Crystallography Open Database

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7116346 CIFC17 H15 Br OP 1 21/c 15.7276; 18.038; 13.687
90; 100.05; 90		1392.4Jing Chen; Chao Chen; Junjie Chen; Guohua Wang; Hongmei Qu
Cu-catalyzed intramolecular aryl-etherification reactions of alkoxyl alkynes with diaryliodonium salts via cleavage of a stable C-O bond
Chem.Commun., 2015, 51, 1356
7116347 CIFC22 H17 F N2 O4 S2P 1 21/c 19.0012; 11.6897; 19.0204
90; 92.744; 90		1999.06Bagineni Prasad; Raju Adepu; Atul Kumar Sharma; Manojit Pal
Creation of molecular complexities via a new Cu-catalyzed cascade reaction: a direct access to novel 2,2'-spirobiindole derivatives
Chem.Commun., 2015, 51, 1259
7116348 CIFC51 H51 Cl2 F6 Fe O P4P 1 21/n 112.7886; 17.372; 22.188
90; 92.649; 90		4924.1Ayham Tohme; Charles T. Hagen; Stephanie Essafi (nee Labouille); Arnaud Bondon; Thierry Roisnel; Duncan Carmichael; Frederic Paul
Easy and quantitative access to Fe(II) and Fe(III) di(aryl)alkynylphosphine oxides featuring [Fe(dppe)Cp*] endgroups: terminal P[double bond, length as m-dash]O functionality blocks the dimerisation of the Fe(III) derivatives
Chem.Commun., 2015, 51, 1316
7116349 CIFC50 H51 Fe O2 P3P 1 21/n 110.6741; 22.0513; 18.8153
90; 104.313; 90		4291.2Ayham Tohme; Charles T. Hagen; Stephanie Essafi (nee Labouille); Arnaud Bondon; Thierry Roisnel; Duncan Carmichael; Frederic Paul
Easy and quantitative access to Fe(II) and Fe(III) di(aryl)alkynylphosphine oxides featuring [Fe(dppe)Cp*] endgroups: terminal P[double bond, length as m-dash]O functionality blocks the dimerisation of the Fe(III) derivatives
Chem.Commun., 2015, 51, 1316
7116350 CIFC52 H53 Fe O P3P -110.9336; 13.3435; 16.5675
76.51; 77.792; 69.833		2183.44Ayham Tohme; Charles T. Hagen; Stephanie Essafi (nee Labouille); Arnaud Bondon; Thierry Roisnel; Duncan Carmichael; Frederic Paul
Easy and quantitative access to Fe(II) and Fe(III) di(aryl)alkynylphosphine oxides featuring [Fe(dppe)Cp*] endgroups: terminal P[double bond, length as m-dash]O functionality blocks the dimerisation of the Fe(III) derivatives
Chem.Commun., 2015, 51, 1316
7116351 CIFC52 H53 Fe O P3C 1 2/c 142.0668; 8.5013; 25.591
90; 111.301; 90		8526.7Ayham Tohme; Charles T. Hagen; Stephanie Essafi (nee Labouille); Arnaud Bondon; Thierry Roisnel; Duncan Carmichael; Frederic Paul
Easy and quantitative access to Fe(II) and Fe(III) di(aryl)alkynylphosphine oxides featuring [Fe(dppe)Cp*] endgroups: terminal P[double bond, length as m-dash]O functionality blocks the dimerisation of the Fe(III) derivatives
Chem.Commun., 2015, 51, 1316
7116352 CIFC29 H26 F6 N7 O3 P Ru SC 1 2/c 113.6846; 22.956; 20.732
90; 98.493; 90		6441.4Yue Zheng; Qianxiong Zhou; Wanhua Lei; Yuanjun Hou; Ke Li; Yongjie Chen; Baowen Zhang; Xuesong Wang
DNA photocleavage in anaerobic conditions by a Ru(II) complex: a new mechanism
Chem.Commun., 2015, 51, 428
7116353 CIFC33 H23.5 N O10.75 TbF d d 28.487; 34.829; 52.441
90; 90; 90		15501Zhiyong Guo; Xuezhi Song; Huaping Lei; Hailong Wang; Shengqun Su; Hui Xu; Guodong Qian; Hongjie Zhang; Banglin Chen
A ketone functionalized luminescent terbium metal-organic framework for sensing of small molecules
Chem.Commun., 2015, 51, 376
7116354 CIFC22 H20 N2 O2P b c n15.715; 12.1408; 9.9342
90; 90; 90		1895.4Digambar Balaji Shinde; Sharath Kandambeth; Pradip Pachfule; Raya Rahul Kumar; Rahul Banerjee
Bifunctional covalent organic frameworks with two dimensional organocatalytic micropores
Chem.Commun., 2015, 51, 310
7116355 CIFC20 H16 N2 O2P 43 21 27.0094; 7.0094; 32.787
90; 90; 90		1610.88Digambar Balaji Shinde; Sharath Kandambeth; Pradip Pachfule; Raya Rahul Kumar; Rahul Banerjee
Bifunctional covalent organic frameworks with two dimensional organocatalytic micropores
Chem.Commun., 2015, 51, 310
7116356 CIFC43 H60 Cl Cu4 N15 O28P 4/m n c13.3088; 13.3088; 20.4387
90; 90; 90		3620.2Di-ming Chen; Wei Shi; Peng Cheng
A cage-based cationic body-centered tetragonal metal-organic framework: single-crystal to single-crystal transformation and selective uptake of organic dyes
Chem.Commun., 2015, 51, 370
7116357 CIFC61 H84 Cl Cu4 N20 O29.5I 4/m m m13.959; 13.959; 20.0475
90; 90; 90		3906.3Di-ming Chen; Wei Shi; Peng Cheng
A cage-based cationic body-centered tetragonal metal-organic framework: single-crystal to single-crystal transformation and selective uptake of organic dyes
Chem.Commun., 2015, 51, 370
7116358 CIFC29 H74 Ge N2 Si8P 1 21/n 112.106; 23.293; 16.666
90; 103.081; 90		4577.6Malgorzata Walewska; Judith Baumgartner; Christoph Marschner
Synthesis of vinyl germylenes
Chem.Commun., 2015, 51, 276
7116359 CIFC32 H64 Ge Si8P 1 21/c 113.326; 18.718; 18.391
90; 102.16; 90		4484.5Malgorzata Walewska; Judith Baumgartner; Christoph Marschner
Synthesis of vinyl germylenes
Chem.Commun., 2015, 51, 276
7116360 CIFC29 H69 Ge P Si8P b c a25.174; 14.054; 25.198
90; 90; 90		8915Malgorzata Walewska; Judith Baumgartner; Christoph Marschner
Synthesis of vinyl germylenes
Chem.Commun., 2015, 51, 276
7116361 CIFC37 H75 Ge P Si8P -19.809; 14.698; 20.257
105.37; 97.24; 109.32		2583.1Malgorzata Walewska; Judith Baumgartner; Christoph Marschner
Synthesis of vinyl germylenes
Chem.Commun., 2015, 51, 276
7116362 CIFC34 H66 Ge Si8P 1 21/n 113.204; 19.641; 18.411
90; 109.7; 90		4495.2Malgorzata Walewska; Judith Baumgartner; Christoph Marschner
Synthesis of vinyl germylenes
Chem.Commun., 2015, 51, 276
7116363 CIFC26 H60 Ge Si8P 1 21/n 19.642; 18.886; 22.043
90; 98.58; 90		3969.1Malgorzata Walewska; Judith Baumgartner; Christoph Marschner
Synthesis of vinyl germylenes
Chem.Commun., 2015, 51, 276
7116364 CIFC30 H28 Cl6 Fe2 N2 OP 1 21/c 110.588; 11.729; 26.02
90; 91.42; 90		3230.3Martin Brzozowski; Jose A. Forni; G. Paul Savage; Anastasios Polyzos
The direct alpha-C(sp3)-H functionalisation of N-aryl tetrahydroisoquinolinesvia an iron-catalysed aerobic nitro-Mannich reaction and continuous flow processing
Chem.Commun., 2015, 51, 334
7116365 CIFC15 H12 O3P 1 21/c 19.0155; 14.112; 9.6804
90; 90.552; 90		1231.5Saikat Khamarui; Rituparna Maiti; Dilip K. Maiti
General base-tuned unorthodox synthesis of amides and ketoesters with water
Chem.Commun., 2015, 51, 384
7116366 CIFC39 H32 Au2 F10 N2P -112.3529; 12.613; 12.95
99.282; 107.229; 100.92		1840.7Zhao Chen; Jing Zhang; Min Song; Jun Yin; Guang-AoYu; Sheng Hua Liu
A novel fluorene-based aggregation-induced emission (AIE)-active gold(I) complex with crystallization-induced emission enhancement (CIEE) and reversible mechanochromism characteristics
Chem.Commun., 2015, 51, 326
7116367 CIFC20 H16 N2P 1 21/c 118.16; 5.8576; 14.864
90; 109.694; 90		1488.7Rajeshwer Vanjari; Tirumaleswararao Guntreddi; Saurabh Kumar; Krishna Nand Singh
Sulphur promoted C(sp3)-C(sp2) cross dehydrogenative cyclisation of acetophenonehydrazones with aldehydes: efficient synthesis of 3,4,5-trisubstituted 1H-pyrazoles
Chem.Commun., 2015, 51, 366
7116368 CIFC62 H60P -14.9784; 11.3963; 19.9225
95.603; 92.746; 93.2		1121.54Gaole Dai; Jingjing Chang; Wenhua Zhang; Shiqiang Bai; Kuo-Wei Huang; Jianwei Xu; Chunyan Chi
Dianthraceno[a,e]pentalenes: synthesis, crystallographic structures and applications in organic field-effect transistors
Chem.Commun., 2015, 51, 503
7116369 CIFC86 H78P -19.7359; 16.193; 22.166
99.203; 101.335; 101.921		3278.4Gaole Dai; Jingjing Chang; Wenhua Zhang; Shiqiang Bai; Kuo-Wei Huang; Jianwei Xu; Chunyan Chi
Dianthraceno[a,e]pentalenes: synthesis, crystallographic structures and applications in organic field-effect transistors
Chem.Commun., 2015, 51, 503
7116370 CIFC15 H14 Cl N3 O5P -16.0904; 7.695; 16.3916
83.899; 82.995; 87.213		757.65Ming Liu; Martin Nieger; Andreas Schmidt
Mesomericbetaine - N-heterocyclic carbene interconversions of 1,2,4-triazolium-phenolates. Sulfur, selenium, and borane adduct formation
Chem.Commun., 2015, 51, 477
7116371 CIFC15 H15 N3 O2C 1 c 119.9626; 4.6037; 15.3349
90; 112.829; 90		1298.91Ming Liu; Martin Nieger; Andreas Schmidt
Mesomericbetaine - N-heterocyclic carbene interconversions of 1,2,4-triazolium-phenolates. Sulfur, selenium, and borane adduct formation
Chem.Commun., 2015, 51, 477
7116372 CIFC33 H13 B F15 N3 OP -111.777; 12.266; 12.551
76.4; 64.72; 64.59		1477.8Ming Liu; Martin Nieger; Andreas Schmidt
Mesomericbetaine - N-heterocyclic carbene interconversions of 1,2,4-triazolium-phenolates. Sulfur, selenium, and borane adduct formation
Chem.Commun., 2015, 51, 477
7116373 CIFC18 H21 B N3 O1.5P -19.0122; 11.123; 17.8748
72.078; 87.907; 79.532		1676.14Ming Liu; Martin Nieger; Andreas Schmidt
Mesomericbetaine - N-heterocyclic carbene interconversions of 1,2,4-triazolium-phenolates. Sulfur, selenium, and borane adduct formation
Chem.Commun., 2015, 51, 477
7116374 CIFC44 H60 B N O2P 1 21/c 118.442; 11.9605; 19.592
90; 116.965; 90		3851.7Brandon R. Barnett; Curtis E. Moore; Arnold L. Rheingold; Joshua S. Figuero
Frustrated Lewis pair behavior of monomeric (boryl)iminomethanes accessed from isocyanide 1,1-hydroboration
Chem.Commun., 2015, 51, 541
7116375 CIFC52 H79 B2 NP 1 21/c 120.9432; 12.5599; 17.1099
90; 91.099; 90		4499.8Brandon R. Barnett; Curtis E. Moore; Arnold L. Rheingold; Joshua S. Figuero
Frustrated Lewis pair behavior of monomeric (boryl)iminomethanes accessed from isocyanide 1,1-hydroboration
Chem.Commun., 2015, 51, 541
7116376 CIFC50 H65 B N2P 1 21/c 112.3306; 13.0545; 25.512
90; 90.626; 90		4106.4Brandon R. Barnett; Curtis E. Moore; Arnold L. Rheingold; Joshua S. Figuero
Frustrated Lewis pair behavior of monomeric (boryl)iminomethanes accessed from isocyanide 1,1-hydroboration
Chem.Commun., 2015, 51, 541
7116377 CIFC52 H69 B N OP 1 21/n 110.6296; 23.2451; 18.409
90; 104.193; 90		4409.8Brandon R. Barnett; Curtis E. Moore; Arnold L. Rheingold; Joshua S. Figuero
Frustrated Lewis pair behavior of monomeric (boryl)iminomethanes accessed from isocyanide 1,1-hydroboration
Chem.Commun., 2015, 51, 541
7116378 CIFC40 H52 B N O2P 1 21/n 110.1073; 16.6024; 20.2451
90; 94.273; 90		3387.79Brandon R. Barnett; Curtis E. Moore; Arnold L. Rheingold; Joshua S. Figuero
Frustrated Lewis pair behavior of monomeric (boryl)iminomethanes accessed from isocyanide 1,1-hydroboration
Chem.Commun., 2015, 51, 541
7116379 CIFC39 H54 B N OP 1 21/c 117.347; 10.634; 19.7137
90; 112.174; 90		3367.6Brandon R. Barnett; Curtis E. Moore; Arnold L. Rheingold; Joshua S. Figuero
Frustrated Lewis pair behavior of monomeric (boryl)iminomethanes accessed from isocyanide 1,1-hydroboration
Chem.Commun., 2015, 51, 541
7116380 CIFC37 H50 B N O2P 1 21/n 113.4374; 14.3288; 18.5873
90; 105.742; 90		3444.6Brandon R. Barnett; Curtis E. Moore; Arnold L. Rheingold; Joshua S. Figuero
Frustrated Lewis pair behavior of monomeric (boryl)iminomethanes accessed from isocyanide 1,1-hydroboration
Chem.Commun., 2015, 51, 541
7116381 CIFC49 H70 B NP -110.9523; 12.2836; 18.2004
77.103; 81.075; 65.736		2170.4Brandon R. Barnett; Curtis E. Moore; Arnold L. Rheingold; Joshua S. Figuero
Frustrated Lewis pair behavior of monomeric (boryl)iminomethanes accessed from isocyanide 1,1-hydroboration
Chem.Commun., 2015, 51, 541
7116382 CIFC52.5 H81 B N2P -110.318; 12.8163; 17.8056
83.969; 86.164; 85.117		2329.1Brandon R. Barnett; Curtis E. Moore; Arnold L. Rheingold; Joshua S. Figuero
Frustrated Lewis pair behavior of monomeric (boryl)iminomethanes accessed from isocyanide 1,1-hydroboration
Chem.Commun., 2015, 51, 541
7116383 CIFC34 H27 N O3 SP 1 21/c 16.1013; 15.039; 23.894
90; 90.877; 90		2192.2Seema Dhiman; S. S. V. Ramasastry
Synthesis of polysubstituted cyclopenta[b]indoles via relay gold(I)/Bronsted acid catalysis
Chem.Commun., 2015, 51, 557
7116384 CIFC21 H20 Cl2 O3P 21 21 2110.9383; 11.4949; 15.5104
90; 90; 90		1950.2Yuxiao Liu; Yongming Deng; Peter Y. Zavalij; Renhua Liu; Michael P. Doyle
An efficient route to highly enantioenrichedtetrahydroazulenes and beta-tetralones by desymmetrization reactions of delta,delta-diaryldiazoaceto-acetates
Chem.Commun., 2015, 51, 565
7116385 CIFC126 H108 Eu2 N18 O12P 21 21 226.0606; 28.4219; 23.3299
90; 90; 90		17280.3Chi-Tung Yeung; Wesley Ting Kwok Chan; Siu-Cheong Yan; Kwan-Leung Yu; King-Him Yim; Wing-Tak Wong; Ga-Lai Law
Lanthanide supramolecular helical diastereoselective breaking induced by point chirality: mixture or P-helix, M-helix
Chem.Commun., 2015, 51, 592
7116386 CIFC138 H90 Eu2 F18 N18 O18 S6P -116.679; 20.3099; 24.4218
87.025; 70.961; 89.269		7809.7Chi-Tung Yeung; Wesley Ting Kwok Chan; Siu-Cheong Yan; Kwan-Leung Yu; King-Him Yim; Wing-Tak Wong; Ga-Lai Law
Lanthanide supramolecular helical diastereoselective breaking induced by point chirality: mixture or P-helix, M-helix
Chem.Commun., 2015, 51, 592
7116387 CIFC44 H40 N6 O4P 1 21 110.3285; 17.8133; 10.5822
90; 100.506; 90		1914.3Chi-Tung Yeung; Wesley Ting Kwok Chan; Siu-Cheong Yan; Kwan-Leung Yu; King-Him Yim; Wing-Tak Wong; Ga-Lai Law
Lanthanide supramolecular helical diastereoselective breaking induced by point chirality: mixture or P-helix, M-helix
Chem.Commun., 2015, 51, 592
7116388 CIFC17 H17 N O3P 21 21 2110.2469; 10.4606; 13.5437
90; 90; 90		1451.7Zhao-Lin He; Chun-Jiang Wang
Ag(I)-catalyzed tandem [6+3] annulation/isomerization of isocyanoacetates with fulvenes: an expedient approach to synthesize fused dihydropyridines
Chem.Commun., 2015, 51, 534
7116389 CIFC98 H167 Ag12 N12 O0.5 P6 Si6P 1 21 115.889; 18.207; 23.994
90; 95.206; 90		6913Bahareh Khalili Najafabadi; John F. Corrigan
N-Heterocyclic carbene stabilized Ag-P nanoclusters
Chem.Commun., 2015, 51, 665
7116390 CIFC141 H250.8 Ag26 N16 P12 Si10P -117.285; 20.433; 29.512
95.465; 91.603; 90.317		10371Bahareh Khalili Najafabadi; John F. Corrigan
N-Heterocyclic carbene stabilized Ag-P nanoclusters
Chem.Commun., 2015, 51, 665
7116391 CIFC15.74 H19.56 N9.19 O Zn2P b c a15.504; 15.364; 18.127
90; 90; 90		4317.9Yichao Lin; Qiuju Zhang; Chongchong Zhao; Huailong Li; Chunlong Kong; Cai Shen; Liang Chen
An exceptionally stable functionalized metal-organic framework for lithium storage
Chem.Commun., 2015, 51, 697
7116392 CIFC30 H24 S2P 1 21/n 18.641; 10.6699; 25.373
90; 97.159; 90		2321.1Sengodagounder Muthusamy; Manickasamy Sivaguru; Eringathodi Suresh
Indium(III) chloride catalyzed highly diastereoselective domino synthesis of indenodithiepines and indenodithiocines
Chem.Commun., 2015, 51, 707
7116393 CIFC33 H29 Cl S2P -19.901; 11.029; 14.297
74.65; 76.568; 68.378		1383.7Sengodagounder Muthusamy; Manickasamy Sivaguru; Eringathodi Suresh
Indium(III) chloride catalyzed highly diastereoselective domino synthesis of indenodithiepines and indenodithiocines
Chem.Commun., 2015, 51, 707
7116394 CIFC39 H34 B N3P 21 21 218.621; 18.3501; 19.69
90; 90; 90		3114.9Xiaoqing Wang; Yanping Wu; Qingsong Liu; Zhenyu Li; Hui Yan; Chonglei Ji; Jicheng Duan; Zhipeng Liu
Aggregation-induced emission (AIE) of pyridyl-enamido-based organoboron luminophores
Chem.Commun., 2015, 51, 784
7116395 CIFC25 H19 B F2 N2P 21 21 2110.9427; 12.7077; 14.9474
90; 90; 90		2078.5Xiaoqing Wang; Yanping Wu; Qingsong Liu; Zhenyu Li; Hui Yan; Chonglei Ji; Jicheng Duan; Zhipeng Liu
Aggregation-induced emission (AIE) of pyridyl-enamido-based organoboron luminophores
Chem.Commun., 2015, 51, 784
7116396 CIFC27 H24 B F2 N3P -112.2723; 14.705; 14.7883
69.664; 67.961; 82.665		2319.6Xiaoqing Wang; Yanping Wu; Qingsong Liu; Zhenyu Li; Hui Yan; Chonglei Ji; Jicheng Duan; Zhipeng Liu
Aggregation-induced emission (AIE) of pyridyl-enamido-based organoboron luminophores
Chem.Commun., 2015, 51, 784
7116397 CIFC37 H29 B N2P 1 21/n 110.9565; 19.2414; 13.7066
90; 95.002; 90		2878.6Xiaoqing Wang; Yanping Wu; Qingsong Liu; Zhenyu Li; Hui Yan; Chonglei Ji; Jicheng Duan; Zhipeng Liu
Aggregation-induced emission (AIE) of pyridyl-enamido-based organoboron luminophores
Chem.Commun., 2015, 51, 784
7116398 CIFC81 H19 NC m c 2115.499; 27.568; 9.7851
90; 90; 90		4180.9T. W. Chamberlain; M. A. Lebedeva; W. Abuajwa; M. Suyetin; W. Lewis; E. Bichoutskaia; M. Schroder; A.; N.; Khlobystov'
Switching intermolecular interactions by confinement in carbon nanotubes
Chem.Commun., 2015, 51, 648
7116399 CIFC168 H192 Cl8 Fe4 N36 O32R 3 :H30.682; 30.682; 23.596
90; 90; 120		19237Dong-Hong Ren; Dan Qiu; Chun-Yan Pang; Zaijun Li; Zhi-Guo Gu
Chiral tetrahedral iron(II) cages: diastereoselective subcomponent self-assembly, structure interconversion and spin-crossover properties
Chem.Commun., 2015, 51, 788
7116400 CIFC168 H192 Cl8 Fe4 N36 O32R 3 :H30.825; 30.825; 22.939
90; 90; 120		18876Dong-Hong Ren; Dan Qiu; Chun-Yan Pang; Zaijun Li; Zhi-Guo Gu
Chiral tetrahedral iron(II) cages: diastereoselective subcomponent self-assembly, structure interconversion and spin-crossover properties
Chem.Commun., 2015, 51, 788
7116401 CIFC211.17 H272.75 Cl8 Fe4 N47.58 O47P 119.6065; 19.7357; 20.2252
116.621; 115.561; 94.4565		5944.6Dong-Hong Ren; Dan Qiu; Chun-Yan Pang; Zaijun Li; Zhi-Guo Gu
Chiral tetrahedral iron(II) cages: diastereoselective subcomponent self-assembly, structure interconversion and spin-crossover properties
Chem.Commun., 2015, 51, 788
7116402 CIFC192 H234 Cl8 Fe4 N42 O44P 119.7723; 19.7731; 20.282
115.476; 116.397; 94.961		6022.1Dong-Hong Ren; Dan Qiu; Chun-Yan Pang; Zaijun Li; Zhi-Guo Gu
Chiral tetrahedral iron(II) cages: diastereoselective subcomponent self-assembly, structure interconversion and spin-crossover properties
Chem.Commun., 2015, 51, 788
7116403 CIFC174 H189 Cl20 Fe4 N39 O32R 3 :H31.4702; 31.4702; 22.296
90; 90; 120		19123Dong-Hong Ren; Dan Qiu; Chun-Yan Pang; Zaijun Li; Zhi-Guo Gu
Chiral tetrahedral iron(II) cages: diastereoselective subcomponent self-assembly, structure interconversion and spin-crossover properties
Chem.Commun., 2015, 51, 788
7116404 CIFC H B N O ZnP 43 21 28.67; 8.67; 12.722
90; 90; 90		956.3Chun-Yang Pan; Li-Juan Zhong; Feng-Hua Zhao; Hong-Mei Yang; Jian Zhou
Zn(1,3-DAP)[B4O7]: a rare chiral zeolitic framework constructed of four-connected [B4O9] clusters with a single-stranded helical channel
Chem.Commun., 2015, 51, 753
7116405 CIFC21 H19 Br N3 O3C 1 2 119.7543; 6.8067; 15.8605
90; 98.736; 90		2107.89Bao-Dong Cui; Yong You; Jian-Qiang Zhao; Jian Zuo; Zhi-Jun Wu; Xiao-Ying Xu; Xiao-Mei Zhang; Wei-Cheng Yuan
3-Pyrrolyl-oxindoles as efficient nucleophiles for organocatalytic asymmetric synthesis of structurally diverse 3,3'-disubstituted oxindole derivatives
Chem.Commun., 2015, 51, 757
7116406 CIFC10 H9 N O3P 1 21/c 19.3511; 11.4869; 8.4156
90; 102.475; 90		882.62Jingjing Shi; Jie Zhou; Yunnan Yan; Jinlong Jia; Xuelei Liu; Huacan Song; H. Eric Xu; Wei Yi
One-pot cascade synthesis of N-methoxyisoquinolinediones via Rh(III)-catalyzed carbenoid insertion C-H activation/cyclization
Chem.Commun., 2015, 51, 668
7116407 CIFC52 H72 B2 Be N4P 1 21/n 112.855; 27.0697; 14.2004
90; 92.555; 90		4936.6T. Arnold; H. Braunschweig; W. C. Ewing; T. Kramer; J. Mies; J. K. Schuster
Beryllium bis(diazaborolyl): old neighbors finally shake hands
Chem.Commun., 2015, 51, 737
7116408 CIFC63 H86 B2 Be N6P 1 21 112.3713; 20.3783; 12.4856
90; 114.919; 90		2854.7T. Arnold; H. Braunschweig; W. C. Ewing; T. Kramer; J. Mies; J. K. Schuster
Beryllium bis(diazaborolyl): old neighbors finally shake hands
Chem.Commun., 2015, 51, 737
7116409 CIFC149 H248 B8 P8 Sn4P 1 21/c 114.0885; 26.577; 20.0509
90; 95.273; 90		7475.89Keith Izod; Casey M. Dixon; Ross W. Harrington; Michael R. Probert
Impact of a rigid backbone on the structure of an agostically-stabilised dialkylstannylene: isolation of an unusual bridged stannyl-stannylene
Chem.Commun., 2015, 51, 679
7116410 CIFC37 H38 N4 Ni O6P 1 21 18.2226; 39.325; 10.4346
90; 91.494; 90		3372.9Tingting Li; Shengbin Zhou; Jiang Wang; Jose Luis Acena; Vadim A. Soloshonok; Hong Liu
Asymmetric synthesis of alpha-(1-oxoisoindolin-3-yl)glycine: synthetic and mechanistic challenges
Chem.Commun., 2015, 51, 1624
7116411 CIFC36 H34 N4 Ni O5P 1 21/n 111.0249; 18.09; 15.8569
90; 91.288; 90		3161.7Tingting Li; Shengbin Zhou; Jiang Wang; Jose Luis Acena; Vadim A. Soloshonok; Hong Liu
Asymmetric synthesis of alpha-(1-oxoisoindolin-3-yl)glycine: synthetic and mechanistic challenges
Chem.Commun., 2015, 51, 1624
7116412 CIFC24 H20 B Cl2 F2 N3 O SP 1 21/n 19.5908; 10.9141; 22.863
90; 99.059; 90		2363.3Hui Liu; Hua Lu; Zhikuan Zhou; Soji Shimizu; Zhifang Li; Nagao Kobayashi; Zhen Shen
Asymmetric core-expanded aza-BODIPY analogues: facile synthesis and optical properties
Chem.Commun., 2015, 51, 1713
7116413 CIFC27 H26 B F2 N3 O2 SP 1 21/n 114.5722; 16.046; 22.1206
90; 107.66; 90		4928.61Hui Liu; Hua Lu; Zhikuan Zhou; Soji Shimizu; Zhifang Li; Nagao Kobayashi; Zhen Shen
Asymmetric core-expanded aza-BODIPY analogues: facile synthesis and optical properties
Chem.Commun., 2015, 51, 1713
7116414 CIFC17 H14 F6 O2 S2P 1 21/c 19.9685; 10.863; 15.8102
90; 98.901; 90		1691.4Ryuhei Kodama; Kimio Sumaru; Kana Morishita; Toshiyuki Kanamori; Kengo Hyodo; Takashi Kamitanaka; Masakazu Morimoto; Satoshi Yokojima; Shinichiro Nakamura; Kingo Uchida
A diarylethene as the SO2 gas generator upon UV irradiation
Chem.Commun., 2015, 51, 1736
7116415 CIFC26 H27 O3 PP 1 21/c 118.332; 6.1364; 20.639
90; 107.621; 90		2212.8Yuzhen Gao; Xueqin Li; Jian Xu; Yile Wu; Weizhu Chen; Guo Tang; Yufen Zhao
Mn(OAc)3-mediated phosphonation-lactonization of alkenoic acids: synthesis of phosphono-gamma-butyrolactones
Chem.Commun., 2015, 51, 1605
7116416 CIFC H Cl SP -111.7098; 12.2432; 19.742
75.953; 72.973; 75.614		2576.9Ru-Qiang Lu; Yi-Nyu Zhou; Xiao-Yun Yan; Ke Shi; Yu-Qing Zheng; Ming Luo; Xin-Chang Wang; Jian Pei; Haiping Xia; Laura Zoppi; Kim K. Baldridge; Jay S. Siegel; Xiao-Yu Cao
Thiophene-fused bowl-shaped polycyclic aromatics with a dibenzo[a,g]corannulene core for organic field-effect transistors
Chem.Commun., 2015, 51, 1681
7116417 CIFC26 H17 NP 1 21/c 113.6965; 7.3314; 18.6691
90; 103.364; 90		1823.89Iyyanar Karthikeyan; Dhanarajan Arunprasath; Govindasamy Sekar
An efficient synthesis of pyrido[1,2-a]indoles through aza-Nazarov type cyclization
Chem.Commun., 2015, 51, 1701
7116418 CIFC27 H16 O4 ZnI b a m36.006; 6.013; 31.426
90; 90; 90		6803.9Xun-Gao Liu; Hui Wang; Bin Chen; Yang Zou; Zhi-Guo Gu; Zujin Zhao; Liang Shen
A luminescent metal-organic framework constructed using a tetraphenylethene-based ligand for sensing volatile organic compounds
Chem.Commun., 2015, 51, 1677
7116419 CIFC11 H13 B Cl2 N2P 1 21/n 17.839; 16.0342; 9.5567
90; 96.056; 90		1194.5Holger Braunschweig; Christina Claes; Alexander Damme; Andrea Deisshurst; Christian Horl; Thomas Kramer
A facile and selective route to remarkably inert monocyclic NHC-stabilized boriranes
Chem.Commun., 2015, 51, 1627
7116420 CIFC13 H17 B Cl2 N2C 1 c 115.0371; 7.5273; 13.1615
90; 108.431; 90		1413.3Holger Braunschweig; Christina Claes; Alexander Damme; Andrea Deissenberger; Rian D. Dewhurst; Christian Horl; Thomas Kramer
A facile and selective route to remarkably inert monocyclic NHC-stabilized boriranes
Chem.Commun., 2015, 51, 1627
7116421 CIFC25 H25 B N2P 1 21/n 110.68; 14.1175; 13.6179
90; 93.975; 90		2048.3Holger Braunschweig; Christina Claes; Alexander Damme; Andrea Deissenberger; Rian D. Dewhurst; Christian Horl; Thomas Kramer
A facile and selective route to remarkably inert monocyclic NHC-stabilized boriranes
Chem.Commun., 2015, 51, 1627
7116422 CIFC27 H29 B N2P 1 21/n 111.205; 13.058; 16.087
90; 106.498; 90		2256.9Holger Braunschweig; Christina Claes; Alexander Damme; Andrea Deissenberger; Rian D. Dewhurst; Christian Horl; Thomas Kramer
A facile and selective route to remarkably inert monocyclic NHC-stabilized boriranes
Chem.Commun., 2015, 51, 1627
7116423 CIFC37 H55 B N2 P2 PtP -115.9324; 15.9875; 16.3672
63.872; 87.926; 79.834		3680.2Holger Braunschweig; Christina Claes; Alexander Damme; Andrea Deissenberger; Rian D. Dewhurst; Christian Horl; Thomas Kramer
A facile and selective route to remarkably inert monocyclic NHC-stabilized boriranes
Chem.Commun., 2015, 51, 1627
7116424 CIFC40.67 H53.33 N5 O4.17 RhR -3 :H34.6494; 34.6494; 16.6624
90; 90; 120		17324.5Eva Jurgens; Barbara Wucher; Frank Rominger; Karl W. Tornroos; Doris Kunz
Selective rearrangement of terminal epoxides into methylketones catalysed by a nucleophilic rhodium-NHC-pincer complex
Chem.Commun., 2015, 51, 1897
7116425 CIFC109 H134 N15 O7 Rh3P 1 21/n 121.7612; 21.6015; 23.3468
90; 90.011; 90		10974.7Eva Jurgens; Barbara Wucher; Frank Rominger; Karl W. Tornroos; Doris Kunz
Selective rearrangement of terminal epoxides into methylketones catalysed by a nucleophilic rhodium-NHC-pincer complex
Chem.Commun., 2015, 51, 1897
7116426 CIFC39 H39 Ir N2 O2 S2P b c a13.4876; 18.3802; 27.8072
90; 90; 90		6893.5Ming Li; Baozhan Zheng; Daibing Luo; Huiqin Sun; Ning Wang; Yan Huang; Jun Dai; Dan Xiao; Shi-Jian Su; Zhiyun Lu
Small molecular neutral microcrystalline iridium(III) complexes as promising molecular oxygen sensors
Chem.Commun., 2015, 51, 1926
7116427 CIFC60 H65 Cl2 Ir N2 O2 S2P -112.8835; 14.7285; 16.0114
103.949; 93.493; 103.298		2847.71Ming Li; Baozhan Zheng; Daibing Luo; Huiqin Sun; Ning Wang; Yan Huang; Jun Dai; Dan Xiao; Shi-Jian Su; Zhiyun Lu
Small molecular neutral microcrystalline iridium(III) complexes as promising molecular oxygen sensors
Chem.Commun., 2015, 51, 1926
7116428 CIFC31.25 H24 Ir N2 O2.25 S2P -118.4383; 18.6855; 19.9281
107.775; 99.052; 117.763		5407.5Ming Li; Baozhan Zheng; Daibing Luo; Huiqin Sun; Ning Wang; Yan Huang; Jun Dai; Dan Xiao; Shi-Jian Su; Zhiyun Lu
Small molecular neutral microcrystalline iridium(III) complexes as promising molecular oxygen sensors
Chem.Commun., 2015, 51, 1926
7116429 CIFC58 H58 N10 O18 S4P -17.8554; 13.428; 14.296
74.64; 83.39; 82.18		1435.6Han-Yuan Gong; Feng Tang; Brett M. Rambo; Rui Cao; Jun-Feng Xiang; Jonathan L. Sessler
Aromatic sulfonate anion-induced pseudorotaxanes: environmentally benign synthesis, selectivity, and structural characterization
Chem.Commun., 2015, 51, 1795
7116430 CIFC58 H74 N10 O26 S4P -110.5682; 12.4098; 13.8043
70.117; 82.636; 85.85		1687.7Han-Yuan Gong; Feng Tang; Brett M. Rambo; Rui Cao; Jun-Feng Xiang; Jonathan L. Sessler
Aromatic sulfonate anion-induced pseudorotaxanes: environmentally benign synthesis, selectivity, and structural characterization
Chem.Commun., 2015, 51, 1795
7116431 CIFC58 H61 N10 O19.5 S4P -112.2027; 13.5862; 19.851
72.658; 78.079; 72.902		2977Han-Yuan Gong; Feng Tang; Brett M. Rambo; Rui Cao; Jun-Feng Xiang; Jonathan L. Sessler
Aromatic sulfonate anion-induced pseudorotaxanes: environmentally benign synthesis, selectivity, and structural characterization
Chem.Commun., 2015, 51, 1795
7116432 CIFC65 H68 N11 O18.5 S4P -114.085; 16.457; 16.585
80.08; 66.96; 72.44		3366.4Han-Yuan Gong; Feng Tang; Brett M. Rambo; Rui Cao; Jun-Feng Xiang; Jonathan L. Sessler
Aromatic sulfonate anion-induced pseudorotaxanes: environmentally benign synthesis, selectivity, and structural characterization
Chem.Commun., 2015, 51, 1795
7116433 CIFC65 H69 N11 O19 S4P -113.9; 16.237; 16.444
79.98; 66.84; 73.12		3257.7Han-Yuan Gong; Feng Tang; Brett M. Rambo; Rui Cao; Jun-Feng Xiang; Jonathan L. Sessler
Aromatic sulfonate anion-induced pseudorotaxanes: environmentally benign synthesis, selectivity, and structural characterization
Chem.Commun., 2015, 51, 1795
7116434 CIFC62 H69 N10 O21.5 S4P -114.166; 16.38; 18.029
103.04; 109.53; 98.05		3733.8Han-Yuan Gong; Feng Tang; Brett M. Rambo; Rui Cao; Jun-Feng Xiang; Jonathan L. Sessler
Aromatic sulfonate anion-induced pseudorotaxanes: environmentally benign synthesis, selectivity, and structural characterization
Chem.Commun., 2015, 51, 1795
7116435 CIFC96 H144 Br4 N8 O22P 1 21/c 110.8583; 18.3496; 22.4335
90; 91.834; 90		4467.5Wei Zhang; Yi Li; Jing-Hua Sun; Cai-Ping Tan; Liang-Nian Ji; Zong-Wan Mao
Supramolecular self-assembled nanoparticles for chemo-photodynamic dual therapy against cisplatin resistant cancer cells
Chem.Commun., 2015, 51, 1807
7116436 CIFC56 H42C 1 2/c 123.491; 10.5581; 16.883
90; 99.21; 90		4133.3Guoying Zhang; Yinjun Xie; Zhengkun Wang; Yang Liu; Hanmin Huang
Diboron as a reductant for nickel-catalyzed reductive coupling: rational design and mechanistic studies
Chem.Commun., 2015, 51, 1850
7116437 CIFC74 H80 O SP -114.3679; 14.8455; 16.0061
75.95; 83.391; 83.523		3277.2Guoying Zhang; Yinjun Xie; Zhengkun Wang; Yang Liu; Hanmin Huang
Diboron as a reductant for nickel-catalyzed reductive coupling: rational design and mechanistic studies
Chem.Commun., 2015, 51, 1850
7116438 CIFC132 H120 N24P 21 21 2123.855; 26.655; 27.082
90; 90; 90		17220Huimin Ding; Yihui Yang; Bijian Li; Feng Pan; Guozhu Zhu; Matthias Zeller; Daqiang Yuan; Cheng Wang
Targeted synthesis of a large triazine-based [4+6] organic molecular cage: structure, porosity and gas separation
Chem.Commun., 2015, 51, 1976
7116439 CIFC65 H90 F6 N8 Na O10 P Rh4P 1 21/c 116.7562; 16.3493; 27.6506
90; 91.707; 90		7571.6Ayana Kashima; Mika Sakate; Hiromi Ota; Akira Fuyuhiro; Yukinari Sunatsuki; Takayoshi Suzuki
Thyminate(2-)-bridged cyclic tetranuclear rhodium(III) complexes formed by a template of a sodium, calcium or lanthanoid ion
Chem.Commun., 2015, 51, 1889
7116440 CIFC65 H92 B F4 N8 Na O11 Rh4P 1 21/c 116.662; 16.4372; 27.4724
90; 94.94; 90		7496.1Ayana Kashima; Mika Sakate; Hiromi Ota; Akira Fuyuhiro; Yukinari Sunatsuki; Takayoshi Suzuki
Thyminate(2-)-bridged cyclic tetranuclear rhodium(III) complexes formed by a template of a sodium, calcium or lanthanoid ion
Chem.Commun., 2015, 51, 1889
7116441 CIFC66 H87 N12 Na O12 Rh4P b c a22.6289; 21.7265; 29.7275
90; 90; 90		14615.4Ayana Kashima; Mika Sakate; Hiromi Ota; Akira Fuyuhiro; Yukinari Sunatsuki; Takayoshi Suzuki
Thyminate(2-)-bridged cyclic tetranuclear rhodium(III) complexes formed by a template of a sodium, calcium or lanthanoid ion
Chem.Commun., 2015, 51, 1889
7116442 CIFC62 H97.5 Ca N10.5 O22 Rh4P -111.3211; 18.6735; 18.7302
89.602; 75.171; 87.676		3824.6Ayana Kashima; Mika Sakate; Hiromi Ota; Akira Fuyuhiro; Yukinari Sunatsuki; Takayoshi Suzuki
Thyminate(2-)-bridged cyclic tetranuclear rhodium(III) complexes formed by a template of a sodium, calcium or lanthanoid ion
Chem.Commun., 2015, 51, 1889
7116443 CIFC62 H83 La N12 O19 Rh4P 21 21 218.7826; 19.9113; 10.6111
90; 90; 90		3968.4Ayana Kashima; Mika Sakate; Hiromi Ota; Akira Fuyuhiro; Yukinari Sunatsuki; Takayoshi Suzuki
Thyminate(2-)-bridged cyclic tetranuclear rhodium(III) complexes formed by a template of a sodium, calcium or lanthanoid ion
Chem.Commun., 2015, 51, 1889
7116444 CIFC62 H83 Eu N12 O19 Rh4P 21 21 218.4641; 19.8783; 10.5405
90; 90; 90		3868.7Ayana Kashima; Mika Sakate; Hiromi Ota; Akira Fuyuhiro; Yukinari Sunatsuki; Takayoshi Suzuki
Thyminate(2-)-bridged cyclic tetranuclear rhodium(III) complexes formed by a template of a sodium, calcium or lanthanoid ion
Chem.Commun., 2015, 51, 1889
7116445 CIFC66 H86 Dy N13 O20 Rh4P 1 21/c 113.9749; 18.7743; 28.0431
90; 93.975; 90		7339.9Ayana Kashima; Mika Sakate; Hiromi Ota; Akira Fuyuhiro; Yukinari Sunatsuki; Takayoshi Suzuki
Thyminate(2-)-bridged cyclic tetranuclear rhodium(III) complexes formed by a template of a sodium, calcium or lanthanoid ion
Chem.Commun., 2015, 51, 1889
7116446 CIFC66 H86 Er N13 O20 Rh4P 1 21/c 113.8619; 18.8672; 28.1155
90; 93.687; 90		7338Ayana Kashima; Mika Sakate; Hiromi Ota; Akira Fuyuhiro; Yukinari Sunatsuki; Takayoshi Suzuki
Thyminate(2-)-bridged cyclic tetranuclear rhodium(III) complexes formed by a template of a sodium, calcium or lanthanoid ion
Chem.Commun., 2015, 51, 1889
7116447 CIFC57 H48 B Cl2 F24 Ir N P SP 41 21 212.9489; 12.9489; 70.484
90; 90; 90		11818.3Areli Flores-Gaspar; Silvia Orgue; Arnald Grabulosa; Antoni Riera; Xavier Verdaguer
Borane as an efficient directing group. Stereoselective 1,2-addition of organometallic reagents to borane P-stereogenic N-phosphanylimines
Chem.Commun., 2015, 51, 1941
7116448 CIFC12 H21 B N PP 21 21 2110.793; 11.0539; 11.3385
90; 90; 90		1352.7Areli Flores-Gaspar; Silvia Orgue; Arnald Grabulosa; Antoni Riera; Xavier Verdaguer
Borane as an efficient directing group. Stereoselective 1,2-addition of organometallic reagents to borane P-stereogenic N-phosphanylimines
Chem.Commun., 2015, 51, 1941
7116449 CIFC34 H34 N2 O4 S4A b a 228.621; 26.533; 9.756
90; 90; 90		7409Yu Jiang; Xiang-Ying Tang; Min Shi
A Rh-catalyzed 1,2-sulfur migration/aza-Diels-Alder cascade initiated by aza-vinyl carbenoids from sulfur-tethered N-sulfonyl-1,2,3-triazoles
Chem.Commun., 2015, 51, 2122
7116450 CIFC36 H38 N2 O4 S4P -19.597; 13.9714; 14.765
105.066; 107.053; 97.126		1784.1Yu Jiang; Xiang-Ying Tang; Min Shi
A Rh-catalyzed 1,2-sulfur migration/aza-Diels-Alder cascade initiated by aza-vinyl carbenoids from sulfur-tethered N-sulfonyl-1,2,3-triazoles
Chem.Commun., 2015, 51, 2122
7116451 CIFC18 H19 N O2 S2P 1 21/c 19.6224; 14.3505; 13.0206
90; 102.158; 90		1757.6Yu Jiang; Xiang-Ying Tang; Min Shi
A Rh-catalyzed 1,2-sulfur migration/aza-Diels-Alder cascade initiated by aza-vinyl carbenoids from sulfur-tethered N-sulfonyl-1,2,3-triazoles
Chem.Commun., 2015, 51, 2122
7116453 CIFC20 H17 N3 O3P 1 21 15.3666; 14.0877; 11.0289
90; 94.065; 90		831.72Daniel Hack; Pankaj Chauhan; Kristina Deckers; Yusuke Mizutani; Gerhard Raabe; Dieter Enders
Combining silver- and organocatalysis: an enantioselective sequential catalytic approach towards pyrano-annulated pyrazoles
Chem.Commun., 2015, 51, 2266
7116454 CIFC15 H18 O4P 1 21/c 18.5618; 8.4049; 18.442
90; 93.163; 90		1325.1Fiene Horeischi; Claudia Guttroff; Bernd Plietker
The enantioselective total synthesis of (+)-clusianone
Chem.Commun., 2015, 51, 2259
7116455 CIFC16 H17 IP 1 21/n 110.6651; 14.1041; 17.531
90; 101.441; 90		2584.6Stephen J. Murray; Hasim Ibrahim
Asymmetric Kita spirolactonisation catalysed by anti-dimethanoanthracene-based iodoarenes
Chem.Commun., 2015, 51, 2376
7116456 CIFC26 H27 N3 O8P 21 21 2110.6406; 11.0802; 21.8683
90; 90; 90		2578.27Pankaj Chauhan; Suruchi Mahajan; Gerhard Raabe; Dieter Enders
Organocatalytic one-pot 1,4-/1,6-/1,2-addition sequence for the stereocontrolled formation of six consecutive stereocenters
Chem.Commun., 2015, 51, 2270
7116457 CIFC229 H308 Cl3 Eu2 N20 O16P -119.854; 24.158; 25.212
99.59; 106.63; 106.33		10710Guifen Lu; Sen Yan; Mengying Shi; Wenhan Yu; Jing Li; Weihua Zhu; Zhongping Ou; Karl M. Kadish
A new class of rare earth tetrapyrrole sandwich complexes containing corrole and phthalocyanine macrocycles: synthesis, physicochemical characterization and X-ray analysis
Chem.Commun., 2015, 51, 2411
7116458 CIFC21 H18 N2P b c a15.517; 8.4691; 23.518
90; 90; 90		3090.6Yang, Xiao-Fei; Hu, Xu-Hong; Feng, Chao; Loh, Teck-Peng
Rhodium(iii)-catalyzed C7-position C-H alkenylation and alkynylation of indolines.
Chemical communications (Cambridge, England), 2015, 51, 2532-2535
7116459 CIFC25 H34 N2 SiP -17.7419; 14.8215; 21.0488
75.571; 80.3817; 85.172		2303.92Yang, Xiao-Fei; Hu, Xu-Hong; Feng, Chao; Loh, Teck-Peng
Rhodium(iii)-catalyzed C7-position C-H alkenylation and alkynylation of indolines.
Chemical communications (Cambridge, England), 2015, 51, 2532-2535
7116460 CIFC24 H27 Cl4 N2 RhP 1 21/c 126.7294; 8.902; 20.8098
90; 90.4289; 90		4951.5Yang, Xiao-Fei; Hu, Xu-Hong; Feng, Chao; Loh, Teck-Peng
Rhodium(iii)-catalyzed C7-position C-H alkenylation and alkynylation of indolines.
Chemical communications (Cambridge, England), 2015, 51, 2532-2535
7116461 CIFC16 H11 B F2 N2 OP -16.9566; 8.3315; 23.1202
95.844; 90.57; 96.433		1324.35Liao, Chia-Wei; Rao M, Rajeswara; Sun, Shih-Sheng
Structural diversity of new solid-state luminophores based on quinoxaline-β-ketoiminate boron difluoride complexes with remarkable fluorescence switching properties.
Chemical communications (Cambridge, England), 2015, 51, 2656-2659
7116462 CIFC17 H13 B F2 N2 OP -17.0915; 10.1014; 10.3857
86.948; 70.988; 86.697		701.75Liao, Chia-Wei; Rao M, Rajeswara; Sun, Shih-Sheng
Structural diversity of new solid-state luminophores based on quinoxaline-β-ketoiminate boron difluoride complexes with remarkable fluorescence switching properties.
Chemical communications (Cambridge, England), 2015, 51, 2656-2659
7116463 CIFC29 H22 B F2 N3 OP 1 21/n 118.0013; 6.9212; 20.263
90; 116.034; 90		2268.42Liao, Chia-Wei; Rao M, Rajeswara; Sun, Shih-Sheng
Structural diversity of new solid-state luminophores based on quinoxaline-β-ketoiminate boron difluoride complexes with remarkable fluorescence switching properties.
Chemical communications (Cambridge, England), 2015, 51, 2656-2659
7116464 CIFC22 H15 B F2 N2 OP -17.1054; 11.1114; 11.9627
96.493; 106.301; 105.521		855.17Liao, Chia-Wei; Rao M, Rajeswara; Sun, Shih-Sheng
Structural diversity of new solid-state luminophores based on quinoxaline-β-ketoiminate boron difluoride complexes with remarkable fluorescence switching properties.
Chemical communications (Cambridge, England), 2015, 51, 2656-2659
7116465 CIFC34 H24 B F2 N3 OP 1 2/n 114.9332; 11.3243; 17.9422
90; 94.526; 90		3024.71Liao, Chia-Wei; Rao M, Rajeswara; Sun, Shih-Sheng
Structural diversity of new solid-state luminophores based on quinoxaline-β-ketoiminate boron difluoride complexes with remarkable fluorescence switching properties.
Chemical communications (Cambridge, England), 2015, 51, 2656-2659
7116466 CIFC20 H15 N OP b c a13.099; 9.359; 24.26
90; 90; 90		2974Yan, Rulong; Li, Xiaoni; Yang, Xiaodong; Kang, Xing; Xiang, Likui; Huang, Guosheng
A novel one-pot method for the synthesis of substituted furopyridines: iodine-mediated oxidation of enaminones by tandem metal-free cyclization.
Chemical communications (Cambridge, England), 2015, 51, 2573-2576
7116467 CIFC20 H14 I N OP 1 21/c 17.4452; 19.3722; 11.2423
90; 91.073; 90		1621.19Yan, Rulong; Li, Xiaoni; Yang, Xiaodong; Kang, Xing; Xiang, Likui; Huang, Guosheng
A novel one-pot method for the synthesis of substituted furopyridines: iodine-mediated oxidation of enaminones by tandem metal-free cyclization.
Chemical communications (Cambridge, England), 2015, 51, 2573-2576
7116468 CIFC64 H80 F12 N3 O15 P3P 1 21 111.316; 24.717; 14.0638
90; 100.065; 90		3873.1Wang, Qi; Cheng, Ming; Xiong, Shuhan; Hu, Xiao-Yu; Jiang, Juli; Wang, Leyong; Pan, Yi
P[double bond, length as m-dash]O functional group-containing cryptands: from supramolecular complexes to poly[2]pseudorotaxanes.
Chemical communications (Cambridge, England), 2015, 51, 2667-2670
7116469 CIFC62 H73 F12 N2 O13 P3P 1 21/n 117.2062; 23.6008; 18.4826
90; 90.615; 90		7505Wang, Qi; Cheng, Ming; Xiong, Shuhan; Hu, Xiao-Yu; Jiang, Juli; Wang, Leyong; Pan, Yi
P[double bond, length as m-dash]O functional group-containing cryptands: from supramolecular complexes to poly[2]pseudorotaxanes.
Chemical communications (Cambridge, England), 2015, 51, 2667-2670
7116470 CIFC25 H26 O2P 1 21/n 112.4084; 6.0932; 26.1861
90; 96.043; 90		1968.85Khan, Imtiaz; Chidipudi, Suresh Reddy; Lam, Hon Wai
Synthesis of spiroindanes by palladium-catalyzed oxidative annulation of non- or weakly activated 1,3-dienes involving C-H functionalization.
Chemical communications (Cambridge, England), 2015, 51, 2613-2616
7116471 CIFC24 H23 Cl O2P 1 21/n 112.4763; 6.01195; 26.1383
90; 97.18; 90		1945.18Khan, Imtiaz; Chidipudi, Suresh Reddy; Lam, Hon Wai
Synthesis of spiroindanes by palladium-catalyzed oxidative annulation of non- or weakly activated 1,3-dienes involving C-H functionalization.
Chemical communications (Cambridge, England), 2015, 51, 2613-2616
7116472 CIFC28 H25 N O2P 1 21/c 19.89753; 24.4163; 9.00094
90; 93.3654; 90		2171.43Khan, Imtiaz; Chidipudi, Suresh Reddy; Lam, Hon Wai
Synthesis of spiroindanes by palladium-catalyzed oxidative annulation of non- or weakly activated 1,3-dienes involving C-H functionalization.
Chemical communications (Cambridge, England), 2015, 51, 2613-2616
7116473 CIFC26 H20 OP 1 21/n 19.3875; 10.893; 18.522
90; 95.417; 90		1885.56Khan, Imtiaz; Chidipudi, Suresh Reddy; Lam, Hon Wai
Synthesis of spiroindanes by palladium-catalyzed oxidative annulation of non- or weakly activated 1,3-dienes involving C-H functionalization.
Chemical communications (Cambridge, England), 2015, 51, 2613-2616
7116476 CIFC25 H35 Cl Ir N3P -18.5409; 11.3926; 13.7162
69.634; 87.763; 71.53		1182.94He, Fan; Braunstein, Pierre; Wesolek, Marcel; Danopoulos, Andreas A.
Imine-functionalised protic NHC complexes of Ir: direct formation by C-H activation.
Chemical communications (Cambridge, England), 2015, 51, 2814
7116477 CIFC25 H36 B Cl F4 Ir N3C 1 2/c 122.1698; 20.5501; 14.5843
90; 110.936; 90		6205.8He, Fan; Braunstein, Pierre; Wesolek, Marcel; Danopoulos, Andreas A.
Imine-functionalised protic NHC complexes of Ir: direct formation by C-H activation.
Chemical communications (Cambridge, England), 2015, 51, 2814
7116478 CIFC33 H47 Cl2 Ir2 N3P 1 21/c 18.7044; 21.9069; 19.1631
90; 115.407; 90		3300.7He, Fan; Braunstein, Pierre; Wesolek, Marcel; Danopoulos, Andreas A.
Imine-functionalised protic NHC complexes of Ir: direct formation by C-H activation.
Chemical communications (Cambridge, England), 2015, 51, 2814
7116479 CIFC50 H68 Ir2 N6P -112.2904; 13.329; 19.4944
86.542; 72.6; 62.575		2693.6He, Fan; Braunstein, Pierre; Wesolek, Marcel; Danopoulos, Andreas A.
Imine-functionalised protic NHC complexes of Ir: direct formation by C-H activation.
Chemical communications (Cambridge, England), 2015, 51, 2814
7116480 CIFC25 H35 F6 Ir N3 PP -110.275; 10.7121; 13.6503
105.834; 110.036; 97.403		1316.23He, Fan; Braunstein, Pierre; Wesolek, Marcel; Danopoulos, Andreas A.
Imine-functionalised protic NHC complexes of Ir: direct formation by C-H activation.
Chemical communications (Cambridge, England), 2015, 51, 2814
7116481 CIFC22 H43 N P2P 1 21/c 113.7199; 12.3613; 28.1443
90; 96.935; 90		4738.2Kreye, Markus; Freytag, Matthias; Jones, Peter G.; Williard, Paul G.; Bernskoetter, Wesley H.; Walter, Marc D.
Homolytic H2 cleavage by a mercury-bridged Ni(i) pincer complex [{(PNP)Ni}2{μ-Hg}].
Chemical communications (Cambridge, England), 2015, 51, 2946
7116482 CIFC36 H68 Li2 N2 P4P 21 21 2124.1538; 13.7672; 12.0771
90; 90; 90		4016Kreye, Markus; Freytag, Matthias; Jones, Peter G.; Williard, Paul G.; Bernskoetter, Wesley H.; Walter, Marc D.
Homolytic H2 cleavage by a mercury-bridged Ni(i) pincer complex [{(PNP)Ni}2{μ-Hg}].
Chemical communications (Cambridge, England), 2015, 51, 2946
7116483 CIFC22 H42 Br N Ni P2P 21 21 2111.4257; 14.471; 15.0601
90; 90; 90		2490.06Kreye, Markus; Freytag, Matthias; Jones, Peter G.; Williard, Paul G.; Bernskoetter, Wesley H.; Walter, Marc D.
Homolytic H2 cleavage by a mercury-bridged Ni(i) pincer complex [{(PNP)Ni}2{μ-Hg}].
Chemical communications (Cambridge, England), 2015, 51, 2946
7116484 CIFC50 H90 Hg N2 Ni2 P4P -113.9339; 16.4179; 24.9947
108.376; 96.539; 97.87		5299.7Kreye, Markus; Freytag, Matthias; Jones, Peter G.; Williard, Paul G.; Bernskoetter, Wesley H.; Walter, Marc D.
Homolytic H2 cleavage by a mercury-bridged Ni(i) pincer complex [{(PNP)Ni}2{μ-Hg}].
Chemical communications (Cambridge, England), 2015, 51, 2946
7116485 CIFC18 H35 N Ni P2P b c a13.2113; 14.5597; 21.1415
90; 90; 90		4066.6Kreye, Markus; Freytag, Matthias; Jones, Peter G.; Williard, Paul G.; Bernskoetter, Wesley H.; Walter, Marc D.
Homolytic H2 cleavage by a mercury-bridged Ni(i) pincer complex [{(PNP)Ni}2{μ-Hg}].
Chemical communications (Cambridge, England), 2015, 51, 2946
7116486 CIFC22 H43 N Ni P2P 21 21 2111.0422; 14.7303; 14.7768
90; 90; 90		2403.52Kreye, Markus; Freytag, Matthias; Jones, Peter G.; Williard, Paul G.; Bernskoetter, Wesley H.; Walter, Marc D.
Homolytic H2 cleavage by a mercury-bridged Ni(i) pincer complex [{(PNP)Ni}2{μ-Hg}].
Chemical communications (Cambridge, England), 2015, 51, 2946
7116487 CIFC19 H35 N Ni O2 P2P b c a15.7937; 13.5622; 20.653
90; 90; 90		4423.82Kreye, Markus; Freytag, Matthias; Jones, Peter G.; Williard, Paul G.; Bernskoetter, Wesley H.; Walter, Marc D.
Homolytic H2 cleavage by a mercury-bridged Ni(i) pincer complex [{(PNP)Ni}2{μ-Hg}].
Chemical communications (Cambridge, England), 2015, 51, 2946
7116488 CIFC23 H45 N Ni P2P 21 21 2111.4225; 14.6398; 14.939
90; 90; 90		2498.15Kreye, Markus; Freytag, Matthias; Jones, Peter G.; Williard, Paul G.; Bernskoetter, Wesley H.; Walter, Marc D.
Homolytic H2 cleavage by a mercury-bridged Ni(i) pincer complex [{(PNP)Ni}2{μ-Hg}].
Chemical communications (Cambridge, England), 2015, 51, 2946
7116489 CIFC22 H33 Cl2 Cr N5 O19P 1 21/n 115.236; 14.7664; 16.0081
90; 118.237; 90		3172.9de Sousa, David P.; Bigelow, Jennifer O.; Sundberg, Jonas; Que, Lawrence; McKenzie, Christine J.
Caught! Crystal trapping of a side-on peroxo bound to Cr(iv).
Chemical communications (Cambridge, England), 2015, 51, 2802
7116490 CIFC24 H28 Cl2 Cr N5 O11P 1 21/c 116.3004; 12.4635; 13.5694
90; 91.647; 90		2755.6de Sousa, David P.; Bigelow, Jennifer O.; Sundberg, Jonas; Que, Lawrence; McKenzie, Christine J.
Caught! Crystal trapping of a side-on peroxo bound to Cr(iv).
Chemical communications (Cambridge, England), 2015, 51, 2802
7116491 CIFC29 H23 N O4P -17.8653; 12.7093; 12.7665
105.75; 100.5; 105.51		1137.98Selvaraju, Subhashini; Niradha Sachinthani, K. A.; Hopson, RaiAnna A; McFarland, Frederick M.; Guo, Song; Rheingold, Arnold L.; Nelson, Toby L.
Eumelanin-inspired core derived from vanillin: a new building block for organic semiconductors.
Chemical communications (Cambridge, England), 2015, 51, 2957
7116492 CIFC168 H96 N9 O53 Zn17R 3 2 :H23.2738; 23.2738; 33.9318
90; 90; 120		15917.4Hu, Jin-Song; Zhang, Lei; Qin, Ling; Zheng, He-Gen; Zhang, Xiang-Biao
A rare three-coordinated zinc cluster-organic framework with two types of secondary building units.
Chemical communications (Cambridge, England), 2015, 51, 2899
7116493 CIFC54 H65 N5 O10 Os3 P2P 1 21/c 112.4416; 15.7773; 28.046
90; 102.532; 90		5374.1Lipeng Wu; Qiang Liu; Anke Spannenberg; alf Jackstell; Matthias Beller
Highly regioselective osmium-catalyzed hydroformylation
Chem.Commun., 2015, 51, 3080
7116494 CIFC60 H50 N2 O10F d d 220.642; 78.16; 8.624
90; 90; 90		13914Zhichao Hu; Guangxi Huang; William P. Lustig; Fangming Wang; Hao Wang; Simon J. Teat; Debasis Banerjee; Deqing Zhang; Jing Li
Achieving exceptionally high luminescence quantum efficiency by immobilizing an AIE molecular chromophore into a metal-organic framework
Chem.Commun., 2015, 51, 3045
7116495 CIFC54 H32 O8 Zn2C 1 2/c 136.929; 31.08; 11.8533
90; 99.228; 90		13429Zhichao Hu; Guangxi Huang; William P. Lustig; Fangming Wang; Hao Wang; Simon J. Teat; Debasis Banerjee; Deqing Zhang; Jing Li
Achieving exceptionally high luminescence quantum efficiency by immobilizing an AIE molecular chromophore into a metal-organic framework
Chem.Commun., 2015, 51, 3045
7116496 CIFC49 H77 Li2 N3 O4P -111.302; 12.6719; 17.2731
91.27; 103.597; 99.07		2369.89Andreas A. Danopoulos; Pierre Braunstein; Elixabete Rezabal; Gilles Frison
Unprecedented directed lateral lithiations of tertiary carbons on NHC platforms
Chem.Commun., 2015, 51, 3049
7116497 CIFC61 H95 Li2 N3 O6P -110.8651; 14.5756; 20.5112
102.51; 100.746; 106.653		2928.9Andreas A. Danopoulos; Pierre Braunstein; Elixabete Rezabal; Gilles Frison
Unprecedented directed lateral lithiations of tertiary carbons on NHC platforms
Chem.Commun., 2015, 51, 3049
7116498 CIFC74 H106 Li4 N6 O2C 1 2/c 131.4483; 18.8909; 26.5581
90; 94.384; 90		15731.7Andreas A. Danopoulos; Pierre Braunstein; Elixabete Rezabal; Gilles Frison
Unprecedented directed lateral lithiations of tertiary carbons on NHC platforms
Chem.Commun., 2015, 51, 3049
7116499 CIFC18 H20 F12 N4 Ni PC m c m10.3657; 13.2968; 16.2518
90; 90; 90		2240Fengzhi Tang; Nigam P. Rath; Liviu M. Mirica
Stable bis(trifluoromethyl)nickel(III) complexes
Chem.Commun., 2015, 51, 3113
7116500 CIFC53 H76 F12 N8 Ni2P 1 21/n 110.2621; 19.5073; 13.473
90; 96.154; 90		2681.6Fengzhi Tang; Nigam P. Rath; Liviu M. Mirica
Stable bis(trifluoromethyl)nickel(III) complexes
Chem.Commun., 2015, 51, 3113
7116501 CIFC28 H40 F12 N4 Ni O PP b c a14.2479; 14.493; 30.515
90; 90; 90		6301.2Fengzhi Tang; Nigam P. Rath; Liviu M. Mirica
Stable bis(trifluoromethyl)nickel(III) complexes
Chem.Commun., 2015, 51, 3113
7116502 CIFC70 H90 N2 O8 Si4 Ti2P -110.0526; 11.8019; 14.793
74.19; 89.42; 75.231		1629.5Christian Godemann; Laura Dura; Dirk Hollmann; Kathleen Grabow; Ursula Bentrup; Haijun Jiao; Axel Schulz; Angelika Bruckner; Torsten Beweries
Highly selective visible light-induced Ti-O bond splitting in an ansa-titanocene dihydroxido complex
Chem.Commun., 2015, 51, 3065
7116503 CIFC25 H36 Cl3 Ir N2P -19.516; 9.914; 14.152
95.215; 95.676; 105.908		1267.9Y. Gothe; T. Marzo; L. Messori; N. Metzler-Nolte
Cytotoxic activity and protein binding through an unusual oxidative mechanism by an iridium(I)-NHC complex
Chem.Commun., 2015, 51, 3151
7116504 CIFC22 H18P 1 21/c 111.2196; 12.1534; 11.867
90; 112.497; 90		1495Marcel Hartmann; Constantin Gabriel Daniliuc; Armido Studer
Preparation of phenanthrenes from ortho-amino-biphenyls and alkynes via base-promoted homolytic aromatic substitution
Chem.Commun., 2015, 51, 3121
7116505 CIFC21 H15 ClP 1 21/c 111.2081; 12.3535; 11.9376
90; 113.383; 90		1517.12Marcel Hartmann; Constantin Gabriel Daniliuc; Armido Studer
Preparation of phenanthrenes from ortho-amino-biphenyls and alkynes via base-promoted homolytic aromatic substitution
Chem.Commun., 2015, 51, 3121
7116506 CIFC29 H24 Br2 O2P -18.9872; 9.0894; 15.463
79.651; 77.966; 77.931		1195.8Katsutoshi Arai; Yoichi Kobayashi; Jiro Abe
Rational molecular designs for drastic acceleration of the color-fading speed of photochromic naphthopyrans
Chem.Commun., 2015, 51, 3057
7116507 CIFC37 H26 OP -19.9865; 10.56; 13.7281
86.2498; 84.3378; 64.127		1295.86Katsutoshi Arai; Yoichi Kobayashi; Jiro Abe
Rational molecular designs for drastic acceleration of the color-fading speed of photochromic naphthopyrans
Chem.Commun., 2015, 51, 3057
7116508 CIFC29 H25 Br O2P 1 21/n 18.4379; 16.1157; 16.807
90; 101.44; 90		2240.06Katsutoshi Arai; Yoichi Kobayashi; Jiro Abe
Rational molecular designs for drastic acceleration of the color-fading speed of photochromic naphthopyrans
Chem.Commun., 2015, 51, 3057
7116509 CIFC41 H26 OC 1 2/c 141.059; 10.4431; 13.0847
90; 98.557; 90		5548Katsutoshi Arai; Yoichi Kobayashi; Jiro Abe
Rational molecular designs for drastic acceleration of the color-fading speed of photochromic naphthopyrans
Chem.Commun., 2015, 51, 3057
7116510 CIFC29 H25 Br O2P 1 21/c 18.4457; 15.2032; 17.4327
90; 92.8463; 90		2235.63Katsutoshi Arai; Yoichi Kobayashi; Jiro Abe
Rational molecular designs for drastic acceleration of the color-fading speed of photochromic naphthopyrans
Chem.Commun., 2015, 51, 3057
7116511 CIFC29 H26 O2P 1 21/n 18.4797; 16.5725; 15.9445
90; 103.454; 90		2179.2Katsutoshi Arai; Yoichi Kobayashi; Jiro Abe
Rational molecular designs for drastic acceleration of the color-fading speed of photochromic naphthopyrans
Chem.Commun., 2015, 51, 3057
7116513 CIFC16 H15 Cl2 N O2 SP -18.2507; 9.1868; 10.7811
92.8871; 100.081; 91.7403		802.9Steven J. Mansfield; Craig D. Campbell; Michael W. Jones; Edward A. Anderson
A robust and modular synthesis of ynamides
Chem.Commun., 2015, 51, 3316
7116514 CIFC5 H5 Cl2 N O2P 21 c n5.8679; 10.425; 11.8622
90; 90; 90		725.64Steven J. Mansfield; Craig D. Campbell; Michael W. Jones; Edward A. Anderson
A robust and modular synthesis of ynamides
Chem.Commun., 2015, 51, 3316
7116515 CIFC21 H40 N O2 SP -15.8562; 8.0977; 23.1501
84.648; 86.401; 84.429		1086.27Stefanie-Ann Alexander; Emma M. Rouse; Jonathan M. White; Nicole Tse; Caroline Kyi; Carl H. Schiesser
Controlling biofilms on cultural materials: the role of 3-(dodecane-1-thiyl)-4-(hydroxymethyl)-2,2,5,5-tetramethyl-1-pyrrolinoxyl
Chem.Commun., 2015, 51, 3355
7116516 CIFC64 H88 N O16P -112.306; 12.532; 25.592
95.097; 99.985; 107.517		3665Shilu Wang; Yiliang Wang; Zhenxia Chen; Yuejian Lin; Linhong Weng; Kang Han; Jian Li; Xueshun Jia; Chunju Li
The marriage of endo-cavity and exo-wall complexation provides a facile strategy for supramolecular polymerization
Chem.Commun., 2015, 51, 3434
7116524 CIFC28 H19 N OP 21 21 218.519; 9.631; 24.207
90; 90; 90		1986.1Yan-Qin He; Yu-Wu Zhong
The synthesis of 2- and 2,7-functionalized pyrene derivatives through Ru(II)-catalyzed C-H activation
Chem.Commun., 2015, 51, 3411
7116525 CIFC79 H51 Cl9 N4P -18.6479; 12.683; 16.619
111.32; 92.12; 99.49		1665.5Yan-Qin He; Yu-Wu Zhong
The synthesis of 2- and 2,7-functionalized pyrene derivatives through Ru(II)-catalyzed C-H activation
Chem.Commun., 2015, 51, 3411
7116526 CIFC41 H28 F6 N5 P RuP -112.308; 13.017; 13.044
111.17; 111.32; 98.55		1718.5Yan-Qin He; Yu-Wu Zhong
The synthesis of 2- and 2,7-functionalized pyrene derivatives through Ru(II)-catalyzed C-H activation
Chem.Commun., 2015, 51, 3411
7116527 CIFC28 H17 NP -13.8489; 17.796; 25.127
86.217; 89.836; 85.622		1712.3Yan-Qin He; Yu-Wu Zhong
The synthesis of 2- and 2,7-functionalized pyrene derivatives through Ru(II)-catalyzed C-H activation
Chem.Commun., 2015, 51, 3411
7116528 CIFC16 H111 Cu4 Dy2 K2 N16 O101.5 Si2 W22C 1 m 120.5847; 13.4613; 22.9069
90; 101.973; 90		6209.3Fei-Yan Yi; Wei Zhu; Song Dang; Jian-Ping Li; Dai Wu; Yun-hui Li; Zhong-Ming Sun
Polyoxometalates-based heterometallic organic-inorganic hybrid materials for rapid adsorption and selective separation of methylene blue from aqueous solutions
Chem.Commun., 2015, 51, 3336
7116529 CIFC26 H126 Cu6 Er2 N24 O97 Si2 W22F d d 243.425; 43.548; 25.625
90; 90; 90		48459Fei-Yan Yi; Wei Zhu; Song Dang; Jian-Ping Li; Dai Wu; Yun-hui Li; Zhong-Ming Sun
Polyoxometalates-based heterometallic organic-inorganic hybrid materials for rapid adsorption and selective separation of methylene blue from aqueous solutions
Chem.Commun., 2015, 51, 3336
7116530 CIFC16 H77 Cu Er N12 O85 Si2 W22P 1 21/c 119.142; 24.362; 21.693
90; 99.006; 90		9992Fei-Yan Yi; Wei Zhu; Song Dang; Jian-Ping Li; Dai Wu; Yun-hui Li; Zhong-Ming Sun
Polyoxometalates-based heterometallic organic-inorganic hybrid materials for rapid adsorption and selective separation of methylene blue from aqueous solutions
Chem.Commun., 2015, 51, 3336
7116531 CIFC40 H34 As2 Br N O2 PdP 1 21/n 112.2363; 15.6103; 19.0632
90; 105.412; 90		3510.36Thomas O. Ronson; Jonathan R. Carney; Adrian C. Whitwood; Richard J.K. Taylor; Ian J. S. Fairlamb
AsCat and FurCat: new Pd catalysts for selective room-temperature Stille cross-couplings of benzyl chlorides with organostannanes
Chem.Commun., 2015, 51, 3466
7116532 CIFC17 H18 F6 O5 S2P 1 21/c 19.8939; 13.25; 15.9721
90; 102.881; 90		2041.16Benito Alcaide; Pedro Almendros; Israel Fernandez; Carlos Lazaro-Milla
Unveiling the uncatalyzed reaction of alkynes with 1,2-dipoles for the room temperature synthesis of cyclobutenes
Chem.Commun., 2015, 51, 3395
7116533 CIFC15 H15 Br F N O2 SP 1 21/c 111.571; 5.2088; 26.139
90; 93.278; 90		1572.8Jorge Saavedra-Olavarria; Gean C. Arteaga; Jhon J. Lopez; Edwin G. Perez
Copper-catalyzed intermolecular and regioselective aminofluorination of styrenes: facile access to beta-fluoro-N-protected phenethylamines
Chem.Commun., 2015, 51, 3379
7116534 CIFC38 H38 O2P -19.6115; 12.5777; 14.3804
110.013; 107.49; 99.474		1486.96Yao Xiong; Xilong Yan; Yawen Ma; Yang Li; Guohui Yin; Ligong Chen
Regulating the piezofluorochromism of 9,10-bis(butoxystyryl)anthracenes by isomerization of butyl groups
Chem.Commun., 2015, 51, 3403
7116535 CIFC38 H38 O2P -19.3559; 9.9674; 16.4761
99.935; 101.993; 96.7		1461.72Yao Xiong; Xilong Yan; Yawen Ma; Yang Li; Guohui Yin; Ligong Chen
Regulating the piezofluorochromism of 9,10-bis(butoxystyryl)anthracenes by isomerization of butyl groups
Chem.Commun., 2015, 51, 3403
7116536 CIFC38 H38 O2P -15.5707; 8.2832; 15.9643
92.864; 96.899; 93.15		729.02Yao Xiong; Xilong Yan; Yawen Ma; Yang Li; Guohui Yin; Ligong Chen
Regulating the piezofluorochromism of 9,10-bis(butoxystyryl)anthracenes by isomerization of butyl groups
Chem.Commun., 2015, 51, 3403
7116537 CIFC28 H50 N3 O6 ReP 1 21/c 111.2427; 25.9864; 11.3945
90; 106.509; 90		3191.75Mirza Cokoja; Iulius I. E. Markovits; Michael H. Anthofer; Saner Poplata; Alexander Pothig; Danny S. Morris; Peter A. Tasker; Wolfgang A. Herrmann; Fritz E. Kuhn; Jason B. Love
Catalytic epoxidation by perrhenate through the formation of organic-phase supramolecular ion pairs
Chem.Commun., 2015, 51, 3399
7116539 CIFC29 H21P 1 21/c 113.911; 9.1555; 16.101
90; 99.76; 90		2021Luigi R. Nassimbeni; Nikoletta B. Bathori; Leena Desiree Patel; Hong Su; Edwin Weber
Separation of xylenes by enclathration
Chem.Commun., 2015, 51, 3627
7116540 CIFC37 H30 O2C 1 2/c 118.733; 8.5251; 17.406
90; 95.92; 90		2764.9Luigi R. Nassimbeni; Nikoletta B. Bathori; Leena Desiree Patel; Hong Su; Edwin Weber
Separation of xylenes by enclathration
Chem.Commun., 2015, 51, 3627
7116541 CIFC64 H46P -111.3462; 14.6342; 27.3605
101.652; 99.918; 92.534		4368.2Luigi R. Nassimbeni; Nikoletta B. Bathori; Leena Desiree Patel; Hong Su; Edwin Weber
Separation of xylenes by enclathration
Chem.Commun., 2015, 51, 3627
7116542 CIFC32 H23P 1 21/c 114.154; 9.1925; 17.307
90; 100.42; 90		2214.7Luigi R. Nassimbeni; Nikoletta B. Bathori; Leena Desiree Patel; Hong Su; Edwin Weber
Separation of xylenes by enclathration
Chem.Commun., 2015, 51, 3627
7116543 CIFC20 H19 B N2 O9C 1 2/c 116.8086; 10.0372; 24.1763
90; 90.321; 90		4078.75Shinya Adachi; Armand B. Cognetta; Micah J. Niphakis; Zhi He; Adam Zajdlik; Jeffrey D. St. Denis; Conor C. G. Scully; Benjamin F. Cravatt; Andrei K. Yudin
Facile synthesis of borofragments and their evaluation in activity-based protein profiling
Chem.Commun., 2015, 51, 3608
7116544 CIFC11 H19 B Cl N5 O8P 1 21/n 114.3477; 6.9395; 17.098
90; 94.14; 90		1697.9Shinya Adachi; Armand B. Cognetta; Micah J. Niphakis; Zhi He; Adam Zajdlik; Jeffrey D. St. Denis; Conor C. G. Scully; Benjamin F. Cravatt; Andrei K. Yudin
Facile synthesis of borofragments and their evaluation in activity-based protein profiling
Chem.Commun., 2015, 51, 3608
7116545 CIFC21 H31 B N6 O9P 1 21/c 119.2489; 7.1031; 20.6727
90; 115.222; 90		2557.04Shinya Adachi; Armand B. Cognetta; Micah J. Niphakis; Zhi He; Adam Zajdlik; Jeffrey D. St. Denis; Conor C. G. Scully; Benjamin F. Cravatt; Andrei K. Yudin
Facile synthesis of borofragments and their evaluation in activity-based protein profiling
Chem.Commun., 2015, 51, 3608
7116546 CIFC144 H132 K N2 Nb2 O4I 2 346.878; 46.878; 46.878
90; 90; 90		103017Keith Searles; Patrick J. Carroll; Chun-Hsing Chen; Maren Pink; Daniel J. Mindiola
Niobium-nitrides derived from nitrogen splitting
Chem.Commun., 2015, 51, 3526
7116547 CIFC149 H144 Cl5 K3 Nb2 O4P -116.7009; 17.9962; 24.535
92.288; 100.453; 114.629		6536.7Keith Searles; Patrick J. Carroll; Chun-Hsing Chen; Maren Pink; Daniel J. Mindiola
Niobium-nitrides derived from nitrogen splitting
Chem.Commun., 2015, 51, 3526
7116548 CIFC151 H140 N2 Nb2 O4P b c a24.645; 25.8062; 37.2338
90; 90; 90		23680.5Keith Searles; Patrick J. Carroll; Chun-Hsing Chen; Maren Pink; Daniel J. Mindiola
Niobium-nitrides derived from nitrogen splitting
Chem.Commun., 2015, 51, 3526
7116549 CIFC165 H156 Cl6 Nb2 O4P 1 2/c 118.1297; 15.6334; 26.09
90; 93.396; 90		7381.7Keith Searles; Patrick J. Carroll; Chun-Hsing Chen; Maren Pink; Daniel J. Mindiola
Niobium-nitrides derived from nitrogen splitting
Chem.Commun., 2015, 51, 3526
7116550 CIFC92 H94 Cl2 Nb O4P 1 21/n 115.8132; 14.3842; 17.9838
90; 111.412; 90		3808.3Keith Searles; Patrick J. Carroll; Chun-Hsing Chen; Maren Pink; Daniel J. Mindiola
Niobium-nitrides derived from nitrogen splitting
Chem.Commun., 2015, 51, 3526
7116551 CIFC19 H16 Br O4P 1 21 15.8959; 11.7317; 12.73
90; 96.833; 90		874.27Jun-Bing Lin; Shi-Ming Xu; Ji-Kang Xie; Hong-Yu Li; Peng-Fei Xu
An organocatalytic Michael-cyclization cascade of 4-oxa-alpha,beta-unsaturated carboxylic acids with aldehydes: facile synthesis of chiral gamma-lactols and trisubstituted gamma-lactones
Chem.Commun., 2015, 51, 3596
7116552 CIFC19 H18 O4P 1 21 15.6167; 25.0791; 11.3191
90; 90.779; 90		1594.28Jun-Bing Lin; Shi-Ming Xu; Ji-Kang Xie; Hong-Yu Li; Peng-Fei Xu
An organocatalytic Michael-cyclization cascade of 4-oxa-alpha,beta-unsaturated carboxylic acids with aldehydes: facile synthesis of chiral gamma-lactols and trisubstituted gamma-lactones
Chem.Commun., 2015, 51, 3596
7116553 CIFC43 H34 O1.5C 1 2/c 127.2227; 16.4194; 6.9476
90; 101.779; 90		3040Arun Naibi Lakshminarayana; Jingjing Chang; Jie Luo; Bin Zheng; Kuo-Wei Huang; Chunyan Chi
Bisindeno-annulated pentacenes with exceptionally high photo-stability and ordered molecular packing: simple synthesis by a regio-selective Scholl reaction
Chem.Commun., 2015, 51, 3604
7116554 CIFC59 H70 O5P -14.6842; 14.8758; 17.803
107.779; 94.984; 91.886		1174.5Arun Naibi Lakshminarayana; Jingjing Chang; Jie Luo; Bin Zheng; Kuo-Wei Huang; Chunyan Chi
Bisindeno-annulated pentacenes with exceptionally high photo-stability and ordered molecular packing: simple synthesis by a regio-selective Scholl reaction
Chem.Commun., 2015, 51, 3604
7116555 CIFC36 H37 N O26 Zn6P 21 21 218.0822; 20.8183; 30.8295
90; 90; 90		5187.3Cui-Lan Chang; Xiao-Yue Qi; Jiang-Wei Zhang; Ya-Ming Qiu; Xian-Jiang Li; Xin Wang; Yu Bai; Jun-Liang Sun; Hu-Wei Liu
Facile synthesis of magnetic homochiral metal-organic frameworks for 'enantioselective fishing'
Chem.Commun., 2015, 51, 3566
7116557 CIFC216 H184 Cu24 N8 O144I 4/m28.096; 28.096; 40.947
90; 90; 90		32323Hyehyun Kim; Minhak Oh; Dongwook Kim; Jeongin Park; Junmo Seong; Sang Kyu Kwak; Myoung Soo Lah
Single crystalline hollow metal-organic frameworks: a metal-organic polyhedron single crystal as a sacrificial template
Chem.Commun., 2015, 51, 3678
7116558 CIFC26 H35 B2 F8 Fe N5 O6P -17.7688; 8.5125; 24.4247
82.716; 85.057; 84.926		1591.34Arun Kumar Bar; Celine Pichon; Nayanmoni Gogoi; Carine Duhayon; S. Ramasesha; Jean-Pascal Sutter
Single-ion magnet behaviour of heptacoordinated Fe(II) complexes: on the importance of supramolecular organization
Chem.Commun., 2015, 51, 3616

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