Crystallography Open Database

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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
7116559 CIFC27 H21 Fe N9 Ni O2C 1 2/c 117.3572; 15.1852; 10.1318
90; 91.117; 90		2669.96Arun 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
7116560 CIFC23 H21 Cl2 Fe N5 O2P 1 21/c 18.6132; 13.1321; 22.5986
90; 108.557; 90		2423.22Arun 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
7116561 CIFC26 H31 N O5P b c n29.508; 8.3721; 19.678
90; 90; 90		4861.3Qiao-Hui Deng; Jia-Rong Chen; Qiang Wei; Quan-Qing Zhao; Liang-Qiu Lu; Wen-Jing Xiao
Visible-light-induced photocatalytic oxytrifluoromethylation of N-allylamides for the synthesis of CF3-containing oxazolines and benzoxazines
Chem.Commun., 2015, 51, 3537
7116570 CIFC67 H74 N2 O8 S2P -115.302; 15.3895; 15.4431
71.988; 60.74; 87.419		2992.4Erik Gabrielsson; Haining Tian; Susanna K. Eriksson; Jiajia Gao; Hong Chen; Fusheng Li; Johan Oscarsson; Junliang Sun; Hakan Rensmo; Lars Kloo; Anders Hagfeldt; Licheng Sun
Dipicolinic acid: a strong anchoring group with tunable redox and spectral behavior for stable dye-sensitized solar cells
Chem.Commun., 2015, 51, 3858
7116572 CIFC16 H14.5 Cl2 Co N5.5 OP -19.611; 13.18; 15.861
75.031; 76.859; 89.895		1886.7Shefali Vaidya; Apoorva Upadhyay; Saurabh Kumar Singh; Tulika Gupta; Subrata Tewary; Stuart K. Langley; James P. S. Walsh; Keith S. Murray; Gopalan Rajaraman; Maheswaran Shanmugam
A synthetic strategy for switching the single ion anisotropy in tetrahedral Co(II) complexes
Chem.Commun., 2015, 51, 3739
7116573 CIFC16 H14.5 Br2 Co N5.5 OP -19.832; 13.304; 15.925
105.24; 103.61; 90.386		1948.1Shefali Vaidya; Apoorva Upadhyay; Saurabh Kumar Singh; Tulika Gupta; Subrata Tewary; Stuart K. Langley; James P. S. Walsh; Keith S. Murray; Gopalan Rajaraman; Maheswaran Shanmugam
A synthetic strategy for switching the single ion anisotropy in tetrahedral Co(II) complexes
Chem.Commun., 2015, 51, 3739
7116574 CIFC15 H13 Cl2 Co N5 SP -18.479; 9.071; 13.536
77.03; 80.74; 67.56		934.4Shefali Vaidya; Apoorva Upadhyay; Saurabh Kumar Singh; Tulika Gupta; Subrata Tewary; Stuart K. Langley; James P. S. Walsh; Keith S. Murray; Gopalan Rajaraman; Maheswaran Shanmugam
A synthetic strategy for switching the single ion anisotropy in tetrahedral Co(II) complexes
Chem.Commun., 2015, 51, 3739
7116575 CIFC15 H13 Br2 Co N5 SP -18.441; 9.015; 13.725
77.19; 80.64; 68.94		946.4Shefali Vaidya; Apoorva Upadhyay; Saurabh Kumar Singh; Tulika Gupta; Subrata Tewary; Stuart K. Langley; James P. S. Walsh; Keith S. Murray; Gopalan Rajaraman; Maheswaran Shanmugam
A synthetic strategy for switching the single ion anisotropy in tetrahedral Co(II) complexes
Chem.Commun., 2015, 51, 3739
7116576 CIFC26 H34 B4 Mo2 O6 Ru2C 1 2/c 117.5892; 15.9899; 11.2183
90; 102.022; 90		3085.94Bijan Mondal; Bijnaneswar Mondal; Koushik Pal; Babu Varghese; Sundargopal Ghosh
An electron-poor di-molybdenum triple-decker with a puckered [B4Ru2] bridging ring is an oblato-closo cluster
Chem.Commun., 2015, 51, 3828
7116577 CIFC22 H36 B4 Mo2 O2P 43 21 29.0041; 9.0041; 31.3056
90; 90; 90		2538.06Bijan Mondal; Bijnaneswar Mondal; Koushik Pal; Babu Varghese; Sundargopal Ghosh
An electron-poor di-molybdenum triple-decker with a puckered [B4Ru2] bridging ring is an oblato-closo cluster
Chem.Commun., 2015, 51, 3828
7116578 CIFC25 H34 B3 Cl Mo2 O5 WP 1 21/n 19.0059; 18.5886; 17.7675
90; 99.389; 90		2934.6Bijan Mondal; Bijnaneswar Mondal; Koushik Pal; Babu Varghese; Sundargopal Ghosh
An electron-poor di-molybdenum triple-decker with a puckered [B4Ru2] bridging ring is an oblato-closo cluster
Chem.Commun., 2015, 51, 3828
7116579 CIFC30 H31 B Mo2 O10 Ru2P c c n17.2668; 30.7845; 12.5659
90; 90; 90		6679.4Bijan Mondal; Bijnaneswar Mondal; Koushik Pal; Babu Varghese; Sundargopal Ghosh
An electron-poor di-molybdenum triple-decker with a puckered [B4Ru2] bridging ring is an oblato-closo cluster
Chem.Commun., 2015, 51, 3828
7116580 CIFC12 H36 Be N2 Si4P 1 21/n 19.8756; 16.6972; 14.5875
90; 109.492; 90		2267.55D. Naglav; A. Neumann; D. Blaser; C. Wolper; R. Haack; G. Jansen; S. Schulz
Bonding situation in Be[N(SiMe3)2]2 - an experimental and computational study
Chem.Commun., 2015, 51, 3889
7116581 CIFC83 H31 Cl2.5 F6 N6P -110.3923; 18.707; 18.841
61.769; 75.03; 74.372		3070.6Takashi Kubo; Shogo Miyazaki; Takuya Kodama; Mitsuya Aoba; Yasukazu Hirao; Hiroyuki Kurata
A facile synthesis of trinaphtho[3.3.3]propellane and its pi-extension and the formation of a two-dimensional honeycomb molecular assembly
Chem.Commun., 2015, 51, 3801
7116582 CIFC86 H36 Cl12 F6 N6 O6C 1 2/c 137.189; 25.4108; 19.26
90; 107.552; 90		17353.4Takashi Kubo; Shogo Miyazaki; Takuya Kodama; Mitsuya Aoba; Yasukazu Hirao; Hiroyuki Kurata
A facile synthesis of trinaphtho[3.3.3]propellane and its pi-extension and the formation of a two-dimensional honeycomb molecular assembly
Chem.Commun., 2015, 51, 3801
7116583 CIFC162 H48 S4P -116.8833; 18.4991; 23.1447
100.718; 96.6104; 91.6599		7046Takashi Kubo; Shogo Miyazaki; Takuya Kodama; Mitsuya Aoba; Yasukazu Hirao; Hiroyuki Kurata
A facile synthesis of trinaphtho[3.3.3]propellane and its pi-extension and the formation of a two-dimensional honeycomb molecular assembly
Chem.Commun., 2015, 51, 3801
7116584 CIFC74 H35 Cl N6P -110.6327; 14.0819; 19.8579
109.255; 90.5719; 109.406		2623.52Takashi Kubo; Shogo Miyazaki; Takuya Kodama; Mitsuya Aoba; Yasukazu Hirao; Hiroyuki Kurata
A facile synthesis of trinaphtho[3.3.3]propellane and its pi-extension and the formation of a two-dimensional honeycomb molecular assembly
Chem.Commun., 2015, 51, 3801
7116585 CIFC70 H132 As4 Ge8 K3 N8 O18 VP -111.9985; 16.7415; 25.3291
80.709; 88.755; 69.258		4692.3Stefan Mitzinger; Lies Broeckaert; Werner Massa; Florian Weigend; Stefanie Dehnen
[V@Ge8As4]^3-^ and [Nb@Ge8As6]^3-^: encapsulation of electron-poor transition metal atoms
Chem.Commun., 2015, 51, 3866
7116586 CIFC63 H124 As6 Ge8 K3 N8 Nb O18P -116.1475; 16.7769; 18.0373
89.184; 80.452; 79.42		4736.1Stefan Mitzinger; Lies Broeckaert; Werner Massa; Florian Weigend; Stefanie Dehnen
[V@Ge8As4]^3-^ and [Nb@Ge8As6]^3-^: encapsulation of electron-poor transition metal atoms
Chem.Commun., 2015, 51, 3866
7116587 CIFC28 H39 N2 O6 P WP 1 21/c 110.9216; 23.5529; 14.5767
90; 126.717; 90		3005.7Jose Manuel Villalba Franco; Takahiro Sasamori; Gregor Schnakenburg; Arturo Espinosa Ferao; Rainer Streubel
Going for strain: synthesis of the first 3-imino-azaphosphiridine complexes and their conversion into oxaphosphirane complex valence isomers
Chem.Commun., 2015, 51, 3878
7116588 CIFC22 H29 N2 O5 P WP -110.9909; 11.0605; 12.874
108.084; 95.194; 118.186		1257.68Jose Manuel Villalba Franco; Takahiro Sasamori; Gregor Schnakenburg; Arturo Espinosa Ferao; Rainer Streubel
Going for strain: synthesis of the first 3-imino-azaphosphiridine complexes and their conversion into oxaphosphirane complex valence isomers
Chem.Commun., 2015, 51, 3878
7116589 CIFC22 H31 N2 O6 P WP 1 21/c 19.5748; 27.7242; 10.5851
90; 115.34; 90		2539.5Jose Manuel Villalba Franco; Takahiro Sasamori; Gregor Schnakenburg; Arturo Espinosa Ferao; Rainer Streubel
Going for strain: synthesis of the first 3-imino-azaphosphiridine complexes and their conversion into oxaphosphirane complex valence isomers
Chem.Commun., 2015, 51, 3878
7116590 CIFC31 H24 Br N O6P 1 21 19.4993; 18.9341; 15.0393
90; 97.203; 90		2683.63Haipeng Hu; Yangbin Liu; Jing Guo; Lili Lin; Yali Xu; Xiaohua Liu; Xiaoming Feng
Enantioselective synthesis of dihydrocoumarin derivatives by chiral scandium(III)-complex catalyzed inverse-electron-demand hetero-Diels-Alder reaction
Chem.Commun., 2015, 51, 3835
7116599 CIFC24 H20 Cl N4 O8 RuP 1 21 110.0833; 9.8576; 12.7262
90; 95.327; 90		1259.48Javier J. Concepcion; Diane K. Zhong; David J. Szalda; James T. Muckerman; Etsuko Fujita
Mechanism of water oxidation by [Ru(bda)(L)2]: the return of the 'blue dimer'
Chem.Commun., 2015, 51, 4105
7116600 CIFC30 H20 Cl N4 O8 RuP 21 21 217.6696; 11.321; 32.206
90; 90; 90		2796.4Javier J. Concepcion; Diane K. Zhong; David J. Szalda; James T. Muckerman; Etsuko Fujita
Mechanism of water oxidation by [Ru(bda)(L)2]: the return of the 'blue dimer'
Chem.Commun., 2015, 51, 4105
7116601 CIFC36 H50 Eu2 N8 O34 ZnC 1 2/c 117.0712; 16.981; 20.3832
90; 108.073; 90		5617.3Peng-Fei Shi; Huan-Cheng Hu; Zhan-Yun Zhang; Gang Xiong; Bin Zhao
Heterometal-organic frameworks as highly sensitive and highly selective luminescent probes to detect I^-^ ions in aqueous solutions
Chem.Commun., 2015, 51, 3985
7116602 CIFC36 H50 N8 O34 Tb2 ZnC 1 2/c 117.0778; 16.9284; 20.3385
90; 108.115; 90		5588.4Peng-Fei Shi; Huan-Cheng Hu; Zhan-Yun Zhang; Gang Xiong; Bin Zhao
Heterometal-organic frameworks as highly sensitive and highly selective luminescent probes to detect I^-^ ions in aqueous solutions
Chem.Commun., 2015, 51, 3985
7116603 CIFC36 H34 I2 N6 O21 Tb2 ZnC 1 2/c 117.2316; 16.7585; 21.2567
90; 106.996; 90		5870.3Peng-Fei Shi; Huan-Cheng Hu; Zhan-Yun Zhang; Gang Xiong; Bin Zhao
Heterometal-organic frameworks as highly sensitive and highly selective luminescent probes to detect I^-^ ions in aqueous solutions
Chem.Commun., 2015, 51, 3985
7116604 CIFC21 H21 As O3 S2P 1 21/n 111.687; 14.366; 12.127
90; 106.254; 90		1954.7Nikhil Lalwani; Yu-Su Chen; Gemma Brooke; Neil A. Cross; David W. Allen; Alan Reynolds; Jesus Ojeda; Graham J. Tizzard; Simon J. Coles; Neil Bricklebank
Triphenylarsonium-functionalised gold nanoparticles: potential nanocarriers for intracellular therapeutics
Chem.Commun., 2015, 51, 4109
7116605 CIFC23 H24 As Br O SP 1 21/n 111.17; 13.6075; 14.4757
90; 91.738; 90		2199.23Nikhil Lalwani; Yu-Su Chen; Gemma Brooke; Neil A. Cross; David W. Allen; Alan Reynolds; Jesus Ojeda; Graham J. Tizzard; Simon J. Coles; Neil Bricklebank
Triphenylarsonium-functionalised gold nanoparticles: potential nanocarriers for intracellular therapeutics
Chem.Commun., 2015, 51, 4109
7116606 CIFC116 Cl4 Fe N7 O72 Si2 W18C 1 2/c 135.5945; 14.4862; 38.2599
90; 113.9; 90		18036.3Rinta Sato; Kosuke Suzuki; Takuo Minato; Masahiro Shinoe; Kazuya Yamaguchi; Noritaka Mizuno
Field-induced slow magnetic relaxation of octahedrally coordinated mononuclear Fe(III)-, Co(II)-, and Mn(III)-containing polyoxometalates
Chem.Commun., 2015, 51, 4081
7116607 CIFC124 Cl12 Co N7 O70 Si2 W18P -114.6616; 18.7039; 19.0694
106.86; 92.59; 98.25		4931.97Rinta Sato; Kosuke Suzuki; Takuo Minato; Masahiro Shinoe; Kazuya Yamaguchi; Noritaka Mizuno
Field-induced slow magnetic relaxation of octahedrally coordinated mononuclear Fe(III)-, Co(II)-, and Mn(III)-containing polyoxometalates
Chem.Commun., 2015, 51, 4081
7116608 CIFC114 Mn N7 O74 Si2 W18C 1 2/c 135.6567; 14.4553; 38.3421
90; 113.89; 90		18069.4Rinta Sato; Kosuke Suzuki; Takuo Minato; Masahiro Shinoe; Kazuya Yamaguchi; Noritaka Mizuno
Field-induced slow magnetic relaxation of octahedrally coordinated mononuclear Fe(III)-, Co(II)-, and Mn(III)-containing polyoxometalates
Chem.Commun., 2015, 51, 4081
7116609 CIFC42 H36 N6 O7 Zn4P -3 c 114.5525; 14.5525; 24.7573
90; 90; 120		4540.56D. Prochowicz; K. Sokolowski; I. Justyniak; A. Kornowicz; D. Fairen-Jimenez; T. Friscic; J. Lewinski
A mechanochemical strategy for IRMOF assembly based on pre-designed oxo-zinc precursors
Chem.Commun., 2015, 51, 4032
7116610 CIFC14 H22 F N2 O5 PP 1 21 17.71; 12.999; 17.692
90; 92.506; 90		1771.4Inmaculada Serrano; David Monge; Eleuterio Alvarez; Rosario Fernandez; Jose M. Lassaletta
Asymmetric organocatalytic synthesis of quaternary alpha-hydroxy phosphonates: en route to alpha-aryl phosphaisoserines
Chem.Commun., 2015, 51, 4077
7116614 CIFC34 H25 B TeP -111.3756; 12.5651; 19.3584
82.926; 75.15; 77.945		2608.5Fu An Tsao; Alan. J. Lough; Douglas W. Stephan
Intramolecular 1,1-carboboration versus intermolecular FLP addition in reactions of boranes and bis(phenylethynyl)telluroether
Chem.Commun., 2015, 51, 4287
7116615 CIFC34 H10 B F15 TeP -112.4545; 13.2182; 20.2994
74.416; 73.514; 81.701		3078.2Fu An Tsao; Alan. J. Lough; Douglas W. Stephan
Intramolecular 1,1-carboboration versus intermolecular FLP addition in reactions of boranes and bis(phenylethynyl)telluroether
Chem.Commun., 2015, 51, 4287
7116616 CIFC34 H15 B F10 TeP -111.3615; 11.5042; 13.1803
77.723; 66.878; 69.212		1475.82Fu An Tsao; Alan. J. Lough; Douglas W. Stephan
Intramolecular 1,1-carboboration versus intermolecular FLP addition in reactions of boranes and bis(phenylethynyl)telluroether
Chem.Commun., 2015, 51, 4287
7116617 CIFC68 H30 B2 F20 Te2C 1 2/c 139.238; 21.195; 20.08
90; 108.82; 90		15807Fu An Tsao; Alan. J. Lough; Douglas W. Stephan
Intramolecular 1,1-carboboration versus intermolecular FLP addition in reactions of boranes and bis(phenylethynyl)telluroether
Chem.Commun., 2015, 51, 4287
7116618 CIFC17 H20 Cl Li N2 O3P 21 21 217.7015; 12.0371; 18.2095
90; 90; 90		1688.09Krzysztof Ziach; Janusz Jurczak
Mirror symmetry breaking upon spontaneous crystallization from a dynamic combinatorial library of macrocyclic imines
Chem.Commun., 2015, 51, 4306
7116619 CIFC37 H40 Cl2 Li2 N4 O14P 1 n 17.6122; 18.1368; 14.751
90; 96.894; 90		2021.81Krzysztof Ziach; Janusz Jurczak
Mirror symmetry breaking upon spontaneous crystallization from a dynamic combinatorial library of macrocyclic imines
Chem.Commun., 2015, 51, 4306
7116620 CIFC39 H52 Cl3 O3P -19.807; 13.8699; 16.6745
109.657; 95.088; 107.141		1996.1Shafali Arora; Shivali Sharma; Venus S. Mithu; Chang Hee-Lee; Kamaljit Singh
Selective functionalization of methylene bridges of calix[6]arenes. Isolation and identification of stable conformers of methyl ether of p-tert-butylcalix[6]arene
Chem.Commun., 2015, 51, 4227
7116621 CIFC78 H92 O6P -113.323; 16.3491; 17.448
72.532; 84.273; 89.557		3606.2Shafali Arora; Shivali Sharma; Venus S. Mithu; Chang Hee-Lee; Kamaljit Singh
Selective functionalization of methylene bridges of calix[6]arenes. Isolation and identification of stable conformers of methyl ether of p-tert-butylcalix[6]arene
Chem.Commun., 2015, 51, 4227
7116622 CIFC55 H55 Cl3 N8P -110.6574; 14.7322; 17.013
66.539; 80.163; 80.329		2399.5Koushik Acharyya; Partha Sarathi Mukherjee
Shape and size directed self-selection in organic cage formation
Chem.Commun., 2015, 51, 4241
7116623 CIFC48 H42 N4 O6P -3 c 113.5006; 13.5006; 29.691
90; 90; 120		4686.6Koushik Acharyya; Partha Sarathi Mukherjee
Shape and size directed self-selection in organic cage formation
Chem.Commun., 2015, 51, 4241
7116624 CIFC56 H56 Cl6 N8 O3P 1 21/c 117.6515; 27.369; 11.1516
90; 102.653; 90		5256.5Koushik Acharyya; Partha Sarathi Mukherjee
Shape and size directed self-selection in organic cage formation
Chem.Commun., 2015, 51, 4241
7116625 CIFC33 H36 N4 O6P 1 21/n 17.2035; 18.776; 21.734
90; 91.764; 90		2938.2Koushik Acharyya; Partha Sarathi Mukherjee
Shape and size directed self-selection in organic cage formation
Chem.Commun., 2015, 51, 4241
7116626 CIFC30 H46 Ge2 N4 Se3P 1 21/c 116.736; 11.336; 18.978
90; 106.354; 90		3454.8Surendar Karwasara; Dhirendra Yadav; Chandan Kumar Jha; Gopalan Rajaraman; Selvarajan Nagendran
Single-step conversion of silathiogermylene to germaacid anhydrides: unusual reactivity
Chem.Commun., 2015, 51, 4310
7116627 CIFC30 H46 Ge2 N4 S3P 1 21/c 116.4; 11.364; 18.733
90; 106.005; 90		3355.9Surendar Karwasara; Dhirendra Yadav; Chandan Kumar Jha; Gopalan Rajaraman; Selvarajan Nagendran
Single-step conversion of silathiogermylene to germaacid anhydrides: unusual reactivity
Chem.Commun., 2015, 51, 4310
7116628 CIFC26 H27 Cl2 Cu N5 O3P -110.671; 11.025; 11.868
89.45; 77.812; 79.52		1341.4Weiwei Fang; Cong Liu; Jiangbo Chen; Zhengwei Lu; Zhi-Ming Li; Xiaoling Bao; Tao Tu
The electronic effects of ligands on metal-coordination geometry: a key role in the visual discrimination of dimethylaminopyridine and its application towards chemo-switch
Chem.Commun., 2015, 51, 4267
7116629 CIFC20 H13 Cl Cu F3 N3 O4 SP 1 21/c 17.59; 20.098; 13.487
90; 94.218; 90		2051.8Weiwei Fang; Cong Liu; Jiangbo Chen; Zhengwei Lu; Zhi-Ming Li; Xiaoling Bao; Tao Tu
The electronic effects of ligands on metal-coordination geometry: a key role in the visual discrimination of dimethylaminopyridine and its application towards chemo-switch
Chem.Commun., 2015, 51, 4267
7116630 CIFC28 H29 Cl2 Cu N5 O2P -110.758; 10.951; 12.045
87.424; 78.339; 79.489		1366.4Weiwei Fang; Cong Liu; Jiangbo Chen; Zhengwei Lu; Zhi-Ming Li; Xiaoling Bao; Tao Tu
The electronic effects of ligands on metal-coordination geometry: a key role in the visual discrimination of dimethylaminopyridine and its application towards chemo-switch
Chem.Commun., 2015, 51, 4267
7116631 CIFC26 H27 Cl2 Cu N5 O2 SP -110.634; 10.982; 11.926
89.311; 77.918; 79.929		1340.5Weiwei Fang; Cong Liu; Jiangbo Chen; Zhengwei Lu; Zhi-Ming Li; Xiaoling Bao; Tao Tu
The electronic effects of ligands on metal-coordination geometry: a key role in the visual discrimination of dimethylaminopyridine and its application towards chemo-switch
Chem.Commun., 2015, 51, 4267
7116632 CIFC16 H8 N4P 1 21/c 14.6304; 14.479; 8.886
90; 90.402; 90		595.7Shuaijun Yang; Danqing Liu; Xiaomin Xu; Qian Miao
Molecular packing and n-channel thin film transistors of chlorinated cyclobuta[1,2-b:3,4-b']diquinoxalines
Chem.Commun., 2015, 51, 4275
7116633 CIFC16 H7 Cl N4P 1 21/n 13.8176; 18.9603; 8.7979
90; 95.327; 90		634.07Shuaijun Yang; Danqing Liu; Xiaomin Xu; Qian Miao
Molecular packing and n-channel thin film transistors of chlorinated cyclobuta[1,2-b:3,4-b']diquinoxalines
Chem.Commun., 2015, 51, 4275
7116634 CIFC16 H6 Cl2 N4P 1 21/n 13.8194; 19.4986; 8.9236
90; 99.974; 90		654.52Shuaijun Yang; Danqing Liu; Xiaomin Xu; Qian Miao
Molecular packing and n-channel thin film transistors of chlorinated cyclobuta[1,2-b:3,4-b']diquinoxalines
Chem.Commun., 2015, 51, 4275
7116635 CIFC16 H4 Cl2 N4P -14.7573; 7.941; 8.892
92.898; 100.56; 94.347		328.6Shuaijun Yang; Danqing Liu; Xiaomin Xu; Qian Miao
Molecular packing and n-channel thin film transistors of chlorinated cyclobuta[1,2-b:3,4-b']diquinoxalines
Chem.Commun., 2015, 51, 4275
7116636 CIFC16 H4 Cl4 N4P -15.8383; 6.0989; 10.5832
82.636; 76.077; 82.498		360.8Shuaijun Yang; Danqing Liu; Xiaomin Xu; Qian Miao
Molecular packing and n-channel thin film transistors of chlorinated cyclobuta[1,2-b:3,4-b']diquinoxalines
Chem.Commun., 2015, 51, 4275
7116637 CIFC46 H50 Cl6 Ir2 N4P -17.991; 9.776; 15.449
100.26; 102.15; 103.55		1113.7Nem Singh; Jae-Ho Jo; Young Ho Song; Hyunuk Kim; Dongwook Kim; Myoung Soo Lah; Ki-Whan Chi
Coordination-driven self-assembly of an iridium-cornered prismatic cage and encapsulation of three heteroguests in its large cavity
Chem.Commun., 2015, 51, 4492
7116638 CIFC254 H220 F18 Ir6 N24 O21 S6P 1 21/n 127.189; 30.491; 29.069
90; 100.26; 90		23713Nem Singh; Jae-Ho Jo; Young Ho Song; Hyunuk Kim; Dongwook Kim; Myoung Soo Lah; Ki-Whan Chi
Coordination-driven self-assembly of an iridium-cornered prismatic cage and encapsulation of three heteroguests in its large cavity
Chem.Commun., 2015, 51, 4492
7116639 CIFC256 H208 Ir6 N26 O4I -4 2 d46.154; 46.154; 49.592
90; 90; 90		105640Nem Singh; Jae-Ho Jo; Young Ho Song; Hyunuk Kim; Dongwook Kim; Myoung Soo Lah; Ki-Whan Chi
Coordination-driven self-assembly of an iridium-cornered prismatic cage and encapsulation of three heteroguests in its large cavity
Chem.Commun., 2015, 51, 4492
7116640 CIFC17 H14 O4P 1 21/n 17.761; 9.02; 21.077
90; 97.965; 90		1461.2Juan Du; Xiuli Zhang; Xi Sun; Lei Wang
Copper-catalyzed direct alpha-ketoesterification of propiophenones with acetophenones via C(sp^3^)-H oxidative cross-coupling
Chem.Commun., 2015, 51, 4372
7116641 CIFC32 H22 N2P 1 21/n 114.6334; 8.9414; 17.7375
90; 105.381; 90		2237.7Wei Huang; Lu Sun; Zhiwen Zheng; Jianhua Su; He Tian
Colour-tunable fluorescence of single molecules based on the vibration induced emission of phenazine
Chem.Commun., 2015, 51, 4462
7116642 CIFC16 H23 B F4 Fe N6P 1 21/n 113.0808; 10.6982; 14.0524
90; 96.336; 90		1954.5Dong Shao; Shao-Liang Zhang; Xin-Hua Zhao; Xin-Yi Wang
Spin canting, metamagnetism, and single-chain magnetic behaviour in a cyano-bridged homospin iron(II) compound
Chem.Commun., 2015, 51, 4360
7116643 CIFC42 H36 B3 N3 O6P 17.3418; 15.788; 31.0079
83.135; 87.475; 89.797		3564.96Xiao-Ye Wang; Fang-Dong Zhuang; Xin-Chang Wang; Xiao-Yu Cao; Jie-Yu Wang; Jian Pei
Synthesis, structure and properties of C3-symmetric heterosuperbenzene with three BN units
Chem.Commun., 2015, 51, 4368
7116644 CIFC232.5 H188 F52.5 N20.5 O P16.75 Pd4 Ru2P -123.8865; 25.4288; 31.7818
96.15; 107.106; 113.591		16341.8Jiajia Yang; Mohan Bhadbhade; William A. Donald; Hasti Iranmanesh; Evan G. Moore; Hong Yan; Jonathon E. Beves
Self-assembled supramolecular cages containing ruthenium(II) polypyridyl complexes
Chem.Commun., 2015, 51, 4465
7116645 CIFC63 H45 F7.5 N11 O2 P1.25 RuC 1 2/c 131.584; 16.937; 26.449
90; 105.27; 90		13649Jiajia Yang; Mohan Bhadbhade; William A. Donald; Hasti Iranmanesh; Evan G. Moore; Hong Yan; Jonathon E. Beves
Self-assembled supramolecular cages containing ruthenium(II) polypyridyl complexes
Chem.Commun., 2015, 51, 4465
7116646 CIFC15 H18 I N O2P 1 21/n 19.3649; 15.0028; 11.1821
90; 92.996; 90		1568.93H.Q. Nimal Gunaratne; Peter Nockemann; Kenneth R. Seddon
Pro-fragrant ionic liquids with stable hemiacetal motifs: water-triggered release of fragrances
Chem.Commun., 2015, 51, 4455
7116647 CIFC24 H23 Cl O8P -19.2814; 11.711; 12.1339
113.081; 96.35; 102.204		1158.1Hong Lu; Jin-Yu Liu; Chen-Guang Li; Jun-Bing Lin; Yong-Min Liang; Peng-Fei Xu
A new chiral C1-symmetric NHC-catalyzed addition to alpha-aryl substituted alpha,beta-disubstituted enals: enantioselective synthesis of fully functionalized dihydropyranones
Chem.Commun., 2015, 51, 4473
7116648 CIFC14 H14 Br2 N2C 2 2 217.3088; 31.966; 12.46
90; 90; 90		2911.1Yusuke Kita; Kosuke Higashida; Kenta Yamaji; Atsuhiro Iimuro; Kazushi Mashima
Asymmetric hydrogenation of quinazolinium salts catalysed by halide-bridged dinuclear iridium complexes bearing chiral diphosphine ligands
Chem.Commun., 2015, 51, 4380
7116649 CIFC72 H76 Br2 Ir2 N4P 1 21 114.4388; 14.3302; 14.9599
90; 94.1029; 90		3087.43Yusuke Kita; Kosuke Higashida; Kenta Yamaji; Atsuhiro Iimuro; Kazushi Mashima
Asymmetric hydrogenation of quinazolinium salts catalysed by halide-bridged dinuclear iridium complexes bearing chiral diphosphine ligands
Chem.Commun., 2015, 51, 4380
7116650 CIFC30 H23 Br N2 O3 SP 1 21/c 115.2526; 8.7689; 19.1451
90; 90.857; 90		2560.3Yuanhao Wang; Xiaoqiang Lei; Yefeng Tang
Rh(II)-catalyzed cycloadditions of 1-tosyl 1,2,3-triazoles with 2H-azirines: switchable reactivity of Rh-azavinylcarbene as [2C]- or aza-[3C]-synthon
Chem.Commun., 2015, 51, 4507
7116651 CIFC29 H24 N2 O2 SP 1 21/c 113.7344; 11.3573; 15.3726
90; 95.591; 90		2386.5Yuanhao Wang; Xiaoqiang Lei; Yefeng Tang
Rh(II)-catalyzed cycloadditions of 1-tosyl 1,2,3-triazoles with 2H-azirines: switchable reactivity of Rh-azavinylcarbene as [2C]- or aza-[3C]-synthon
Chem.Commun., 2015, 51, 4507
7116652 CIFC20 H23 N O6 S2P 1 21 19.1418; 9.388; 12.6939
90; 110.69; 90		1019.17Chao Song; Wen Yang; Nannan Zhou; Rui Qian; Yajun Zhang; Kaiyan Lou; Rui Wang; Wei Wang
Fluorescent theranostic agents for Hg2+ detection and detoxification treatment
Chem.Commun., 2015, 51, 4443
7116653 CIFC98 H126 O6P -110.3348; 19.1818; 22.503
80.708; 78.639; 78.993		4257.4Liang Han; Yuewei Zhang; Weiping Chen; Xiao Cheng; Kaiqing Ye; Jingying Zhang; Yue Wang
Assembly of twisted luminescent architectures based on acenaphtho[1,2-k]fluoranthene derivatives
Chem.Commun., 2015, 51, 4477
7116654 CIFC74 H66 B F27 Ir N6 O6P -114.2926; 17.57617; 30.9787
96.4495; 91.4551; 106.009		7420.04Simone A. Hauser; Ivan Prokes; Adrian B. Chaplin
Low-coordinate iridium NHC complexes derived from selective and reversible C-H bond activation of fluoroarenes
Chem.Commun., 2015, 51, 4425
7116655 CIFC71 H58 B Cl2 F26 Ir N6 O4P 1 21/n 119.5682; 18.7483; 20.39
90; 104.772; 90		7233.2Simone A. Hauser; Ivan Prokes; Adrian B. Chaplin
Low-coordinate iridium NHC complexes derived from selective and reversible C-H bond activation of fluoroarenes
Chem.Commun., 2015, 51, 4425
7116656 CIFC77 H70 B F26 Ir N6 O6P 1 21/c 120.7249; 22.1162; 18.7709
90; 116.331; 90		7711.1Simone A. Hauser; Ivan Prokes; Adrian B. Chaplin
Low-coordinate iridium NHC complexes derived from selective and reversible C-H bond activation of fluoroarenes
Chem.Commun., 2015, 51, 4425
7116657 CIFC71 H63 B F27 Ir N6 O6P -114.3353; 17.5209; 30.9758
95.9306; 91.1596; 106.158		7423Simone A. Hauser; Ivan Prokes; Adrian B. Chaplin
Low-coordinate iridium NHC complexes derived from selective and reversible C-H bond activation of fluoroarenes
Chem.Commun., 2015, 51, 4425
7116658 CIFC67 H63 B F24 Ir N7 O6P 1 21/c 113.782; 20.0926; 25.2535
90; 91.1355; 90		6991.73Simone A. Hauser; Ivan Prokes; Adrian B. Chaplin
Low-coordinate iridium NHC complexes derived from selective and reversible C-H bond activation of fluoroarenes
Chem.Commun., 2015, 51, 4425
7116659 CIFC15 H22 B F N2P -17.486; 9.564; 10.597
75.8; 76.99; 75.35		700.8Masahito Murai; Tetsuya Omura; Yoichiro Kuninobu; Kazuhiko Takai
Rhenium-catalysed dehydrogenative borylation of primary and secondary C(sp^3^)-H bonds adjacent to a nitrogen atom
Chem.Commun., 2015, 51, 4583
7116660 CIFC46 H79 Fe9 N2 O50P 32 2 118.927; 18.927; 24.693
90; 90; 120		7661Jiong-Peng Zhao; Song-De Han; Xue Jiang; Jian Xu; Ze Chang; Xian-He Bu
A three dimensional magnetically frustrated metal-organic framework via the vertices augmentation of underlying net
Chem.Commun., 2015, 51, 4627
7116661 CIFC H N OP 21 21 2110.5611; 15.5632; 22.4083
90; 90; 90		3683.1Pei-Qiang Huang; Su-Yu Huang; Long-Hui Gao; Zhong-Yi Mao; Zong Chang; Ai-E Wang
Enantioselective total synthesis of (+)-methoxystemofoline and (+)-isomethoxystemofoline
Chem.Commun., 2015, 51, 4576
7116662 CIFC70 H110 Li2 O2 Pb2 Si4P -112.2658; 16.7325; 20.375
99.254; 107.15; 107.882		3654.6Masaichi Saito; Marisa Nakada; Takuya Kuwabara; Mao Minoura
A reversible two-electron redox system involving a divalent lead species
Chem.Commun., 2015, 51, 4674
7116663 CIFC36 H56 Li2 O2 Pb Si2P -112.4117; 12.4449; 13.7628
82.874; 67.352; 75.447		1898.1Masaichi Saito; Marisa Nakada; Takuya Kuwabara; Mao Minoura
A reversible two-electron redox system involving a divalent lead species
Chem.Commun., 2015, 51, 4674
7116664 CIFC16 H17 N O2 SP 1 21/n 114.3451; 5.6024; 19.171
90; 110.01; 90		1447.7Xiang-Wei Liu; Jiang-Ling Shi; Jiang-Bo Wei; Chao Yang; Jia-Xuan Yan; Kun Peng; Le Dai; Chen-Guang Li; Bi-Qin Wang; Zhang-Jie Shi
Diversified syntheses of multifunctionalized thiazole derivatives via regioselective and programmed C-H activation
Chem.Commun., 2015, 51, 4599
7116665 CIFFe1.172 H Li0.828 O SP 4/n m m :13.7038; 3.7038; 8.8852
90; 90; 90		121.888U. Pachmayr; D. Johrendt
[(Li0.8Fe0.2)OH]FeS and the ferromagnetic superconductors [(Li0.8Fe0.2)OH]Fe(S1-xSex) (0 < x ? 1)
Chem.Commun., 2015, 51, 4689
7116666 CIFC148 H96 Mn6 N20 O18P 1 21/c 127.159; 13.925; 41.043
90; 112.375; 90		14353L. A. Barrios; J. Salinas-Uber; O. Roubeau; S. J. Teat; G. Aromi
Molecular self-recognition: a chiral [Mn(II)6] wheel via donor-acceptor pi^...^pi contacts and H-bonds
Chem.Commun., 2015, 51, 4631
7116667 CIFC49 H62 N6 O3P 1 21/n 114.623; 16.641; 18.326
90; 101.777; 90		4365.6L. A. Barrios; J. Salinas-Uber; O. Roubeau; S. J. Teat; G. Aromi
Molecular self-recognition: a chiral [Mn(II)6] wheel via donor-acceptor pi^...^pi contacts and H-bonds
Chem.Commun., 2015, 51, 4631
7116668 CIFC72 H96 O Si4P 21 21 2113.7114; 19.2562; 25.0769
90; 90; 90		6621Takashi Matsuno; Yutaro Koyama; Satoru Hiroto; Jatish Kumar; Tsuyoshi Kawai; Hiroshi Shinokubo
Isolation of a 1,4-diketone intermediate in oxidative dimerization of 2-hydroxyanthracene and its conversion to oxahelicene
Chem.Commun., 2015, 51, 4607
7116669 CIFC72 H98 O2 Si4P 1 21/c 113.426; 18.425; 28.086
90; 94.327; 90		6928Takashi Matsuno; Yutaro Koyama; Satoru Hiroto; Jatish Kumar; Tsuyoshi Kawai; Hiroshi Shinokubo
Isolation of a 1,4-diketone intermediate in oxidative dimerization of 2-hydroxyanthracene and its conversion to oxahelicene
Chem.Commun., 2015, 51, 4607
7116670 CIFC67.2 H91.2 N1.6 O2.4 Si3.2P 1 21/c 113.31; 29.8304; 19.4965
90; 93.59; 90		7725.8Takashi Matsuno; Yutaro Koyama; Satoru Hiroto; Jatish Kumar; Tsuyoshi Kawai; Hiroshi Shinokubo
Isolation of a 1,4-diketone intermediate in oxidative dimerization of 2-hydroxyanthracene and its conversion to oxahelicene
Chem.Commun., 2015, 51, 4607
7116671 CIFC72 H96 O Si4P 1 21/c 119.768; 21.986; 16.67
90; 111.807; 90		6727Takashi Matsuno; Yutaro Koyama; Satoru Hiroto; Jatish Kumar; Tsuyoshi Kawai; Hiroshi Shinokubo
Isolation of a 1,4-diketone intermediate in oxidative dimerization of 2-hydroxyanthracene and its conversion to oxahelicene
Chem.Commun., 2015, 51, 4607
7116672 CIFC72 H98 O2 Si4P -113.171; 14.918; 17.544
85.743; 79.779; 84.496		3371Takashi Matsuno; Yutaro Koyama; Satoru Hiroto; Jatish Kumar; Tsuyoshi Kawai; Hiroshi Shinokubo
Isolation of a 1,4-diketone intermediate in oxidative dimerization of 2-hydroxyanthracene and its conversion to oxahelicene
Chem.Commun., 2015, 51, 4607
7116688 CIFC29 H28 Cl2 N P Ru SP 1 21/n 112.6476; 11.7959; 18.6459
90; 102.933; 90		2711.21Zhang, Hui-Jun; Lin, Weidong; Wu, Zhengjian; Ruan, Wenqing; Wen, Ting-Bin
Silver-mediated direct phosphorylation of benzothiazoles and thiazoles with diarylphosphine oxides.
Chemical communications (Cambridge, England), 2015, 51, 3450-3453
7116689 CIFC15 H12 N O P SC 1 2/c 110.4363; 13.1058; 20.7087
90; 96.816; 90		2812.44Zhang, Hui-Jun; Lin, Weidong; Wu, Zhengjian; Ruan, Wenqing; Wen, Ting-Bin
Silver-mediated direct phosphorylation of benzothiazoles and thiazoles with diarylphosphine oxides.
Chemical communications (Cambridge, England), 2015, 51, 3450-3453
7116702 CIFC27 H22 N4 O8 ZnP 1 21/c 111.361; 15.532; 16.269
90; 94.661; 90		2861.3Bappaditya Gole; Udishnu Sanyal; Partha Sarathi Mukherjee
A smart approach to achieve an exceptionally high loading of metal nanoparticles supported by functionalized extended frameworks for efficient catalysis
Chem.Commun., 2015, 51, 4872
7116703 CIFC23 H14 N2 O5 ZnC 1 2/c 129.971; 16.271; 15.804
90; 115.749; 90		6942Bappaditya Gole; Udishnu Sanyal; Partha Sarathi Mukherjee
A smart approach to achieve an exceptionally high loading of metal nanoparticles supported by functionalized extended frameworks for efficient catalysis
Chem.Commun., 2015, 51, 4872
7116706 CIFC25 H24 N2 OP -19.491; 9.5574; 10.9648
91.766; 93.926; 97.631		982.69Subban Kathiravan; Shishir Ghosh; Graeme Hogarth; Ian A. Nicholls
Copper catalysed amidation of aryl halides through chelation assistance
Chem.Commun., 2015, 51, 4834
7116707 CIFC19 H20 N2 O SP 1 21/c 116.8737; 9.68667; 10.28958
90; 96.9165; 90		1669.59Subban Kathiravan; Shishir Ghosh; Graeme Hogarth; Ian A. Nicholls
Copper catalysed amidation of aryl halides through chelation assistance
Chem.Commun., 2015, 51, 4834
7116708 CIFC23 H40 Cl Ir N2P 1 21/n 111.8497; 12.2144; 16.718
90; 91.591; 90		2418.8Yannick D. Bidal; Mathieu Lesieur; Mohand Melaimi; David B. Cordes; Alexandra M. Z. Slawin; Guy Bertrand; Catherine S. J. Cazin
A simple access to transition metal cyclopropenylidene complexes
Chem.Commun., 2015, 51, 4778
7116709 CIFC15 H28 Cl Cu N2P 1 21/c 16.043; 18.944; 15.635
90; 100.45; 90		1760.2Yannick D. Bidal; Mathieu Lesieur; Mohand Melaimi; David B. Cordes; Alexandra M. Z. Slawin; Guy Bertrand; Catherine S. J. Cazin
A simple access to transition metal cyclopropenylidene complexes
Chem.Commun., 2015, 51, 4778
7116710 CIFC30.5 H57 Cl5 N4 Pd2P -18.6743; 15.139; 15.947
86.794; 85.946; 80.765		2059.7Yannick D. Bidal; Mathieu Lesieur; Mohand Melaimi; David B. Cordes; Alexandra M. Z. Slawin; Guy Bertrand; Catherine S. J. Cazin
A simple access to transition metal cyclopropenylidene complexes
Chem.Commun., 2015, 51, 4778
7116711 CIFC15 H28 Au Cl N2P 1 21/n 111.3202; 12.8913; 12.5373
90; 90.2151; 90		1829.6Yannick D. Bidal; Mathieu Lesieur; Mohand Melaimi; David B. Cordes; Alexandra M. Z. Slawin; Guy Bertrand; Catherine S. J. Cazin
A simple access to transition metal cyclopropenylidene complexes
Chem.Commun., 2015, 51, 4778
7116712 CIFC31 H56 Au F3 N4 O3 SP 1 21/c 113.2941; 9.5096; 14.5324
90; 93.61; 90		1833.56Yannick D. Bidal; Mathieu Lesieur; Mohand Melaimi; David B. Cordes; Alexandra M. Z. Slawin; Guy Bertrand; Catherine S. J. Cazin
A simple access to transition metal cyclopropenylidene complexes
Chem.Commun., 2015, 51, 4778
7116713 CIFC6 H6 Fe Na3 O17C 1 2/c 117.4212; 12.5545; 14.9217
90; 101.047; 90		3203.1Qingchun Ge; Tai-Shung Chung
Oxalic acid complexes: promising draw solutes for forward osmosis (FO) in protein enrichment
Chem.Commun., 2015, 51, 4854
7116714 CIFC6 H10 Cr Na3 O17C 1 2/c 117.2551; 12.4639; 15.1228
90; 100.454; 90		3198.4Qingchun Ge; Tai-Shung Chung
Oxalic acid complexes: promising draw solutes for forward osmosis (FO) in protein enrichment
Chem.Commun., 2015, 51, 4854
7116715 CIFC24 H18P n a 217.4869; 19.718; 11.2222
90; 90; 90		1656.7Lingzhi Li; Ming Chen; Haoke Zhang; Han Nie; Jing Zhi Sun; Anjun Qin; Ben Zhong Tang
Influence of the number and substitution position of phenyl groups on the aggregation-enhanced emission of benzene-cored luminogens
Chem.Commun., 2015, 51, 4830
7116716 CIFC20 H25 NP 21 21 2110.529; 11.655; 12.596
90; 90; 90		1545.7Mirja Enders; Christian J. Friedmann; Philipp N. Plessow; Angela Bihlmeier; Martin Nieger; Wim Klopper; Stefan Brase
Unprecedented pseudo-ortho and ortho metallation of [2.2]paracyclophanes ‒ a methyl group matters
Chem.Commun., 2015, 51, 4793
7116717 CIFC26 H29 N SP 1 21/c 17.535; 14.973; 18.844
90; 95.77; 90		2115.2Mirja Enders; Christian J. Friedmann; Philipp N. Plessow; Angela Bihlmeier; Martin Nieger; Wim Klopper; Stefan Brase
Unprecedented pseudo-ortho and ortho metallation of [2.2]paracyclophanes ‒ a methyl group matters
Chem.Commun., 2015, 51, 4793
7116718 CIFC20 H25 N SP 1 21/n 18.104; 8.358; 24.688
90; 96.2; 90		1662.4Mirja Enders; Christian J. Friedmann; Philipp N. Plessow; Angela Bihlmeier; Martin Nieger; Wim Klopper; Stefan Brase
Unprecedented pseudo-ortho and ortho metallation of [2.2]paracyclophanes ‒ a methyl group matters
Chem.Commun., 2015, 51, 4793
7116719 CIFC20 H25 N SP 1 21/n 17.812; 11.736; 18.668
90; 96.49; 90		1700.5Mirja Enders; Christian J. Friedmann; Philipp N. Plessow; Angela Bihlmeier; Martin Nieger; Wim Klopper; Stefan Brase
Unprecedented pseudo-ortho and ortho metallation of [2.2]paracyclophanes ‒ a methyl group matters
Chem.Commun., 2015, 51, 4793
7116720 CIFC32 H28 O4P 1 21/n 110.2761; 15.204; 15.2549
90; 96.857; 90		2366.34Murat Cakici; Zhi-Gang Gu; Martin Nieger; Jochen Burck; Lars Heinke; Stefan Brase
Planar-chiral building blocks for metal-organic frameworks
Chem.Commun., 2015, 51, 4796
7116729 CIFC48.93 H35.72 Cu2 N2 O8.93P -110.7482; 12.23; 16.366
95.11; 96.968; 102.936		2066.2Yuichi Takasaki; Satoshi Takamizawa
Reversible crystal deformation of a single-crystal host of copper(II) 1-naphthoate-pyrazine through crystal phase transition induced by methanol vapor sorption
Chem.Commun., 2015, 51, 5024
7116730 CIFC48 H32 Cu2 N2 O8P -110.4745; 11.6064; 17.037
97.583; 104.918; 90.081		1982.5Yuichi Takasaki; Satoshi Takamizawa
Reversible crystal deformation of a single-crystal host of copper(II) 1-naphthoate-pyrazine through crystal phase transition induced by methanol vapor sorption
Chem.Commun., 2015, 51, 5024
7116731 CIFC48 H32 Cu2 N2 O8P -110.6065; 11.6485; 17.4513
80.612; 75.215; 89.821		2055.1Yuichi Takasaki; Satoshi Takamizawa
Reversible crystal deformation of a single-crystal host of copper(II) 1-naphthoate-pyrazine through crystal phase transition induced by methanol vapor sorption
Chem.Commun., 2015, 51, 5024
7116732 CIFC36 H24 Co3 N13 Na O15.25P 6313.1191; 13.1191; 16.014
90; 90; 120		2386.92Ru-Xin Yao; Xin Cui; Jun Wang; Xian-Ming Zhang
A homochiral magnet based on D3 symmetric [(NaO3)Co3] clusters: from spontaneous resolution to absolute chiral induction
Chem.Commun., 2015, 51, 5108
7116733 CIFC36 H27 Co3 N13 Na O15P 6313.1177; 13.1177; 16.005
90; 90; 120		2385.07Ru-Xin Yao; Xin Cui; Jun Wang; Xian-Ming Zhang
A homochiral magnet based on D3 symmetric [(NaO3)Co3] clusters: from spontaneous resolution to absolute chiral induction
Chem.Commun., 2015, 51, 5108
7116734 CIFC6 H5 B K N3P -19.5267; 9.9704; 10.1727
81.041; 68.165; 83.636		884.51Johannes Landmann; Jan A. P. Sprenger; Rudiger Bertermann; Nikolai Ignatiev; Vera Bernhardt-Pitchougina; Eduard Bernhardt; Helge Willner; Maik Finze
Convenient access to the tricyanoborate dianion B(CN)3^2-^ and selected reactions as a boron-centred nucleophile
Chem.Commun., 2015, 51, 4989
7116735 CIFC28 H36 B4 K4 N12 O2P 1 21/c 17.5693; 25.062; 22.116
90; 94.3; 90		4183.6Johannes Landmann; Jan A. P. Sprenger; Rudiger Bertermann; Nikolai Ignatiev; Vera Bernhardt-Pitchougina; Eduard Bernhardt; Helge Willner; Maik Finze
Convenient access to the tricyanoborate dianion B(CN)3^2-^ and selected reactions as a boron-centred nucleophile
Chem.Commun., 2015, 51, 4989
7116736 CIFC9 B F5 K N3P 1 21/c 111.894; 12.782; 7.5458
90; 103.98; 90		1113.2Johannes Landmann; Jan A. P. Sprenger; Rudiger Bertermann; Nikolai Ignatiev; Vera Bernhardt-Pitchougina; Eduard Bernhardt; Helge Willner; Maik Finze
Convenient access to the tricyanoborate dianion B(CN)3^2-^ and selected reactions as a boron-centred nucleophile
Chem.Commun., 2015, 51, 4989
7116737 CIFC6 H5 B K N3P -19.5044; 9.976; 10.1345
81.033; 68.217; 83.514		879.8Johannes Landmann; Jan A. P. Sprenger; Rudiger Bertermann; Nikolai Ignatiev; Vera Bernhardt-Pitchougina; Eduard Bernhardt; Helge Willner; Maik Finze
Convenient access to the tricyanoborate dianion B(CN)3^2-^ and selected reactions as a boron-centred nucleophile
Chem.Commun., 2015, 51, 4989
7116738 CIFC9 H8 B2 K2 N6 OP 1 21/n 19.8586; 13.1307; 12.1811
90; 93.991; 90		1573.02Johannes Landmann; Jan A. P. Sprenger; Rudiger Bertermann; Nikolai Ignatiev; Vera Bernhardt-Pitchougina; Eduard Bernhardt; Helge Willner; Maik Finze
Convenient access to the tricyanoborate dianion B(CN)3^2-^ and selected reactions as a boron-centred nucleophile
Chem.Commun., 2015, 51, 4989
7116739 CIFC26.5 H36.5 Br2 Fe N3.5 O1.5P 1 21 115.777; 10.03; 17.685
90; 100.09; 90		2755.3Ziqing Zuo; Lei Zhang; Xuebing Leng; Zheng Huang
Iron-catalyzed asymmetric hydrosilylation of ketones
Chem.Commun., 2015, 51, 5073
7116740 CIFC47 H45 Br2 Fe N3 OP 433.2315; 33.2315; 18.2906
90; 90; 90		20198.9Ziqing Zuo; Lei Zhang; Xuebing Leng; Zheng Huang
Iron-catalyzed asymmetric hydrosilylation of ketones
Chem.Commun., 2015, 51, 5073
7116741 CIFC2 H10 B10 N2 Na2 O17C 1 2/c 121.9507; 6.4172; 11.0598
90; 103.407; 90		1515.45Jun-Hua Wang; Qi Wei; Jian-Wen Cheng; Huan He; Bai-Feng Yang; Guo-Yu Yang
Na2B10O17^.^H2en: a three-dimensional open-framework layered borate co-templated by inorganic cations and organic amines
Chem.Commun., 2015, 51, 5066
7116742 CIFC32 H33 Fe N4 O9.5P 1 21 18.4996; 14.4218; 26.0595
90; 97.616; 90		3166.2R. Gautam; E. A. Akam; A. V. Astashkin; J. J. Loughrey; E. Tomat
Sirtuin inhibitor sirtinol is an intracellular iron chelator
Chem.Commun., 2015, 51, 5104
7116743 CIFC69 H118 N12 Na7I -4 2 d32.759; 32.759; 29.376
90; 90; 90		31525Andreas Stascha
A pyrazolate-stabilized sodium hydride complex
Chem.Commun., 2015, 51, 5056
7116744 CIFC12.17 H20.33 N2 NaP 1 21/c 115.184; 19.831; 26.107
90; 100.11; 90		7739Andreas Stascha
A pyrazolate-stabilized sodium hydride complex
Chem.Commun., 2015, 51, 5056
7116745 CIFC56 H38 Cu2 N3 O11P -116.1748; 17.1245; 17.3765
61.699; 79.187; 79.168		4135.1Valentina Brega; Matthias Zeller; Yufan He; H. Peter Lu; Jeremy K. Klosterman
Multi-responsive metal-organic lantern cages in solution
Chem.Commun., 2015, 51, 5077
7116746 CIFC150.55 H187.34 Cu4 N5.82 O34.04P 1 21/c 118.2648; 27.0741; 16.6959
90; 110.078; 90		7754.4Valentina Brega; Matthias Zeller; Yufan He; H. Peter Lu; Jeremy K. Klosterman
Multi-responsive metal-organic lantern cages in solution
Chem.Commun., 2015, 51, 5077
7116747 CIFC136.45 H149.05 Cu4 N16.15 O34.15C 1 2/c 122.7256; 27.998; 23.4326
90; 91.88; 90		14901.5Valentina Brega; Matthias Zeller; Yufan He; H. Peter Lu; Jeremy K. Klosterman
Multi-responsive metal-organic lantern cages in solution
Chem.Commun., 2015, 51, 5077
7116748 CIFC108 H84 Cu4 N4 O24.61 S4P -114.935; 16.106; 16.995
105.989; 109.453; 104.285		3437Valentina Brega; Matthias Zeller; Yufan He; H. Peter Lu; Jeremy K. Klosterman
Multi-responsive metal-organic lantern cages in solution
Chem.Commun., 2015, 51, 5077
7116749 CIFC21 H44 Li N5P b c a10.5102; 18.8729; 23.8796
90; 90; 90		4736.7Stuart D. Robertson; Alan R. Kennedy; John J. Liggat; Robert E. Mulvey
Facile synthesis of a genuinely alkane-soluble but isolable lithium hydride transfer reagent
Chem.Commun., 2015, 51, 5452
7116750 CIFC30 H31 B O2 ZrP b c a10.3097; 15.5055; 32.3133
90; 90; 90		5165.51Gang He; Benjamin D. Wiltshire; Paul Choi; Aliaksandr Savin; Shuai Sun; Arash Mohammadpour; Michael J. Ferguson; Robert McDonald; Samira Farsinezhad; Alex Brown; Karthik Shankar; Eric Rivard
Phosphorescence within benzotellurophenes and color tunable tellurophenes under ambient conditions
Chem.Commun., 2015, 51, 5444
7116751 CIFC20 H21 B O2 TeP b c a8.2167; 20.788; 22.069
90; 90; 90		3769.6Gang He; Benjamin D. Wiltshire; Paul Choi; Aliaksandr Savin; Shuai Sun; Arash Mohammadpour; Michael J. Ferguson; Robert McDonald; Samira Farsinezhad; Alex Brown; Karthik Shankar; Eric Rivard
Phosphorescence within benzotellurophenes and color tunable tellurophenes under ambient conditions
Chem.Commun., 2015, 51, 5444
7116752 CIFC20 H14 TeP -15.7439; 11.1587; 12.0325
80.1921; 87.5978; 79.981		748.3Gang He; Benjamin D. Wiltshire; Paul Choi; Aliaksandr Savin; Shuai Sun; Arash Mohammadpour; Michael J. Ferguson; Robert McDonald; Samira Farsinezhad; Alex Brown; Karthik Shankar; Eric Rivard
Phosphorescence within benzotellurophenes and color tunable tellurophenes under ambient conditions
Chem.Commun., 2015, 51, 5444
7116753 CIFC28 H34 B2 O4 TeP 1 21/n 110.6313; 21.4729; 13.1595
90; 113.042; 90		2764.4Gang He; Benjamin D. Wiltshire; Paul Choi; Aliaksandr Savin; Shuai Sun; Arash Mohammadpour; Michael J. Ferguson; Robert McDonald; Samira Farsinezhad; Alex Brown; Karthik Shankar; Eric Rivard
Phosphorescence within benzotellurophenes and color tunable tellurophenes under ambient conditions
Chem.Commun., 2015, 51, 5444
7116754 CIFC28 H34 B2 O4 TeP -17.0792; 12.1454; 16.953
75.2698; 82.0304; 80.2126		1382.2Gang He; Benjamin D. Wiltshire; Paul Choi; Aliaksandr Savin; Shuai Sun; Arash Mohammadpour; Michael J. Ferguson; Robert McDonald; Samira Farsinezhad; Alex Brown; Karthik Shankar; Eric Rivard
Phosphorescence within benzotellurophenes and color tunable tellurophenes under ambient conditions
Chem.Commun., 2015, 51, 5444
7116755 CIFC18 H18 B Cu F5 N4 O3I 1 2/a 115.4006; 9.5362; 28.09
90; 90.988; 90		4124.8Cameron M. Moore; Nathaniel K. Szymczak
Redox-induced fluoride ligand dissociation stabilized by intramolecular hydrogen bonding
Chem.Commun., 2015, 51, 5490
7116756 CIFC18 H18 Cu F N4 O3P 1 21/n 18.793; 14.8014; 13.3814
90; 93.525; 90		1738.28Cameron M. Moore; Nathaniel K. Szymczak
Redox-induced fluoride ligand dissociation stabilized by intramolecular hydrogen bonding
Chem.Commun., 2015, 51, 5490
7116757 CIFC15 H11 N O3P b c a9.89; 7.3; 32.941
90; 90; 90		2378.2Soumitra Agasti; Upendra Sharma; Togati Naveen; Debabrata Maiti
Orthogonal selectivity with cinnamic acids in 3-substituted benzofuran synthesis through C-H olefination of phenols
Chem.Commun., 2015, 51, 5375
7116758 CIFC34 H36 B2 F15 Li O6P 1 21/n 112.4374; 19.273; 15.5445
90; 93.373; 90		3719.7Junhao Zheng; Yuwen Wang; Zhen Hua Li; Huadong Wang
Application of a nucleophilic boryl complex in the frustrated Lewis pair: activation of H-H, B-H and C[double bond, length as m-dash]C bonds with B(C6F5)3 and boryl-borate lithium
Chem.Commun., 2015, 51, 5505
7116759 CIFC23 H23 N3 O7P 1 21 18.223; 20.352; 14.3
90; 105.02; 90		2311.4Audrey Dumoulin; Claudia Lalli; Pascal Retailleau; Geraldine Masson
Catalytic, highly enantioselective, direct amination of enecarbamates
Chem.Commun., 2015, 51, 5383
7116760 CIFC25 H48 B11 Li N2 O3P n m a15.1947; 12.6157; 16.666
90; 90; 90		3194.74Matthew J. Asay; Steven P. Fisher; Sarah E. Lee; Fook S. Tham; Dan Borchardt; Vincent Lavallo
Synthesis of unsymmetrical N-carboranyl NHCs: directing effect of the carborane anion
Chem.Commun., 2015, 51, 5359
7116761 CIFC34.93 H66.85 B11 Li2 N2 O5.48P n n 215.9089; 26.7369; 10.561
90; 90; 90		4492.2Matthew J. Asay; Steven P. Fisher; Sarah E. Lee; Fook S. Tham; Dan Borchardt; Vincent Lavallo
Synthesis of unsymmetrical N-carboranyl NHCs: directing effect of the carborane anion
Chem.Commun., 2015, 51, 5359
7116762 CIFC13 H19 N O3 SP 21 21 2111.3743; 14.0235; 18.6496
90; 90; 90		2974.75Pablo Barrio; Elsa Rodriguez; Kodai Saito; Santos Fustero; Takahiko Akiyama
Gamma-Silylboronates in the chiral Bronsted acid-catalysed allylboration of aldehydes
Chem.Commun., 2015, 51, 5246
7116763 CIFC37 H51 F3 Mn N7 O4 SP -113.1912; 13.5415; 23.494
93.278; 103.037; 104.963		3920.1Yun Ji Park; Ellen M. Matson; Mark J. Nilges; Alison R. Fout
Exploring Mn-O bonding in the context of an electronically flexible secondary coordination sphere: synthesis of a Mn(III)-oxo
Chem.Commun., 2015, 51, 5310
7116764 CIFC48 H74 K Mn N7 O4P 1 21/c 123.141; 9.7932; 22.661
90; 105.914; 90		4938.7Yun Ji Park; Ellen M. Matson; Mark J. Nilges; Alison R. Fout
Exploring Mn-O bonding in the context of an electronically flexible secondary coordination sphere: synthesis of a Mn(III)-oxo
Chem.Commun., 2015, 51, 5310
7116765 CIFC40 H59 Mn N7 O2P 1 21/c 19.7762; 9.2337; 42.2828
90; 90.193; 90		3816.9Yun Ji Park; Ellen M. Matson; Mark J. Nilges; Alison R. Fout
Exploring Mn-O bonding in the context of an electronically flexible secondary coordination sphere: synthesis of a Mn(III)-oxo
Chem.Commun., 2015, 51, 5310
7116766 CIFC42 H59 F6 Mn N7 O7 S2P 21 21 2110.6932; 16.2784; 27.67
90; 90; 90		4816.5Yun Ji Park; Ellen M. Matson; Mark J. Nilges; Alison R. Fout
Exploring Mn-O bonding in the context of an electronically flexible secondary coordination sphere: synthesis of a Mn(III)-oxo
Chem.Commun., 2015, 51, 5310
7116767 CIFC8 H26 Fe3 N6 Se4C 2 2 219.1399; 18.122; 11.5436
90; 90; 90		1912Joshua T. Greenfield; Chongin Pak; Saeed Kamali; Kathleen Lee; Kirill Kovnir
Control over connectivity and magnetism of tetrahedral FeSe2 chains through coordination Fe-amine complexes
Chem.Commun., 2015, 51, 5355
7116768 CIFC6 H18 Fe3 N4 Se4P 1 21/c 19.0393; 10.6303; 16.641
90; 102.652; 90		1560.2Joshua T. Greenfield; Chongin Pak; Saeed Kamali; Kathleen Lee; Kirill Kovnir
Control over connectivity and magnetism of tetrahedral FeSe2 chains through coordination Fe-amine complexes
Chem.Commun., 2015, 51, 5355
7116769 CIFC21 H21 I N O3P -111.5839; 15.7615; 32.762
91.604; 91.02; 101.055		5866.7K. Ackermann; A. Giannoulis; D. B. Cordes; A. M. Z. Slawin; B. E. Bode
Assessing dimerisation degree and cooperativity in a biomimetic small-molecule model by pulsed EPR
Chem.Commun., 2015, 51, 5257
7116770 CIFC44.5 H36 Cl N4 O3P 42/n :236.726; 36.726; 5.6924
90; 90; 90		7678K. Ackermann; A. Giannoulis; D. B. Cordes; A. M. Z. Slawin; B. E. Bode
Assessing dimerisation degree and cooperativity in a biomimetic small-molecule model by pulsed EPR
Chem.Commun., 2015, 51, 5257
7116771 CIFC14 H30 N2 O23 U2P -16.2109; 9.997; 11.3778
97.9088; 93.7875; 104.294		674.38M. Basile; D. K. Unruh; K. Gojdas; E. Flores; L. Streicher; T. Z. Forbes
Chemical controls on uranyl citrate speciation and the self-assembly of nanoscale macrocycles and sandwich complexes in aqueous solutions
Chem.Commun., 2015, 51, 5306
7116772 CIFC16 H34 N2 O24 U2P -16.3074; 10.0063; 11.992
94.6846; 98.8324; 104.503		718.32M. Basile; D. K. Unruh; K. Gojdas; E. Flores; L. Streicher; T. Z. Forbes
Chemical controls on uranyl citrate speciation and the self-assembly of nanoscale macrocycles and sandwich complexes in aqueous solutions
Chem.Commun., 2015, 51, 5306
7116773 CIFC22 H30 N2 O22 U2P -16.7978; 9.8815; 11.7825
100.662; 99.5051; 91.0417		766.15M. Basile; D. K. Unruh; K. Gojdas; E. Flores; L. Streicher; T. Z. Forbes
Chemical controls on uranyl citrate speciation and the self-assembly of nanoscale macrocycles and sandwich complexes in aqueous solutions
Chem.Commun., 2015, 51, 5306
7116774 CIFC60 H96 N12 Na4 O94 U6P -119.987; 20.5879; 21.1208
68.467; 64.419; 67.96		7044.4M. Basile; D. K. Unruh; K. Gojdas; E. Flores; L. Streicher; T. Z. Forbes
Chemical controls on uranyl citrate speciation and the self-assembly of nanoscale macrocycles and sandwich complexes in aqueous solutions
Chem.Commun., 2015, 51, 5306
7116775 CIFC36 H27 Mg3 Na5 O81 U9P 63/m17.4123; 17.4123; 17.8443
90; 90; 120		4685.4M. Basile; D. K. Unruh; K. Gojdas; E. Flores; L. Streicher; T. Z. Forbes
Chemical controls on uranyl citrate speciation and the self-assembly of nanoscale macrocycles and sandwich complexes in aqueous solutions
Chem.Commun., 2015, 51, 5306
7116776 CIFC66 H55 N2 Np O7 P5P 1 21/n 113.61157; 16.5891; 26.4952
90; 91.6657; 90		5980.19Sean D. Woodall; Adam N. Swinburne; Nidhu lal Banik; Andrew Kerridge; Poppy Di Pietro; Christian Adam; Peter Kaden; Louise S. Natrajan
Neptunyl(VI) centred visible LMCT emission directly observable in the presence of uranyl(VI)
Chem.Commun., 2015, 51, 5402
7116777 CIFC67 H57 Cl2 N2 O7 P5 UP 1 21/n 19.7808; 23.697; 26.1815
90; 95.334; 90		6042Sean D. Woodall; Adam N. Swinburne; Nidhu lal Banik; Andrew Kerridge; Poppy Di Pietro; Christian Adam; Peter Kaden; Louise S. Natrajan
Neptunyl(VI) centred visible LMCT emission directly observable in the presence of uranyl(VI)
Chem.Commun., 2015, 51, 5402
7116778 CIFC23 H47 B Fe O2 P2P n m a13.8799; 16.5053; 11.7284
90; 90; 90		2686.9Thomas J. Mazzacano; Neal P. Mankad
Thermal C-H borylation using a CO-free iron boryl complex
Chem.Commun., 2015, 51, 5379
7116779 CIFC17 H35 B Fe O8 P2P 1 21/c 110.5518; 14.372; 16.31
90; 108.637; 90		2343.7Thomas J. Mazzacano; Neal P. Mankad
Thermal C-H borylation using a CO-free iron boryl complex
Chem.Commun., 2015, 51, 5379
7116780 CIFC23 H24 B F18 Fe O8 P3P 1 21/n 110.7235; 18.0733; 18.7761
90; 100.2; 90		3581.5Thomas J. Mazzacano; Neal P. Mankad
Thermal C-H borylation using a CO-free iron boryl complex
Chem.Commun., 2015, 51, 5379
7116781 CIFC24 H36 N5 O Re S4P -111.5743; 11.7501; 12.5007
86.489; 86.743; 60.987		1483.23Yan, Yong; Mague, Joel T.; Donahue, James P.; Sproules, Stephen
Unprecedented Spin Localisation in a Paramagnetic Dirhenium Complex with Multiple Metal Bonds
Chem.Commun., 2015, 51, 5482
7116782 CIFC17 H20 O4P 1 21/n 18.3539; 11.145; 16.1987
90; 101.731; 90		1476.67M. Presset; B. Michelet; R. Guillot; C. Bour; S. Bezzenine-Lafollee; V. Gandon
Gallium(III)- and calcium(II)-catalyzed Meyer-Schuster rearrangements followed by intramolecular aldol condensation or endo-Michael addition
Chem.Commun., 2015, 51, 5318
7116783 CIFC26 H29 F12 N7 O2 P2 PdP 1 21/c 117.4973; 9.579; 20.1652
90; 98.859; 90		3339.5Michael R. Chapman; Christopher M. Pask; Alireza Ariafard; Charlotte E. Willans
sigma-Alkenyl endo-palladacycle formation via regiospecific functionalisation of an unreactive NHC-tethered C(sp2)-H bond
Chem.Commun., 2015, 51, 5513
7116784 CIFC14 H15 F6 N4 O P PdP 1 21/m 112.097; 6.8619; 21.461
90; 91.882; 90		1780.5Michael R. Chapman; Christopher M. Pask; Alireza Ariafard; Charlotte E. Willans
sigma-Alkenyl endo-palladacycle formation via regiospecific functionalisation of an unreactive NHC-tethered C(sp2)-H bond
Chem.Commun., 2015, 51, 5513
7116785 CIFC14 H15 F6 N4 O Pd SbP 1 21 113.0668; 6.8152; 21.0073
90; 90.568; 90		1870.7Michael R. Chapman; Christopher M. Pask; Alireza Ariafard; Charlotte E. Willans
sigma-Alkenyl endo-palladacycle formation via regiospecific functionalisation of an unreactive NHC-tethered C(sp2)-H bond
Chem.Commun., 2015, 51, 5513
7116786 CIFC13 H13 N OP 21 21 215.018; 11.717; 18.072
90; 90; 90		1062.6Robert M. Edkins; Elliott Hayden; Jonathan W. Steed; Katharina Fucke
Conserved hydrogen bonding in tetrahydrocarbazolone derivatives: influence of solution-state assembly on crystal form nucleation
Chem.Commun., 2015, 51, 5314
7116787 CIFC13 H13 N OP 1 21/c 19.4905; 4.937; 21.8359
90; 95.103; 90		1019.06Robert M. Edkins; Elliott Hayden; Jonathan W. Steed; Katharina Fucke
Conserved hydrogen bonding in tetrahydrocarbazolone derivatives: influence of solution-state assembly on crystal form nucleation
Chem.Commun., 2015, 51, 5314
7116788 CIFC13 H13 N OP 1 21/n 110.5236; 7.17; 13.5856
90; 93.912; 90		1022.7Robert M. Edkins; Elliott Hayden; Jonathan W. Steed; Katharina Fucke
Conserved hydrogen bonding in tetrahydrocarbazolone derivatives: influence of solution-state assembly on crystal form nucleation
Chem.Commun., 2015, 51, 5314
7116789 CIFC13 H13 N OP 1 21/c 14.918; 17.5881; 11.975
90; 97.432; 90		1027.12Robert M. Edkins; Elliott Hayden; Jonathan W. Steed; Katharina Fucke
Conserved hydrogen bonding in tetrahydrocarbazolone derivatives: influence of solution-state assembly on crystal form nucleation
Chem.Commun., 2015, 51, 5314
7116790 CIFC13 H13 N OP 1 21/n 19.3763; 6.5586; 16.7932
90; 102.558; 90		1008Robert M. Edkins; Elliott Hayden; Jonathan W. Steed; Katharina Fucke
Conserved hydrogen bonding in tetrahydrocarbazolone derivatives: influence of solution-state assembly on crystal form nucleation
Chem.Commun., 2015, 51, 5314
7116791 CIFC13 H13 N OP 1 21/n 112.7256; 5.4479; 14.793
90; 103.039; 90		999.12Robert M. Edkins; Elliott Hayden; Jonathan W. Steed; Katharina Fucke
Conserved hydrogen bonding in tetrahydrocarbazolone derivatives: influence of solution-state assembly on crystal form nucleation
Chem.Commun., 2015, 51, 5314
7116792 CIFC13 H13 N OP b c a14.6822; 6.6231; 20.97
90; 90; 90		2039.2Robert M. Edkins; Elliott Hayden; Jonathan W. Steed; Katharina Fucke
Conserved hydrogen bonding in tetrahydrocarbazolone derivatives: influence of solution-state assembly on crystal form nucleation
Chem.Commun., 2015, 51, 5314
7116793 CIFC50 H61 Cu N4 O2P 1 21/c 119.5203; 11.1949; 20.5166
90; 99.303; 90		4424.5Vincent Cesar; Valentina Mallardo; Adela Nano; Georges Dahm; Noel Lugan; Guy Lavigne; Stephane Bellemin-Laponnaz
IMes-acac: hybrid combination of diaminocarbene and acetylacetonato sub-units into a new anionic ambidentate NHC ligand
Chem.Commun., 2015, 51, 5271
7116794 CIFC50 H62 B Cu F4 N4 O2P -110.373; 18.414; 26.739
96.931; 91.874; 102.56		4940Vincent Cesar; Valentina Mallardo; Adela Nano; Georges Dahm; Noel Lugan; Guy Lavigne; Stephane Bellemin-Laponnaz
IMes-acac: hybrid combination of diaminocarbene and acetylacetonato sub-units into a new anionic ambidentate NHC ligand
Chem.Commun., 2015, 51, 5271
7116795 CIFC13 H31 Cl Cu N4 O6P n a 2117.0837; 12.5402; 9.2795
90; 90; 90		1988Athina Anastasaki; Vasiliki Nikolaou; Francesca Brandford-Adams; Gabit Nurumbetov; Qiang Zhang; Guy J. Clarkson; David J. Fox; Paul Wilson; Kristian Kempe; David M. Haddleton
Photo-induced living radical polymerization of acrylates utilizing a discrete copper(II)-formate complex
Chem.Commun., 2015, 51, 5626
7116796 CIFC18 H14 Cu2 N0 O10I m m a18.8261; 22.1934; 10.0062
90; 90; 90		4180.7Hui-Min Wen; Bin Li; Hailong Wang; Chuande Wu; Khalid Alfooty; Rajamani Krishna; Banglin Chen
A microporous metal-organic framework with rare lvt topology for highly selective C2H2/C2H4 separation at room temperature
Chem.Commun., 2015, 51, 5610
7116797 CIFC35 H41 Cu5 N40 O0F d d d16.18; 43.077; 45.485
90; 90; 90		31702B. X. Dong; S. Y. Zhang; W. L. Liu; Y. C. Wu; J. Ge; L. Song; Y. L. Teng
Gas storage and separation in a water-stable [Cu^I^5BTT3]^4-^ anion framework comprising a giant multi-prismatic nanoscale cage
Chem.Commun., 2015, 51, 5691
7116798 CIFC36 H51 N O2 ZrP 1 21 110.82; 11.235; 15.074
90; 110.637; 90		1714.9Xiaoguang Zhou; Bing Wei; Xiu-Li Sun; Yong Tang; Zuowei Xie
Asymmetric hydroamination catalyzed by a new chiral zirconium system: reaction scope and mechanism
Chem.Commun., 2015, 51, 5751
7116799 CIFC42 H57 N O2 ZrP 3225.473; 25.473; 15.017
90; 90; 120		8439Xiaoguang Zhou; Bing Wei; Xiu-Li Sun; Yong Tang; Zuowei Xie
Asymmetric hydroamination catalyzed by a new chiral zirconium system: reaction scope and mechanism
Chem.Commun., 2015, 51, 5751
7116800 CIFC50 H57 N O2 Si ZrP 21 21 2110.4723; 20.7272; 21.2971
90; 90; 90		4622.8Xiaoguang Zhou; Bing Wei; Xiu-Li Sun; Yong Tang; Zuowei Xie
Asymmetric hydroamination catalyzed by a new chiral zirconium system: reaction scope and mechanism
Chem.Commun., 2015, 51, 5751
7116801 CIFC51 H57 N O2 ZrP 21 21 219.9279; 20.7319; 20.8378
90; 90; 90		4288.9Xiaoguang Zhou; Bing Wei; Xiu-Li Sun; Yong Tang; Zuowei Xie
Asymmetric hydroamination catalyzed by a new chiral zirconium system: reaction scope and mechanism
Chem.Commun., 2015, 51, 5751
7116802 CIFC53 H61 N O2 ZrP 1 21 110.0708; 16.4364; 29.62
90; 91.34; 90		4901.6Xiaoguang Zhou; Bing Wei; Xiu-Li Sun; Yong Tang; Zuowei Xie
Asymmetric hydroamination catalyzed by a new chiral zirconium system: reaction scope and mechanism
Chem.Commun., 2015, 51, 5751
7116803 CIFC56 H59 N O2 ZrP 1 21 112.3987; 10.2035; 35.906
90; 91.315; 90		4541.3Xiaoguang Zhou; Bing Wei; Xiu-Li Sun; Yong Tang; Zuowei Xie
Asymmetric hydroamination catalyzed by a new chiral zirconium system: reaction scope and mechanism
Chem.Commun., 2015, 51, 5751
7116804 CIFC50 H55 N O2 ZrP 1 21 19.9153; 39.191; 10.9485
90; 93.596; 90		4246.1Xiaoguang Zhou; Bing Wei; Xiu-Li Sun; Yong Tang; Zuowei Xie
Asymmetric hydroamination catalyzed by a new chiral zirconium system: reaction scope and mechanism
Chem.Commun., 2015, 51, 5751
7116805 CIFC49 H51 N O2 ZrP 1 21 110.249; 10.086; 20.139
90; 102.78; 90		2030.2Xiaoguang Zhou; Bing Wei; Xiu-Li Sun; Yong Tang; Zuowei Xie
Asymmetric hydroamination catalyzed by a new chiral zirconium system: reaction scope and mechanism
Chem.Commun., 2015, 51, 5751
7116806 CIFC51 H55 N O2 ZrP 21 21 2110.4071; 20.0669; 20.1804
90; 90; 90		4214.4Xiaoguang Zhou; Bing Wei; Xiu-Li Sun; Yong Tang; Zuowei Xie
Asymmetric hydroamination catalyzed by a new chiral zirconium system: reaction scope and mechanism
Chem.Commun., 2015, 51, 5751
7116807 CIFC53 H59 N O2 ZrP 21 21 2110.5049; 20.1449; 20.7934
90; 90; 90		4400.3Xiaoguang Zhou; Bing Wei; Xiu-Li Sun; Yong Tang; Zuowei Xie
Asymmetric hydroamination catalyzed by a new chiral zirconium system: reaction scope and mechanism
Chem.Commun., 2015, 51, 5751
7116808 CIFC61 H59 N O2 ZrP 21 21 219.9859; 10.2631; 46.379
90; 90; 90		4753.2Xiaoguang Zhou; Bing Wei; Xiu-Li Sun; Yong Tang; Zuowei Xie
Asymmetric hydroamination catalyzed by a new chiral zirconium system: reaction scope and mechanism
Chem.Commun., 2015, 51, 5751
7116809 CIFC44 H43 N O2 ZrC 1 2/c 129.258; 24.694; 23.148
90; 117.297; 90		14862Xiaoguang Zhou; Bing Wei; Xiu-Li Sun; Yong Tang; Zuowei Xie
Asymmetric hydroamination catalyzed by a new chiral zirconium system: reaction scope and mechanism
Chem.Commun., 2015, 51, 5751
7116810 CIFC72 H87 N5 O4 Zr2P -112.0652; 13.096; 23.377
100.831; 93.008; 111.473		3346.2Xiaoguang Zhou; Bing Wei; Xiu-Li Sun; Yong Tang; Zuowei Xie
Asymmetric hydroamination catalyzed by a new chiral zirconium system: reaction scope and mechanism
Chem.Commun., 2015, 51, 5751
7116811 CIFC42 H34 O12 Zn3P 32 2 118.1019; 18.1019; 24.668
90; 90; 120		7000.2Hongmin Su; Fuxing Sun; Jiangtao Jia; Hongming He; Aifei Wang; Guangshan Zhu
A highly porous medical metal-organic framework constructed from bioactive curcumin
Chem.Commun., 2015, 51, 5774
7116812 CIFC13 H14 N2 O7P 21 21 215.0946; 14.4569; 18.2887
90; 90; 90		1347E.-K. Kim; R. Krishnamurthy
Synthesis of orotidine by intramolecular nucleosidation
Chem.Commun., 2015, 51, 5618
7116813 CIFC16 H29 N O7P 21 21 216.1806; 14.641; 20.36
90; 90; 90		1842.4Nikoletta B. Bathori; Luigi R. Nassimbeni; Jacco van de Streek
One hydrogen bond does not a separation make, or does it? Resolution of amines by diacetoneketogulonic acid
Chem.Commun., 2015, 51, 5664
7116814 CIFC17 H31 N O7P 21 21 216.3376; 15.4586; 20.0153
90; 90; 90		1960.9Nikoletta B. Bathori; Luigi R. Nassimbeni; Jacco van de Streek
One hydrogen bond does not a separation make, or does it? Resolution of amines by diacetoneketogulonic acid
Chem.Commun., 2015, 51, 5664
7116815 CIFC24 H31 N O7P 21 21 217.6206; 11.4755; 26.5274
90; 90; 90		2319.8Nikoletta B. Bathori; Luigi R. Nassimbeni; Jacco van de Streek
One hydrogen bond does not a separation make, or does it? Resolution of amines by diacetoneketogulonic acid
Chem.Commun., 2015, 51, 5664

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