1 21/c 116.4245; 7.25848; 13.1153
90; 108.39; 90		1483.72Das, Amrita; Ghosh, Indrajit; König, Burkhard
Synthesis of pyrrolo[1,2-a]quinolines and ullazines by visible light mediated one- and twofold annulation of N-arylpyrroles with arylalkynes.
Chemical communications (Cambridge, England), 2016, 52, 8695-8698
7124753 CIFC25 H24 Cl N3 OP 21 21 2110.3206; 11.6585; 18.3971
90; 90; 90		2213.59Ma, Jiajia; Harms, Klaus; Meggers, Eric
Enantioselective rhodium/ruthenium photoredox catalysis en route to chiral 1,2-aminoalcohols.
Chemical communications (Cambridge, England), 2016, 52, 10183-10186
7124754 CIFC48.4 H49.6 Cl2 F6 N4 O P Rh S2P -117.1583; 17.7095; 18.8292
66.918; 69.054; 76.796		4889.7Ma, Jiajia; Harms, Klaus; Meggers, Eric
Enantioselective rhodium/ruthenium photoredox catalysis en route to chiral 1,2-aminoalcohols.
Chemical communications (Cambridge, England), 2016, 52, 10183-10186
7124755 CIFC16 H46 Mo2 N2 Ni2 O16P 1 21/n 112.0683; 10.1464; 12.6315
90; 91.893; 90		1545.88Kuznetsov, Denis A.; Konev, Dmitry V.; Komarova, Natal'ya S.; Ionov, Andrey M.; Mozhchil, Rais N.; Fedyanin, Ivan V.
Ni-based heterogeneous catalyst from a designed molecular precursor for the efficient electrochemical water oxidation.
Chemical communications (Cambridge, England), 2016, 52, 9255-9258
7124756 CIFC106 H74.5 B3.5 F13.88 I0.5 N21 O4 Pd2C 1 2/c 142.9184; 20.7337; 28.9827
90; 125.086; 90		21104.1Li, Yu-Hao; Jiang, Ji-Jun; Fan, Yan-Zhong; Wei, Zhang-Wen; Chen, Cheng-Xia; Yu, Hui-Juan; Zheng, Shao-Ping; Fenske, Dieter; Su, Cheng-Yong; Barboiu, Mihail
Solvent- and anion-induced interconversions of metal-organic cages.
Chemical communications (Cambridge, England), 2016, 52, 8745-8748
7124757 CIFC98 H75 B4 F16 N17 O4 Pd2C 1 2/c 143.0462; 20.744; 28.9748
90; 125.766; 90		20993.7Li, Yu-Hao; Jiang, Ji-Jun; Fan, Yan-Zhong; Wei, Zhang-Wen; Chen, Cheng-Xia; Yu, Hui-Juan; Zheng, Shao-Ping; Fenske, Dieter; Su, Cheng-Yong; Barboiu, Mihail
Solvent- and anion-induced interconversions of metal-organic cages.
Chemical communications (Cambridge, England), 2016, 52, 8745-8748
7124758 CIFC106 H56 N6 O2P -116.792; 19.978; 23.171
102.93; 101.11; 112.55		6654Burgun, Alexandre; Valente, Peter; Evans, Jack D.; Huang, David M.; Sumby, Christopher J.; Doonan, Christian J.
Endohedrally functionalised porous organic cages.
Chemical communications (Cambridge, England), 2016, 52, 8850-8853
7124759 CIFC110 H60 N2 O2P b c n31.58; 18.296; 20.075
90; 90; 90		11599Burgun, Alexandre; Valente, Peter; Evans, Jack D.; Huang, David M.; Sumby, Christopher J.; Doonan, Christian J.
Endohedrally functionalised porous organic cages.
Chemical communications (Cambridge, England), 2016, 52, 8850-8853
7124760 CIFC116 H66 N2 O2I 41/a c d :239.28; 39.28; 39.78
90; 90; 90		61377Burgun, Alexandre; Valente, Peter; Evans, Jack D.; Huang, David M.; Sumby, Christopher J.; Doonan, Christian J.
Endohedrally functionalised porous organic cages.
Chemical communications (Cambridge, England), 2016, 52, 8850-8853
7124761 CIFC17 H21 N O3P -18.0877; 8.9461; 10.5339
93.626; 92.834; 94.652		756.99Kaishap, Partha Pratim; Sarma, Bipul; Gogoi, Sanjib
The amide C-N bond of isatins as the directing group and the internal oxidant in Ru-catalyzed C-H activation and annulation reactions: access to 8-amido isocoumarins.
Chemical communications (Cambridge, England), 2016, 52, 9809-9812
7124762 CIFC798 H638 Ca17 N72 O322P 1 21/c 144.593; 51.642; 38.959
90; 107.1; 90		85751Mandal, Pradeep K.; Kauffmann, Brice; Destecroix, Harry; Ferrand, Yann; Davis, Anthony P.; Huc, Ivan
Crystal structure of a complex between β-glucopyranose and a macrocyclic receptor with dendritic multicharged water solubilizing chains.
Chemical communications (Cambridge, England), 2016, 52, 9355-9358
7124763 CIFC54 H72 Br N9 O8P 1 21/n 112.865; 18.623; 22.483
90; 90.143; 90		5387Kim, Ajeong; Ali, Rashid; Park, Seok Ho; Kim, Yong-Hoon; Park, Jung Su
Probing and evaluating anion-π interaction in meso-dinitrophenyl functionalized calix[4]pyrrole isomers.
Chemical communications (Cambridge, England), 2016, 52, 11139-11142
7124764 CIFC54 H72 Cl N9 O8P 1 21/n 113.0109; 18.833; 22.702
90; 90.423; 90		5562.6Kim, Ajeong; Ali, Rashid; Park, Seok Ho; Kim, Yong-Hoon; Park, Jung Su
Probing and evaluating anion-π interaction in meso-dinitrophenyl functionalized calix[4]pyrrole isomers.
Chemical communications (Cambridge, England), 2016, 52, 11139-11142
7124765 CIFC54 H72 I N9 O8P c a 2121.335; 15.168; 37.948
90; 90; 90		12280Kim, Ajeong; Ali, Rashid; Park, Seok Ho; Kim, Yong-Hoon; Park, Jung Su
Probing and evaluating anion-π interaction in meso-dinitrophenyl functionalized calix[4]pyrrole isomers.
Chemical communications (Cambridge, England), 2016, 52, 11139-11142
7124766 CIFC54 H72 Cl0.63 F0.37 N9 O8P 1 21/n 112.9168; 18.9009; 22.5896
90; 90.65; 90		5514.7Kim, Ajeong; Ali, Rashid; Park, Seok Ho; Kim, Yong-Hoon; Park, Jung Su
Probing and evaluating anion-π interaction in meso-dinitrophenyl functionalized calix[4]pyrrole isomers.
Chemical communications (Cambridge, England), 2016, 52, 11139-11142
7124767 CIFC72 H116 Cl3 N10 O18 P2P -118.5581; 19.3272; 23.1017
86.218; 87.845; 81.721		8178.5Kim, Ajeong; Ali, Rashid; Park, Seok Ho; Kim, Yong-Hoon; Park, Jung Su
Probing and evaluating anion-π interaction in meso-dinitrophenyl functionalized calix[4]pyrrole isomers.
Chemical communications (Cambridge, England), 2016, 52, 11139-11142
7124768 CIFC58 H60 Cl6 N10 O14P -111.224; 13.636; 22.374
101.011; 98.751; 91.381		3317Kim, Ajeong; Ali, Rashid; Park, Seok Ho; Kim, Yong-Hoon; Park, Jung Su
Probing and evaluating anion-π interaction in meso-dinitrophenyl functionalized calix[4]pyrrole isomers.
Chemical communications (Cambridge, England), 2016, 52, 11139-11142
7124769 CIFC70 H110 N10 O16 S2P 1 21/n 114.239; 21.245; 24.51
90; 92.19; 90		7409Kim, Ajeong; Ali, Rashid; Park, Seok Ho; Kim, Yong-Hoon; Park, Jung Su
Probing and evaluating anion-π interaction in meso-dinitrophenyl functionalized calix[4]pyrrole isomers.
Chemical communications (Cambridge, England), 2016, 52, 11139-11142
7124770 CIFC54 H72 N10 O11P 1 21/n 112.8705; 18.6776; 23.141
90; 90.418; 90		5562.7Kim, Ajeong; Ali, Rashid; Park, Seok Ho; Kim, Yong-Hoon; Park, Jung Su
Probing and evaluating anion-π interaction in meso-dinitrophenyl functionalized calix[4]pyrrole isomers.
Chemical communications (Cambridge, England), 2016, 52, 11139-11142
7124771 CIFC56 H75 N9 O10P 1 21/n 112.773; 19.067; 23.221
90; 91.69; 90		5653Kim, Ajeong; Ali, Rashid; Park, Seok Ho; Kim, Yong-Hoon; Park, Jung Su
Probing and evaluating anion-π interaction in meso-dinitrophenyl functionalized calix[4]pyrrole isomers.
Chemical communications (Cambridge, England), 2016, 52, 11139-11142
7124772 CIFC87 H129 N4 O16 Zn2P -114.3039; 17.603; 20.104
64.648; 74.715; 86.046		4407.1Gonawala, Sunalee; Leopoldino, Verônica R; Kpogo, Kenneth; Verani, Cláudio N
Langmuir-Blodgett films of salophen-based metallosurfactants as surface pretreatment coatings for corrosion mitigation.
Chemical communications (Cambridge, England), 2016, 52, 11155-11158
7124773 CIFC44 H28 Br4 N8 O12 Pb4 PdP -17.634; 13.084; 14.166
105.216; 105.376; 94.884		1298.1Dong, Ying; Li, Yue; Wei, Yong-Liang; Wang, Jian-Cheng; Ma, Jian-Ping; Ji, Jun; Yao, Bing-Jian; Dong, Yu-Bin
A N-heterocyclic tetracarbene Pd(ii) moiety containing a Pd(ii)-Pb(ii) bimetallic MOF for three-component cyclotrimerization via benzyne.
Chemical communications (Cambridge, England), 2016, 52, 10505-10508
7124774 CIFC126 H250 N10 O102 S4 V24I -4 3 m21.927; 21.927; 21.927
90; 90; 90		10542Zhang, Yu-Teng; Wang, Xin-Long; Li, Shuang-Bao; Gong, Ya-Ru; Song, Bai-Qiao; Shao, Kui-Zhan; Su, Zhong-Min
Anderson-like alkoxo-polyoxovanadate clusters serving as unprecedented second building units to construct metal-organic polyhedra.
Chemical communications (Cambridge, England), 2016, 52, 9632-9635
7124775 CIFC123.5 H250.5 N15.5 O101.5 S4 V24I -4 3 m21.841; 21.841; 21.841
90; 90; 90		10419Zhang, Yu-Teng; Wang, Xin-Long; Li, Shuang-Bao; Gong, Ya-Ru; Song, Bai-Qiao; Shao, Kui-Zhan; Su, Zhong-Min
Anderson-like alkoxo-polyoxovanadate clusters serving as unprecedented second building units to construct metal-organic polyhedra.
Chemical communications (Cambridge, England), 2016, 52, 9632-9635
7124776 CIFC121 H152 Br6 O101 S4 V24I -4 3 m22.108; 22.108; 22.108
90; 90; 90		10806Zhang, Yu-Teng; Wang, Xin-Long; Li, Shuang-Bao; Gong, Ya-Ru; Song, Bai-Qiao; Shao, Kui-Zhan; Su, Zhong-Min
Anderson-like alkoxo-polyoxovanadate clusters serving as unprecedented second building units to construct metal-organic polyhedra.
Chemical communications (Cambridge, England), 2016, 52, 9632-9635
7124777 CIFC106.5 H221.5 N8.5 O100.5 S4 V24I -421.848; 21.848; 19.081
90; 90; 90		9108Zhang, Yu-Teng; Wang, Xin-Long; Li, Shuang-Bao; Gong, Ya-Ru; Song, Bai-Qiao; Shao, Kui-Zhan; Su, Zhong-Min
Anderson-like alkoxo-polyoxovanadate clusters serving as unprecedented second building units to construct metal-organic polyhedra.
Chemical communications (Cambridge, England), 2016, 52, 9632-9635
7124778 CIFC183.5 H280.5 N9.5 O101.5 S4 V24I -428.983; 28.983; 25.744
90; 90; 90		21625Zhang, Yu-Teng; Wang, Xin-Long; Li, Shuang-Bao; Gong, Ya-Ru; Song, Bai-Qiao; Shao, Kui-Zhan; Su, Zhong-Min
Anderson-like alkoxo-polyoxovanadate clusters serving as unprecedented second building units to construct metal-organic polyhedra.
Chemical communications (Cambridge, England), 2016, 52, 9632-9635
7124779 CIFC48 H69 N O6 Si2P 21 21 2110.50766; 14.738; 35.4339
90; 90; 90		5487.36Gan, Zubao; Chu, Zhiwen; Hu, Jia; Su, Zhishan; Hu, Changwei; Gao, Lu; Song, Zhenlei
Tunable reactivity of geminal bis(silyl) enol derivatives leading to selective exo-IEDDA or Sakurai allylation with a β,γ-unsaturated ketoester.
Chemical communications (Cambridge, England), 2016, 52, 10137-10140
7124780 CIFC226 H226 Cl16 F24 N26 O68 Pd4 S8P -117.8945; 19.5103; 20.507
90.134; 99.808; 110.635		6587.2Szalóki, György; Croué, Vincent; Allain, Magali; Goeb, Sébastien; Sallé, Marc
Neutral versus polycationic coordination cages: a comparison regarding neutral guest inclusion.
Chemical communications (Cambridge, England), 2016, 52, 10012-10015
7124781 CIFC210 H199 Cl16 F24 N21 O32 Pd4 S8P 1 21/c 116.3201; 29.0112; 27.2545
90; 105.883; 90		12411.4Szalóki, György; Croué, Vincent; Allain, Magali; Goeb, Sébastien; Sallé, Marc
Neutral versus polycationic coordination cages: a comparison regarding neutral guest inclusion.
Chemical communications (Cambridge, England), 2016, 52, 10012-10015
7124782 CIFC21 H28 B2 F8 N2 O2P -16.8103; 12.0335; 15.7289
70.566; 78.711; 88.033		1191.39Catalán, Aldo C; Tiburcio, Jorge
Self-assembly of pseudo-rotaxane and rotaxane complexes using an electrostatic slippage approach.
Chemical communications (Cambridge, England), 2016, 52, 9526-9529
7124783 CIFC24 H25 N3 O4I 1 2/a 122.3944; 10.7588; 19.4913
90; 105.44; 90		4526.69Ren, Shichao; Song, Shengjin; Ye, Lu; Feng, Chao; Loh, Teck-Peng
Copper-catalyzed oxyamination of electron-deficient alkenes with N-acyloxyamines.
Chemical communications (Cambridge, England), 2016, 52, 10373-10376
7124784 CIFC118 H108 Cl6 Co3 Ir2 N24 O29C 1 2/c 131.23; 17.481; 26.747
90; 102.845; 90		14237Li, Xuezhao; Wu, Jinguo; Chen, Liyong; Zhong, Xiaoming; He, Cheng; Zhang, Rong; Duan, Chunying
Engineering an iridium-containing metal-organic molecular capsule for induced-fit geometrical conversion and dual catalysis.
Chemical communications (Cambridge, England), 2016, 52, 9628-9631
7124785 CIFC121 H107 Cl4 Co3 Ir2 N25 O22P 43 21 220.973; 20.973; 30.067
90; 90; 90		13225Li, Xuezhao; Wu, Jinguo; Chen, Liyong; Zhong, Xiaoming; He, Cheng; Zhang, Rong; Duan, Chunying
Engineering an iridium-containing metal-organic molecular capsule for induced-fit geometrical conversion and dual catalysis.
Chemical communications (Cambridge, England), 2016, 52, 9628-9631
7124786 CIFC29 H20 OP -19.5812; 10.2719; 12.371
114.389; 96.569; 105.237		1034.9Chen, Ling; Cao, Jian; Xu, Zheng; Zheng, Zhan-Jiang; Cui, Yu-Ming; Xu, Li-Wen
Lewis acid catalyzed [2+2] cycloaddition of ynamides and propargyl silyl ethers: synthesis of alkylidenecyclobutenones and their reactivity in ring-opening and ring expansion.
Chemical communications (Cambridge, England), 2016, 52, 9574-9577
7124787 CIFC33 H31 N OP -19.688; 9.724; 14.142
92.269; 93.742; 99.428		1309.8Chen, Ling; Cao, Jian; Xu, Zheng; Zheng, Zhan-Jiang; Cui, Yu-Ming; Xu, Li-Wen
Lewis acid catalyzed [2+2] cycloaddition of ynamides and propargyl silyl ethers: synthesis of alkylidenecyclobutenones and their reactivity in ring-opening and ring expansion.
Chemical communications (Cambridge, England), 2016, 52, 9574-9577
7124788 CIFC29 H22 O2P -18.5465; 11.111; 12.403
109.873; 101.743; 90.448		1080.7Chen, Ling; Cao, Jian; Xu, Zheng; Zheng, Zhan-Jiang; Cui, Yu-Ming; Xu, Li-Wen
Lewis acid catalyzed [2+2] cycloaddition of ynamides and propargyl silyl ethers: synthesis of alkylidenecyclobutenones and their reactivity in ring-opening and ring expansion.
Chemical communications (Cambridge, England), 2016, 52, 9574-9577
7124789 CIFC21 H23 N O4C 1 c 18.12275; 19.6409; 11.31395
90; 92.5884; 90		1803.16Firth, James D.; Craven, Philip G. E.; Lilburn, Matthew; Pahl, Axel; Marsden, Stephen P.; Nelson, Adam
A biosynthesis-inspired approach to over twenty diverse natural product-like scaffolds.
Chemical communications (Cambridge, England), 2016, 52, 9837-9840
7124790 CIFC22 H25 N O4P 1 21/c 111.06181; 9.47232; 18.5215
90; 97.9172; 90		1922.2Firth, James D.; Craven, Philip G. E.; Lilburn, Matthew; Pahl, Axel; Marsden, Stephen P.; Nelson, Adam
A biosynthesis-inspired approach to over twenty diverse natural product-like scaffolds.
Chemical communications (Cambridge, England), 2016, 52, 9837-9840
7124791 CIFC21 H22 F3 N O4P -111.7112; 15.2229; 22.2156
78.173; 76.486; 89.949		3764.55Firth, James D.; Craven, Philip G. E.; Lilburn, Matthew; Pahl, Axel; Marsden, Stephen P.; Nelson, Adam
A biosynthesis-inspired approach to over twenty diverse natural product-like scaffolds.
Chemical communications (Cambridge, England), 2016, 52, 9837-9840
7124792 CIFC21 H23 N O4P b c n22.8332; 9.84289; 16.7747
90; 90; 90		3770.02Firth, James D.; Craven, Philip G. E.; Lilburn, Matthew; Pahl, Axel; Marsden, Stephen P.; Nelson, Adam
A biosynthesis-inspired approach to over twenty diverse natural product-like scaffolds.
Chemical communications (Cambridge, England), 2016, 52, 9837-9840
7124793 CIFC22 H28 N2 O4P 1 21/c 120.1612; 9.24516; 10.76938
90; 96.7643; 90		1993.37Firth, James D.; Craven, Philip G. E.; Lilburn, Matthew; Pahl, Axel; Marsden, Stephen P.; Nelson, Adam
A biosynthesis-inspired approach to over twenty diverse natural product-like scaffolds.
Chemical communications (Cambridge, England), 2016, 52, 9837-9840
7124794 CIFC22 H25 N O4P 1 21/n 19.8686; 23.9445; 33.107
90; 90.065; 90		7823.1Firth, James D.; Craven, Philip G. E.; Lilburn, Matthew; Pahl, Axel; Marsden, Stephen P.; Nelson, Adam
A biosynthesis-inspired approach to over twenty diverse natural product-like scaffolds.
Chemical communications (Cambridge, England), 2016, 52, 9837-9840
7124795 CIFC22 H28 N2 O4P 1 21 19.67334; 11.20885; 18.6086
90; 94.3265; 90		2011.93Firth, James D.; Craven, Philip G. E.; Lilburn, Matthew; Pahl, Axel; Marsden, Stephen P.; Nelson, Adam
A biosynthesis-inspired approach to over twenty diverse natural product-like scaffolds.
Chemical communications (Cambridge, England), 2016, 52, 9837-9840
7124796 CIFC14 H23 O6 P Si2 WP 21 21 219.7786; 9.9521; 21.9977
90; 90; 90		2140.76Kyri, A. W.; Schnakenburg, G.; Streubel, R.
A novel route to C-unsubstituted 1,2-oxaphosphetane and 1,2-oxaphospholane complexes.
Chemical communications (Cambridge, England), 2016, 52, 8593-8595
7124797 CIFC14 H24 I O6 P Si2 WP -19.179; 10.433; 14.066
86.293; 81.81; 65.584		1214Kyri, A. W.; Schnakenburg, G.; Streubel, R.
A novel route to C-unsubstituted 1,2-oxaphosphetane and 1,2-oxaphospholane complexes.
Chemical communications (Cambridge, England), 2016, 52, 8593-8595
7124798 CIFC15 H25 O6 P Si2 WP 21 21 219.2343; 10.3502; 23.1652
90; 90; 90		2214.06Kyri, A. W.; Schnakenburg, G.; Streubel, R.
A novel route to C-unsubstituted 1,2-oxaphosphetane and 1,2-oxaphospholane complexes.
Chemical communications (Cambridge, England), 2016, 52, 8593-8595
7124799 CIFC49 H71 Br2 Fe3 N6 O SP -111.9958; 12.5852; 17.0913
104.697; 102.692; 91.2459		2426.6Lee, Yousoon; Abboud, Khalil A.; García-Serres, Ricardo; Murray, Leslie J.
A three-coordinate Fe(ii) center within a [3Fe-(μ3-S)] cluster that provides an accessible coordination site.
Chemical communications (Cambridge, England), 2016, 52, 9295-9298
7124800 CIFC50.88 H74.76 Br1.03 Fe3 N6 O1.47 SP -111.651; 12.6465; 17.0493
94.401; 95.909; 96.266		2473.99Lee, Yousoon; Abboud, Khalil A.; García-Serres, Ricardo; Murray, Leslie J.
A three-coordinate Fe(ii) center within a [3Fe-(μ3-S)] cluster that provides an accessible coordination site.
Chemical communications (Cambridge, England), 2016, 52, 9295-9298
7124801 CIFC31 H29 Br2 N O4P 4312.339; 12.339; 18.0683
90; 90; 90		2750.9Li, Meng; Lu, Hai-Yan; Zhang, Chao; Shi, Lin; Tang, Zhiyong; Chen, Chuan-Feng
Helical aromatic imide based enantiomers with full-color circularly polarized luminescence.
Chemical communications (Cambridge, England), 2016, 52, 9921-9924
7124802 CIFC31 H29 Br2 N O4P 4112.347; 12.347; 18.073
90; 90; 90		2755.2Li, Meng; Lu, Hai-Yan; Zhang, Chao; Shi, Lin; Tang, Zhiyong; Chen, Chuan-Feng
Helical aromatic imide based enantiomers with full-color circularly polarized luminescence.
Chemical communications (Cambridge, England), 2016, 52, 9921-9924
7124803 CIFC23 H19 N O SP 21 21 215.6327; 14.2928; 21.544
90; 90; 90		1734.4León, Thierry; Fernández, Elena
The Pauson-Khand reaction using alkynylboronic esters: solving a long-standing regioselectivity issue.
Chemical communications (Cambridge, England), 2016, 52, 9363-9366
7124804 CIFC22 H25 B O3P -19.7865; 12.5627; 16.1123
90.4912; 102.202; 93.6195		1931.82León, Thierry; Fernández, Elena
The Pauson-Khand reaction using alkynylboronic esters: solving a long-standing regioselectivity issue.
Chemical communications (Cambridge, England), 2016, 52, 9363-9366
7124805 CIFC26 H21 B N2 OP 1 21/c 119.3909; 10.1233; 20.4987
90; 95.235; 90		4007.1León, Thierry; Fernández, Elena
The Pauson-Khand reaction using alkynylboronic esters: solving a long-standing regioselectivity issue.
Chemical communications (Cambridge, England), 2016, 52, 9363-9366
7124806 CIFC8 H4 In O5I 41 2 215.4625; 15.4625; 12.337
90; 90; 90		2949.6Peralta, Ricardo A.; Campos-Reales-Pineda, Alberto; Pfeiffer, Heriberto; Álvarez, J Raziel; Zárate, J Antonio; Balmaseda, Jorge; González-Zamora, Eduardo; Martínez, Ana; Martínez-Otero, Diego; Jancik, Vojtech; Ibarra, Ilich A.
CO2 capture enhancement in InOF-1 via the bottleneck effect of confined ethanol.
Chemical communications (Cambridge, England), 2016, 52, 10273-10276
7124807 CIFC10 H10 In O6I 41 2 215.483; 15.483; 12.308
90; 90; 90		2950.5Peralta, Ricardo A.; Campos-Reales-Pineda, Alberto; Pfeiffer, Heriberto; Álvarez, J Raziel; Zárate, J Antonio; Balmaseda, Jorge; González-Zamora, Eduardo; Martínez, Ana; Martínez-Otero, Diego; Jancik, Vojtech; Ibarra, Ilich A.
CO2 capture enhancement in InOF-1 via the bottleneck effect of confined ethanol.
Chemical communications (Cambridge, England), 2016, 52, 10273-10276
7124808 CIFC60 H62 Au Cl P S3P 1 21 19.8334; 21.319; 12.7266
90; 95.59; 90		2655.3Aillard, Paul; Dova, Davide; Magné, Valentin; Retailleau, Pascal; Cauteruccio, Silvia; Licandro, Emanuela; Voituriez, Arnaud; Marinetti, Angela
The synthesis of substituted phosphathiahelicenes via regioselective bromination of a preformed helical scaffold: a new approach to modular ligands for enantioselective gold-catalysis.
Chemical communications (Cambridge, England), 2016, 52, 10984-10987
7124809 CIFC12 H6 Cl2 Cu2 N2 O10 PdR -3 m :H18.899; 18.899; 31.69
90; 90; 120		9802Spanopoulos, I.; Bratsos, I.; Tampaxis, C.; Vourloumis, D.; Klontzas, E.; Froudakis, G. E.; Charalambopoulou, G.; Steriotis, T. A.; Trikalitis, P. N.
Exceptional gravimetric and volumetric CO2 uptake in a palladated NbO-type MOF utilizing cooperative acidic and basic, metal-CO2 interactions.
Chemical communications (Cambridge, England), 2016, 52, 10559-10562
7124810 CIFC16 H34 Mg N2 O2 P2 S2P 1 21/n 113.2446; 10.2823; 17.0713
90; 97.7952; 90		2303.37Benson, Callum G. M.; Plajer, Alex J.; García-Rodríguez, Raúl; Bond, Andrew D.; Singh, Sanjay; Gade, Lutz H.; Wright, Dominic S.
A versatile hard-soft N/S-ligand for metal coordination and cluster formation.
Chemical communications (Cambridge, England), 2016, 52, 9683-9686
7124811 CIFC20 H28 N2 P2 S2 SnP -18.5948; 9.7615; 14.7996
85.955; 87.786; 73.175		1185.33Benson, Callum G. M.; Plajer, Alex J.; García-Rodríguez, Raúl; Bond, Andrew D.; Singh, Sanjay; Gade, Lutz H.; Wright, Dominic S.
A versatile hard-soft N/S-ligand for metal coordination and cluster formation.
Chemical communications (Cambridge, England), 2016, 52, 9683-9686
7124812 CIFC96 H209 N16 Na17 O8 P16 S17P 4 c c23.7918; 23.7918; 37.5449
90; 90; 90		21252.3Benson, Callum G. M.; Plajer, Alex J.; García-Rodríguez, Raúl; Bond, Andrew D.; Singh, Sanjay; Gade, Lutz H.; Wright, Dominic S.
A versatile hard-soft N/S-ligand for metal coordination and cluster formation.
Chemical communications (Cambridge, England), 2016, 52, 9683-9686
7124813 CIFC11 H9 N OP 1 21/c 15.8141; 23.591; 6.8413
90; 114.257; 90		855.5Stephens, David E.; Lakey-Beitia, Johant; Burch, Jessica E.; Arman, Hadi D.; Larionov, Oleg V.
Mechanistic insights into the potassium tert-butoxide-mediated synthesis of N-heterobiaryls.
Chemical communications (Cambridge, England), 2016, 52, 9945-9948
7124814 CIFC17 H14 Cl N O3P 1 21/c 115.84; 13.517; 7.047
90; 101.395; 90		1479.1Stephens, David E.; Lakey-Beitia, Johant; Burch, Jessica E.; Arman, Hadi D.; Larionov, Oleg V.
Mechanistic insights into the potassium tert-butoxide-mediated synthesis of N-heterobiaryls.
Chemical communications (Cambridge, England), 2016, 52, 9945-9948
7124815 CIFC24 H24 N2P 1 21/c 112.648; 5.914; 13.125
90; 94.02; 90		979Stephens, David E.; Lakey-Beitia, Johant; Burch, Jessica E.; Arman, Hadi D.; Larionov, Oleg V.
Mechanistic insights into the potassium tert-butoxide-mediated synthesis of N-heterobiaryls.
Chemical communications (Cambridge, England), 2016, 52, 9945-9948
7124816 CIFC10 H13 N O4P 1 21 14.8503; 17.114; 6.4411
90; 105.911; 90		514.2Stephens, David E.; Lakey-Beitia, Johant; Burch, Jessica E.; Arman, Hadi D.; Larionov, Oleg V.
Mechanistic insights into the potassium tert-butoxide-mediated synthesis of N-heterobiaryls.
Chemical communications (Cambridge, England), 2016, 52, 9945-9948
7124817 CIFC10 H13 N O3P -16.69; 8.863; 9.115
107.219; 111.191; 92.478		474.4Stephens, David E.; Lakey-Beitia, Johant; Burch, Jessica E.; Arman, Hadi D.; Larionov, Oleg V.
Mechanistic insights into the potassium tert-butoxide-mediated synthesis of N-heterobiaryls.
Chemical communications (Cambridge, England), 2016, 52, 9945-9948
7124818 CIFC22 H16 N2P 1 21/c 120.26; 5.434; 16.088
90; 110.528; 90		1658.7Stephens, David E.; Lakey-Beitia, Johant; Burch, Jessica E.; Arman, Hadi D.; Larionov, Oleg V.
Mechanistic insights into the potassium tert-butoxide-mediated synthesis of N-heterobiaryls.
Chemical communications (Cambridge, England), 2016, 52, 9945-9948
7124819 CIFC26 H28 N2I 1 2/a 118.301; 6.133; 18.738
90; 94.032; 90		2098Stephens, David E.; Lakey-Beitia, Johant; Burch, Jessica E.; Arman, Hadi D.; Larionov, Oleg V.
Mechanistic insights into the potassium tert-butoxide-mediated synthesis of N-heterobiaryls.
Chemical communications (Cambridge, England), 2016, 52, 9945-9948
7124820 CIFC10 H13 N O3P 1 21/c 16.8201; 16.879; 9.0566
90; 106.25; 90		1000.9Stephens, David E.; Lakey-Beitia, Johant; Burch, Jessica E.; Arman, Hadi D.; Larionov, Oleg V.
Mechanistic insights into the potassium tert-butoxide-mediated synthesis of N-heterobiaryls.
Chemical communications (Cambridge, England), 2016, 52, 9945-9948
7124821 CIFC77 H66 B4 Cl6P -112.3724; 16.262; 18.3411
68.034; 76.109; 68.507		3161.58Zhang, Zuolun; Wang, Zheng; Haehnel, Martin; Eichhorn, Antonius; Edkins, Robert M.; Steffen, Andreas; Krueger, Anke; Lin, Zhenyang; Marder, Todd B.
Synthesis and fluxional behaviour of novel chloroborole dimers.
Chemical communications (Cambridge, England), 2016, 52, 9707-9710
7124822 CIFC38 H28 B2 Br4 Cl2P -110.7763; 11.4318; 15.5909
74.252; 81.811; 69.779		1732.1Zhang, Zuolun; Wang, Zheng; Haehnel, Martin; Eichhorn, Antonius; Edkins, Robert M.; Steffen, Andreas; Krueger, Anke; Lin, Zhenyang; Marder, Todd B.
Synthesis and fluxional behaviour of novel chloroborole dimers.
Chemical communications (Cambridge, England), 2016, 52, 9707-9710
7124823 CIFC14 H36 Cu N6 O8P -19.4885; 10.1789; 11.6397
85.237; 74.922; 77.744		1060.29Yu, Fengshou; Li, Fei; Hu, Jixiang; Bai, Lichen; Zhu, Yong; Sun, Licheng
Electrocatalytic water oxidation by a macrocyclic Cu(ii) complex in neutral phosphate buffer.
Chemical communications (Cambridge, England), 2016, 52, 10377-10380
7124824 CIFC41 H36 F16 N2P 1 21/c 112.7034; 15.8896; 29.1048
90; 94.795; 90		5854.3Kim, Youngsuk; Lee, Eunsung
Activation of C-F bonds in fluoroarenes by N-heterocyclic carbenes as an effective route to synthesize abnormal NHC complexes.
Chemical communications (Cambridge, England), 2016, 52, 10922-10925
7124825 CIFC45 H42 Au Cl F14 N2 OP 1 21/c 115.0816; 14.3924; 20.4104
90; 96.525; 90		4401.6Kim, Youngsuk; Lee, Eunsung
Activation of C-F bonds in fluoroarenes by N-heterocyclic carbenes as an effective route to synthesize abnormal NHC complexes.
Chemical communications (Cambridge, England), 2016, 52, 10922-10925
7124826 CIFC34 H41 F5 N2C 1 2/c 118.227; 17.04; 20.143
90; 101.779; 90		6124Kim, Youngsuk; Lee, Eunsung
Activation of C-F bonds in fluoroarenes by N-heterocyclic carbenes as an effective route to synthesize abnormal NHC complexes.
Chemical communications (Cambridge, England), 2016, 52, 10922-10925
7124827 CIFC29 H16P 1 21/c 111.856; 7.3071; 20.186
90; 96.412; 90		1737.8Rajeshkumar, Venkatachalam; Stuparu, Mihaiela C.
A photochemical approach to aromatic extension of the corannulene nucleus.
Chemical communications (Cambridge, England), 2016, 52, 9957-9960
7124828 CIFC30 H14 SP c a 219.2775; 26.8593; 7.3125
90; 90; 90		1822.18Rajeshkumar, Venkatachalam; Stuparu, Mihaiela C.
A photochemical approach to aromatic extension of the corannulene nucleus.
Chemical communications (Cambridge, England), 2016, 52, 9957-9960
7124829 CIFC29 H16 SP 1 21/n 114.111; 7.318; 18.169
90; 100.411; 90		1845.3Rajeshkumar, Venkatachalam; Stuparu, Mihaiela C.
A photochemical approach to aromatic extension of the corannulene nucleus.
Chemical communications (Cambridge, England), 2016, 52, 9957-9960
7124830 CIFC30 H19 NP 1 21/n 114.3543; 7.4826; 17.7472
90; 97.963; 90		1887.8Rajeshkumar, Venkatachalam; Stuparu, Mihaiela C.
A photochemical approach to aromatic extension of the corannulene nucleus.
Chemical communications (Cambridge, England), 2016, 52, 9957-9960
7124831 CIFC13 H12 Cd N2 O2I 41/a :224.583; 24.583; 10.8704
90; 90; 90		6569.2Xiao, Qiong; Wu, Yuan; Li, Mian; O'Keeffe, Michael; Li, Dan
A metal-organic framework with rod secondary building unit based on the Boerdijk-Coxeter helix.
Chemical communications (Cambridge, England), 2016, 52, 11543-11546
7124832 CIFC13 H12 Cd N2 O2I 41/a :224.0666; 24.0666; 10.5856
90; 90; 90		6131.2Xiao, Qiong; Wu, Yuan; Li, Mian; O'Keeffe, Michael; Li, Dan
A metal-organic framework with rod secondary building unit based on the Boerdijk-Coxeter helix.
Chemical communications (Cambridge, England), 2016, 52, 11543-11546
7124833 CIFC13 H12 Cd N2 O2I 41/a :224.6108; 24.6108; 10.76785
90; 90; 90		6521.99Xiao, Qiong; Wu, Yuan; Li, Mian; O'Keeffe, Michael; Li, Dan
A metal-organic framework with rod secondary building unit based on the Boerdijk-Coxeter helix.
Chemical communications (Cambridge, England), 2016, 52, 11543-11546
7124834 CIFC13 H12 Cd N2 O2I 41/a :224.029; 24.029; 10.5501
90; 90; 90		6091.6Xiao, Qiong; Wu, Yuan; Li, Mian; O'Keeffe, Michael; Li, Dan
A metal-organic framework with rod secondary building unit based on the Boerdijk-Coxeter helix.
Chemical communications (Cambridge, England), 2016, 52, 11543-11546
7124835 CIFC15 H9 Cd2 N13 O12P c c n9.1873; 12.5692; 20.0824
90; 90; 90		2319.1Frost, Jamie M.; Kobera, Libor; Pialat, Amélie; Zhang, Yixin; Southern, Scott A.; Gabidullin, Bulat; Bryce, David L.; Murugesu, Muralee
From discrete molecule, to polymer, to MOF: mapping the coordination chemistry of Cd(II) using (113)Cd solid-state NMR.
Chemical communications (Cambridge, England), 2016, 52, 10680-10683
7124836 CIFC10 H6 Cd N4 O4I m -3 m30.1172; 30.1172; 30.1172
90; 90; 90		27317.7Frost, Jamie M.; Kobera, Libor; Pialat, Amélie; Zhang, Yixin; Southern, Scott A.; Gabidullin, Bulat; Bryce, David L.; Murugesu, Muralee
From discrete molecule, to polymer, to MOF: mapping the coordination chemistry of Cd(II) using (113)Cd solid-state NMR.
Chemical communications (Cambridge, England), 2016, 52, 10680-10683
7124837 CIFC45 H51.47 F12 Mo N3 O3 P4P 1 21/c 115.3031; 15.9629; 20.6295
90; 104.622; 90		4876.2Pal, Raja; Laureanti, Joseph A.; Groy, Thomas L.; Jones, Anne K.; Trovitch, Ryan J.
Hydrogen production from water using a bis(imino)pyridine molybdenum electrocatalyst.
Chemical communications (Cambridge, England), 2016, 52, 11555-11558
7124838 CIFC39 H41 Mo N3 O P2P 1 21/c 111.1519; 16.9788; 18.245
90; 105.844; 90		3323.4Pal, Raja; Laureanti, Joseph A.; Groy, Thomas L.; Jones, Anne K.; Trovitch, Ryan J.
Hydrogen production from water using a bis(imino)pyridine molybdenum electrocatalyst.
Chemical communications (Cambridge, England), 2016, 52, 11555-11558
7124839 CIFC15 H10 O5C 1 2/c 127.783; 4.6822; 20.212
90; 118.891; 90		2302Li, Meiqi; Zhang, Qi; Wang, Jian-Rong; Mei, Xuefeng
Mechanochromism triggered fluorescent color switching among polymorphs of a natural fluorescence pigment.
Chemical communications (Cambridge, England), 2016, 52, 11288-11291
7124840 CIFC15 H10 O5P 1 21/n 116.4721; 3.6915; 19.4294
90; 96.188; 90		1174.56Li, Meiqi; Zhang, Qi; Wang, Jian-Rong; Mei, Xuefeng
Mechanochromism triggered fluorescent color switching among polymorphs of a natural fluorescence pigment.
Chemical communications (Cambridge, England), 2016, 52, 11288-11291
7124841 CIFC15 H10 O5P 1 21/n 112.6343; 3.6437; 31.2026
90; 95.706; 90		1429.31Li, Meiqi; Zhang, Qi; Wang, Jian-Rong; Mei, Xuefeng
Mechanochromism triggered fluorescent color switching among polymorphs of a natural fluorescence pigment.
Chemical communications (Cambridge, England), 2016, 52, 11288-11291
7124842 CIFC15 H10 O5P 1 21/n 116.6384; 3.6887; 19.406
90; 95.544; 90		1185.45Li, Meiqi; Zhang, Qi; Wang, Jian-Rong; Mei, Xuefeng
Mechanochromism triggered fluorescent color switching among polymorphs of a natural fluorescence pigment.
Chemical communications (Cambridge, England), 2016, 52, 11288-11291
7124843 CIFC44 H36 Cl F24 N7 P2P -112.175; 12.483; 18.276
75.34; 78.55; 71.31		2524.5Amendola, Valeria; Bergamaschi, Greta; Boiocchi, Massimo; Legnani, Laura; Presti, Eliana Lo; Miljkovic, Ana; Monzani, Enrico; Pancotti, Francesca
Chloride-binding in organic-water mixtures: the powerful synergy of C-H donor groups within a bowl-shaped cavity.
Chemical communications (Cambridge, England), 2016, 52, 10910-10913
7124844 CIFC44 H36 Br F24 N7 P2P -112.226; 12.514; 18.219
75.477; 78.586; 71.715		2540.5Amendola, Valeria; Bergamaschi, Greta; Boiocchi, Massimo; Legnani, Laura; Presti, Eliana Lo; Miljkovic, Ana; Monzani, Enrico; Pancotti, Francesca
Chloride-binding in organic-water mixtures: the powerful synergy of C-H donor groups within a bowl-shaped cavity.
Chemical communications (Cambridge, England), 2016, 52, 10910-10913
7124845 CIFC18 H17 Cl2 N O4 SP 1 21/c 113.725; 7.0845; 20.233
90; 108.593; 90		1864.7Xia, Dong; Li, Yang; Miao, Tao; Li, Pinhua; Wang, Lei
Direct synthesis of sulfonated dihydroisoquinolinones from N-allylbenzamide and arylsulfinic acids via TBHP-promoted cascade radical addition and cyclization.
Chemical communications (Cambridge, England), 2016, 52, 11559-11562
7124846 CIFC42 H40 Br2 N2 O6P 1 21 19.5936; 17.0134; 12.402
90; 111.095; 90		1888.6Li, Jun-Long; Yang, Kai-Chuan; Li, Yi; Li, Qiang; Zhu, Hong-Ping; Han, Bo; Peng, Cheng; Zhi, Yong-Gang; Gou, Xiao-Jun
Asymmetric synthesis of bicyclic dihydropyrans via organocatalytic inverse-electron-demand oxo-Diels-Alder reactions of enolizable aliphatic aldehydes.
Chemical communications (Cambridge, England), 2016, 52, 10617-10620
7124847 CIFC31 H27 I N2 O2 SP 1 21/c 19.6062; 11.1759; 25.6122
90; 92.1354; 90		2747.76Li, Honghe; Li, Xiaoxiao; Zhao, Zhigang; Ma, Ting; Sun, Chenyang; Yang, Bowen
Intermolecular iodofunctionalization of allenamides with indoles, pyrroles, and furans: synthesis of iodine-substituted Z-enamides.
Chemical communications (Cambridge, England), 2016, 52, 10167-10170
7124848 CIFC19 H18 I N3 O2 SP -18.421; 10; 11.8424
100.66; 103.744; 90.605		950.42Li, Honghe; Li, Xiaoxiao; Zhao, Zhigang; Ma, Ting; Sun, Chenyang; Yang, Bowen
Intermolecular iodofunctionalization of allenamides with indoles, pyrroles, and furans: synthesis of iodine-substituted Z-enamides.
Chemical communications (Cambridge, England), 2016, 52, 10167-10170
7124849 CIFC20 H13 F N4 SP -19.927; 13.059; 13.682
69.528; 89.026; 78.107		1623.1Yoshida, Suguru; Yano, Takahisa; Nishiyama, Yoshitake; Misawa, Yoshihiro; Kondo, Masakazu; Matsushita, Takeshi; Igawa, Kazunobu; Tomooka, Katsuhiko; Hosoya, Takamitsu
Thiazolobenzyne: a versatile intermediate for multisubstituted benzothiazoles.
Chemical communications (Cambridge, England), 2016, 52, 11199-11202
7124850 CIFC32 H64 B Li O8P 1 21/n 110.6111; 22.4729; 14.576
90; 92.676; 90		3472.03Basnet, Prakash; Thapa, Surendra; Dickie, Diane A.; Giri, Ramesh
The copper-catalysed Suzuki-Miyaura coupling of alkylboron reagents: disproportionation of anionic (alkyl)(alkoxy)borates to anionic dialkylborates prior to transmetalation.
Chemical communications (Cambridge, England), 2016, 52, 11072-11075
7124851 CIFC28 H56 B2 Li2 O6P -18.3308; 9.3831; 10.3351
98.43; 106.326; 90.671		765.74Basnet, Prakash; Thapa, Surendra; Dickie, Diane A.; Giri, Ramesh
The copper-catalysed Suzuki-Miyaura coupling of alkylboron reagents: disproportionation of anionic (alkyl)(alkoxy)borates to anionic dialkylborates prior to transmetalation.
Chemical communications (Cambridge, England), 2016, 52, 11072-11075
7124852 CIFC19 H27 N O9 ZnP -110.4273; 10.8211; 10.8805
85.208; 74.992; 67.508		1095.45Foster, Jonathan A.; Henke, Sebastian; Schneemann, Andreas; Fischer, Roland A.; Cheetham, Anthony K.
Liquid exfoliation of alkyl-ether functionalised layered metal-organic frameworks to nanosheets.
Chemical communications (Cambridge, England), 2016, 52, 10474-10477
7124853 CIFC27 H24 Au F5 N2P 1 21/c 122.2207; 12.08219; 20.7776
90; 114.995; 90		5055.81Johnson, Alice; Gimeno, M Concepción
An efficient and sustainable synthesis of NHC gold complexes.
Chemical communications (Cambridge, England), 2016, 52, 9664-9667
7124854 CIFC11 H8 Au F5 N2P 1 21/c 112.1492; 7.1342; 13.5219
90; 97.48; 90		1162.03Johnson, Alice; Gimeno, M Concepción
An efficient and sustainable synthesis of NHC gold complexes.
Chemical communications (Cambridge, England), 2016, 52, 9664-9667
7124855 CIFC15 H16 Au F5 N2P -19.2638; 9.9251; 10.7976
104.458; 104.138; 114.79		801.05Johnson, Alice; Gimeno, M Concepción
An efficient and sustainable synthesis of NHC gold complexes.
Chemical communications (Cambridge, England), 2016, 52, 9664-9667
7124856 CIFC29 H32 Au F5 N2P 1 21/c 116.6316; 6.73754; 23.1802
90; 107.797; 90		2473.18Johnson, Alice; Gimeno, M Concepción
An efficient and sustainable synthesis of NHC gold complexes.
Chemical communications (Cambridge, England), 2016, 52, 9664-9667
7124857 CIFC32 H20 F N3 OP 1 21/c 127.5965; 5.8463; 14.617
90; 93.918; 90		2352.76Yu, Ling; Wu, Zhongbin; Xie, Guohua; Zhong, Cheng; Zhu, Zece; Cong, Hengjiang; Ma, Dongge; Yang, Chuluo
Achieving a balance between small singlet-triplet energy splitting and high fluorescence radiative rate in a quinoxaline-based orange-red thermally activated delayed fluorescence emitter.
Chemical communications (Cambridge, England), 2016, 52, 11012-11015
7124858 CIFC55.18 H49.76 B2 Cl3.96 Cu2 F8 Mo4 N4.6 O8 P4P 31 2 113.2466; 13.2466; 38.4491
90; 90; 120		5842.9Elsayed Moussa, M.; Attenberger, B.; Peresypkina, E. V.; Fleischmann, M.; Balázs, G; Scheer, M.
Facile synthesis of one-dimensional organometallic-organic hybrid polymers based on a diphosphorus complex and flexible bipyridyl linkers.
Chemical communications (Cambridge, England), 2016, 52, 10004-10007
7124859 CIFC28.2 H25.9 B Cl0.4 Cu F4 Mo2 N2.5 O4 P2P -112.15; 12.9837; 13.0995
112.581; 95.502; 112.579		1688.53Elsayed Moussa, M.; Attenberger, B.; Peresypkina, E. V.; Fleischmann, M.; Balázs, G; Scheer, M.
Facile synthesis of one-dimensional organometallic-organic hybrid polymers based on a diphosphorus complex and flexible bipyridyl linkers.
Chemical communications (Cambridge, England), 2016, 52, 10004-10007
7124860 CIFC28.1 H22.2 B Cl0.2 Cu F4 Mo2 N2 O8 P2P -111.051; 12.9411; 14.5125
107.454; 109.734; 92.922		1836.64Elsayed Moussa, M.; Attenberger, B.; Peresypkina, E. V.; Fleischmann, M.; Balázs, G; Scheer, M.
Facile synthesis of one-dimensional organometallic-organic hybrid polymers based on a diphosphorus complex and flexible bipyridyl linkers.
Chemical communications (Cambridge, England), 2016, 52, 10004-10007
7124861 CIFC57 H46 B2 Cl2 Cu2 F8 Mo4 N4 O16 P4C 1 2/c 123.3364; 15.9366; 20.1067
90; 116.735; 90		6678.3Elsayed Moussa, M.; Attenberger, B.; Peresypkina, E. V.; Fleischmann, M.; Balázs, G; Scheer, M.
Facile synthesis of one-dimensional organometallic-organic hybrid polymers based on a diphosphorus complex and flexible bipyridyl linkers.
Chemical communications (Cambridge, England), 2016, 52, 10004-10007
7124862 CIFC36 H17 B2 F20 NP 1 21/n 114.9491; 11.0572; 20.4604
90; 102.897; 90		3296.69Körte, Leif A; Blomeyer, Sebastian; Heidemeyer, Shari; Mix, Andreas; Neumann, Beate; Mitzel, Norbert W.
Intramolecular cooperativity in frustrated Lewis pairs.
Chemical communications (Cambridge, England), 2016, 52, 9949-9952
7124863 CIFC13 H22 B10 O2P -17.0022; 11.1149; 12.7151
72.088; 85.357; 77.321		918.58Zheng, Fangrui; Leung, Tsz-Fai; Chan, Ka-Wing; Sung, Herman H. Y.; Williams, Ian D.; Xie, Zuowei; Jia, Guochen
Phosphine-catalyzed cage carbon functionalization of o-carborane: facile synthesis of alkenylcarboranes.
Chemical communications (Cambridge, England), 2016, 52, 10767-10770
7124864 CIFC14 H24 B10 O2P -16.9249; 11.0485; 13.4241
70.985; 82.699; 79.375		951.9Zheng, Fangrui; Leung, Tsz-Fai; Chan, Ka-Wing; Sung, Herman H. Y.; Williams, Ian D.; Xie, Zuowei; Jia, Guochen
Phosphine-catalyzed cage carbon functionalization of o-carborane: facile synthesis of alkenylcarboranes.
Chemical communications (Cambridge, England), 2016, 52, 10767-10770
7124865 CIFC15 H27 B10 N O2P -17.3998; 11.4524; 12.796
101.746; 102.967; 101.723		998.81Zheng, Fangrui; Leung, Tsz-Fai; Chan, Ka-Wing; Sung, Herman H. Y.; Williams, Ian D.; Xie, Zuowei; Jia, Guochen
Phosphine-catalyzed cage carbon functionalization of o-carborane: facile synthesis of alkenylcarboranes.
Chemical communications (Cambridge, England), 2016, 52, 10767-10770
7124866 CIFC13 H21 B10 Cl O2P 1 21/n 114.2465; 6.9536; 19.296
90; 103.257; 90		1860.6Zheng, Fangrui; Leung, Tsz-Fai; Chan, Ka-Wing; Sung, Herman H. Y.; Williams, Ian D.; Xie, Zuowei; Jia, Guochen
Phosphine-catalyzed cage carbon functionalization of o-carborane: facile synthesis of alkenylcarboranes.
Chemical communications (Cambridge, England), 2016, 52, 10767-10770
7124867 CIFC13 H21 B10 Br O2P 1 21/n 114.3765; 6.99225; 19.7177
90; 105.687; 90		1908.28Zheng, Fangrui; Leung, Tsz-Fai; Chan, Ka-Wing; Sung, Herman H. Y.; Williams, Ian D.; Xie, Zuowei; Jia, Guochen
Phosphine-catalyzed cage carbon functionalization of o-carborane: facile synthesis of alkenylcarboranes.
Chemical communications (Cambridge, England), 2016, 52, 10767-10770
7124868 CIFC19 H26 B10 O2P 1 21/c 115.59137; 7.11207; 20.7564
90; 106.786; 90		2203.55Zheng, Fangrui; Leung, Tsz-Fai; Chan, Ka-Wing; Sung, Herman H. Y.; Williams, Ian D.; Xie, Zuowei; Jia, Guochen
Phosphine-catalyzed cage carbon functionalization of o-carborane: facile synthesis of alkenylcarboranes.
Chemical communications (Cambridge, England), 2016, 52, 10767-10770
7124869 CIFC17 H24 B10 O2P -17.5123; 11.5047; 13.1285
109.896; 91.522; 105.035		1022.13Zheng, Fangrui; Leung, Tsz-Fai; Chan, Ka-Wing; Sung, Herman H. Y.; Williams, Ian D.; Xie, Zuowei; Jia, Guochen
Phosphine-catalyzed cage carbon functionalization of o-carborane: facile synthesis of alkenylcarboranes.
Chemical communications (Cambridge, England), 2016, 52, 10767-10770
7124870 CIFC18 H26 B10 O3C 1 2/c 126.4656; 8.57309; 20.8506
90; 111.965; 90		4387.43Zheng, Fangrui; Leung, Tsz-Fai; Chan, Ka-Wing; Sung, Herman H. Y.; Williams, Ian D.; Xie, Zuowei; Jia, Guochen
Phosphine-catalyzed cage carbon functionalization of o-carborane: facile synthesis of alkenylcarboranes.
Chemical communications (Cambridge, England), 2016, 52, 10767-10770
7124871 CIFC11 H20 B10 O3P 1 21/n 122.1533; 6.78019; 23.3341
90; 100.05; 90		3451.09Zheng, Fangrui; Leung, Tsz-Fai; Chan, Ka-Wing; Sung, Herman H. Y.; Williams, Ian D.; Xie, Zuowei; Jia, Guochen
Phosphine-catalyzed cage carbon functionalization of o-carborane: facile synthesis of alkenylcarboranes.
Chemical communications (Cambridge, England), 2016, 52, 10767-10770
7124872 CIFC11 H20 B10 O2 SP 1 21/n 114.009; 7.0087; 17.9756
90; 100.292; 90		1736.5Zheng, Fangrui; Leung, Tsz-Fai; Chan, Ka-Wing; Sung, Herman H. Y.; Williams, Ian D.; Xie, Zuowei; Jia, Guochen
Phosphine-catalyzed cage carbon functionalization of o-carborane: facile synthesis of alkenylcarboranes.
Chemical communications (Cambridge, England), 2016, 52, 10767-10770
7124873 CIFC11 H20 B10 O2 SP 1 21/n 114.1171; 7.06182; 17.8292
90; 100.102; 90		1749.88Zheng, Fangrui; Leung, Tsz-Fai; Chan, Ka-Wing; Sung, Herman H. Y.; Williams, Ian D.; Xie, Zuowei; Jia, Guochen
Phosphine-catalyzed cage carbon functionalization of o-carborane: facile synthesis of alkenylcarboranes.
Chemical communications (Cambridge, England), 2016, 52, 10767-10770
7124874 CIFC12 H21 B10 N O2C 1 2/c 122.0219; 6.88628; 24.2999
90; 104.579; 90		3566.4Zheng, Fangrui; Leung, Tsz-Fai; Chan, Ka-Wing; Sung, Herman H. Y.; Williams, Ian D.; Xie, Zuowei; Jia, Guochen
Phosphine-catalyzed cage carbon functionalization of o-carborane: facile synthesis of alkenylcarboranes.
Chemical communications (Cambridge, England), 2016, 52, 10767-10770
7124875 CIFC124 Cl12 N7 O73 Si2 Sn6 W18P 1 21 118.7517; 28.4384; 21.539
90; 115.122; 90		10399.6Suzuki, Kosuke; Hanaya, Takumi; Sato, Rinta; Minato, Takuo; Yamaguchi, Kazuya; Mizuno, Noritaka
Hexanuclear tin(ii) and mixed valence tin(ii,iv) oxide clusters within polyoxometalates.
Chemical communications (Cambridge, England), 2016, 52, 10688-10691
7124876 CIFC115 N10 O77 Si2 Sn6 W18P -117.6999; 18.7362; 29.8744
82.659; 88.278; 74.291		9458.9Suzuki, Kosuke; Hanaya, Takumi; Sato, Rinta; Minato, Takuo; Yamaguchi, Kazuya; Mizuno, Noritaka
Hexanuclear tin(ii) and mixed valence tin(ii,iv) oxide clusters within polyoxometalates.
Chemical communications (Cambridge, England), 2016, 52, 10688-10691
7124877 CIFC64 H36 F4 N2 O8 Zn2P -113.967; 15.48; 20.893
89.948; 83.096; 89.209		4484Wang, Fangming; Liu, Wei; Teat, Simon J.; Xu, Feng; Wang, Hao; Wang, Xinlong; An, Litao; Li, Jing
Chromophore-immobilized luminescent metal-organic frameworks as potential lighting phosphors and chemical sensors.
Chemical communications (Cambridge, England), 2016, 52, 10249-10252
7124878 CIFC66 H38 F4 N2 O8 Zn2P -116.317; 16.8197; 20.0452
89.982; 85.952; 85.919		5473.6Wang, Fangming; Liu, Wei; Teat, Simon J.; Xu, Feng; Wang, Hao; Wang, Xinlong; An, Litao; Li, Jing
Chromophore-immobilized luminescent metal-organic frameworks as potential lighting phosphors and chemical sensors.
Chemical communications (Cambridge, England), 2016, 52, 10249-10252
7124879 CIFC23 H22 S2P 1 21 110.023; 7.569; 13.421
90; 108.949; 90		963Xu, Wei; Chen, Ming; Sun, Ning; Liu, Yuanhong
Gold-catalyzed cyclization of 1,6-diynyl dithioacetals via 1,7-carbene transfer and aromatic C-H functionalization.
Chemical communications (Cambridge, England), 2016, 52, 11000-11003
7124880 CIFC15 H16 O S2P 1 21/c 115.567; 7.3046; 12.5049
90; 107.222; 90		1358.2Xu, Wei; Chen, Ming; Sun, Ning; Liu, Yuanhong
Gold-catalyzed cyclization of 1,6-diynyl dithioacetals via 1,7-carbene transfer and aromatic C-H functionalization.
Chemical communications (Cambridge, England), 2016, 52, 11000-11003
7124881 CIFC52 H40 O2 S4P 1 21 110.601; 19.272; 11.193
90; 117.501; 90		2028.4Xu, Wei; Chen, Ming; Sun, Ning; Liu, Yuanhong
Gold-catalyzed cyclization of 1,6-diynyl dithioacetals via 1,7-carbene transfer and aromatic C-H functionalization.
Chemical communications (Cambridge, England), 2016, 52, 11000-11003
7124882 CIFC26 H20 O S2C 1 2/c 122.945; 11.378; 16.575
90; 111.887; 90		4015Xu, Wei; Chen, Ming; Sun, Ning; Liu, Yuanhong
Gold-catalyzed cyclization of 1,6-diynyl dithioacetals via 1,7-carbene transfer and aromatic C-H functionalization.
Chemical communications (Cambridge, England), 2016, 52, 11000-11003
7124883 CIFC28 H38 Au F6 N O2 P SbP 1 21/n 112.9088; 13.5954; 18.3182
90; 93.268; 90		3209.6Xu, Wei; Chen, Ming; Sun, Ning; Liu, Yuanhong
Gold-catalyzed cyclization of 1,6-diynyl dithioacetals via 1,7-carbene transfer and aromatic C-H functionalization.
Chemical communications (Cambridge, England), 2016, 52, 11000-11003
7124884 CIFC26 H20 S2P 1 21/n 111.9307; 11.8029; 13.8044
90; 98.163; 90		1924.2Xu, Wei; Chen, Ming; Sun, Ning; Liu, Yuanhong
Gold-catalyzed cyclization of 1,6-diynyl dithioacetals via 1,7-carbene transfer and aromatic C-H functionalization.
Chemical communications (Cambridge, England), 2016, 52, 11000-11003
7124885 CIFC29 H20 S2P 1 21/c 115.8061; 6.3393; 21.023
90; 95.291; 90		2097.5Xu, Wei; Chen, Ming; Sun, Ning; Liu, Yuanhong
Gold-catalyzed cyclization of 1,6-diynyl dithioacetals via 1,7-carbene transfer and aromatic C-H functionalization.
Chemical communications (Cambridge, England), 2016, 52, 11000-11003
7124886 CIFC28 H24 O3 S2P -19.8628; 11.701; 12.236
108.538; 104.931; 90.24		1287.9Xu, Wei; Chen, Ming; Sun, Ning; Liu, Yuanhong
Gold-catalyzed cyclization of 1,6-diynyl dithioacetals via 1,7-carbene transfer and aromatic C-H functionalization.
Chemical communications (Cambridge, England), 2016, 52, 11000-11003
7124887 CIFC13 H11 Cl N4 OP 1 21 16.1447; 8.6445; 12.6178
90; 101.032; 90		657.84Vishwanath, Manjunatha; Sivamuthuraman, Koilpitchai; Kesavan, Venkitasamy
An efficient construction of N,N-bicyclic pyrazolidinones comprising enaminonitriles via asymmetric [3+2] cycloaddition.
Chemical communications (Cambridge, England), 2016, 52, 12314-12317
7124888 CIFC50 H96 Br8 Dy6 N14 O32P -111.225; 12.338; 18.269
72.433; 82.638; 89.18		2391.5Li, Xiao-Lei; Wu, Jianfeng; Tang, Jinkui; Le Guennic, Boris; Shi, Wei; Cheng, Peng
A planar triangular Dy3 + Dy3 single-molecule magnet with a toroidal magnetic moment.
Chemical communications (Cambridge, England), 2016, 52, 9570-9573
7124889 CIFC16 H16 Co Dy N8 O5P 1 21/m 16.897; 15.6685; 9.6096
90; 102.131; 90		1015.28Chorazy, Szymon; Wang, Junhao; Ohkoshi, Shin-Ichi
Yellow to greenish-blue colour-tunable photoluminescence and 4f-centered slow magnetic relaxation in a cyanido-bridged Dy(III)(4-hydroxypyridine)-Co(III) layered material.
Chemical communications (Cambridge, England), 2016, 52, 10795-10798
7124890 CIFC45 H62 Cl2 N4 O4 ZrP 1 21/n 112.9667; 18.0916; 18.8976
90; 95.342; 90		4413.9Schneider, Fabian; Zhao, Tiankun; Huhn, Thomas
Cytotoxic heteroleptic heptacoordinate salan zirconium(iv)-bis-chelates - synthesis, aqueous stability and X-ray structure analysis.
Chemical communications (Cambridge, England), 2016, 52, 10151-10154
7124891 CIFC29 H33 N3 O6 ZrP 1 21/n 19.4729; 22.863; 12.408
90; 93.774; 90		2681.5Schneider, Fabian; Zhao, Tiankun; Huhn, Thomas
Cytotoxic heteroleptic heptacoordinate salan zirconium(iv)-bis-chelates - synthesis, aqueous stability and X-ray structure analysis.
Chemical communications (Cambridge, England), 2016, 52, 10151-10154
7124892 CIFC31 H29 B2 F10 N O2P -19.8867; 10.3242; 16.1713
76.107; 86.224; 73.616		1537.3Fleige, Mirco; Möbus, Juri; Vom Stein, Thorsten; Glorius, Frank; Stephan, Douglas W.
Lewis acid catalysis: catalytic hydroboration of alkynes initiated by Piers' borane.
Chemical communications (Cambridge, England), 2016, 52, 10830-10833
7124893 CIFC20 H16 Br N2 O2P 1 21/n 121; 7.6152; 23.7899
90; 112.403; 90		3517.3Das, Tapas; Kayet, Anirban; Mishra, Ruchika; Singh, Vinod K.
Highly fluorescent 1,2-dihydropyrimido[1,6-α]indole: an efficient metal free synthesis and photophysical study.
Chemical communications (Cambridge, England), 2016, 52, 11231-11234
7124894 CIFC120 H101 B Cl6 N12 O5C m c 2126.6592; 23.6211; 19.6982
90; 90; 90		12404.3Zhang, Yuehong; Oh, Juwon; Wang, Kang; Shin, Dongju; Zhan, Xiaopeng; Zheng, Yingting; Kim, Dongho; Jiang, Jianzhuang
The first porphyrin-subphthalocyaninatoboron(iii)-fused hybrid with unique conformation and intramolecular charge transfer behavior.
Chemical communications (Cambridge, England), 2016, 52, 10517-10520
7124895 CIFC19 H16 O3P -17.0903; 10.2299; 11.0836
67.824; 77.107; 79.532		721.45Jiang, Chongguo; Xiong, Zhiling; Jin, Shengfei; Gao, Peng; Tang, Yingzhan; Wang, Yanshi; Du, Chuan; Wang, Xiaoyu; Liu, Yang; Lin, Bin; Liu, Yongxiang; Cheng, Maosheng
A Au(i)-catalyzed hydrogen bond-directed tandem strategy to synthesize indeno-chromen-4-one and indeno-quinolin-4-one derivatives.
Chemical communications (Cambridge, England), 2016, 52, 11516-11519
7124896 CIFC78 H66 Eu N7 O18P 21 320.898; 20.898; 20.898
90; 90; 90		9127Sun, Yan-Qiong; Wan, Fang; Li, Xin-Xiong; Lin, Jian; Wu, Tao; Zheng, Shou-Tian; Bu, Xianhui
A lanthanide complex for metal encapsulations and anion exchanges.
Chemical communications (Cambridge, England), 2016, 52, 10125-10128
7124897 CIFC78 H60 Cd Eu N7.5 O26P 21 320.509; 20.509; 20.509
90; 90; 90		8626.48Sun, Yan-Qiong; Wan, Fang; Li, Xin-Xiong; Lin, Jian; Wu, Tao; Zheng, Shou-Tian; Bu, Xianhui
A lanthanide complex for metal encapsulations and anion exchanges.
Chemical communications (Cambridge, England), 2016, 52, 10125-10128
7124898 CIFC26 H20 Cl4 Hg2 N2 O5C 1 2/c 120.25; 12.1502; 13.984
90; 123.951; 90		2854.1Sun, Yan-Qiong; Wan, Fang; Li, Xin-Xiong; Lin, Jian; Wu, Tao; Zheng, Shou-Tian; Bu, Xianhui
A lanthanide complex for metal encapsulations and anion exchanges.
Chemical communications (Cambridge, England), 2016, 52, 10125-10128
7124899 CIFC52 H48 N8 O25 Pb2P 1 21/c 116.777; 12.3446; 13.27
90; 96.886; 90		2728.5Sun, Yan-Qiong; Wan, Fang; Li, Xin-Xiong; Lin, Jian; Wu, Tao; Zheng, Shou-Tian; Bu, Xianhui
A lanthanide complex for metal encapsulations and anion exchanges.
Chemical communications (Cambridge, England), 2016, 52, 10125-10128
7124900 CIFC14 H12P 1 21/c 118.222; 5.648; 20.014
90; 97.925; 90		2040.1Chen, Gen-Qiang; Fang, Wei; Wei, Yin; Tang, Xiang-Ying; Shi, Min
Gold(i)-catalyzed dehydrogenative cycloisomerization of 1,5-enynes.
Chemical communications (Cambridge, England), 2016, 52, 10799-10802
7124901 CIFC41 H30 B Cl3 N4 O2P -19.821; 12.383; 15.111
79.156; 84.922; 73.193		1726.7Saikawa, Makoto; Nakamura, Takashi; Uchida, Junji; Yamamura, Masaki; Nabeshima, Tatsuya
Synthesis of figure-of-eight helical bisBODIPY macrocycles and their chiroptical properties.
Chemical communications (Cambridge, England), 2016, 52, 10727-10730
7124902 CIFC61.5 H46.5 B Cl4.5 N4 O6P -113.411; 20.416; 21.32
75.181; 83.052; 88.03		5602Saikawa, Makoto; Nakamura, Takashi; Uchida, Junji; Yamamura, Masaki; Nabeshima, Tatsuya
Synthesis of figure-of-eight helical bisBODIPY macrocycles and their chiroptical properties.
Chemical communications (Cambridge, England), 2016, 52, 10727-10730
7124903 CIFC40.5 H30 B Cl N4 O2P 19.887; 11.839; 15.495
77.762; 80.071; 66.473		1617.3Saikawa, Makoto; Nakamura, Takashi; Uchida, Junji; Yamamura, Masaki; Nabeshima, Tatsuya
Synthesis of figure-of-eight helical bisBODIPY macrocycles and their chiroptical properties.
Chemical communications (Cambridge, England), 2016, 52, 10727-10730
7124904 CIFC60 H42 B2 N4 O6P 1 21 111.4322; 16.3704; 12.5755
90; 100.994; 90		2310.31Saikawa, Makoto; Nakamura, Takashi; Uchida, Junji; Yamamura, Masaki; Nabeshima, Tatsuya
Synthesis of figure-of-eight helical bisBODIPY macrocycles and their chiroptical properties.
Chemical communications (Cambridge, England), 2016, 52, 10727-10730
7124905 CIFC62 H44 B2 Cl6 N4 O6P 1 21/n 127.3653; 13.783; 31.7984
90; 114.516; 90		10912.3Saikawa, Makoto; Nakamura, Takashi; Uchida, Junji; Yamamura, Masaki; Nabeshima, Tatsuya
Synthesis of figure-of-eight helical bisBODIPY macrocycles and their chiroptical properties.
Chemical communications (Cambridge, England), 2016, 52, 10727-10730
7124906 CIFC33 H53 B K N3 O SiP 21 21 2111.5483; 15.6266; 19.1969
90; 90; 90		3464.3Dawkins, Michael J. C.; Middleton, Ewart; Kefalidis, Christos E.; Dange, Deepak; Juckel, Martin M.; Maron, Laurent; Jones, Cameron
Two-coordinate terminal zinc hydride complexes: synthesis, structure and preliminary reactivity studies.
Chemical communications (Cambridge, England), 2016, 52, 10490-10492
7124907 CIFC47 H59 N O3 Si ZnP -4 21 c21.1923; 21.1923; 18.9615
90; 90; 90		8515.9Dawkins, Michael J. C.; Middleton, Ewart; Kefalidis, Christos E.; Dange, Deepak; Juckel, Martin M.; Maron, Laurent; Jones, Cameron
Two-coordinate terminal zinc hydride complexes: synthesis, structure and preliminary reactivity studies.
Chemical communications (Cambridge, England), 2016, 52, 10490-10492
7124908 CIFC33 H53 B Br N3 O Si ZnP 1 21/c 115.203; 11.974; 19.965
90; 100.3; 90		3575.9Dawkins, Michael J. C.; Middleton, Ewart; Kefalidis, Christos E.; Dange, Deepak; Juckel, Martin M.; Maron, Laurent; Jones, Cameron
Two-coordinate terminal zinc hydride complexes: synthesis, structure and preliminary reactivity studies.
Chemical communications (Cambridge, England), 2016, 52, 10490-10492
7124909 CIFC84 H98 N2 O2 Si2 Zn2P -113.39; 14.317; 20.067
80.79; 79.66; 71.54		3567.7Dawkins, Michael J. C.; Middleton, Ewart; Kefalidis, Christos E.; Dange, Deepak; Juckel, Martin M.; Maron, Laurent; Jones, Cameron
Two-coordinate terminal zinc hydride complexes: synthesis, structure and preliminary reactivity studies.
Chemical communications (Cambridge, England), 2016, 52, 10490-10492
7124910 CIFC42 H48.98 Br0.02 N Si ZnP -114.0869; 15.8901; 17.1769
72.101; 81.448; 81.036		3593.29Dawkins, Michael J. C.; Middleton, Ewart; Kefalidis, Christos E.; Dange, Deepak; Juckel, Martin M.; Maron, Laurent; Jones, Cameron
Two-coordinate terminal zinc hydride complexes: synthesis, structure and preliminary reactivity studies.
Chemical communications (Cambridge, England), 2016, 52, 10490-10492
7124911 CIFC45 H54 Br N O3 Si ZnI 41/a :220.9835; 20.9835; 37.613
90; 90; 90		16561.3Dawkins, Michael J. C.; Middleton, Ewart; Kefalidis, Christos E.; Dange, Deepak; Juckel, Martin M.; Maron, Laurent; Jones, Cameron
Two-coordinate terminal zinc hydride complexes: synthesis, structure and preliminary reactivity studies.
Chemical communications (Cambridge, England), 2016, 52, 10490-10492
7124912 CIFC55.75 H62 N O2 Si ZnP n a 2127.289; 12.855; 28.084
90; 90; 90		9852Dawkins, Michael J. C.; Middleton, Ewart; Kefalidis, Christos E.; Dange, Deepak; Juckel, Martin M.; Maron, Laurent; Jones, Cameron
Two-coordinate terminal zinc hydride complexes: synthesis, structure and preliminary reactivity studies.
Chemical communications (Cambridge, England), 2016, 52, 10490-10492
7124913 CIFC44 H53 N Si ZnP b c a18.699; 10.648; 37.755
90; 90; 90		7517Dawkins, Michael J. C.; Middleton, Ewart; Kefalidis, Christos E.; Dange, Deepak; Juckel, Martin M.; Maron, Laurent; Jones, Cameron
Two-coordinate terminal zinc hydride complexes: synthesis, structure and preliminary reactivity studies.
Chemical communications (Cambridge, England), 2016, 52, 10490-10492
7124914 CIFC38 H41 N Si ZnP -19.9787; 11.6997; 14.992
88.8; 85.337; 72.292		1661.8Dawkins, Michael J. C.; Middleton, Ewart; Kefalidis, Christos E.; Dange, Deepak; Juckel, Martin M.; Maron, Laurent; Jones, Cameron
Two-coordinate terminal zinc hydride complexes: synthesis, structure and preliminary reactivity studies.
Chemical communications (Cambridge, England), 2016, 52, 10490-10492
7124915 CIFC28 H23 Br N2 O2P 1 21/c 18.1067; 15.997; 18.8373
90; 99.636; 90		2408.41Zhou, Xiaorong; Peng, Zhixing; Zhao, Hongyang; Zhang, Zhiyin; Lu, Ping; Wang, Yanguang
Rh-Catalyzed annulations of N-methoxybenzamides with ketenimines: synthesis of 3-aminoisoindolinones and 3-diarylmethyleneisoindolinones with strong aggregation induced emission properties.
Chemical communications (Cambridge, England), 2016, 52, 10676-10679
7124916 CIFC32 H23 N OP 1 21/n 113.2048; 9.7962; 36.3
90; 90.681; 90		4695.3Zhou, Xiaorong; Peng, Zhixing; Zhao, Hongyang; Zhang, Zhiyin; Lu, Ping; Wang, Yanguang
Rh-Catalyzed annulations of N-methoxybenzamides with ketenimines: synthesis of 3-aminoisoindolinones and 3-diarylmethyleneisoindolinones with strong aggregation induced emission properties.
Chemical communications (Cambridge, England), 2016, 52, 10676-10679
7124917 CIFC44 H31 N OP 1 21/n 19.7155; 11.1424; 33.67
90; 94.871; 90		3631.7Zhou, Xiaorong; Peng, Zhixing; Zhao, Hongyang; Zhang, Zhiyin; Lu, Ping; Wang, Yanguang
Rh-Catalyzed annulations of N-methoxybenzamides with ketenimines: synthesis of 3-aminoisoindolinones and 3-diarylmethyleneisoindolinones with strong aggregation induced emission properties.
Chemical communications (Cambridge, England), 2016, 52, 10676-10679
7124918 CIFC42 H90 Cl4 N6 O2 ReP -110.4031; 11.9265; 11.9819
64.8219; 75.0617; 82.2082		1299.34Feng, Xiaowen; Liu, Jun-Liang; Pedersen, Kasper S.; Nehrkorn, Joscha; Schnegg, Alexander; Holldack, Karsten; Bendix, Jesper; Sigrist, Marc; Mutka, Hannu; Samohvalov, Dumitru; Aguilà, David; Tong, Ming-Liang; Long, Jeffrey R.; Clérac, Rodolphe
Multifaceted magnetization dynamics in the mononuclear complex [Re<sup>IV</sup>Cl<sub>4</sub>(CN)<sub>2</sub>]<sup>2</sup>.
Chemical communications (Cambridge, England), 2016, 52, 12905-12908
7124919 CIFC13 H9 F3 N2 OP -15.617; 7.3899; 14.156
75.267; 80.383; 88.88		560.1Ragupathi, Ayyakkannu; Sagadevan, Arunachalam; Lin, Chun-Cheng; Hwu, Jih-Ru; Hwang, Kuo Chu
Copper(i)-catalysed oxidative C-N coupling of 2-aminopyridine with terminal alkynes featuring a C[triple bond, length as m-dash]C bond cleavage promoted by visible light.
Chemical communications (Cambridge, England), 2016, 52, 11756-11759
7124920 CIFC5 H16 Cl5 N2 SbP 21 21 217.662; 13.433; 13.883
90; 90; 90		1428.9Mei, Guang-Quan; Zhang, Han-Yue; Liao, Wei-Qiang
A symmetry breaking phase transition-triggered high-temperature solid-state quadratic nonlinear optical switch coupled with a switchable dielectric constant in an organic-inorganic hybrid compound.
Chemical communications (Cambridge, England), 2016, 52, 11135-11138
7124921 CIFC5 H16 Cl5 N2 SbP n m a13.514; 7.818; 13.8
90; 90; 90		1458Mei, Guang-Quan; Zhang, Han-Yue; Liao, Wei-Qiang
A symmetry breaking phase transition-triggered high-temperature solid-state quadratic nonlinear optical switch coupled with a switchable dielectric constant in an organic-inorganic hybrid compound.
Chemical communications (Cambridge, England), 2016, 52, 11135-11138
7124922 CIFC70 H78 N2 O2 Ti2P 1 21/c 111.09321; 22.0757; 28.1078
90; 92.8099; 90		6875.05Liu, Cham-Chuen; Chan, Michael C. W.; Lo, Po-Kam; Lau, Kai-Chung; Yiu, Shek-Man
Multifaceted chelating μ-(η(3):η(3)-antifacial)-(cis-C4R2H2) coordination motif in binuclear complexes.
Chemical communications (Cambridge, England), 2016, 52, 11056-11059
7124923 CIFC72 H83 N2 O2.5 Zr2P -111.3506; 15.5365; 19.1544
79.469; 79.993; 81.353		3245.81Liu, Cham-Chuen; Chan, Michael C. W.; Lo, Po-Kam; Lau, Kai-Chung; Yiu, Shek-Man
Multifaceted chelating μ-(η(3):η(3)-antifacial)-(cis-C4R2H2) coordination motif in binuclear complexes.
Chemical communications (Cambridge, England), 2016, 52, 11056-11059
7124924 CIFC73.5 H85.5 Hf2 N2 O2P 1 21/c 114.6909; 16.2174; 27.5623
90; 103.614; 90		6382.2Liu, Cham-Chuen; Chan, Michael C. W.; Lo, Po-Kam; Lau, Kai-Chung; Yiu, Shek-Man
Multifaceted chelating μ-(η(3):η(3)-antifacial)-(cis-C4R2H2) coordination motif in binuclear complexes.
Chemical communications (Cambridge, England), 2016, 52, 11056-11059
7124925 CIFC211 H82 Cl5 N6 Na2 O12 Sc6P 1 21/c 115.1344; 20.6079; 21.8351
90; 90.019; 90		6810.1Konarev, Dmitri V.; Zorina, Leokadiya V.; Khasanov, Salavat S.; Popov, Alexey A.; Otsuka, Akihiro; Yamochi, Hideki; Saito, Gunzi; Lyubovskaya, Rimma N.
A crystalline anionic complex of scandium nitride endometallofullerene: experimental observation of single-bonded (Sc3N@Ih-C80(-))2 dimers.
Chemical communications (Cambridge, England), 2016, 52, 10763-10766
7124926 CIFC67.5 H108 O13 S6 Zn4P -113.8362; 15.0709; 20.3113
89.161; 79.646; 73.544		3992.8Kelly, Rory P.; Kazeminejad, Neda; Lamsfus, Carlos A.; Maron, Laurent; Roesky, Peter W.
Activation of SO<sub>2</sub> by [Zn(Cp*)<sub>2</sub>] and [(Cp*)Zn<sup>I</sup>-Zn<sup>I</sup>(Cp*)].
Chemical communications (Cambridge, England), 2016, 52, 13090-13093
7124927 CIFC16 H40 N4 O8 S3 Zn2P 1 21/c 112.903; 15.8305; 13.4913
90; 103.699; 90		2677.4Kelly, Rory P.; Kazeminejad, Neda; Lamsfus, Carlos A.; Maron, Laurent; Roesky, Peter W.
Activation of SO<sub>2</sub> by [Zn(Cp*)<sub>2</sub>] and [(Cp*)Zn<sup>I</sup>-Zn<sup>I</sup>(Cp*)].
Chemical communications (Cambridge, England), 2016, 52, 13090-13093
7124928 CIFC29 H20 O2P -18.6037; 9.6242; 13.0214
79.03; 81.504; 74.717		1015.65Chen, Ling; Cui, Yu-Ming; Xu, Zheng; Cao, Jian; Zheng, Zhan-Jiang; Xu, Li-Wen
An efficient approach toward formation of polycyclic coumarin derivatives via carbocation-initiated [4+2] cycloaddition and atom-economical photo-irradiated cyclization.
Chemical communications (Cambridge, England), 2016, 52, 11131-11134
7124929 CIFC17 H14 O4P 1 21/n 18.1218; 27.7422; 12.2315
90; 95.062; 90		2745.2Ji, Wei; Liu, Guofeng; Wang, Fang; Zhu, Zhu; Feng, Chuanliang
Galactose-decorated light-responsive hydrogelator precursors for selectively killing cancer cells.
Chemical communications (Cambridge, England), 2016, 52, 12574-12577
7124930 CIFC29 H33 N3 O2P -19.6437; 11.6855; 12.1217
87.115; 71.784; 82.973		1287.7Quinodoz, P.; Wright, K.; Drouillat, B.; David, O.; Marrot, J.; Couty, F.
Synthesis of homopropargylamines from 2-cyanoazetidines.
Chemical communications (Cambridge, England), 2016, 52, 10072-10075
7124931 CIFC28 H26P c a 2120.325; 11.622; 8.52
90; 90; 90		2012.6Wang, Guohua; Chen, Chao; Peng, Jing
Copper-catalyzed intramolecular aryl-bicyclization of diynes with diaryliodonium salts via vinyl cations.
Chemical communications (Cambridge, England), 2016, 52, 10277-10280
7124932 CIFC192 H240 Cl4 N36 Ni4 O16I 2 323.432; 23.432; 23.432
90; 90; 90		12865.5Xi, Sai-Fei; Bao, Ling-Yu; Lin, Jian-Guo; Liu, Qing-Zhu; Qiu, Ling; Zhang, Feng-Li; Wang, Yu-Xia; Ding, Zheng-Dong; Li, Ke; Gu, Zhi-Guo
Enantiomers of tetrahedral metal-organic cages: a new class of highly efficient G-quadruplex ligands with potential anticancer activities.
Chemical communications (Cambridge, England), 2016, 52, 10261-10264
7124933 CIFC192 H240 Cl4 N36 Ni4 O16I 2 323.4359; 23.4359; 23.4359
90; 90; 90		12872Xi, Sai-Fei; Bao, Ling-Yu; Lin, Jian-Guo; Liu, Qing-Zhu; Qiu, Ling; Zhang, Feng-Li; Wang, Yu-Xia; Ding, Zheng-Dong; Li, Ke; Gu, Zhi-Guo
Enantiomers of tetrahedral metal-organic cages: a new class of highly efficient G-quadruplex ligands with potential anticancer activities.
Chemical communications (Cambridge, England), 2016, 52, 10261-10264
7124934 CIFC204 H264 B6 F24 N36 Ni4 O12P 118.9274; 19.8289; 22.328
110.839; 102.662; 108.564		6881.7Xi, Sai-Fei; Bao, Ling-Yu; Lin, Jian-Guo; Liu, Qing-Zhu; Qiu, Ling; Zhang, Feng-Li; Wang, Yu-Xia; Ding, Zheng-Dong; Li, Ke; Gu, Zhi-Guo
Enantiomers of tetrahedral metal-organic cages: a new class of highly efficient G-quadruplex ligands with potential anticancer activities.
Chemical communications (Cambridge, England), 2016, 52, 10261-10264
7124935 CIFC240 H276 Cl4 N36 Ni4 O6F 41 3 239.2624; 39.2624; 39.2624
90; 90; 90		60524Xi, Sai-Fei; Bao, Ling-Yu; Lin, Jian-Guo; Liu, Qing-Zhu; Qiu, Ling; Zhang, Feng-Li; Wang, Yu-Xia; Ding, Zheng-Dong; Li, Ke; Gu, Zhi-Guo
Enantiomers of tetrahedral metal-organic cages: a new class of highly efficient G-quadruplex ligands with potential anticancer activities.
Chemical communications (Cambridge, England), 2016, 52, 10261-10264
7124936 CIFC241 H264 F3 N36 Ni4 O3 SP 119.222; 20.854; 22.254
106.518; 103.878; 112.172		7289.5Xi, Sai-Fei; Bao, Ling-Yu; Lin, Jian-Guo; Liu, Qing-Zhu; Qiu, Ling; Zhang, Feng-Li; Wang, Yu-Xia; Ding, Zheng-Dong; Li, Ke; Gu, Zhi-Guo
Enantiomers of tetrahedral metal-organic cages: a new class of highly efficient G-quadruplex ligands with potential anticancer activities.
Chemical communications (Cambridge, England), 2016, 52, 10261-10264
7124937 CIFC29 H28 F4 N2 O5P 1 21/c 112.4966; 9.7777; 22.6334
90; 100.263; 90		2721.3Hua, Hui-Liang; Zhang, Bo-Sheng; He, Yu-Tao; Qiu, Yi-Feng; Hu, Jing-Yuan; Yang, Yu-Chen; Liang, Yong-Min
Copper-catalyzed difluoromethylation of propargylamide-substituted indoles: synthesis of mono- and bis-difluoromethylated indoloazepinone derivatives.
Chemical communications (Cambridge, England), 2016, 52, 10396-10399
7124938 CIFC24 H22 F2 N2 O3P b c a12.2175; 15.8782; 22.0697
90; 90; 90		4281.34Hua, Hui-Liang; Zhang, Bo-Sheng; He, Yu-Tao; Qiu, Yi-Feng; Hu, Jing-Yuan; Yang, Yu-Chen; Liang, Yong-Min
Copper-catalyzed difluoromethylation of propargylamide-substituted indoles: synthesis of mono- and bis-difluoromethylated indoloazepinone derivatives.
Chemical communications (Cambridge, England), 2016, 52, 10396-10399
7124939 CIFC28 H25 Cl F4 N2 O5P 1 21/c 112.8985; 14.8772; 27.961
90; 97.992; 90		5313.4Hua, Hui-Liang; Zhang, Bo-Sheng; He, Yu-Tao; Qiu, Yi-Feng; Hu, Jing-Yuan; Yang, Yu-Chen; Liang, Yong-Min
Copper-catalyzed difluoromethylation of propargylamide-substituted indoles: synthesis of mono- and bis-difluoromethylated indoloazepinone derivatives.
Chemical communications (Cambridge, England), 2016, 52, 10396-10399
7124940 CIFC29 H28 N2 OP 1 21 18.118; 16.336; 8.515
90; 91.597; 90		1128.8Wilkie, Ross P.; Neal, Andrew R.; Johnston, Craig A.; Voute, Nicholas; Lancefield, Christopher S.; Stell, Matthew D.; Medda, Federico; Makiyi, Edward F.; Turner, Emma M.; Stephen Ojo, O.; Slawin, Alexandra M. Z.; Lebl, Tomas; Mullen, Peter; Harrison, David J.; Ireland, Chris M.; Westwood, Nicholas J.
Total synthesis of dehaloperophoramidine using a highly diastereoselective Hosomi-Sakurai reaction.
Chemical communications (Cambridge, England), 2016, 52, 10747-10750
7124941 CIFC41 H38 N4 O2R -3 :H24.722; 24.722; 13.524
90; 90; 120		7158Wilkie, Ross P.; Neal, Andrew R.; Johnston, Craig A.; Voute, Nicholas; Lancefield, Christopher S.; Stell, Matthew D.; Medda, Federico; Makiyi, Edward F.; Turner, Emma M.; Stephen Ojo, O.; Slawin, Alexandra M. Z.; Lebl, Tomas; Mullen, Peter; Harrison, David J.; Ireland, Chris M.; Westwood, Nicholas J.
Total synthesis of dehaloperophoramidine using a highly diastereoselective Hosomi-Sakurai reaction.
Chemical communications (Cambridge, England), 2016, 52, 10747-10750
7124942 CIFC28 H27 B F4 N4P 1 21/c 16.691; 29.96; 12.952
90; 104.2; 90		2517Wilkie, Ross P.; Neal, Andrew R.; Johnston, Craig A.; Voute, Nicholas; Lancefield, Christopher S.; Stell, Matthew D.; Medda, Federico; Makiyi, Edward F.; Turner, Emma M.; Stephen Ojo, O.; Slawin, Alexandra M. Z.; Lebl, Tomas; Mullen, Peter; Harrison, David J.; Ireland, Chris M.; Westwood, Nicholas J.
Total synthesis of dehaloperophoramidine using a highly diastereoselective Hosomi-Sakurai reaction.
Chemical communications (Cambridge, England), 2016, 52, 10747-10750
7124943 CIFC29 H31 N3 O SP 1 21 113.438; 14.165; 13.5796
90; 93.657; 90		2579.6Wilkie, Ross P.; Neal, Andrew R.; Johnston, Craig A.; Voute, Nicholas; Lancefield, Christopher S.; Stell, Matthew D.; Medda, Federico; Makiyi, Edward F.; Turner, Emma M.; Stephen Ojo, O.; Slawin, Alexandra M. Z.; Lebl, Tomas; Mullen, Peter; Harrison, David J.; Ireland, Chris M.; Westwood, Nicholas J.
Total synthesis of dehaloperophoramidine using a highly diastereoselective Hosomi-Sakurai reaction.
Chemical communications (Cambridge, England), 2016, 52, 10747-10750
7124944 CIFC56 H82 N4 Na4 O6P 1 2/c 118.372; 10.659; 28.255
90; 100.193; 90		5446Lichtenberg, C.; Krummenacher, I.
Aminotroponiminates as tunable, redox-active ligands: reversible single electron transfer and reductive dimerisation.
Chemical communications (Cambridge, England), 2016, 52, 10044-10047
7124945 CIFC25 H39 Co N6 O4P 1 21/n 114.5396; 9.6307; 20.8295
90; 109.316; 90		2752.5Das, Debasree; Pattanayak, Santanu; Singh, Kundan K.; Garai, Bikash; Sen Gupta, Sayam
Electrocatalytic water oxidation by a molecular cobalt complex through a high valent cobalt oxo intermediate.
Chemical communications (Cambridge, England), 2016, 52, 11787-11790
7124946 CIFC167 H278 Al4 N8 O12I 1 2/a 129.9091; 11.0908; 25.9834
90; 108.075; 90		8193.8McKeown, Paul; Davidson, Matthew G.; Kociok-Köhn, Gabriele; Jones, Matthew D.
Aluminium salalens vs. salans: "Initiator Design" for the isoselective polymerisation of rac-lactide.
Chemical communications (Cambridge, England), 2016, 52, 10431-10434
7124947 CIFC33 H51 Al N2 O3P 1 21/c 112.1388; 19.0837; 14.1406
90; 102.663; 90		3196.04McKeown, Paul; Davidson, Matthew G.; Kociok-Köhn, Gabriele; Jones, Matthew D.
Aluminium salalens vs. salans: "Initiator Design" for the isoselective polymerisation of rac-lactide.
Chemical communications (Cambridge, England), 2016, 52, 10431-10434
7124948 CIFC38 H61 Al N2 O2P 1 21/c 113.8779; 13.002; 20.8532
90; 98.2288; 90		3724McKeown, Paul; Davidson, Matthew G.; Kociok-Köhn, Gabriele; Jones, Matthew D.
Aluminium salalens vs. salans: "Initiator Design" for the isoselective polymerisation of rac-lactide.
Chemical communications (Cambridge, England), 2016, 52, 10431-10434
7124949 CIFC43 H61 Al N2 O3P -110.9794; 14.2923; 15.1168
115.692; 100.605; 102.864		1974.85McKeown, Paul; Davidson, Matthew G.; Kociok-Köhn, Gabriele; Jones, Matthew D.
Aluminium salalens vs. salans: "Initiator Design" for the isoselective polymerisation of rac-lactide.
Chemical communications (Cambridge, England), 2016, 52, 10431-10434
7124950 CIFC23 H20 Br N O P TcC 1 2/c 122.001; 13.607; 17.541
90; 126.91; 90		4198.8Ackermann, J.; Hagenbach, A.; Abram, U.
{Tc(NO)(Cp)(PPh3)}(+) - a novel technetium(i) core.
Chemical communications (Cambridge, England), 2016, 52, 10285-10288
7124951 CIFC24 H20 B F4 N O2 P TcP 1 21/c 19.27; 17.374; 14.27
90; 100.29; 90		2261.3Ackermann, J.; Hagenbach, A.; Abram, U.
{Tc(NO)(Cp)(PPh3)}(+) - a novel technetium(i) core.
Chemical communications (Cambridge, England), 2016, 52, 10285-10288
7124952 CIFC29 H25 N O P TcP 1 21 19.179; 13.937; 10.048
90; 112.89; 90		1184.2Ackermann, J.; Hagenbach, A.; Abram, U.
{Tc(NO)(Cp)(PPh3)}(+) - a novel technetium(i) core.
Chemical communications (Cambridge, England), 2016, 52, 10285-10288
7124953 CIFC36.5 H31 Br3 Cl N O3 P2 TcP 1 21/c 112.551; 14.394; 44.488
90; 97.55; 90		7967.5Ackermann, J.; Hagenbach, A.; Abram, U.
{Tc(NO)(Cp)(PPh3)}(+) - a novel technetium(i) core.
Chemical communications (Cambridge, England), 2016, 52, 10285-10288
7124954 CIFC25 H28 N2 O4 SP 21 21 218.782; 10.8274; 26.0299
90; 90; 90		2475.08Rainoldi, G.; Faltracco, M.; Lo Presti, L.; Silvani, A.; Lesma, G.
Highly diastereoselective entry into chiral spirooxindole-based 4-methyleneazetidines via formal [2+2] annulation reaction.
Chemical communications (Cambridge, England), 2016, 52, 11575-11578
7124955 CIFC18 H12 Cu2 N0 O10 SiP 63/m m c18.5185; 18.5185; 19.1215
90; 90; 120		5678.9Gao, Chao-Ying; Tian, Hong-Rui; Ai, Jing; Li, Lei-Jiao; Dang, Song; Lan, Ya-Qian; Sun, Zhong-Ming
A microporous Cu-MOF with optimized open metal sites and pore spaces for high gas storage and active chemical fixation of CO2.
Chemical communications (Cambridge, England), 2016, 52, 11147-11150
7124956 CIFC8 H16 Cu F6 N4 O4 VP 4/n b m :29.7325; 9.7325; 8.2154
90; 90; 90		778.18Manson, Jamie L.; Schlueter, John A.; Garrett, Kerry E.; Goddard, Paul A.; Lancaster, Tom; Möller, Johannes S; Blundell, Stephen J.; Steele, Andrew J.; Franke, Isabel; Pratt, Francis L.; Singleton, John; Bendix, Jesper; Lapidus, Saul H.; Uhlarz, Marc; Ayala-Valenzuela, Oscar; McDonald, Ross D.; Gurak, Mary; Baines, Christopher
Bimetallic MOFs (H<sub>3</sub>O)<sub>x</sub>[Cu(MF<sub>6</sub>)(pyrazine)<sub>2</sub>]·(4 - x)H<sub>2</sub>O (M = V<sup>4+</sup>, x = 0; M = Ga<sup>3+</sup>, x = 1): co-existence of ordered and disordered quantum spins in the V<sup>4+</sup> system.
Chemical communications (Cambridge, England), 2016, 52, 12653-12656
7124957 CIFC8 H17 Cu F6 Ga N4 O4P 4/n b m :29.7134; 9.7134; 8.2415
90; 90; 90		777.59Manson, Jamie L.; Schlueter, John A.; Garrett, Kerry E.; Goddard, Paul A.; Lancaster, Tom; Möller, Johannes S; Blundell, Stephen J.; Steele, Andrew J.; Franke, Isabel; Pratt, Francis L.; Singleton, John; Bendix, Jesper; Lapidus, Saul H.; Uhlarz, Marc; Ayala-Valenzuela, Oscar; McDonald, Ross D.; Gurak, Mary; Baines, Christopher
Bimetallic MOFs (H<sub>3</sub>O)<sub>x</sub>[Cu(MF<sub>6</sub>)(pyrazine)<sub>2</sub>]·(4 - x)H<sub>2</sub>O (M = V<sup>4+</sup>, x = 0; M = Ga<sup>3+</sup>, x = 1): co-existence of ordered and disordered quantum spins in the V<sup>4+</sup> system.
Chemical communications (Cambridge, England), 2016, 52, 12653-12656
7124958 CIFC24 H20 N2 O2P 1 21/c 110.3006; 17.4826; 10.8631
90; 92.484; 90		1954.4Huo, Congde; Dong, Jie; Su, Yingpeng; Tang, Jing; Chen, Fengjuan
Iron-catalyzed oxidative sp<sup>3</sup> carbon-hydrogen bond functionalization of 3,4-dihydro-1,4-benzoxazin-2-ones.
Chemical communications (Cambridge, England), 2016, 52, 13341-13344
7124959 CIFC19 H22 N2 O2 SP 1 21 19.5967; 9.265; 10.1709
90; 102.244; 90		883.76Zhao, Quan-Qing; Hu, Xiao-Qiang; Yang, Meng-Nan; Chen, Jia-Rong; Xiao, Wen-Jing
A visible-light photocatalytic N-radical cascade of hydrazones for the synthesis of dihydropyrazole-fused benzosultams.
Chemical communications (Cambridge, England), 2016, 52, 12749-12752
7124960 CIFC19 H20 N2 O2 SP -19.31; 13.2449; 14.8906
69.506; 77.927; 89.163		1678.5Zhao, Quan-Qing; Hu, Xiao-Qiang; Yang, Meng-Nan; Chen, Jia-Rong; Xiao, Wen-Jing
A visible-light photocatalytic N-radical cascade of hydrazones for the synthesis of dihydropyrazole-fused benzosultams.
Chemical communications (Cambridge, England), 2016, 52, 12749-12752
7124961 CIFC104 H92 Br8 Cl2 N4 OP -110.9254; 13.4449; 15.8457
95.9; 100.524; 95.947		2258.4Krzeszewski, Maciej; Swider, Paweł; Dobrzycki, Łukasz; Cyrański, Michał K; Danikiewicz, Witold; Gryko, Daniel T.
The role of steric hindrance in the intramolecular oxidative aromatic coupling of pyrrolo[3,2-b]pyrroles.
Chemical communications (Cambridge, England), 2016, 52, 11539-11542
7124962 CIFC46 H51 Ge N2 O PP 1 21/n 113.91699; 19.62321; 14.94628
90; 94.7717; 90		4067.62Li, Zhongshu; Chen, Xiaodan; Li, Yaqi; Su, Cheng-Yong; Grützmacher, Hansjörg
N-Heterocyclic carbene phosphaketene adducts as precursors to carbene-phosphinidene adducts and a rearranged π-system.
Chemical communications (Cambridge, England), 2016, 52, 11343-11346
7124963 CIFC46 H51 N2 O P SiP -19.4352; 12.6209; 17.8147
85.36; 78.369; 76.089		2015.71Li, Zhongshu; Chen, Xiaodan; Li, Yaqi; Su, Cheng-Yong; Grützmacher, Hansjörg
N-Heterocyclic carbene phosphaketene adducts as precursors to carbene-phosphinidene adducts and a rearranged π-system.
Chemical communications (Cambridge, England), 2016, 52, 11343-11346
7124964 CIFC46 H51 N2 O P SnP 1 21/n 114.0166; 19.8309; 14.945
90; 94.185; 90		4143.06Li, Zhongshu; Chen, Xiaodan; Li, Yaqi; Su, Cheng-Yong; Grützmacher, Hansjörg
N-Heterocyclic carbene phosphaketene adducts as precursors to carbene-phosphinidene adducts and a rearranged π-system.
Chemical communications (Cambridge, England), 2016, 52, 11343-11346
7124965 CIFC49 H61 N2 O P SnP -110.64809; 11.6076; 19.4163
91.4216; 92.8956; 110.289		2245.77Li, Zhongshu; Chen, Xiaodan; Li, Yaqi; Su, Cheng-Yong; Grützmacher, Hansjörg
N-Heterocyclic carbene phosphaketene adducts as precursors to carbene-phosphinidene adducts and a rearranged π-system.
Chemical communications (Cambridge, England), 2016, 52, 11343-11346
7124966 CIFC45 H51 Ge N2 PP 1 21/n 124.0628; 12.8152; 25.4632
90; 94.7933; 90		7824.62Li, Zhongshu; Chen, Xiaodan; Li, Yaqi; Su, Cheng-Yong; Grützmacher, Hansjörg
N-Heterocyclic carbene phosphaketene adducts as precursors to carbene-phosphinidene adducts and a rearranged π-system.
Chemical communications (Cambridge, England), 2016, 52, 11343-11346
7124967 CIFC160 H164 N8 O1.5 P4 Sn4P -113.0114; 17.0048; 18.7117
111.389; 94.838; 110.638		3498.2Li, Zhongshu; Chen, Xiaodan; Li, Yaqi; Su, Cheng-Yong; Grützmacher, Hansjörg
N-Heterocyclic carbene phosphaketene adducts as precursors to carbene-phosphinidene adducts and a rearranged π-system.
Chemical communications (Cambridge, England), 2016, 52, 11343-11346
7124968 CIFC51 H41 N7 O2P 1 21/c 111.998; 14.423; 21.871
90; 92.101; 90		3782Mosca, Lorenzo; Čejka, Jan; Dolenský, Bohumil; Havlík, Martin; Jakubek, Milan; Kaplánek, Robert; Král, Vladimír; Anzenbacher, Pavel
Bowl-shaped Tröger's bases and their recognition properties.
Chemical communications (Cambridge, England), 2016, 52, 10664-10667
7124969 CIFC69 H52 N8 O4P 1 21/c 121.3761; 12.4047; 21.2424
90; 113.697; 90		5157.8Mosca, Lorenzo; Čejka, Jan; Dolenský, Bohumil; Havlík, Martin; Jakubek, Milan; Kaplánek, Robert; Král, Vladimír; Anzenbacher, Pavel
Bowl-shaped Tröger's bases and their recognition properties.
Chemical communications (Cambridge, England), 2016, 52, 10664-10667
7124970 CIFC46 H38 Cl2 N6P -117.9422; 18.3629; 20.9128
107.088; 100.483; 116.305		5498.3Mosca, Lorenzo; Čejka, Jan; Dolenský, Bohumil; Havlík, Martin; Jakubek, Milan; Kaplánek, Robert; Král, Vladimír; Anzenbacher, Pavel
Bowl-shaped Tröger's bases and their recognition properties.
Chemical communications (Cambridge, England), 2016, 52, 10664-10667
7124971 CIFC17 H14 Ag N7 O4I 41/a :231.37; 31.37; 7.8467
90; 90; 90		7721.8Li, Cheng-Peng; Wang, Si; Guo, Wei; Yan, Yan; Du, Miao
Dual structure evolution of a Ag(i) supramolecular framework triggered by anion-exchange: replacement of terminal ligand and switching of network interpenetration degree.
Chemical communications (Cambridge, England), 2016, 52, 11060-11063
7124972 CIFC17 H15 Ag N7 O3.5I 41/a :231.065; 31.065; 8.0003
90; 90; 90		7720.6Li, Cheng-Peng; Wang, Si; Guo, Wei; Yan, Yan; Du, Miao
Dual structure evolution of a Ag(i) supramolecular framework triggered by anion-exchange: replacement of terminal ligand and switching of network interpenetration degree.
Chemical communications (Cambridge, England), 2016, 52, 11060-11063
7124973 CIFC19 H14 Ag F3 N6 O3P 42/n :222.8131; 22.8131; 7.7879
90; 90; 90		4053.1Li, Cheng-Peng; Wang, Si; Guo, Wei; Yan, Yan; Du, Miao
Dual structure evolution of a Ag(i) supramolecular framework triggered by anion-exchange: replacement of terminal ligand and switching of network interpenetration degree.
Chemical communications (Cambridge, England), 2016, 52, 11060-11063
7124974 CIFC29 H41 F6 Fe N4 O2 PP 1 21/c 121.0286; 8.7204; 17.6555
90; 99.237; 90		3195.6Kwon, Yubin M.; Delgado, Mayra; Zakharov, Lev N.; Seda, Takele; Gilbertson, John D.
Nitrite reduction by a pyridinediimine complex with a proton-responsive secondary coordination sphere.
Chemical communications (Cambridge, England), 2016, 52, 11016-11019
7124975 CIFC29.5 H41 Cl Fe N4 O2P 1 21/c 19.6385; 13.7609; 23.41
90; 92.164; 90		3102.8Kwon, Yubin M.; Delgado, Mayra; Zakharov, Lev N.; Seda, Takele; Gilbertson, John D.
Nitrite reduction by a pyridinediimine complex with a proton-responsive secondary coordination sphere.
Chemical communications (Cambridge, England), 2016, 52, 11016-11019
7124976 CIFC29 H44 Br3 Fe N5P -110.0331; 13.3181; 14.1
64.813; 81.091; 81.046		1675.9Kwon, Yubin M.; Delgado, Mayra; Zakharov, Lev N.; Seda, Takele; Gilbertson, John D.
Nitrite reduction by a pyridinediimine complex with a proton-responsive secondary coordination sphere.
Chemical communications (Cambridge, England), 2016, 52, 11016-11019
7124977 CIFC27 H40 F6 Fe N6 O2 PP -18.4876; 12.8367; 16.0181
112.855; 90.553; 99.918		1578.52Kwon, Yubin M.; Delgado, Mayra; Zakharov, Lev N.; Seda, Takele; Gilbertson, John D.
Nitrite reduction by a pyridinediimine complex with a proton-responsive secondary coordination sphere.
Chemical communications (Cambridge, England), 2016, 52, 11016-11019
7124978 CIFC25 H25 Cl Hg N2 O3P -19.4629; 11.35; 12.3473
103.843; 109.616; 99.745		1166.87Hong, Jung-Ho; Kurapati, Sathish; Jo, Yunhee; Shin, June-Ho; Cho, Dong-Gyu
Accelerated hydration reaction of an unsymmetrical tolan evidenced by a Hg(ii)-trapped macrocycle and its application as a Hg(ii)-selective indicator.
Chemical communications (Cambridge, England), 2016, 52, 10759-10762
7124979 CIFC127 H139 Cd2 Cr4 N8 Na5 O42F 2 2 240.623; 41.321; 51.868
90; 90; 90		87065Xia, Qingchun; Liu, Yan; Li, Zijian; Gong, Wei; Cui, Yong
A Cr(salen)-based metal-organic framework as a versatile catalyst for efficient asymmetric transformations.
Chemical communications (Cambridge, England), 2016, 52, 13167-13170
7124980 CIFC8 H8 N2 O4P 1 21/c 14.7242; 12.369; 13.831
90; 82.466; 90		801.2Kennedy, Stuart R.; Miquelot, Adeline; Aguilar, Juan A.; Steed, Jonathan W.
Trimeric cyclamers: solution aggregation and high Z' crystals based on guest structure and basicity.
Chemical communications (Cambridge, England), 2016, 52, 11846-11849
7124981 CIFC12 H16 N2 O5P 1 21/c 122.309; 19.1478; 9.01
90; 91.398; 90		3847.6Kennedy, Stuart R.; Miquelot, Adeline; Aguilar, Juan A.; Steed, Jonathan W.
Trimeric cyclamers: solution aggregation and high Z' crystals based on guest structure and basicity.
Chemical communications (Cambridge, England), 2016, 52, 11846-11849
7124982 CIFC10 H11 N3 O4P -113.3689; 15.143; 18.786
77.079; 74.563; 63.839		3265.5Kennedy, Stuart R.; Miquelot, Adeline; Aguilar, Juan A.; Steed, Jonathan W.
Trimeric cyclamers: solution aggregation and high Z' crystals based on guest structure and basicity.
Chemical communications (Cambridge, England), 2016, 52, 11846-11849
7124983 CIFC11 H14 N2 O5P 1 21/n 114.6759; 31.285; 15.9269
90; 99.324; 90		7216Kennedy, Stuart R.; Miquelot, Adeline; Aguilar, Juan A.; Steed, Jonathan W.
Trimeric cyclamers: solution aggregation and high Z' crystals based on guest structure and basicity.
Chemical communications (Cambridge, England), 2016, 52, 11846-11849
7124984 CIFC12.2 H11.5 N2.7 O5.4P -4 21 c17.707; 17.707; 7.3732
90; 90; 90		2311.8Kennedy, Stuart R.; Miquelot, Adeline; Aguilar, Juan A.; Steed, Jonathan W.
Trimeric cyclamers: solution aggregation and high Z' crystals based on guest structure and basicity.
Chemical communications (Cambridge, England), 2016, 52, 11846-11849
7124985 CIFC20 H22 N4 O4P -14.5668; 20.531; 20.9009
76.149; 88.228; 88.156		1901.2Kennedy, Stuart R.; Miquelot, Adeline; Aguilar, Juan A.; Steed, Jonathan W.
Trimeric cyclamers: solution aggregation and high Z' crystals based on guest structure and basicity.
Chemical communications (Cambridge, England), 2016, 52, 11846-11849
7124986 CIFC8 H10 N2 O5P 21 21 214.5426; 10.729; 18.692
90; 90; 90		911Kennedy, Stuart R.; Miquelot, Adeline; Aguilar, Juan A.; Steed, Jonathan W.
Trimeric cyclamers: solution aggregation and high Z' crystals based on guest structure and basicity.
Chemical communications (Cambridge, England), 2016, 52, 11846-11849
7124987 CIFC28 H24 N4 O4 Pd2P 1 21/c 113.9426; 18.5793; 18.8456
90; 146.18; 90		2717.16Monas, Andrea; Užarević, Krunoslav; Halasz, Ivan; Kulcsár, Marina Juribašić; Ćurić, Manda
Vapour-induced solid-state C-H bond activation for the clean synthesis of an organopalladium biothiol sensor.
Chemical communications (Cambridge, England), 2016, 52, 12960-12963
7124988 CIFC28 H24 N4 O4 Pd2P b c a15.7028; 12.1884; 27.7307
90; 90; 90		5307.4Monas, Andrea; Užarević, Krunoslav; Halasz, Ivan; Kulcsár, Marina Juribašić; Ćurić, Manda
Vapour-induced solid-state C-H bond activation for the clean synthesis of an organopalladium biothiol sensor.
Chemical communications (Cambridge, England), 2016, 52, 12960-12963
7124989 CIFC30 H36 B2 Br4 Fe N6 O6C 1 2/c 126.14; 8.4019; 18.4972
90; 117.658; 90		3598.3Cecot, Giacomo; Alameddine, Bassam; Prior, Stéphanie; Zorzi, Rita De; Geremia, Silvano; Scopelliti, Rosario; Fadaei, Farzaneh T.; Solari, Euro; Severin, Kay
Large heterometallic coordination cages with gyrobifastigium-like geometry.
Chemical communications (Cambridge, England), 2016, 52, 11243-11246
7124990 CIFC50 H52 B2 Fe N10 O6P 1 21/c 18.84673; 38.91135; 14.15673
90; 105.312; 90		4700.3Cecot, Giacomo; Alameddine, Bassam; Prior, Stéphanie; Zorzi, Rita De; Geremia, Silvano; Scopelliti, Rosario; Fadaei, Farzaneh T.; Solari, Euro; Severin, Kay
Large heterometallic coordination cages with gyrobifastigium-like geometry.
Chemical communications (Cambridge, England), 2016, 52, 11243-11246
7124991 CIFC408 H368 B8 F48 Fe4 N40 O72 P16 Pt8 S16P -128.3614; 28.8276; 41.0379
101.861; 92.914; 104.12		31663Cecot, Giacomo; Alameddine, Bassam; Prior, Stéphanie; Zorzi, Rita De; Geremia, Silvano; Scopelliti, Rosario; Fadaei, Farzaneh T.; Solari, Euro; Severin, Kay
Large heterometallic coordination cages with gyrobifastigium-like geometry.
Chemical communications (Cambridge, England), 2016, 52, 11243-11246
7124992 CIFC24 H24 B2 Br4 Fe N6 O6I 1 2/a 114.7088; 12.8848; 18.6454
90; 102.859; 90		3445.05Cecot, Giacomo; Alameddine, Bassam; Prior, Stéphanie; Zorzi, Rita De; Geremia, Silvano; Scopelliti, Rosario; Fadaei, Farzaneh T.; Solari, Euro; Severin, Kay
Large heterometallic coordination cages with gyrobifastigium-like geometry.
Chemical communications (Cambridge, England), 2016, 52, 11243-11246
7124993 CIFC44 H40 B2 Fe N10 O6P 1 21/c 19.4866; 10.6979; 47.959
90; 94.425; 90		4852.7Cecot, Giacomo; Alameddine, Bassam; Prior, Stéphanie; Zorzi, Rita De; Geremia, Silvano; Scopelliti, Rosario; Fadaei, Farzaneh T.; Solari, Euro; Severin, Kay
Large heterometallic coordination cages with gyrobifastigium-like geometry.
Chemical communications (Cambridge, England), 2016, 52, 11243-11246
7124994 CIFC95 H34 O2P 1 21/c 110.8278; 30.7175; 16.9665
90; 102.171; 90		5516.3Vidal, Sara; Izquierdo, Marta; Law, Wai Kit; Jiang, Kui; Filippone, Salvatore; Perles, Josefina; Yan, He; Martín, Nazario
Photochemical site-selective synthesis of [70]methanofullerenes.
Chemical communications (Cambridge, England), 2016, 52, 12733-12736
7124995 CIFC140 H136 K4 O11P -113.3928; 15.4263; 15.9182
72.759; 71.007; 66.158		2792.2Sumy, Daniel P.; Finke, Aaron D.; Whalley, Adam C.
The reductive aromatization of tridecacyclene.
Chemical communications (Cambridge, England), 2016, 52, 12368-12371
7124996 CIFC93 H128.56 O3 UP 1 21/c 116.6756; 37.752; 12.3496
90; 93.136; 90		7762.9Hoerger, Christopher J.; La Pierre, Henry S.; Maron, Laurent; Scheurer, Andreas; Heinemann, Frank W.; Meyer, Karsten
Reductive disproportionation of nitric oxide mediated by low-valent uranium.
Chemical communications (Cambridge, England), 2016, 52, 10854-10857
7124997 CIFC81 H105 O4 UP 1 21/c 121.4453; 13.7404; 25.313
90; 119.622; 90		6484.1Hoerger, Christopher J.; La Pierre, Henry S.; Maron, Laurent; Scheurer, Andreas; Heinemann, Frank W.; Meyer, Karsten
Reductive disproportionation of nitric oxide mediated by low-valent uranium.
Chemical communications (Cambridge, England), 2016, 52, 10854-10857
7124998 CIFC9 H20 B N O2I b a 210.1195; 29.385; 7.4892
90; 90; 90		2227Romero, Erik A.; Peltier, Jesse L.; Jazzar, Rodolphe; Bertrand, Guy
Catalyst-free dehydrocoupling of amines, alcohols, and thiols with pinacol borane and 9-borabicyclononane (9-BBN).
Chemical communications (Cambridge, England), 2016, 52, 10563-10565
7124999 CIFC24 H18 Br PP 1 21/n 110.9091; 8.4128; 20.1396
90; 94.569; 90		1842.46Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125000 CIFC24 H18 As BrP 1 21/n 110.8919; 8.4344; 20.3175
90; 94.242; 90		1861.39Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125001 CIFC24 H18 Br SbP 1 21/n 110.9265; 8.5022; 20.5734
90; 93.534; 90		1907.62Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125002 CIFC33 H29 As TeP 1 21/n 112.0462; 8.7352; 25.0693
90; 98.504; 90		2608.94Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125003 CIFC33 H29 Sb TeP -18.7261; 11.7875; 14.189
79.576; 74.286; 75.358		1349.35Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125004 CIFC28 H26 Cl O P TeP 1 21/c 18.7067; 12.5095; 22.0558
90; 94.318; 90		2395.42Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125005 CIFC25 H20 Cl3 P TeP -18.5366; 11.678; 12.597
89.5; 87.76; 85.74		1251.4Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125006 CIFC48 H36 P2 TeP -111.7394; 12.5066; 14.3469
91.146; 101.003; 117.065		1827.45Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125007 CIFC18 H22 Cl P TeP 1 21/c 114.502; 8.33; 14.464
90; 91.826; 90		1746.4Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125008 CIFC18 H22 Br P TeP 1 21/n 17.786; 13.9267; 16.4054
90; 97.078; 90		1765.3Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125009 CIFC18 H22 I P TeP 1 21/n 17.9634; 14.047; 16.871
90; 99.976; 90		1858.7Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125010 CIFC38 H48 Cl4 I6 P2 Te3C 1 2/c 122.509; 11.4213; 22.101
90; 110.786; 90		5312Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125011 CIFC18 H22 I3 P TeP 1 21/n 19.8954; 15.5322; 14.5588
90; 93.366; 90		2233.8Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125012 CIFC25 H18 F3 O3 P S TeP 1 21/n 18.5859; 13.5523; 20.3142
90; 99.133; 90		2333.77Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125013 CIFC25 H18 As F3 O3 S TeP 1 21/n 18.6484; 13.5162; 20.5103
90; 99.069; 90		2367.55Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125014 CIFC28 H24 F3 O3 S Sb TeC 1 2/c 122.9864; 12.573; 20.1946
90; 115.397; 90		5272.4Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125015 CIFC40 H26 B F15 Na O7 PP 1 21/c 110.0891; 18.9802; 20.8742
90; 93.041; 90		3991.6Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125016 CIFC440 H572 Au92 S44C 1 2/c 145.325; 28.1243; 88.076
90; 91.544; 90		112233Liao, Lingwen; Chen, Jishi; Wang, Chengming; Zhuang, Shengli; Yan, Nan; Yao, Chuanhao; Xia, Nan; Li, Lingling; Bao, Xiaoli; Wu, Zhikun
Transition-sized Au<sub>92</sub> nanoparticle bridging non-fcc-structured gold nanoclusters and fcc-structured gold nanocrystals.
Chemical communications (Cambridge, England), 2016, 52, 12036-12039
7125017 CIFC15 H20 N2 O2 SP -16.2192; 9.1506; 13.4968
98.63; 96.96; 92.679		752.15Meyer, Andreas Uwe; Berger, Anna Lucia; König, Burkhard
Metal-free C-H sulfonamidation of pyrroles by visible light photoredox catalysis.
Chemical communications (Cambridge, England), 2016, 52, 10918-10921
7125018 CIFC18 H24 N2 O2 SP 1 21/n 110.79743; 13.38129; 11.85342
90; 96.5156; 90		1701.56Meyer, Andreas Uwe; Berger, Anna Lucia; König, Burkhard
Metal-free C-H sulfonamidation of pyrroles by visible light photoredox catalysis.
Chemical communications (Cambridge, England), 2016, 52, 10918-10921
7125019 CIFC19 H20 N2 O2 SP 1 21/c 115.7933; 8.92836; 12.9799
90; 110.209; 90		1717.6Meyer, Andreas Uwe; Berger, Anna Lucia; König, Burkhard
Metal-free C-H sulfonamidation of pyrroles by visible light photoredox catalysis.
Chemical communications (Cambridge, England), 2016, 52, 10918-10921
7125020 CIFC30 H40 N4 O4 S2P 1 21/n 118.0343; 7.581; 23.5816
90; 109.174; 90		3045.18Meyer, Andreas Uwe; Berger, Anna Lucia; König, Burkhard
Metal-free C-H sulfonamidation of pyrroles by visible light photoredox catalysis.
Chemical communications (Cambridge, England), 2016, 52, 10918-10921
7125021 CIFC12 H16 N2 O2 S2P 1 21/c 114.6626; 5.3944; 18.2386
90; 113.435; 90		1323.6Meyer, Andreas Uwe; Berger, Anna Lucia; König, Burkhard
Metal-free C-H sulfonamidation of pyrroles by visible light photoredox catalysis.
Chemical communications (Cambridge, England), 2016, 52, 10918-10921
7125022 CIFC29 H21 Br N2 O4P 21 21 217.08473; 16.7619; 22.085
90; 90; 90		2622.67Wang, Kai-Kai; Wang, Pan; Ouyang, Qin; Du, Wei; Chen, Ying-Chun
Substrate-controlled switchable asymmetric annulations to access polyheterocyclic skeletons.
Chemical communications (Cambridge, England), 2016, 52, 11104-11107
7125023 CIFC23 H17 N3 O2P 21 21 2110.06732; 10.59058; 22.9703
90; 90; 90		2449.06Wang, Kai-Kai; Wang, Pan; Ouyang, Qin; Du, Wei; Chen, Ying-Chun
Substrate-controlled switchable asymmetric annulations to access polyheterocyclic skeletons.
Chemical communications (Cambridge, England), 2016, 52, 11104-11107
7125024 CIFC40 H38.4 Cl4 Cr2 F8 N4 O21.2 Tb2P -19.6481; 11.3861; 13.3598
67.617; 78.339; 87.41		1328.23Langley, Stuart K.; Wielechowski, Daniel P.; Moubaraki, Boujemaa; Murray, Keith S.
Enhancing the magnetic blocking temperature and magnetic coercivity of {CrLn} single-molecule magnets via bridging ligand modification.
Chemical communications (Cambridge, England), 2016, 52, 10976-10979
7125025 CIFC40 H37.2 Cl4 Cr2 Dy2 F8 N4 O20.6P -19.543; 11.414; 13.306
67.56; 77.95; 87.25		1309.3Langley, Stuart K.; Wielechowski, Daniel P.; Moubaraki, Boujemaa; Murray, Keith S.
Enhancing the magnetic blocking temperature and magnetic coercivity of {CrLn} single-molecule magnets via bridging ligand modification.
Chemical communications (Cambridge, England), 2016, 52, 10976-10979
7125026 CIFC40 H37.67 Cl4 Cr2 F8 Ho2 N4 O20.83P -19.667; 11.331; 13.316
67.54; 78.27; 87.69		1318.7Langley, Stuart K.; Wielechowski, Daniel P.; Moubaraki, Boujemaa; Murray, Keith S.
Enhancing the magnetic blocking temperature and magnetic coercivity of {CrLn} single-molecule magnets via bridging ligand modification.
Chemical communications (Cambridge, England), 2016, 52, 10976-10979
7125027 CIFC70 H114 Cr2 Dy2 N4 O23P -111.164; 11.907; 16.534
70.77; 73.76; 82.43		1990.5Langley, Stuart K.; Wielechowski, Daniel P.; Moubaraki, Boujemaa; Murray, Keith S.
Enhancing the magnetic blocking temperature and magnetic coercivity of {CrLn} single-molecule magnets via bridging ligand modification.
Chemical communications (Cambridge, England), 2016, 52, 10976-10979
7125028 CIFC12 H24 B10 O8P 1 21/n 111.7899; 13.5842; 13.728
90; 104.058; 90		2132.78Cao, Ke; Xu, Tao-Tao; Wu, Ji; Jiang, Linhai; Yang, Junxiao
Palladium catalyzed/silver tuned selective mono-/tetra-acetoxylation of o-carboranes via B-H activation.
Chemical communications (Cambridge, England), 2016, 52, 11446-11449
7125029 CIFC20 H32 B10 O8P -112.7205; 13.3454; 16.395
98.928; 92.479; 90.262		2746.7Cao, Ke; Xu, Tao-Tao; Wu, Ji; Jiang, Linhai; Yang, Junxiao
Palladium catalyzed/silver tuned selective mono-/tetra-acetoxylation of o-carboranes via B-H activation.
Chemical communications (Cambridge, England), 2016, 52, 11446-11449
7125030 CIFC6 H18 B10 O2P -17.3484; 7.6219; 12.005
83.262; 88.589; 88.161		667.2Cao, Ke; Xu, Tao-Tao; Wu, Ji; Jiang, Linhai; Yang, Junxiao
Palladium catalyzed/silver tuned selective mono-/tetra-acetoxylation of o-carboranes via B-H activation.
Chemical communications (Cambridge, England), 2016, 52, 11446-11449
7125031 CIFC6 H18 B10 O2P 1 21/n 17.7915; 21.7; 8.0127
90; 94.885; 90		1349.83Cao, Ke; Xu, Tao-Tao; Wu, Ji; Jiang, Linhai; Yang, Junxiao
Palladium catalyzed/silver tuned selective mono-/tetra-acetoxylation of o-carboranes via B-H activation.
Chemical communications (Cambridge, England), 2016, 52, 11446-11449
7125032 CIFC25 H28 F6 N4 O2 P RuC 1 2/c 130.6243; 19.9078; 11.5863
90; 102.813; 90		6887.83Xie, Jianhui; Lo, Po-Kam; Lam, William W. Y.; Man, Wai-Lun; Ma, Li; Yiu, Shek-Man; Lau, Kai-Chung; Lau, Tai-Chu
Oxidation of hydroquinones by a (salen)ruthenium(vi) nitrido complex.
Chemical communications (Cambridge, England), 2016, 52, 11430-11433
7125033 CIFC22 H16 Br Cl N2 OP 21 21 218.048; 9.69; 25.348
90; 90; 90		1976.8Bao, Xiaoze; Wei, Shiqiang; Zou, Liwei; He, Yuli; Xue, Fuzhao; Qu, Jingping; Wang, Baomin
Asymmetric chlorination of 4-substituted pyrazolones catalyzed by natural cinchona alkaloid.
Chemical communications (Cambridge, England), 2016, 52, 11426-11429
7125034 CIFC5.5 H12 F6 N2 O0.5 PC 1 2/c 116.155; 6.7318; 19.587
90; 109.09; 90		2013Regnier, Vianney; Molton, Florian; Philouze, Christian; Martin, David
An air-persistent oxyallyl radical cation with simple di(methyl)amino substituents.
Chemical communications (Cambridge, England), 2016, 52, 11422-11425
7125035 CIFC24 H17 N OP n a 2115.3015; 12.1976; 9.6252
90; 90; 90		1796.5Liu, Ren-Rong; Xu, Teng-Fei; Wang, Yong-Gang; Xiang, Bin; Gao, Jian-Rong; Jia, Yi-Xia
Palladium-catalyzed dearomative arylalkynylation of indoles.
Chemical communications (Cambridge, England), 2016, 52, 13664-13667
7125036 CIFC31 H30 Cl3 F6 N6 O P RuP -110.63; 12.402; 14.118
77.336; 74.113; 79.124		1730.1Ng, Chee Koon; Wu, Jie; Hor, T. S. Andy; Luo, He-Kuan
A binary catalyst system of a cationic Ru-CNC pincer complex with an alkali metal salt for selective hydroboration of carbon dioxide.
Chemical communications (Cambridge, England), 2016, 52, 11842-11845
7125037 CIFC31 H30 Cl4 F6 N5 O2 P RuP b c a16.6675; 11.1422; 38.2172
90; 90; 90		7097.4Ng, Chee Koon; Wu, Jie; Hor, T. S. Andy; Luo, He-Kuan
A binary catalyst system of a cationic Ru-CNC pincer complex with an alkali metal salt for selective hydroboration of carbon dioxide.
Chemical communications (Cambridge, England), 2016, 52, 11842-11845
7125038 CIFC27 H32 Br N3 O6 SP 1 21/n 113.4851; 8.5343; 25.6709
90; 103.401; 90		2873.9Fuentes de Arriba, Ángel L; Simón, Luis; Rubio, Omayra H.; Monleón, Laura M; Alcázar, Victoria; Sanz, Francisca; Raposo, César A; Morán, Joaquín R
A bio-inspired enantioselective small-molecule artificial receptor for β adrenergic agonists and antagonists and its application for enantioselective extraction.
Chemical communications (Cambridge, England), 2016, 52, 12582-12585
7125039 CIFC92 H108 Br2 N10 O15 S2P 1 21 18.3467; 25.1787; 22.297
90; 92.223; 90		4682.4Fuentes de Arriba, Ángel L; Simón, Luis; Rubio, Omayra H.; Monleón, Laura M; Alcázar, Victoria; Sanz, Francisca; Raposo, César A; Morán, Joaquín R
A bio-inspired enantioselective small-molecule artificial receptor for β adrenergic agonists and antagonists and its application for enantioselective extraction.
Chemical communications (Cambridge, England), 2016, 52, 12582-12585
7125040 CIFC44.16 N8 O76 Zr12C 1 2/m 121.28954; 14.55846; 8.10658
90; 84.173; 90		2499.59Waitschat, S.; Reinsch, H.; Stock, N.
Water-based synthesis and characterisation of a new Zr-MOF with a unique inorganic building unit.
Chemical communications (Cambridge, England), 2016, 52, 12698-12701
7125041 CIFC28 H21 Br O3P -17.336; 11.8041; 13.6969
104.265; 98.881; 96.225		1122.36Wu, Ya-Nan; Xu, Ting; Fu, Rong; Wang, Nan-Nan; Hao, Wen-Juan; Wang, Shu-Liang; Li, Guigen; Tu, Shu-Jiang; Jiang, Bo
Dual rhodium/copper catalysis: synthesis of benzo[b]fluorenes and 2-naphthalenylmethanones via de-diazotized cycloadditions.
Chemical communications (Cambridge, England), 2016, 52, 11943-11946

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