Crystallography Open Database

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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
7116816 CIFC20 H29 N O7P 1 21 114.4045; 6.2322; 23.4872
90; 103.762; 90		2048Nikoletta 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
7116817 CIFC24 H31 N O7P 1 21 113.74; 6.188; 15.056
90; 113.998; 90		1169.5Nikoletta 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
7116818 CIFC20 H29 N O7P 1 21 114.634; 6.2305; 11.855
90; 102.86; 90		1053.8Nikoletta 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
7116819 CIFC32 H24 B2 N2P 1 21/n 19.938; 15.052; 16.599
90; 94.82; 90		2474.2Cong Ma; Jianying Zhang; Jianfeng Li; Chunming Cui
Multiple C-H borylation of phenylhydrazones to boron-nitrogen analogues of benzopentalene
Chem.Commun., 2015, 51, 5732
7116820 CIFC24 H18 B2 N2 SP -19.492; 10.356; 10.494
76.69; 80.05; 77.48		971.7Cong Ma; Jianying Zhang; Jianfeng Li; Chunming Cui
Multiple C-H borylation of phenylhydrazones to boron-nitrogen analogues of benzopentalene
Chem.Commun., 2015, 51, 5732
7116821 CIFC28 H25 B N2P n a 2111.268; 23.152; 8.5403
90; 90; 90		2228Cong Ma; Jianying Zhang; Jianfeng Li; Chunming Cui
Multiple C-H borylation of phenylhydrazones to boron-nitrogen analogues of benzopentalene
Chem.Commun., 2015, 51, 5732
7116822 CIFC20 H17 B N2P -110.344; 17.825; 18.052
94.99; 98.18; 90.06		3281.8Cong Ma; Jianying Zhang; Jianfeng Li; Chunming Cui
Multiple C-H borylation of phenylhydrazones to boron-nitrogen analogues of benzopentalene
Chem.Commun., 2015, 51, 5732
7116823 CIFC30 H38 N2 O5 S2P 1 21 113.0848; 13.5713; 16.2698
90; 94.205; 90		2881.38Yi Li; Marcel Hartmann; Constantin Gabriel Daniliuc; Armido Studer
Radical aminooxygenation of alkenes with N-fluoro-benzenesulfonimide (NFSI) and TEMPONa
Chem.Commun., 2015, 51, 5706
7116824 CIFC35 H47 I N2 ZnP n a m13.0009; 24.7338; 10.817
90; 90; 90		3478.33Matthew P. Blake; Nikolas Kaltsoyannis; Philip Mountford
Synthesis, molecular and electronic structure, and reactions of a Zn-Hg-Zn bonded complex
Chem.Commun., 2015, 51, 5743
7116825 CIFC36 H46 Fe N2 O2 ZnP b c a20.9493; 14.21072; 22.37442
90; 90; 90		6660.97Matthew P. Blake; Nikolas Kaltsoyannis; Philip Mountford
Synthesis, molecular and electronic structure, and reactions of a Zn-Hg-Zn bonded complex
Chem.Commun., 2015, 51, 5743
7116826 CIFC58 H82 Hg N4 Zn2P 1 21/n 112.784; 17.3101; 13.0055
90; 101.117; 90		2824.01Matthew P. Blake; Nikolas Kaltsoyannis; Philip Mountford
Synthesis, molecular and electronic structure, and reactions of a Zn-Hg-Zn bonded complex
Chem.Commun., 2015, 51, 5743
7116827 CIFC39 H45 Br6 N3 O3C 1 2/c 134.3269; 16.0953; 17.3532
90; 115.959; 90		8620.3Ryohei Yamakado; Shin-ichi Matsuoka; Masato Suzuki; Daisuke Takeuchi; Hyuma Masu; Isao Azumaya; Koji Takagi
Diastereoselective cyclization of an aminobenzoic acid derivative and chiroptical properties of triple-stranded helical bis(phenylethynyl)benzene
Chem.Commun., 2015, 51, 5710
7116830 CIFC18 H13 N3 OP 1 21/c 18.3217; 9.5453; 17.1799
90; 100.577; 90		1341.47Sreekumar Pankajakshan; Zhi Guang Chng; Rakesh Ganguly; Teck Peng Loh
Copper-catalyzed aerobic carboxygenation and N-arylation of [1,2,3]triazolo[1,5-a]pyridines towards pyridinium triazolinone ylides
Chem.Commun., 2015, 51, 5929
7116831 CIFC12 H9 N3 OC 1 2/c 111.477; 8.789; 19.955
90; 103.778; 90		1955Sreekumar Pankajakshan; Zhi Guang Chng; Rakesh Ganguly; Teck Peng Loh
Copper-catalyzed aerobic carboxygenation and N-arylation of [1,2,3]triazolo[1,5-a]pyridines towards pyridinium triazolinone ylides
Chem.Commun., 2015, 51, 5929
7116832 CIFC26 H23 NP 1 21/n 115.205; 7.3621; 18.007
90; 96.56; 90		2002.5Jia Zheng; Liangbin Huang; Zun Li; Wanqing Wu; Jianxiao Li; Huanfeng Jiang
Synthesis of 3-bromosubstituted pyrroles via palladium-catalyzed intermolecular oxidative cyclization of bromoalkynes with N-allylamines
Chem.Commun., 2015, 51, 5894
7116833 CIFC30 H22 O2P -111.7482; 13.7728; 15.9289
102.716; 104.883; 113.218		2134.1Shohei Eda; Fumiaki Eguchi; Hiroshi Haneda; Toshiyuki Hamura
A new synthetic route to substituted tetracenes and pentacenes via stereoselective [4+2] cycloadditions of 1,4-dihydro-1,4-epoxynaphthalene and isobenzofuran
Chem.Commun., 2015, 51, 5963
7116834 CIFC30 H22 O2P -110.448; 12.7886; 16.6149
84.832; 71.771; 84.18		2093.72Shohei Eda; Fumiaki Eguchi; Hiroshi Haneda; Toshiyuki Hamura
A new synthetic route to substituted tetracenes and pentacenes via stereoselective [4+2] cycloadditions of 1,4-dihydro-1,4-epoxynaphthalene and isobenzofuran
Chem.Commun., 2015, 51, 5963
7116835 CIFC42 H30 O2P 1 21/c 110.5584; 9.542; 29.2511
90; 91.525; 90		2945.95Shohei Eda; Fumiaki Eguchi; Hiroshi Haneda; Toshiyuki Hamura
A new synthetic route to substituted tetracenes and pentacenes via stereoselective [4+2] cycloadditions of 1,4-dihydro-1,4-epoxynaphthalene and isobenzofuran
Chem.Commun., 2015, 51, 5963
7116836 CIFC43 H38 Cl2 Li N8 O2 ScP -112.0145; 13.1895; 14.9239
64.581; 70.692; 88.526		1997Rachel H. Platel; Thiago Teixeira Tasso; Wen Zhou; Taniyuki Furuyama; Nagao Kobayashi; Daniel B. Leznoff
Metallophthalocyanin-ocenes: scandium phthalocyanines with an eta^5^-bound Cp ring
Chem.Commun., 2015, 51, 5986
7116837 CIFC37 H21 N8 ScP -18.976; 15.873; 19.618
83.59; 86.358; 83.85		2758Rachel H. Platel; Thiago Teixeira Tasso; Wen Zhou; Taniyuki Furuyama; Nagao Kobayashi; Daniel B. Leznoff
Metallophthalocyanin-ocenes: scandium phthalocyanines with an eta^5^-bound Cp ring
Chem.Commun., 2015, 51, 5986
7116838 CIFC45 H37 N8 O0.75 ScP b c m16.1402; 21.4116; 21.6902
90; 90; 90		7495.9Rachel H. Platel; Thiago Teixeira Tasso; Wen Zhou; Taniyuki Furuyama; Nagao Kobayashi; Daniel B. Leznoff
Metallophthalocyanin-ocenes: scandium phthalocyanines with an eta^5^-bound Cp ring
Chem.Commun., 2015, 51, 5986
7116839 CIFC32 H26 N4 Ni S2P b c a18.0049; 9.0457; 32.7494
90; 90; 90		5333.8Stephane A. Baudron; Herve Ruffin; Mir Wais Hosseini
On Zn(II) 2,2'-bisdipyrrin circular helicates
Chem.Commun., 2015, 51, 5906
7116840 CIFC32 H26 N4 Ni S2P -19.7891; 11.7331; 12.5712
104.486; 99.689; 102.531		1326.3Stephane A. Baudron; Herve Ruffin; Mir Wais Hosseini
On Zn(II) 2,2'-bisdipyrrin circular helicates
Chem.Commun., 2015, 51, 5906
7116841 CIFC32 H24 N4 Ni S2P -19.9075; 12.3331; 12.436
64.149; 69.893; 79.482		1283.19Stephane A. Baudron; Herve Ruffin; Mir Wais Hosseini
On Zn(II) 2,2'-bisdipyrrin circular helicates
Chem.Commun., 2015, 51, 5906
7116842 CIFC33 H27 Cl3 N4 S2P -18.9232; 12.3869; 14.6782
75.749; 75.097; 86.521		1519.57Stephane A. Baudron; Herve Ruffin; Mir Wais Hosseini
On Zn(II) 2,2'-bisdipyrrin circular helicates
Chem.Commun., 2015, 51, 5906
7116843 CIFC64 H48 N8 S4 Zn2P 1 21/n 115.1355; 14.9332; 24.9048
90; 106.399; 90		5400Stephane A. Baudron; Herve Ruffin; Mir Wais Hosseini
On Zn(II) 2,2'-bisdipyrrin circular helicates
Chem.Commun., 2015, 51, 5906
7116844 CIFC205 H172 N24 O4 S12 Zn6P -113.3649; 18.2896; 18.8109
96.448; 99.538; 94.693		4482.1Stephane A. Baudron; Herve Ruffin; Mir Wais Hosseini
On Zn(II) 2,2'-bisdipyrrin circular helicates
Chem.Commun., 2015, 51, 5906
7116845 CIFC34 H26 N4 Ni O4P -19.2124; 11.1476; 14.7168
86.166; 76.5; 70.682		1386.77Stephane A. Baudron; Herve Ruffin; Mir Wais Hosseini
On Zn(II) 2,2'-bisdipyrrin circular helicates
Chem.Commun., 2015, 51, 5906
7116846 CIFC34 H24 N4 Ni O4C 1 2/c 134.4732; 9.868; 7.9143
90; 100.724; 90		2645.28Stephane A. Baudron; Herve Ruffin; Mir Wais Hosseini
On Zn(II) 2,2'-bisdipyrrin circular helicates
Chem.Commun., 2015, 51, 5906
7116847 CIFC34 H26 N4 O4P 1 2/c 120.8248; 7.2192; 19.4469
90; 105.825; 90		2812.81Stephane A. Baudron; Herve Ruffin; Mir Wais Hosseini
On Zn(II) 2,2'-bisdipyrrin circular helicates
Chem.Commun., 2015, 51, 5906
7116848 CIFC68 H48 N8 O8 Zn2C 1 2/c 123.8065; 16.6644; 42.744
90; 100.563; 90		16670.1Stephane A. Baudron; Herve Ruffin; Mir Wais Hosseini
On Zn(II) 2,2'-bisdipyrrin circular helicates
Chem.Commun., 2015, 51, 5906
7116849 CIFC105 H75 Cl9 N12 O12 Zn3C 1 2/c 118.1355; 21.5289; 25.5659
90; 100.008; 90		9830Stephane A. Baudron; Herve Ruffin; Mir Wais Hosseini
On Zn(II) 2,2'-bisdipyrrin circular helicates
Chem.Commun., 2015, 51, 5906
7116850 CIFC136 H96 N16 O16 Zn4I 2 2 215.3648; 19.7305; 23.6393
90; 90; 90		7166.4Stephane A. Baudron; Herve Ruffin; Mir Wais Hosseini
On Zn(II) 2,2'-bisdipyrrin circular helicates
Chem.Commun., 2015, 51, 5906
7116851 CIFC136 H96 N16 O16 Zn4I 2 2 215.337; 19.7279; 23.6518
90; 90; 90		7156.2Stephane A. Baudron; Herve Ruffin; Mir Wais Hosseini
On Zn(II) 2,2'-bisdipyrrin circular helicates
Chem.Commun., 2015, 51, 5906
7116852 CIFC36 H15 As B F15 OP 1 21/n 113.134; 16.309; 14.601
90; 96.167; 90		3109.5Ralf Kather; Tomas Svoboda; Maren Wehrhahn; Elena Rychagova; Enno Lork; Libor Dostal; Sergey Ketkov; Jens Beckmann
Lewis-acid induced disaggregation of dimeric arylantimony oxides
Chem.Commun., 2015, 51, 5932
7116853 CIFC36 H15 B F15 O SbP 1 21/n 112.248; 17.312; 15.058
90; 95.34; 90		3179Ralf Kather; Tomas Svoboda; Maren Wehrhahn; Elena Rychagova; Enno Lork; Libor Dostal; Sergey Ketkov; Jens Beckmann
Lewis-acid induced disaggregation of dimeric arylantimony oxides
Chem.Commun., 2015, 51, 5932
7116854 CIFC30 H19 B F15 N2 O SbP -19.814; 10.784; 16.68
84.08; 87.26; 77.49		1713.6Ralf Kather; Tomas Svoboda; Maren Wehrhahn; Elena Rychagova; Enno Lork; Libor Dostal; Sergey Ketkov; Jens Beckmann
Lewis-acid induced disaggregation of dimeric arylantimony oxides
Chem.Commun., 2015, 51, 5932
7116855 CIFC25 H24 N2 O2 S3P 1 21/n 111.461; 12.938; 15.619
90; 93.48; 90		2311.8Chuan Liu; Qin Yin; Li-Xin Dai; Shu-Li You
Synthesis of pyrroloindolines and furoindolines via cascade dearomatization of indole derivatives with carbenium ion
Chem.Commun., 2015, 51, 5971
7116856 CIFC93 H97 Al N10 O2 UP 1 21/c 121.6483; 15.4318; 24.4807
90; 98.594; 90		8086.5Markus Zegke; Gary S. Nichol; Polly L. Arnold; Jason B. Love
Catalytic one-electron reduction of uranyl(VI) to Group 1 uranyl(V) complexes via Al(III) coordination
Chem.Commun., 2015, 51, 5876
7116857 CIFC74 H88 Al N9 O3 UP 1 21/n 112.5004; 40.0423; 14.2199
90; 105.173; 90		6869.57Markus Zegke; Gary S. Nichol; Polly L. Arnold; Jason B. Love
Catalytic one-electron reduction of uranyl(VI) to Group 1 uranyl(V) complexes via Al(III) coordination
Chem.Commun., 2015, 51, 5876
7116858 CIFC124 H124 Li2 N18 O4 U2P -111.963; 14.243; 17.926
99.705; 90.311; 114.231		2736Markus Zegke; Gary S. Nichol; Polly L. Arnold; Jason B. Love
Catalytic one-electron reduction of uranyl(VI) to Group 1 uranyl(V) complexes via Al(III) coordination
Chem.Commun., 2015, 51, 5876
7116859 CIFC84.47 H84.47 Li0.87 N16.49 O2 UC 1 c 114.2782; 24.4176; 22.8717
90; 90.634; 90		7973.5Markus Zegke; Gary S. Nichol; Polly L. Arnold; Jason B. Love
Catalytic one-electron reduction of uranyl(VI) to Group 1 uranyl(V) complexes via Al(III) coordination
Chem.Commun., 2015, 51, 5876
7116860 CIFC62 H62 B0 N12 Na O2 UC 1 c 114.427; 24.602; 23.182
90; 90.881; 90		8227Markus Zegke; Gary S. Nichol; Polly L. Arnold; Jason B. Love
Catalytic one-electron reduction of uranyl(VI) to Group 1 uranyl(V) complexes via Al(III) coordination
Chem.Commun., 2015, 51, 5876
7116861 CIFC77 H76 K N15 O2 UP 21 21 2113.693; 21.7419; 24.2382
90; 90; 90		7216Markus Zegke; Gary S. Nichol; Polly L. Arnold; Jason B. Love
Catalytic one-electron reduction of uranyl(VI) to Group 1 uranyl(V) complexes via Al(III) coordination
Chem.Commun., 2015, 51, 5876
7116862 CIFC18 H11.33 Co O6.67P -3 1 c16.789; 16.789; 15.144
90; 90; 120		3696.8Min Chen; Hui Zhao; Chun-Sen Liu; Xi Wang; Heng-Zhen Shi; Miao Du
Template-directed construction of conformational supramolecular isomers for bilayer porous metal-organic frameworks with distinct gas sorption behaviors
Chem.Commun., 2015, 51, 6014
7116863 CIFC18 H11.33 Co O6.67R -3 c :H17.431; 17.431; 48.043
90; 90; 120		12641.7Min Chen; Hui Zhao; Chun-Sen Liu; Xi Wang; Heng-Zhen Shi; Miao Du
Template-directed construction of conformational supramolecular isomers for bilayer porous metal-organic frameworks with distinct gas sorption behaviors
Chem.Commun., 2015, 51, 6014
7116864 CIFC18 H11.33 Co O6.67P -3 1 c16.7639; 16.7639; 14.9592
90; 90; 120		3640.7Min Chen; Hui Zhao; Chun-Sen Liu; Xi Wang; Heng-Zhen Shi; Miao Du
Template-directed construction of conformational supramolecular isomers for bilayer porous metal-organic frameworks with distinct gas sorption behaviors
Chem.Commun., 2015, 51, 6014
7116865 CIFC18 H11.33 Co O6.67P -3 1 c16.7335; 16.7335; 14.9637
90; 90; 120		3628.6Min Chen; Hui Zhao; Chun-Sen Liu; Xi Wang; Heng-Zhen Shi; Miao Du
Template-directed construction of conformational supramolecular isomers for bilayer porous metal-organic frameworks with distinct gas sorption behaviors
Chem.Commun., 2015, 51, 6014
7116866 CIFC18 H11.33 Co O6.67R -3 c :H17.2813; 17.2813; 47.354
90; 90; 120		12247.3Min Chen; Hui Zhao; Chun-Sen Liu; Xi Wang; Heng-Zhen Shi; Miao Du
Template-directed construction of conformational supramolecular isomers for bilayer porous metal-organic frameworks with distinct gas sorption behaviors
Chem.Commun., 2015, 51, 6014
7116867 CIFC18 H11.33 Co O6.67R -3 c :H17.3321; 17.3321; 47.616
90; 90; 120		12387.6Min Chen; Hui Zhao; Chun-Sen Liu; Xi Wang; Heng-Zhen Shi; Miao Du
Template-directed construction of conformational supramolecular isomers for bilayer porous metal-organic frameworks with distinct gas sorption behaviors
Chem.Commun., 2015, 51, 6014
7116870 CIFC54 H52P 21 21 2113.2582; 14.2403; 42.561
90; 90; 90		8035.5K. W. J. Heard; J. J. Morrison; L. Weston; C. H. Lo; L. Pirvu; J. Raftery; M. S. Little; J. J. W. McDouall; S. G. Yeates; P. Quayle
An orthogonal C-H borylation - cross-coupling strategy for the preparation of tetrasubstituted 'A2B2'-chrysene derivatives with tuneable photophysical properties
Chem.Commun., 2015, 51, 6115
7116871 CIFC42 H42 Cl2P 1 21/c 115.5669; 11.5716; 18.0171
90; 96.615; 90		3223.9K. W. J. Heard; J. J. Morrison; L. Weston; C. H. Lo; L. Pirvu; J. Raftery; M. S. Little; J. J. W. McDouall; S. G. Yeates; P. Quayle
An orthogonal C-H borylation - cross-coupling strategy for the preparation of tetrasubstituted 'A2B2'-chrysene derivatives with tuneable photophysical properties
Chem.Commun., 2015, 51, 6115
7116872 CIFC20 H8 Cl2 F6P -18.5128; 11.4844; 13.1495
97.59; 96.803; 103.045		1226.68K. W. J. Heard; J. J. Morrison; L. Weston; C. H. Lo; L. Pirvu; J. Raftery; M. S. Little; J. J. W. McDouall; S. G. Yeates; P. Quayle
An orthogonal C-H borylation - cross-coupling strategy for the preparation of tetrasubstituted 'A2B2'-chrysene derivatives with tuneable photophysical properties
Chem.Commun., 2015, 51, 6115
7116873 CIFC34 H45 Fe N2P -110.1306; 11.1529; 13.6025
93.475; 92.686; 101.503		1500.52Shenglai Yao; Tibor Szilvasi; Nils Lindenmaier; Yun Xiong; Shigeyoshi Inoue; Mario Adelhardt; Jorg Sutter; Karsten Meyer; Matthias Driess
Reductive cleavage of P4 by iron(I) centres: synthesis and structural characterisation of Fe2(P2)2 complexes with two bridging P22- ligands
Chem.Commun., 2015, 51, 6153
7116874 CIFC54 H74 Fe2 N4 P4P 1 21/n 114.4521; 12.9461; 14.8567
90; 105.421; 90		2679.6Shenglai Yao; Tibor Szilvasi; Nils Lindenmaier; Yun Xiong; Shigeyoshi Inoue; Mario Adelhardt; Jorg Sutter; Karsten Meyer; Matthias Driess
Reductive cleavage of P4 by iron(I) centres: synthesis and structural characterisation of Fe2(P2)2 complexes with two bridging P22- ligands
Chem.Commun., 2015, 51, 6153
7116875 CIFC43 H69 Fe K0.5 N2 O4 P2P 1 21/c 113.2205; 18.4486; 18.4434
90; 90.303; 90		4498.28Shenglai Yao; Tibor Szilvasi; Nils Lindenmaier; Yun Xiong; Shigeyoshi Inoue; Mario Adelhardt; Jorg Sutter; Karsten Meyer; Matthias Driess
Reductive cleavage of P4 by iron(I) centres: synthesis and structural characterisation of Fe2(P2)2 complexes with two bridging P22- ligands
Chem.Commun., 2015, 51, 6153
7116876 CIFC19 H18 Cl O2P 43 21 211.6351; 11.6351; 48.952
90; 90; 90		6626.9Yang Yang; Jinpeng Li; Biao Du; Changchun Yuan; Bo Liu; Song Qin
An entry to vinylcyclopropane through palladium-catalyzed intramolecular cyclopropanation of alkenes with unstabilized allylic tosylhydrazones
Chem.Commun., 2015, 51, 6179
7116877 CIFC19 H17 Br N2 O3P 21 21 215.613; 16.048; 18.9931
90; 90; 90		1710.8Srimanta Manna; Rishikesh Narayan; Christopher Golz; Carsten Strohmann; Andrey P. Antonchick
Regioselective annulation of nitrosopyridine with alkynes: straightforward synthesis of N-oxide-imidazopyridines
Chem.Commun., 2015, 51, 6119
7116878 CIFC56 H72 S8 Si4C 1 2/c 143.196; 6.377; 24.5113
90; 115.408; 90		6099Kengo Asai; Aiko Fukazawa; Shigehiro Yamaguchi
A cyclic octithiophene containing beta,beta'-linkages
Chem.Commun., 2015, 51, 6096
7116879 CIFC46 H45 B F15 P3 PdP 1 21/n 19.7351; 29.7778; 16.3484
90; 104.943; 90		4579Peng Cui; Cezar C. Comanescu; Vlad M. Iluc
Frustrated Lewis pair-like reactions of nucleophilic palladium carbenes with B(C6F5)3
Chem.Commun., 2015, 51, 6206
7116880 CIFC33 H53 Cl P2 PdP 1 21/c 112.3466; 11.6819; 23.5089
90; 91.4208; 90		3389.7Peng Cui; Cezar C. Comanescu; Vlad M. Iluc
Frustrated Lewis pair-like reactions of nucleophilic palladium carbenes with B(C6F5)3
Chem.Commun., 2015, 51, 6206
7116881 CIFC36 H61 P3 PdC 1 2/c 128.976; 14.6255; 31.853
90; 106.946; 90		12913Peng Cui; Cezar C. Comanescu; Vlad M. Iluc
Frustrated Lewis pair-like reactions of nucleophilic palladium carbenes with B(C6F5)3
Chem.Commun., 2015, 51, 6206
7116882 CIFC54 H61 B F15 P3 PdP 1 21/c 114.7706; 13.9199; 28.5994
90; 93.208; 90		5871Peng Cui; Cezar C. Comanescu; Vlad M. Iluc
Frustrated Lewis pair-like reactions of nucleophilic palladium carbenes with B(C6F5)3
Chem.Commun., 2015, 51, 6206
7116883 CIFC60 H58 B F24 P3 PdP 1 21/n 113.1862; 12.7167; 37.1231
90; 94.967; 90		6201.6Peng Cui; Cezar C. Comanescu; Vlad M. Iluc
Frustrated Lewis pair-like reactions of nucleophilic palladium carbenes with B(C6F5)3
Chem.Commun., 2015, 51, 6206
7116884 CIFC68 H74 B F24 P3 PdP -113.7002; 17.7228; 18.52
65.531; 74.7; 88.259		3931.8Peng Cui; Cezar C. Comanescu; Vlad M. Iluc
Frustrated Lewis pair-like reactions of nucleophilic palladium carbenes with B(C6F5)3
Chem.Commun., 2015, 51, 6206
7116885 CIFC29 H46 O5 SiP -110.3975; 11.144; 13.6268
113.777; 91.585; 102.55		1398.6Hideki Abe; Yuri Horii; Megumi Hagiwara; Toyoharu Kobayashi; Hisanaka Ito
Stereoselective synthesis of a highly oxygenated decahydrocyclopenta[g]chromene derivative: the common tricyclic framework of leucosceptrine and leucosesterterpenone
Chem.Commun., 2015, 51, 6108
7116886 CIFC74 H127 Cl3 Mg3 O11P -114.3956; 15.2219; 18.5435
88.65; 74.452; 85.197		3900.96Baofei Pan; Junjie Zhang; Jinhua Huang; John T. Vaughey; Lu Zhang; Sang-Don Han; Anthony K. Burrell; Zhengcheng Zhang; Chen Liao
A Lewis acid-free and phenolate-based magnesium electrolyte for rechargeable magnesium batteries
Chem.Commun., 2015, 51, 6214
7116887 CIFC16 H12 Cl N O3P -110.3981; 10.4368; 15.4169
78.123; 81.589; 61.978		1442.9Wen-Zhen Zhang; Tian Xia; Xu-Tong Yang; Xiao-Bing Lu
Synthesis of oxazolidine-2,4-diones by a tandem phosphorus-mediated carboxylative condensation-cyclization reaction using atmospheric carbon dioxide
Chem.Commun., 2015, 51, 6175
7116888 CIFC28 H20 O2P -110.5146; 11.1198; 18.1537
73.905; 80.721; 89.893		2010.6Jing Wang; Dekun Qin; Jingbo Lan; Yangyang Cheng; Shuai Zhang; Qiang Guo; Jie Wu; Di Wu; Jingsong You
Rh-catalysed direct cyclisation of 1,4-naphthoquinone and 9,10-phenanthraquinone with alkyne: facile access to 1,8-dioxapyrenes and 1,12-dioxaperylenes as orange and red-emitting luminophores
Chem.Commun., 2015, 51, 6337
7116889 CIFC29 H31 N O3P 1 21/c 113.186; 14.909; 12.985
90; 110.29; 90		2394.3Kai Zhang; Hang Wang; Jingfeng Zheng; Lei Yu; Hanfeng Ding
Hypervalent iodine mediated alkene difunctionalization of vinylphenols: diastereoselective synthesis of substituted indoles and indolizines
Chem.Commun., 2015, 51, 6399
7116890 CIFC29 H23 Br N2 SP -19.2263; 11.3952; 12.1843
99.988; 101.997; 95.944		1221.01Ying Zhang; Jun-Hao Wang; Ji Zheng; Dan Li
A Br-substituted phenanthroimidazole derivative with aggregation induced emission from intermolecular halogen-hydrogen interactions
Chem.Commun., 2015, 51, 6350
7116891 CIFC29 H24 N2 SP 1 21/n 18.6586; 22.4244; 12.0588
90; 100.455; 90		2302.51Ying Zhang; Jun-Hao Wang; Ji Zheng; Dan Li
A Br-substituted phenanthroimidazole derivative with aggregation induced emission from intermolecular halogen-hydrogen interactions
Chem.Commun., 2015, 51, 6350
7116892 CIFC28 H28 Cl N O9P -111.5552; 11.6532; 11.9655
77.69; 68.849; 63.172		1338.48Marie Cordier; Aurelie Dos Santos; Laurent El Kaim; Noisette Narboni
Passerini/Tsuji-Trost strategies towards achieving lactams and cyclopentane derivatives
Chem.Commun., 2015, 51, 6411
7116893 CIFC19 H20 I N OP 1 21/c 110.6819; 9.4115; 17.492
90; 92.723; 90		1756.5Renhong Sun; Jun Liu; Shuang Yang; Ming Chen; Ning Sun; Haoyi Chen; Xin Xie; Xu You; Shi Li; Yuanhong Liu
Cp2TiCl2-catalyzed cis-hydroalumination of propargylic amines with Red-Al: stereoselective synthesis of Z-configured allylic amines
Chem.Commun., 2015, 51, 6426
7116894 CIFC16 H26 Al O4 TiP -19.6563; 9.8287; 10.6494
64.408; 74.407; 73.803		862.5Renhong Sun; Jun Liu; Shuang Yang; Ming Chen; Ning Sun; Haoyi Chen; Xin Xie; Xu You; Shi Li; Yuanhong Liu
Cp2TiCl2-catalyzed cis-hydroalumination of propargylic amines with Red-Al: stereoselective synthesis of Z-configured allylic amines
Chem.Commun., 2015, 51, 6426
7116895 CIFC18 H16 O3 S3P -14.5264; 13.238; 14.614
85.804; 82.143; 84.097		861.3Hai-Bin Yang; Yu-Chao Yuan; Yin Wei; Min Shi
Amine-catalyzed tunable reactions of allenoates with dithioesters: formal [4+2] and [2+2] cycloadditions for the synthesis of 2,3-dihydro-1,4-oxathiines and enantioenriched thietanes
Chem.Commun., 2015, 51, 6430
7116896 CIFC22 H27 N O4 SC 1 2/c 131.687; 6.2286; 23.0782
90; 106.427; 90		4368.9Hai-Bin Yang; Yu-Chao Yuan; Yin Wei; Min Shi
Amine-catalyzed tunable reactions of allenoates with dithioesters: formal [4+2] and [2+2] cycloadditions for the synthesis of 2,3-dihydro-1,4-oxathiines and enantioenriched thietanes
Chem.Commun., 2015, 51, 6430
7116897 CIFC212.07 H84 Cl4 O66.07 Ru11.36P -116.3234; 16.3914; 18.3063
64.293; 83.74; 83.301		4373.8Chia-Hsiang Chen; Amineh Aghabali; Catalina Suarez; Marilyn M. Olmstead; Alan L. Balch; Luis Echegoyen
Synthesis and characterization of bis-triruthenium cluster derivatives of an all equatorial [60]fullerene tetramalonate
Chem.Commun., 2015, 51, 6489
7116898 CIFC97 H40 O25 Ru3P 1 21/c 122.538; 34.0435; 18.4298
90; 92.787; 90		14124Chia-Hsiang Chen; Amineh Aghabali; Catalina Suarez; Marilyn M. Olmstead; Alan L. Balch; Luis Echegoyen
Synthesis and characterization of bis-triruthenium cluster derivatives of an all equatorial [60]fullerene tetramalonate
Chem.Commun., 2015, 51, 6489
7116899 CIFC37 H25 N2 O4 ZnP -19.8824; 11.548; 15.648
89.784; 76.441; 75.603		1678.7Suresh Sanda; Srinivasulu Parshamoni; Soumava Biswas; Sanjit Konar
Highly selective detection of palladium and picric acid by a luminescent MOF: a dual functional fluorescent sensor
Chem.Commun., 2015, 51, 6576
7116900 CIFC31 H39 Cl2 N3 NiP 21 21 2113.6222; 14.2676; 15.7854
90; 90; 90		3068Blake R. Reed; Sebastian A. Stoian; Richard L. Lord; Stanislav Groysman
The aldimine effect in bis(imino)pyridine complexes: non-planar nickel(I) complexes of a bis(aldimino)pyridine ligand
Chem.Commun., 2015, 51, 6496
7116901 CIFC32 H39 Br2 Cl2 N3 NiP 1 21/n 19.787; 26.3927; 13.7739
90; 108.906; 90		3365.9Blake R. Reed; Sebastian A. Stoian; Richard L. Lord; Stanislav Groysman
The aldimine effect in bis(imino)pyridine complexes: non-planar nickel(I) complexes of a bis(aldimino)pyridine ligand
Chem.Commun., 2015, 51, 6496
7116902 CIFC39 H47 Cl N3 Ni O2P -19.7349; 12.3308; 15.6197
87.49; 75.776; 85.562		1811.45Blake R. Reed; Sebastian A. Stoian; Richard L. Lord; Stanislav Groysman
The aldimine effect in bis(imino)pyridine complexes: non-planar nickel(I) complexes of a bis(aldimino)pyridine ligand
Chem.Commun., 2015, 51, 6496
7116903 CIFC39 H47 Br N3 Ni O2P -19.8908; 12.3807; 15.5767
86.987; 75.727; 85.167		1841Blake R. Reed; Sebastian A. Stoian; Richard L. Lord; Stanislav Groysman
The aldimine effect in bis(imino)pyridine complexes: non-planar nickel(I) complexes of a bis(aldimino)pyridine ligand
Chem.Commun., 2015, 51, 6496
7116904 CIFC37 H49 Br N3 Ni O1.5P -19.7274; 14.232; 14.9719
111.974; 99.695; 101.376		1816.3Blake R. Reed; Sebastian A. Stoian; Richard L. Lord; Stanislav Groysman
The aldimine effect in bis(imino)pyridine complexes: non-planar nickel(I) complexes of a bis(aldimino)pyridine ligand
Chem.Commun., 2015, 51, 6496
7116905 CIFC44 H44 Cu5 N6 O14P 1 21/n 16.2137; 16.2226; 22.6452
90; 91.2531; 90		2282.1Christian Plenk; Jasmin Krause; Martin Beck; Eva Rentschler
Rational linkage of magnetic molecules using click chemistry
Chem.Commun., 2015, 51, 6524
7116906 CIFC23 H17 F3 O SP -19.4049; 10.3048; 10.563
79.807; 74.337; 82.314		966.1Dao-Qian Chen; Pin Gao; Ping-Xin Zhou; Xian-Rong Song; Yi-Feng Qiu; Xue-Yuan Liu; Yong-Min Liang
Regioselective access to CF3S-substituted dihydrofurans from homopropargylic alcohols with trifluoromethanesulfenamide
Chem.Commun., 2015, 51, 6637
7116907 CIFC64 H82 N8 S8P -4 3 n22.6217; 22.6217; 22.6217
90; 90; 90		11576.5Yunus Zorlu; Ufuk Kumru; Umit Isci; Burcin Divrik; Erwann Jeanneau; Florian Albrieux; Yavuz Dede; Vefa Ahsen; Fabienne Dumoulin
1,4,8,11,15,18,22,25-Alkylsulfanyl phthalocyanines: effect of macrocycle distortion on spectroscopic and packing properties
Chem.Commun., 2015, 51, 6580
7116908 CIFC80 H114 N8 S8P -112.7956; 17.1258; 18.8008
112.281; 91.994; 94.129		3793.8Yunus Zorlu; Ufuk Kumru; Umit Isci; Burcin Divrik; Erwann Jeanneau; Florian Albrieux; Yavuz Dede; Vefa Ahsen; Fabienne Dumoulin
1,4,8,11,15,18,22,25-Alkylsulfanyl phthalocyanines: effect of macrocycle distortion on spectroscopic and packing properties
Chem.Commun., 2015, 51, 6580
7116909 CIFC12 H9 N3 O2P b c a11.5359; 15.7377; 23.975
90; 90; 90		4352.6Cheng Xu; Feng-Cheng Jia; Qun Cai; Deng-Kui Li; Zhi-Wen Zhou; An-Xin Wu
Intramolecular decarboxylative coupling as the key step in copper-catalyzed domino reaction: facile access to 2-(1,3,4-oxadiazol-2-yl)aniline derivatives
Chem.Commun., 2015, 51, 6629
7116910 CIFC25 H19 N OP c a 2113.273; 18.584; 7.3811
90; 90; 90		1820.7Liangwei Zhang; Xiangdong Li; Yuanhong Liu; Dayong Zhang
Palladium-catalyzed highly efficient synthesis of functionalized indolizines via cross-coupling/cycloisomerization cascade
Chem.Commun., 2015, 51, 6633
7116911 CIFC24 H32 Cl NP 21 21 217.0083; 8.9587; 32.914
90; 90; 90		2066.5Liangwei Zhang; Xiangdong Li; Yuanhong Liu; Dayong Zhang
Palladium-catalyzed highly efficient synthesis of functionalized indolizines via cross-coupling/cycloisomerization cascade
Chem.Commun., 2015, 51, 6633
7116912 CIFC20 H20 F3 N OP -110.018; 10.446; 35.11
83.334; 86.119; 76.252		3542Liangwei Zhang; Xiangdong Li; Yuanhong Liu; Dayong Zhang
Palladium-catalyzed highly efficient synthesis of functionalized indolizines via cross-coupling/cycloisomerization cascade
Chem.Commun., 2015, 51, 6633
7116913 CIFC21 H31 Cl N O2P -17.085; 12.661; 12.767
94.479; 93.887; 100.786		1117.6Liangwei Zhang; Xiangdong Li; Yuanhong Liu; Dayong Zhang
Palladium-catalyzed highly efficient synthesis of functionalized indolizines via cross-coupling/cycloisomerization cascade
Chem.Commun., 2015, 51, 6633
7116914 CIFC22 H19 N2P 1 21/n 19.7108; 11.3687; 14.8851
90; 97.059; 90		1630.85Likui Xiang; Yanning Niu; Xiaobo Pang; Xiaodong Yang; Rulong Yan
I2-catalyzed synthesis of substituted imidazoles from vinyl azides and benzylamines
Chem.Commun., 2015, 51, 6598
7116915 CIFC12 H14 Br N OP b c a8.8904; 13.0832; 19.2524
90; 90; 90		2239.3Rahul Kisan Kawade; Deepak B. Huple; Rong-Jing Lin; Rai-Shung Liu
Cu-catalyzed oxidative Povarov reactions between N-alkyl N-methylanilines and saturated oxa- and thiacycles
Chem.Commun., 2015, 51, 6625
7116916 CIFC16 H14 Co2 O7P -18.893; 16.495; 19.797
101.28; 102.13; 103.697		2664.8Pierangelo Gobbo; Tommaso Romagnoli; Stephanie M. Barbon; Jacquelyn T. Price; Jennifer Keir; Joe B. Gilroy; Mark S. Workentin
Expanding the scope of strained-alkyne chemistry: a protection-deprotection strategy via the formation of a dicobalt-hexacarbonyl complex
Chem.Commun., 2015, 51, 6647
7116917 CIFC16 H14 Co2 O7P -19.074; 12.983; 16.699
110.879; 96.205; 98.023		1793.4Pierangelo Gobbo; Tommaso Romagnoli; Stephanie M. Barbon; Jacquelyn T. Price; Jennifer Keir; Joe B. Gilroy; Mark S. Workentin
Expanding the scope of strained-alkyne chemistry: a protection-deprotection strategy via the formation of a dicobalt-hexacarbonyl complex
Chem.Commun., 2015, 51, 6647
7116918 CIFC23 H17 Co2 N O11C 1 2/c 139.343; 8.101; 16.72
90; 110.966; 90		4976Pierangelo Gobbo; Tommaso Romagnoli; Stephanie M. Barbon; Jacquelyn T. Price; Jennifer Keir; Joe B. Gilroy; Mark S. Workentin
Expanding the scope of strained-alkyne chemistry: a protection-deprotection strategy via the formation of a dicobalt-hexacarbonyl complex
Chem.Commun., 2015, 51, 6647
7116919 CIFC28 H17 OP b c n11.6165; 12.7592; 12.4644
90; 90; 90		1847.44Tatsuya Aotake; Mitsuharu Suzuki; Naoki Aratani; Junpei Yuasa; Daiki Kuzuhara; Hironobu Hayashi; Haruyuki Nakano; Tsuyoshi Kawai; Jishan Wu; Hiroko Yamada
9,9'-Anthryl-anthroxyl radicals: strategic stabilization of highly reactive phenoxyl radicals
Chem.Commun., 2015, 51, 6734
7116920 CIFC58.5 H37.5 Cl7.5 O2P -111.5782; 14.3354; 16.4867
96.3005; 101.787; 113.704		2395.88Tatsuya Aotake; Mitsuharu Suzuki; Naoki Aratani; Junpei Yuasa; Daiki Kuzuhara; Hironobu Hayashi; Haruyuki Nakano; Tsuyoshi Kawai; Jishan Wu; Hiroko Yamada
9,9'-Anthryl-anthroxyl radicals: strategic stabilization of highly reactive phenoxyl radicals
Chem.Commun., 2015, 51, 6734
7116921 CIFC52 H41 OP 1 21/n 110.6594; 21.7535; 16.0991
90; 100.123; 90		3674.93Tatsuya Aotake; Mitsuharu Suzuki; Naoki Aratani; Junpei Yuasa; Daiki Kuzuhara; Hironobu Hayashi; Haruyuki Nakano; Tsuyoshi Kawai; Jishan Wu; Hiroko Yamada
9,9'-Anthryl-anthroxyl radicals: strategic stabilization of highly reactive phenoxyl radicals
Chem.Commun., 2015, 51, 6734
7116922 CIFC57 H46 Cl15 OP 1 21/c 113.966; 19.591; 21.6636
90; 109.308; 90		5593.9Tatsuya Aotake; Mitsuharu Suzuki; Naoki Aratani; Junpei Yuasa; Daiki Kuzuhara; Hironobu Hayashi; Haruyuki Nakano; Tsuyoshi Kawai; Jishan Wu; Hiroko Yamada
9,9'-Anthryl-anthroxyl radicals: strategic stabilization of highly reactive phenoxyl radicals
Chem.Commun., 2015, 51, 6734
7116923 CIFC21 H22 N2 O4 SP 1 21/c 113.153; 17.8912; 9.1269
90; 109.86; 90		2020Xin-Hua Hao; Pin Gao; Xian-Rong Song; Yi-Feng Qiu; Dong-Po Jin; Xue-Yuan Liu; Yong-Min Liang
Metal-free nitro-carbocyclization of 1,6-enynes with tBuONO and TEMPO
Chem.Commun., 2015, 51, 6839
7116924 CIFC45 H40 Ag0 Cl7 F0 N5 O11 P0 Sb U Zn0P -110.3488; 15.1997; 16.7191
89.696; 77.054; 84.978		2552.93Christina M. Davis; Kei Ohkubo; I-Ting Ho; Zhan Zhang; Masatoshi Ishida; Yuanyuan Fang; Vincent M. Lynch; Karl M. Kadish; Jonathan L. Sessler; Shunichi Fukuzumi
Near-infrared-induced electron transfer of an uranyl macrocyclic complex without energy transfer to dioxygen
Chem.Commun., 2015, 51, 6757
7116925 CIFC32 H31 B Fe N7 SP 1 21/n 19.3767; 16.0545; 19.6816
90; 96.784; 90		2942.1M. Sallmann; B. Braun; C. Limberg
Dioxygenation of cysteamine to hypotaurine at a tris(pyrazolyl)borate iron(II) unit - cysteamine dioxygenase mimicking?
Chem.Commun., 2015, 51, 6785
7116926 CIFC36 H52 Eu2 N8 O22P -113.2205; 13.9973; 14.9
99.68; 91.009; 117.103		2405.6Yin-Ling Hou; Hang Xu; Rui-Rui Cheng; Bin Zhao
Controlled lanthanide-organic framework nanospheres as reversible and sensitive luminescent sensors for practical applications
Chem.Commun., 2015, 51, 6769
7116927 CIFC33 H47 N7 O22 Tb2P -113.009; 13.7701; 15.0439
99.513; 90.402; 116.522		2368.1Yin-Ling Hou; Hang Xu; Rui-Rui Cheng; Bin Zhao
Controlled lanthanide-organic framework nanospheres as reversible and sensitive luminescent sensors for practical applications
Chem.Commun., 2015, 51, 6769
7116928 CIFC19 H19 F3 N2P b c a10.9173; 8.53033; 34.7268
90; 90; 90		3234.04Kazuki Isa; Maki Minakawa; Motoi Kawatsura
Palladium-catalyzed amination of 2,3,3-trifluoroallyl esters: synthesis of trifluoromethylenamines via an intramolecular fluorine shift and CF3 group construction
Chem.Commun., 2015, 51, 6761
7116929 CIFC55 H77 Ge N O4 SiP -111.9476; 13.7236; 16.2518
81.454; 83.839; 80.731		2591.21Terrance J. Hadlington; Benedikt Schwarze; Ekaterina I. Izgorodina; Cameron Jones
Two-coordinate hydrido-germylenes
Chem.Commun., 2015, 51, 6854
7116930 CIFC50 H66 Ge N O3 SiP -110.074; 14.516; 18.777
109.23; 96.79; 97.99		2527.7Terrance J. Hadlington; Benedikt Schwarze; Ekaterina I. Izgorodina; Cameron Jones
Two-coordinate hydrido-germylenes
Chem.Commun., 2015, 51, 6854
7116931 CIFC45 H55 Ge N O3 SiP 1 21/n 110.7047; 21.7462; 17.079
90; 92.615; 90		3971.6Terrance J. Hadlington; Benedikt Schwarze; Ekaterina I. Izgorodina; Cameron Jones
Two-coordinate hydrido-germylenes
Chem.Commun., 2015, 51, 6854
7116932 CIFC45 H55 N O3 SiP 1 21/n 112.369; 21.768; 14.724
90; 96.32; 90		3940.3Terrance J. Hadlington; Benedikt Schwarze; Ekaterina I. Izgorodina; Cameron Jones
Two-coordinate hydrido-germylenes
Chem.Commun., 2015, 51, 6854
7116933 CIFC53 H70 Li N O5 SiP 1 21/c 111.531; 24.287; 17.056
90; 98.37; 90		4725.7Terrance J. Hadlington; Benedikt Schwarze; Ekaterina I. Izgorodina; Cameron Jones
Two-coordinate hydrido-germylenes
Chem.Commun., 2015, 51, 6854
7116934 CIFC32 H26 N2 O2P 1 21/c 118.889; 7.1199; 18.6541
90; 104.646; 90		2427.2Ting Li; Zhen Wang; Mingliang Zhang; Hui-Jun Zhang; Ting-Bin Wen
Rh/Cu-catalyzed multiple C-H, C-C, and C-N bond cleavage: facile synthesis of pyrido[2,1-a]indoles from 1-(pyridin-2-yl)-1H-indoles and gamma-substituted propargyl alcohols
Chem.Commun., 2015, 51, 6777
7116935 CIFC42 H30 N2P -111.0719; 11.9763; 12.7664
95.06; 92.632; 117.362		1490.4Ting Li; Zhen Wang; Mingliang Zhang; Hui-Jun Zhang; Ting-Bin Wen
Rh/Cu-catalyzed multiple C-H, C-C, and C-N bond cleavage: facile synthesis of pyrido[2,1-a]indoles from 1-(pyridin-2-yl)-1H-indoles and gamma-substituted propargyl alcohols
Chem.Commun., 2015, 51, 6777
7116936 CIFC30.3 H25.6 Cl0.6 N4 O2 RhP -19.6401; 11.069; 12.562
82.69; 77.98; 83.72		1295.6Ting Li; Zhen Wang; Mingliang Zhang; Hui-Jun Zhang; Ting-Bin Wen
Rh/Cu-catalyzed multiple C-H, C-C, and C-N bond cleavage: facile synthesis of pyrido[2,1-a]indoles from 1-(pyridin-2-yl)-1H-indoles and gamma-substituted propargyl alcohols
Chem.Commun., 2015, 51, 6777
7116937 CIFC30 H21 Cl N2P -18.8053; 11.2771; 12.0975
67.401; 89.113; 83.151		1100.51Ting Li; Zhen Wang; Mingliang Zhang; Hui-Jun Zhang; Ting-Bin Wen
Rh/Cu-catalyzed multiple C-H, C-C, and C-N bond cleavage: facile synthesis of pyrido[2,1-a]indoles from 1-(pyridin-2-yl)-1H-indoles and gamma-substituted propargyl alcohols
Chem.Commun., 2015, 51, 6777
7116938 CIFC32 H26 N2 OP 1 21/c 19.9489; 17.1959; 14.4905
90; 109.121; 90		2342.3Ting Li; Zhen Wang; Mingliang Zhang; Hui-Jun Zhang; Ting-Bin Wen
Rh/Cu-catalyzed multiple C-H, C-C, and C-N bond cleavage: facile synthesis of pyrido[2,1-a]indoles from 1-(pyridin-2-yl)-1H-indoles and gamma-substituted propargyl alcohols
Chem.Commun., 2015, 51, 6777
7116939 CIFC72 H60 Ag O4 P4 ReR 3 :H14.2192; 14.2192; 51.1145
90; 90; 120		8950F. Deiser; F. Kraus; H. Schmidbaur
Bis(triphenylphosphine)silver(I) perrhenate, a cyclic dimer
Chem.Commun., 2015, 51, 6746
7116940 CIFC72 H60 Ag2 O8 P4 Re2P -112.1764; 12.4966; 13.2647
89.938; 62.745; 68.528		1635.6F. Deiser; F. Kraus; H. Schmidbaur
Bis(triphenylphosphine)silver(I) perrhenate, a cyclic dimer
Chem.Commun., 2015, 51, 6746
7116941 CIFC28.84 H42.57 N O6 S SiP 1 21/c 115.627; 13.4083; 15.769
90; 110.208; 90		3100.7Urszula K. Klimczak; Bartosz K. Zambron
Effective 1,5-stereocontrol in Pd(0)/InI promoted reactions of chiral N-Ts-4-vinylazetidin-2-ones with aldehydes. An efficient entry into nonracemic semi-protected (3Z)-2,6-anti-enediols
Chem.Commun., 2015, 51, 6796
7116942 CIFC22 H12 K N9 O1.94P 42/n :220.9259; 20.9259; 9.6322
90; 90; 90		4217.9Yumi Yakiyama; Gil Ryeong Lee; Sung Yeon Kim; Yoshitaka Matsushita; Yasushi Morita; Moon Jeong Park; Masaki Kawano
Formation of a nanometer-thick water layer at high humidity on a dynamic crystalline material composed of multi-interactive molecules
Chem.Commun., 2015, 51, 6828
7116943 CIFC22 K N9 O2P 1 2/a 120.904; 15.931; 9.711
90; 104.65; 90		3129Yumi Yakiyama; Gil Ryeong Lee; Sung Yeon Kim; Yoshitaka Matsushita; Yasushi Morita; Moon Jeong Park; Masaki Kawano
Formation of a nanometer-thick water layer at high humidity on a dynamic crystalline material composed of multi-interactive molecules
Chem.Commun., 2015, 51, 6828
7116944 CIFC22 K N9 O6P 1 2/a 120.656; 15.978; 16.801
90; 100.68; 90		5449Yumi Yakiyama; Gil Ryeong Lee; Sung Yeon Kim; Yoshitaka Matsushita; Yasushi Morita; Moon Jeong Park; Masaki Kawano
Formation of a nanometer-thick water layer at high humidity on a dynamic crystalline material composed of multi-interactive molecules
Chem.Commun., 2015, 51, 6828
7116945 CIFC22 K N9 O8.5P 1 2/n 124.131; 19.458; 16.672
90; 122.52; 90		6601Yumi Yakiyama; Gil Ryeong Lee; Sung Yeon Kim; Yoshitaka Matsushita; Yasushi Morita; Moon Jeong Park; Masaki Kawano
Formation of a nanometer-thick water layer at high humidity on a dynamic crystalline material composed of multi-interactive molecules
Chem.Commun., 2015, 51, 6828
7116946 CIFC10 H9 N OP b c a15.005; 12.061; 18.219
90; 90; 90		3297.2Yanli Xu; Weigao Hu; Xiaodong Tang; Jinwu Zhao; Wanqing Wu; Huanfeng Jiang
Palladium-catalyzed Csp2-H carbonylation of aromatic oximes: selective access to benzo[d][1,2]oxazin-1-ones and 3-methyleneisoindolin-1-ones
Chem.Commun., 2015, 51, 6843
7116947 CIFC10 H18 B16 Cu O5P m -3 n28.973; 28.973; 28.973
90; 90; 90		24321Clingerman, Daniel J.; Morris, William; Mondloch, Joseph E.; Kennedy, Robert D.; Sarjeant, Amy A.; Stern, Charlotte; Hupp, Joseph T.; Farha, Omar K.; Mirkin, Chad A.
Stabilization of a highly porous metal-organic framework utilizing a carborane-based linker.
Chemical communications (Cambridge, England), 2015, 51, 6521-6523
7116948 CIFC12 H30 B24P 1 21/c 111.9932; 19.6594; 12.4615
90; 118.684; 90		2577.6Clingerman, Daniel J.; Morris, William; Mondloch, Joseph E.; Kennedy, Robert D.; Sarjeant, Amy A.; Stern, Charlotte; Hupp, Joseph T.; Farha, Omar K.; Mirkin, Chad A.
Stabilization of a highly porous metal-organic framework utilizing a carborane-based linker.
Chemical communications (Cambridge, England), 2015, 51, 6521-6523
7116949 CIFC75 H63 Mn3 N12 O12P -112.281; 12.919; 30.425
94.65; 93.93; 92.4		4794.5Bloch, Witold M.; Burgun, Alexandre; Doonan, Christian J.; Sumby, Christopher J.
Probing post-synthetic metallation in metal-organic frameworks: insights from X-ray crystallography.
Chemical communications (Cambridge, England), 2015, 51, 5486-5489
7116950 CIFC77 H69 Cl5.25 Mn5.5 N13 O16.5P 1 21/m 112.338; 33.33; 25.857
90; 97.45; 90		10543Bloch, Witold M.; Burgun, Alexandre; Doonan, Christian J.; Sumby, Christopher J.
Probing post-synthetic metallation in metal-organic frameworks: insights from X-ray crystallography.
Chemical communications (Cambridge, England), 2015, 51, 5486-5489
7116951 CIFC37.5 H33 Cl Mn2 N6 O7.5P 1 21/m 112.355; 33.452; 12.952
90; 97.63; 90		5306Bloch, Witold M.; Burgun, Alexandre; Doonan, Christian J.; Sumby, Christopher J.
Probing post-synthetic metallation in metal-organic frameworks: insights from X-ray crystallography.
Chemical communications (Cambridge, England), 2015, 51, 5486-5489
7116952 CIFC21 H22 N4 O4P 21 21 215.9906; 15.7335; 21.9353
90; 90; 90		2067.5Bag, Subhendu Sekhar; Jana, Subhashis; Yashmeen, Afsana; De, Suranjan
Triazolo-β-aza-ε-amino acid and its aromatic analogue as novel scaffolds for β-turn peptidomimetics.
Chemical communications (Cambridge, England), 2015, 51, 5242-5245
7116961 CIFC42 H46 N4 O13 S3P 21 21 218.6884; 19.6749; 25.149
90; 90; 90		4299.1Zhiyuan Hu; Rory L. Arrowsmith; James A. Tyson; Vincenzo Mirabello; Haobo Ge; Ian M. Eggleston; Stanley W. Botchway; G. Dan Pantos; Sofia I. Pascu
A fluorescent Arg-Gly-Asp (RGD) peptide-naphthalenediimide (NDI) conjugate for imaging integrin alpha-v-beta3in vitro
Chem.Commun., 2015, 51, 6901
7116963 CIFC120 H76 O36 S12 Zr6F m -3 m32.7165; 32.7165; 32.7165
90; 90; 90		35018.7Bo Gui; Ka-Kit Yee; Yan-Lung Wong; Shek-Man Yiu; Matthias Zeller; Cheng Wang; Zhengta Xu
Tackling poison and leach: catalysis by dangling thiol-palladium functions within a porous metal-organic solid
Chem.Commun., 2015, 51, 6917
7116964 CIFC72 H80 Cl2 N4 Ni2P 1 21/n 116.1963; 12.2535; 16.3252
90; 94.689; 90		3229.1Wei Gao; Lan Xin; Zhiqiang Hao; Guodong Li; Ji-Hu Su; Lijing Zhou; Ying Mu
The ligand redox behavior and role in 1,2-bis[(2,6-diisopropylphenyl)imino]-acenaphthene nickel-TMA(MAO) systems for ethylene polymerization
Chem.Commun., 2015, 51, 7004
7116965 CIFC64.5 H63 Cl N2 Ni PP -111.2339; 13.5323; 19.012
72.179; 88.564; 84.99		2741Wei Gao; Lan Xin; Zhiqiang Hao; Guodong Li; Ji-Hu Su; Lijing Zhou; Ying Mu
The ligand redox behavior and role in 1,2-bis[(2,6-diisopropylphenyl)imino]-acenaphthene nickel-TMA(MAO) systems for ethylene polymerization
Chem.Commun., 2015, 51, 7004
7116966 CIFC38 H46 Al Br2 N2 NiP b c n13.7598; 18.9444; 14.2281
90; 90; 90		3708.9Wei Gao; Lan Xin; Zhiqiang Hao; Guodong Li; Ji-Hu Su; Lijing Zhou; Ying Mu
The ligand redox behavior and role in 1,2-bis[(2,6-diisopropylphenyl)imino]-acenaphthene nickel-TMA(MAO) systems for ethylene polymerization
Chem.Commun., 2015, 51, 7004
7116967 CIFC18 H10 O2P 21 21 215.2561; 9.121; 24.027
90; 90; 90		1151.9Ruth Dorel; Carlos Manzano; Maricarmen Grisoli; We-Hyo Soe; Christian Joachim; Antonio M. Echavarren
Tetrabenzocircumpyrene: a nanographene fragment with an embedded peripentacene core
Chem.Commun., 2015, 51, 6932
7116968 CIFC54 H32P 1 21/c 19.2045; 16.8399; 22.397
90; 90.064; 90		3471.6Ruth Dorel; Carlos Manzano; Maricarmen Grisoli; We-Hyo Soe; Christian Joachim; Antonio M. Echavarren
Tetrabenzocircumpyrene: a nanographene fragment with an embedded peripentacene core
Chem.Commun., 2015, 51, 6932
7116969 CIFC78 H81.4P -17.6054; 18.7609; 21.2252
72.252; 84.027; 87.9		2868.66Ruth Dorel; Carlos Manzano; Maricarmen Grisoli; We-Hyo Soe; Christian Joachim; Antonio M. Echavarren
Tetrabenzocircumpyrene: a nanographene fragment with an embedded peripentacene core
Chem.Commun., 2015, 51, 6932
7116970 CIFC66.15 H56.83 Cl0.45P 1 21/c 19.3755; 26.1158; 20.0039
90; 101.625; 90		4797.5Ruth Dorel; Carlos Manzano; Maricarmen Grisoli; We-Hyo Soe; Christian Joachim; Antonio M. Echavarren
Tetrabenzocircumpyrene: a nanographene fragment with an embedded peripentacene core
Chem.Commun., 2015, 51, 6932
7116971 CIFC62 H36P -110.1459; 14.0677; 15.4819
66.782; 77.518; 85.704		1982.63Ruth Dorel; Carlos Manzano; Maricarmen Grisoli; We-Hyo Soe; Christian Joachim; Antonio M. Echavarren
Tetrabenzocircumpyrene: a nanographene fragment with an embedded peripentacene core
Chem.Commun., 2015, 51, 6932
7116972 CIFC68 H54 Cl4C 1 2/c 147.051; 9.3095; 27.9099
90; 125.063; 90		10006.5Ruth Dorel; Carlos Manzano; Maricarmen Grisoli; We-Hyo Soe; Christian Joachim; Antonio M. Echavarren
Tetrabenzocircumpyrene: a nanographene fragment with an embedded peripentacene core
Chem.Commun., 2015, 51, 6932
7116973 CIFC44 H56 O6 S2P -19.2441; 9.4374; 11.5116
81.533; 81.481; 87.419		982.09Michal Hucko; Hana Dvorakova; Vaclav Eigner; Pavel Lhotak
2,14-Dithiacalix[4]arene and its homooxa analogues: synthesis and dynamic NMR study of conformational behaviour
Chem.Commun., 2015, 51, 7051
7116974 CIFC43 H54 O5 S2P 1 21/a 113.3707; 18.8446; 16.9728
90; 107.545; 90		4077.62Michal Hucko; Hana Dvorakova; Vaclav Eigner; Pavel Lhotak
2,14-Dithiacalix[4]arene and its homooxa analogues: synthesis and dynamic NMR study of conformational behaviour
Chem.Commun., 2015, 51, 7051
7116975 CIFC32 H30 N OI 41/a :227.745; 27.745; 6.4943
90; 90; 90		4999Subham Bhattacharjee; Santanu Bhattacharya
Role of synergistic pi-pi stacking and X-H^...^Cl (X = C, N, O) H-bonding interactions in gelation and gel phase crystallization
Chem.Commun., 2015, 51, 7019
7116976 CIFC30 H40 Cl2.08 N2 O3P -19.7572; 11.9316; 13.8051
89.961; 102.504; 110.06		1469.11Subham Bhattacharjee; Santanu Bhattacharya
Role of synergistic pi-pi stacking and X-H^...^Cl (X = C, N, O) H-bonding interactions in gelation and gel phase crystallization
Chem.Commun., 2015, 51, 7019
7116977 CIFC17 H16 N2 O3 SC 1 2/c 126.8782; 8.2244; 19.4674
90; 132.644; 90		3165.5Jisu Jeong; Donggun Lee; Sukbok Chang
Copper-catalyzed oxygen atom transfer of N-oxides leading to a facile deoxygenation procedure applicable to both heterocyclic and amine N-oxides
Chem.Commun., 2015, 51, 7035
7116978 CIFC18 H14 F3 N3 O3P 1 21/n 111.296; 13.615; 11.516
90; 105.89; 90		1703Devalina Ray; T. Manikandan; Arup Roy; Krishna N. Tripathi; Ravi P. Singh
Ligand-promoted intramolecular dehydrogenative cross-coupling using a Cu catalyst: direct access to polycyclic heteroarenes
Chem.Commun., 2015, 51, 7065
7116981 CIFC39 H29 N O3 P2P 21 21 2111.279; 16.1962; 17.5843
90; 90; 90		3212.2G. Gangadhararao; R. N. Prasad Tulichala; K. C. Kumara Swamy
Spontaneous resolution upon crystallization of allenyl-bis-phosphine oxides
Chem.Commun., 2015, 51, 7168
7116982 CIFC39 H29 N O4 P2P 21 21 2111.281; 16.1001; 17.7437
90; 90; 90		3222.7G. Gangadhararao; R. N. Prasad Tulichala; K. C. Kumara Swamy
Spontaneous resolution upon crystallization of allenyl-bis-phosphine oxides
Chem.Commun., 2015, 51, 7168
7116983 CIFC40 H31 N O4 P2P 21 21 2111.1755; 15.95; 18.117
90; 90; 90		3229.3G. Gangadhararao; R. N. Prasad Tulichala; K. C. Kumara Swamy
Spontaneous resolution upon crystallization of allenyl-bis-phosphine oxides
Chem.Commun., 2015, 51, 7168
7116984 CIFC40 H30 Cl N O4 P2P -19.9475; 13.0705; 14.9853
106.24; 94.143; 110.585		1719.37G. Gangadhararao; R. N. Prasad Tulichala; K. C. Kumara Swamy
Spontaneous resolution upon crystallization of allenyl-bis-phosphine oxides
Chem.Commun., 2015, 51, 7168
7116985 CIFC42 H32 Br Cl6 N O4 P2P -111.5145; 13.3968; 14.6374
86.833; 75.632; 87.59		2183G. Gangadhararao; R. N. Prasad Tulichala; K. C. Kumara Swamy
Spontaneous resolution upon crystallization of allenyl-bis-phosphine oxides
Chem.Commun., 2015, 51, 7168
7116986 CIFC39 H33 N O4 P2P 21 21 2111.335; 17.7472; 16.1457
90; 90; 90		3247.9G. Gangadhararao; R. N. Prasad Tulichala; K. C. Kumara Swamy
Spontaneous resolution upon crystallization of allenyl-bis-phosphine oxides
Chem.Commun., 2015, 51, 7168
7116987 CIFC39 H33 N O4 P2P 21 21 2111.3101; 17.7378; 16.0426
90; 90; 90		3218.4G. Gangadhararao; R. N. Prasad Tulichala; K. C. Kumara Swamy
Spontaneous resolution upon crystallization of allenyl-bis-phosphine oxides
Chem.Commun., 2015, 51, 7168
7116988 CIFC39 H33 Cl N O4 P2P -19.7782; 12.6735; 15.218
72.422; 88.076; 69.077		1673.42G. Gangadhararao; R. N. Prasad Tulichala; K. C. Kumara Swamy
Spontaneous resolution upon crystallization of allenyl-bis-phosphine oxides
Chem.Commun., 2015, 51, 7168
7116989 CIFC39 H33 N O4 P2P 21 21 2111.326; 15.94; 17.593
90; 90; 90		3176.2G. Gangadhararao; R. N. Prasad Tulichala; K. C. Kumara Swamy
Spontaneous resolution upon crystallization of allenyl-bis-phosphine oxides
Chem.Commun., 2015, 51, 7168
7116990 CIFC28 H19 N3P 1 21/c 115.3114; 12.9392; 10.8302
90; 102.639; 90		2093.7Lijun Shi; Xiang Zhong; Houde She; Ziqiang Lei; Fuwei Li
Manganese catalyzed C-H functionalization of indoles with alkynes to synthesize bis/trisubstituted indolylalkenes and carbazoles: the acid is the key to control selectivity
Chem.Commun., 2015, 51, 7136
7116991 CIFC17 H10 Mn N3 O4P 1 21/c 111.7689; 10.7605; 13.511
90; 107.25; 90		1634.1Lijun Shi; Xiang Zhong; Houde She; Ziqiang Lei; Fuwei Li
Manganese catalyzed C-H functionalization of indoles with alkynes to synthesize bis/trisubstituted indolylalkenes and carbazoles: the acid is the key to control selectivity
Chem.Commun., 2015, 51, 7136
7116992 CIFC12 H22 B10P 21 21 219.009; 12.9189; 14.1739
90; 90; 90		1649.65Ke Cao; Yawen Huang; Junxiao Yang; Ji Wu
Palladium catalyzed selective mono-arylation of o-carboranes via B-H activation
Chem.Commun., 2015, 51, 7257
7116993 CIFC13 H24 B10 O2P 1 21/c 17.3151; 13.218; 19.6674
90; 93.078; 90		1898.92Ke Cao; Yawen Huang; Junxiao Yang; Ji Wu
Palladium catalyzed selective mono-arylation of o-carboranes via B-H activation
Chem.Commun., 2015, 51, 7257
7116994 CIFC12 H22 B10 OC 1 2/c 124.2272; 13.0711; 23.5734
90; 108.334; 90		7086.2Ke Cao; Yawen Huang; Junxiao Yang; Ji Wu
Palladium catalyzed selective mono-arylation of o-carboranes via B-H activation
Chem.Commun., 2015, 51, 7257
7116995 CIFC10 H20 B10P b c a24.322; 8.2628; 15.382
90; 90; 90		3091.3Ke Cao; Yawen Huang; Junxiao Yang; Ji Wu
Palladium catalyzed selective mono-arylation of o-carboranes via B-H activation
Chem.Commun., 2015, 51, 7257
7116996 CIFC13 H24 B10 O2P 1 21/n 17.0474; 19.9445; 13.4339
90; 94.295; 90		1882.92Ke Cao; Yawen Huang; Junxiao Yang; Ji Wu
Palladium catalyzed selective mono-arylation of o-carboranes via B-H activation
Chem.Commun., 2015, 51, 7257
7116997 CIFC70 H66 Cl4 N6 O4P -110.963; 10.985; 15.643
94.45; 104.45; 119.51		1542Chenhao Zhang; Ke Shi; Kang Cai; Jiajun Xie; Ting Lei; Qifan Yan; Jie-Yu Wang; Jian Pei; Dahui Zhao
Cyano- and chloro-substituted coronene diimides as solution-processable electron-transporting semiconductors
Chem.Commun., 2015, 51, 7144
7116998 CIFC36 H36 As Cl2 N SiP -18.8947; 12.7255; 15.2825
78.686; 73.993; 70.48		1556.81Deepak Dange; Amelia Davey; Joseph A. B. Abdalla; Simon Aldridge; Cameron Jones
Utilisation of a lithium boryl as a reducing agent in low oxidation state group 15 chemistry: synthesis and characterisation of an amido-distibene and a boryl-dibismuthene
Chem.Commun., 2015, 51, 7128
7116999 CIFC38 H40 Br2 N Sb SiP -110.1762; 11.2391; 15.5145
95.865; 95.903; 100.813		1720.21Deepak Dange; Amelia Davey; Joseph A. B. Abdalla; Simon Aldridge; Cameron Jones
Utilisation of a lithium boryl as a reducing agent in low oxidation state group 15 chemistry: synthesis and characterisation of an amido-distibene and a boryl-dibismuthene
Chem.Commun., 2015, 51, 7128
7117000 CIFC44 H52 Br2 N Sb SiP 1 21/c 110.104; 17.041; 23.615
90; 101.92; 90		3978.4Deepak Dange; Amelia Davey; Joseph A. B. Abdalla; Simon Aldridge; Cameron Jones
Utilisation of a lithium boryl as a reducing agent in low oxidation state group 15 chemistry: synthesis and characterisation of an amido-distibene and a boryl-dibismuthene
Chem.Commun., 2015, 51, 7128
7117001 CIFC38 H40 Bi Br2 N SiP -110.1646; 11.259; 15.5011
95.931; 96.15; 100.498		1720.51Deepak Dange; Amelia Davey; Joseph A. B. Abdalla; Simon Aldridge; Cameron Jones
Utilisation of a lithium boryl as a reducing agent in low oxidation state group 15 chemistry: synthesis and characterisation of an amido-distibene and a boryl-dibismuthene
Chem.Commun., 2015, 51, 7128
7117002 CIFC44 H52 Bi Br2 N SiP 1 21/c 110.13; 17.182; 23.696
90; 102.26; 90		4030.3Deepak Dange; Amelia Davey; Joseph A. B. Abdalla; Simon Aldridge; Cameron Jones
Utilisation of a lithium boryl as a reducing agent in low oxidation state group 15 chemistry: synthesis and characterisation of an amido-distibene and a boryl-dibismuthene
Chem.Commun., 2015, 51, 7128
7117003 CIFC51 H42 Bi Br2 N SiP -110.3779; 12.172; 18.3157
82.925; 88.322; 66.682		2108Deepak Dange; Amelia Davey; Joseph A. B. Abdalla; Simon Aldridge; Cameron Jones
Utilisation of a lithium boryl as a reducing agent in low oxidation state group 15 chemistry: synthesis and characterisation of an amido-distibene and a boryl-dibismuthene
Chem.Commun., 2015, 51, 7128
7117004 CIFC82 H90 B Bi2 N3 SiP -113.6508; 14.2481; 20.2258
97.059; 95.917; 112.943		3545.8Deepak Dange; Amelia Davey; Joseph A. B. Abdalla; Simon Aldridge; Cameron Jones
Utilisation of a lithium boryl as a reducing agent in low oxidation state group 15 chemistry: synthesis and characterisation of an amido-distibene and a boryl-dibismuthene
Chem.Commun., 2015, 51, 7128
7117005 CIFC63.5 H73.5 As B N3 SiP -112.3574; 12.667; 19.7946
99.963; 104.228; 100.574		2874Deepak Dange; Amelia Davey; Joseph A. B. Abdalla; Simon Aldridge; Cameron Jones
Utilisation of a lithium boryl as a reducing agent in low oxidation state group 15 chemistry: synthesis and characterisation of an amido-distibene and a boryl-dibismuthene
Chem.Commun., 2015, 51, 7128
7117006 CIFC65.25 H80 As B N3 SiP -112.4034; 13.37; 20.102
77.434; 77.587; 65.731		2936.5Deepak Dange; Amelia Davey; Joseph A. B. Abdalla; Simon Aldridge; Cameron Jones
Utilisation of a lithium boryl as a reducing agent in low oxidation state group 15 chemistry: synthesis and characterisation of an amido-distibene and a boryl-dibismuthene
Chem.Commun., 2015, 51, 7128
7117007 CIFC98 H128 N2 Sb2 Si2P -112.6918; 13.6933; 14.0983
72.74; 77.066; 67.955		2151.2Deepak Dange; Amelia Davey; Joseph A. B. Abdalla; Simon Aldridge; Cameron Jones
Utilisation of a lithium boryl as a reducing agent in low oxidation state group 15 chemistry: synthesis and characterisation of an amido-distibene and a boryl-dibismuthene
Chem.Commun., 2015, 51, 7128
7117008 CIFC52 H72 B2 Bi2 N4P -110.501; 12.7973; 21.8679
88.502; 76.645; 67.584		2636.9Deepak Dange; Amelia Davey; Joseph A. B. Abdalla; Simon Aldridge; Cameron Jones
Utilisation of a lithium boryl as a reducing agent in low oxidation state group 15 chemistry: synthesis and characterisation of an amido-distibene and a boryl-dibismuthene
Chem.Commun., 2015, 51, 7128
7117018 CIFC27 H36 Br2 F6 In N2 SbP -19.5651; 10.502; 18.1036
94.315; 95.583; 115.957		1613.18Bastien Michelet; Jean-Remy Colard-Itte; Guillaume Thiery; Regis Guillot; Christophe Bour; Vincent Gandon
Dibromoindium(III) cations as a pi-Lewis acid: characterization of [IPr^.^InBr2][SbF6] and its catalytic activity towards alkynes and alkenes
Chem.Commun., 2015, 51, 7401
7117019 CIFC36 H24 Co3 Mn3 N17 Na O19R -317.343; 17.343; 31.6652
90; 90; 120		8248.2Jiang Liu; Mei Qu; Rodolphe Clerac; Xian Ming Zhang
A two-dimensional honeycomb coordination network based on fused triacontanuclear heterometallic {Co12Mn18} wheels
Chem.Commun., 2015, 51, 7356
7117020 CIFGd2 H8 O7C m c m16.583; 12.975; 7.3106
90; 90; 90		1573Yan Yang; Qian-Chong Zhang; Yin-Yin Pan; La-Sheng Long; Lan-Sun Zheng
Magnetocaloric effect and thermal conductivity of Gd(OH)3 and Gd2O(OH)4(H2O)2
Chem.Commun., 2015, 51, 7317
7117021 CIFGd H3 O3P 63/m6.2993; 6.2993; 3.6057
90; 90; 120		123.91Yan Yang; Qian-Chong Zhang; Yin-Yin Pan; La-Sheng Long; Lan-Sun Zheng
Magnetocaloric effect and thermal conductivity of Gd(OH)3 and Gd2O(OH)4(H2O)2
Chem.Commun., 2015, 51, 7317
7117022 CIFC8 H10 N14 O4P -15.4207; 6.797; 10.53
82.822; 77.868; 71.33		358.65Jiaheng Zhang; Damon A. Parrish; Jean'ne M. Shreeve
Curious cases of 3,6-dinitropyrazolo[4,3-c]pyrazole-based energetic cocrystals with high nitrogen content: an alternative to salt formation
Chem.Commun., 2015, 51, 7337
7117023 CIFC8 H10 N14 O4P 1 21/c 16.2903; 7.2315; 15.5555
90; 92.037; 90		707.15Jiaheng Zhang; Damon A. Parrish; Jean'ne M. Shreeve
Curious cases of 3,6-dinitropyrazolo[4,3-c]pyrazole-based energetic cocrystals with high nitrogen content: an alternative to salt formation
Chem.Commun., 2015, 51, 7337
7117024 CIFC54 H40 Cd Cl2 N12 O10P 43 21 215.8664; 15.8664; 21.7986
90; 90; 90		5487.6Fan Yang; Qi-Kui Liu; Dan Wu; An-Yan Li; Yu-Bin Dong
p-Benzoquinone adsorption-separation, sensing and its photoinduced transformation within a robust Cd(II)-MOF in a SC-SC fashion
Chem.Commun., 2015, 51, 7443
7117025 CIFC56 H46 Cd Cl2 N12 O11P 43 21 215.8983; 15.8983; 21.6675
90; 90; 90		5476.59Fan Yang; Qi-Kui Liu; Dan Wu; An-Yan Li; Yu-Bin Dong
p-Benzoquinone adsorption-separation, sensing and its photoinduced transformation within a robust Cd(II)-MOF in a SC-SC fashion
Chem.Commun., 2015, 51, 7443
7117026 CIFC54 H41.2 Cd Cl2 N12 O10P 41 21 215.90821; 15.90821; 21.6184
90; 90; 90		5470.99Fan Yang; Qi-Kui Liu; Dan Wu; An-Yan Li; Yu-Bin Dong
p-Benzoquinone adsorption-separation, sensing and its photoinduced transformation within a robust Cd(II)-MOF in a SC-SC fashion
Chem.Commun., 2015, 51, 7443
7117027 CIFC24 H20 N9 P SnP -110.756; 11.0605; 12.354
91.668; 108.414; 116.545		1222.1Benjamin Peerless; Theo Keane; Anthony J. H. M. Meijer; Peter Portius
Homoleptic low-valent polyazides of group 14 elements
Chem.Commun., 2015, 51, 7435
7117028 CIFC24 H20 Ge N9 PP -17.7712; 11.4711; 14.2003
93.278; 99.357; 100.865		1221.59Benjamin Peerless; Theo Keane; Anthony J. H. M. Meijer; Peter Portius
Homoleptic low-valent polyazides of group 14 elements
Chem.Commun., 2015, 51, 7435
7117029 CIFC16 H17 O3 PP 1 21 15.826; 17.749; 14.404
90; 93.154; 90		1487.2Junli Hou; Yang Chen; Dongmei Ma; Burghard Cordes; Jingyun Wang; Xin Wang; Fritz E. Kuhn; Hao Guo; Mingdong Zhou
Methyltrioxorhenium-catalyzed highly selective dihydroxylation of 1,2-allenylic diphenyl phosphine oxides
Chem.Commun., 2015, 51, 7439
7117030 CIFC16 H17 O3 PP 1 21 15.8589; 17.826; 14.463
90; 93.258; 90		1508.1Junli Hou; Yang Chen; Dongmei Ma; Burghard Cordes; Jingyun Wang; Xin Wang; Fritz E. Kuhn; Hao Guo; Mingdong Zhou
Methyltrioxorhenium-catalyzed highly selective dihydroxylation of 1,2-allenylic diphenyl phosphine oxides
Chem.Commun., 2015, 51, 7439
7117031 CIFC27 H19 B F2 N2 SP -110.1096; 12.4472; 18.3814
95.587; 95.919; 96.9		2269.9Xiaoqing Wang; Qingsong Liu; Hui Yan; Zhipeng Liu; Mingguang Yao; Qingfu Zhang; Shuwen Gong; Weijiang He
Piezochromic luminescence behaviors of two new benzothiazole-enamido boron difluoride complexes: intra- and inter-molecular effects induced by hydrostatic compression
Chem.Commun., 2015, 51, 7497
7117032 CIFC66 H66 B2 F4 N8 O S2C 1 2 129.997; 8.4716; 12.7084
90; 112.788; 90		2977.4Xiaoqing Wang; Qingsong Liu; Hui Yan; Zhipeng Liu; Mingguang Yao; Qingfu Zhang; Shuwen Gong; Weijiang He
Piezochromic luminescence behaviors of two new benzothiazole-enamido boron difluoride complexes: intra- and inter-molecular effects induced by hydrostatic compression
Chem.Commun., 2015, 51, 7497
7117033 CIFC9.66667 H13 Br N4.33333 PP -110.1735; 12.6747; 16.2901
83.778; 72.596; 73.177		1918.05Justin F. Binder; Ala'aeddeen Swidan; Martin Tang; Jennifer H. Nguyen; Charles L. B. Macdonald
Remarkably stable chelating bis-N-heterocyclic carbene adducts of phosphorus(I) cations
Chem.Commun., 2015, 51, 7741
7117034 CIFC21 H20 Br N4 PP 1 21/c 112.2417; 4.8288; 33.91
90; 98.281; 90		1983.6Justin F. Binder; Ala'aeddeen Swidan; Martin Tang; Jennifer H. Nguyen; Charles L. B. Macdonald
Remarkably stable chelating bis-N-heterocyclic carbene adducts of phosphorus(I) cations
Chem.Commun., 2015, 51, 7741
7117035 CIFC10 H12 F3 N4 O3 P SP -18.2477; 8.4833; 10.7821
97.866; 104.396; 93.252		720.59Justin F. Binder; Ala'aeddeen Swidan; Martin Tang; Jennifer H. Nguyen; Charles L. B. Macdonald
Remarkably stable chelating bis-N-heterocyclic carbene adducts of phosphorus(I) cations
Chem.Commun., 2015, 51, 7741
7117036 CIFC49 H48 B N4 O PP -111.0003; 13.6439; 14.0585
77.876; 79.118; 87.493		2025.82Justin F. Binder; Ala'aeddeen Swidan; Martin Tang; Jennifer H. Nguyen; Charles L. B. Macdonald
Remarkably stable chelating bis-N-heterocyclic carbene adducts of phosphorus(I) cations
Chem.Commun., 2015, 51, 7741
7117037 CIFC46 H42 B Cl2 N4 PP -111.012; 13.4813; 13.8114
78.513; 77.138; 87.889		1958.84Justin F. Binder; Ala'aeddeen Swidan; Martin Tang; Jennifer H. Nguyen; Charles L. B. Macdonald
Remarkably stable chelating bis-N-heterocyclic carbene adducts of phosphorus(I) cations
Chem.Commun., 2015, 51, 7741
7117038 CIFC20 H24 Au Cl F6 N8 O6 P2 S2C 1 2/c 120.7657; 14.6302; 13.2427
90; 123.628; 90		3349.9Justin F. Binder; Ala'aeddeen Swidan; Martin Tang; Jennifer H. Nguyen; Charles L. B. Macdonald
Remarkably stable chelating bis-N-heterocyclic carbene adducts of phosphorus(I) cations
Chem.Commun., 2015, 51, 7741
7117039 CIFC88 H0.5 Cl12 Co14 N48 O4P -117.9278; 18.574; 28.0345
74.801; 87.6211; 61.281		7861.1Fu-Ping Huang; Peng-Fei Yao; Hai-Ye Li; Qing Yu; He-Dong Bian; Hong Liang
An intuitional hierarchical assembly of cluster-organic frameworks with a thickness of 1.97 nm from a discrete Co14 cluster
Chem.Commun., 2015, 51, 7598
7117040 CIFC31.33 H26 Cl2 Co4.67 N16 O3.33P -323.2046; 23.2046; 17.2439
90; 90; 120		8041.1Fu-Ping Huang; Peng-Fei Yao; Hai-Ye Li; Qing Yu; He-Dong Bian; Hong Liang
An intuitional hierarchical assembly of cluster-organic frameworks with a thickness of 1.97 nm from a discrete Co14 cluster
Chem.Commun., 2015, 51, 7598
7117041 CIFC29 H16 B F10 N O2P -111.0372; 11.6357; 11.866
111.316; 103.831; 100.243		1318.13Lu Wang; Kai Wang; Houyu Zhang; Chuanjun Jiao; Bo Zou; Kaiqi Ye; Hongyu Zhang; Yue Wang
The facile realization of RGB luminescence based on one yellow emissive four-coordinate organoboron material
Chem.Commun., 2015, 51, 7701
7117042 CIFC29 H16 B F10 N O2P -110.4884; 11.0467; 11.5358
95.268; 98.354; 99.426		1295.34Lu Wang; Kai Wang; Houyu Zhang; Chuanjun Jiao; Bo Zou; Kaiqi Ye; Hongyu Zhang; Yue Wang
The facile realization of RGB luminescence based on one yellow emissive four-coordinate organoboron material
Chem.Commun., 2015, 51, 7701
7117043 CIFC26 H28 N2 O3P 1 21/c 17.2482; 12.373; 24.27
90; 97.43; 90		2158.3Timothy K. Beng; Hironori Takeuchi; Manuel Weber; Richmond Sarpong
Stereocontrolled synthesis of vicinally functionalized piperidines by nucleophilic beta-addition of alkyllithiums to alpha-aryl substituted piperidine enecarbamates
Chem.Commun., 2015, 51, 7653
7117044 CIFC27 H30 N2 O3P -17.215; 12.5739; 13.1379
70.358; 86.908; 85.384		1118.43Timothy K. Beng; Hironori Takeuchi; Manuel Weber; Richmond Sarpong
Stereocontrolled synthesis of vicinally functionalized piperidines by nucleophilic beta-addition of alkyllithiums to alpha-aryl substituted piperidine enecarbamates
Chem.Commun., 2015, 51, 7653
7117045 CIFC36 H32 SiP 1 21/c 114.0394; 10.71244; 18.6534
90; 107.182; 90		2680.2Shunsuke Sueki; Yoichiro Kuninobu
Rhodium-catalysed synthesis of multi-substituted silylindenes from aryl alkynes and hydrosilanes via C-H bond activation
Chem.Commun., 2015, 51, 7685
7117046 CIFC39 H35 B Fe N6 O3P b c a11.861; 22.463; 25.58
90; 90; 90		6815Debobrata Sheet; Shrabanti Bhattacharya; Tapan Kanti Paine
Dioxygen activation and two consecutive oxidative decarboxylations of phenylpyruvate by nonheme iron(II) complexes: functional models of hydroxymandelate synthase (HMS) and CloR
Chem.Commun., 2015, 51, 7681
7117047 CIFC48 H67 N O2 ZrP 21 21 2111.2139; 17.371; 23.2242
90; 90; 90		4524Qiu Sun; Yaorong Wang; Dan Yuan; Yingming Yao; Qi Shen
Zirconium catalysed intermolecular hydroamination reactions of secondary amines with alkynes
Chem.Commun., 2015, 51, 7633
7117048 CIFC19 H18 Mn N9 S5C 1 2/c 111.928; 13.662; 17.417
90; 105.321; 90		2737.4Dariusz Matoga; Marcin Oszajca; Marcin Molenda
Ground to conduct: mechanochemical synthesis of a metal-organic framework with high proton conductivity
Chem.Commun., 2015, 51, 7637
7117049 CIFC14 H8 Mn N6 O4 S2P 1 21/c 19.723; 14.061; 7.1516
90; 97.92; 90		968.4Dariusz Matoga; Marcin Oszajca; Marcin Molenda
Ground to conduct: mechanochemical synthesis of a metal-organic framework with high proton conductivity
Chem.Commun., 2015, 51, 7637
7117050 CIFC28 H28 N4 O S8P 1 21/n 18.8402; 14.927; 23.777
90; 96.92; 90		3114.7Anup Rana; Sangsu Lee; Dongho Kim; Pradeepta K. Panda
Beta-Octakis(methylthio)porphycenes: synthesis, characterisation and third order nonlinear optical studies
Chem.Commun., 2015, 51, 7705
7117051 CIFC14 H16 N2 O2 S4P 1 21/c 14.918; 8.5807; 19.8851
90; 97.072; 90		832.76Anup Rana; Sangsu Lee; Dongho Kim; Pradeepta K. Panda
Beta-Octakis(methylthio)porphycenes: synthesis, characterisation and third order nonlinear optical studies
Chem.Commun., 2015, 51, 7705
7117052 CIFC18 H18 Cl2 Co N4P -111.574; 15.2041; 19.9081
90.06; 103.277; 110.696		3176.6Sharon Lai-Fung Chan; Tsz Lung Lam; Chen Yang; Siu-Cheong Yan; Nga Man Cheng
A robust and efficient cobalt molecular catalyst for CO2 reduction
Chem.Commun., 2015, 51, 7799
7117053 CIFC18 H18 Fe SiP 21 21 219.6741; 10.9465; 29.0292
90; 90; 90		3074.1Takanori Shibata; Tsubasa Shizuno; Tomoya Sasaki
Enantioselective synthesis of planar-chiral benzosiloloferrocenes by Rh-catalyzed intramolecular C-H silylation
Chem.Commun., 2015, 51, 7802
7117054 CIFC22 H26P 1 21/c 112.4844; 8.092; 17.7356
90; 92.499; 90		1790.01Takashi Otani; Kanako Ueki; Kinryo Cho; Kan Kanai; Kotaro Tateno; Takao Saito
Construction of dibenzo-fused seven- to nine-membered carbocycles via Bronsted acid-promoted intramolecular Friedel-Crafts-type alkenylation
Chem.Commun., 2015, 51, 7895
7117055 CIFC21 H24P 1 21/n 15.881; 16.344; 17.969
90; 95.555; 90		1719Takashi Otani; Kanako Ueki; Kinryo Cho; Kan Kanai; Kotaro Tateno; Takao Saito
Construction of dibenzo-fused seven- to nine-membered carbocycles via Bronsted acid-promoted intramolecular Friedel-Crafts-type alkenylation
Chem.Commun., 2015, 51, 7895
7117056 CIFC74 H48 Cl8 F8 N4 O18 Ru4P -110.641; 14.224; 15.449
91.028; 110.013; 109.772		2043.8Hiroki Fukunaga; Takafumi Yoshino; Hajime Sagayama; Jun-ichi Yamaura; Taka-hisa Arima; Wataru Kosaka; Hitoshi Miyasaka
A charge-disproportionate ordered state with delta = 0.75 in a chemically sensitive donor/acceptor D^delta^+2A^2delta-^ layered framework
Chem.Commun., 2015, 51, 7795
7117057 CIFC74 H48 Cl8 F8 N4 O18 Ru4P -19.994; 14.265; 14.433
82.602; 79.222; 82.472		1992.4Hiroki Fukunaga; Takafumi Yoshino; Hajime Sagayama; Jun-ichi Yamaura; Taka-hisa Arima; Wataru Kosaka; Hitoshi Miyasaka
A charge-disproportionate ordered state with delta = 0.75 in a chemically sensitive donor/acceptor D^delta^+2A^2delta-^ layered framework
Chem.Commun., 2015, 51, 7795
7117058 CIFC70 H40 F8 N4 O18 Ru4P -110.551; 13.573; 30.865
80.126; 79.263; 74.635		4152.6Hiroki Fukunaga; Takafumi Yoshino; Hajime Sagayama; Jun-ichi Yamaura; Taka-hisa Arima; Wataru Kosaka; Hitoshi Miyasaka
A charge-disproportionate ordered state with delta = 0.75 in a chemically sensitive donor/acceptor D^delta^+2A^2delta-^ layered framework
Chem.Commun., 2015, 51, 7795
7117059 CIFC102 H108 Co2 N18 Ni4 O24 Tb2P 1 21/c 116.8968; 22.282; 19.3332
90; 106.728; 90		6970.8Sebastien Dhers; Jean-Pierre Costes; Philippe Guionneau; Carley Paulsen; Laure Vendier; Jean-Pascal Sutter
On the importance of ferromagnetic exchange between transition metals in field-free SMMs: examples of ring-shaped hetero-trimetallic [(LnNi2){W(CN)8}]2 compounds
Chem.Commun., 2015, 51, 7875
7117060 CIFC120 H134 Dy2 N34 Ni4 O20 W2P -116.712; 20.624; 20.852
87.814; 89.178; 74.215		6910.9Sebastien Dhers; Jean-Pierre Costes; Philippe Guionneau; Carley Paulsen; Laure Vendier; Jean-Pascal Sutter
On the importance of ferromagnetic exchange between transition metals in field-free SMMs: examples of ring-shaped hetero-trimetallic [(LnNi2){W(CN)8}]2 compounds
Chem.Commun., 2015, 51, 7875
7117061 CIFC120 H134 N34 Ni4 O20 Tb2 W2P -116.7341; 20.6199; 20.8979
87.881; 89.214; 74.309		6937.4Sebastien Dhers; Jean-Pierre Costes; Philippe Guionneau; Carley Paulsen; Laure Vendier; Jean-Pascal Sutter
On the importance of ferromagnetic exchange between transition metals in field-free SMMs: examples of ring-shaped hetero-trimetallic [(LnNi2){W(CN)8}]2 compounds
Chem.Commun., 2015, 51, 7875
7117062 CIFC120 H134 N34 Ni4 O20 W2 Y2P -116.71; 20.663; 20.852
87.797; 89.185; 74.158		6921.1Sebastien Dhers; Jean-Pierre Costes; Philippe Guionneau; Carley Paulsen; Laure Vendier; Jean-Pascal Sutter
On the importance of ferromagnetic exchange between transition metals in field-free SMMs: examples of ring-shaped hetero-trimetallic [(LnNi2){W(CN)8}]2 compounds
Chem.Commun., 2015, 51, 7875
7117066 CIFC23 H18 N2 O SP 1 21/c 116.26; 8.0578; 16.7298
90; 118.216; 90		1931.47Xiaohan Ye; Jeffrey L. Petersen; Xiaodong Shi
Nickel-catalyzed directed sulfenylation of sp2 and sp3 C-H bonds
Chem.Commun., 2015, 51, 7863
7117067 CIFC22 H15 Cl N2 O SP 1 21/n 112.0459; 10.3781; 15.4051
90; 107.395; 90		1837.78Xiaohan Ye; Jeffrey L. Petersen; Xiaodong Shi
Nickel-catalyzed directed sulfenylation of sp2 and sp3 C-H bonds
Chem.Commun., 2015, 51, 7863
7117068 CIFC32 H47 Au N2 SP -19.6005; 11.3245; 15.2126
74.9336; 82.8296; 77.8418		1556.94Kazunori Miyamoto; Masaya Hirobe; Masanobu Uchiyama; Masahito Ochiai
Stereoselective synthesis and reaction of gold(I) (Z)-enethiolates
Chem.Commun., 2015, 51, 7962
7117069 CIFC8 H6 F3 I O6 SP -15.4618; 9.7781; 11.8765
98.2; 93.463; 91.657		626.19Akira Yoshimura; Khiem C. Nguyen; Scott C. Klasen; Akio Saito; Victor N. Nemykin; Viktor V. Zhdankin
Preparation, structure, and versatile reactivity of pseudocyclic benziodoxole triflate, new hypervalent iodine reagent
Chem.Commun., 2015, 51, 7835
7117071 CIFC40 H50 Cl2 Cu N2 O2C 1 2 113.608; 10.347; 14.528
90; 117.341; 90		1817.1Koichi Tanaka; Tomoharu Iwashita; Erika Yoshida; Tomomi Ishikawa; Shinya Otuka; Zofia Urbanczyk-Lipkowska; Hiroki Takahashi
Solvent-dependent strong asymmetric amplification in the catalytic enantioselective Henry reaction using the trans-N,N'-bis-biphenyl-4-ylmethyl-cyclohexane-1,2-diamine-CuCl2 complex
Chem.Commun., 2015, 51, 7907
7117072 CIFC36 H42 Cl2 Cu N2 O2P 1 21 113.8568; 15.8847; 15.2073
90; 96.046; 90		3328.68Koichi Tanaka; Tomoharu Iwashita; Erika Yoshida; Tomomi Ishikawa; Shinya Otuka; Zofia Urbanczyk-Lipkowska; Hiroki Takahashi
Solvent-dependent strong asymmetric amplification in the catalytic enantioselective Henry reaction using the trans-N,N'-bis-biphenyl-4-ylmethyl-cyclohexane-1,2-diamine-CuCl2 complex
Chem.Commun., 2015, 51, 7907
7117073 CIFC32 H34 Cl2 Cu N2C 1 2/c 125.878; 10.4574; 10.7037
90; 102.636; 90		2826.44Koichi Tanaka; Tomoharu Iwashita; Erika Yoshida; Tomomi Ishikawa; Shinya Otuka; Zofia Urbanczyk-Lipkowska; Hiroki Takahashi
Solvent-dependent strong asymmetric amplification in the catalytic enantioselective Henry reaction using the trans-N,N'-bis-biphenyl-4-ylmethyl-cyclohexane-1,2-diamine-CuCl2 complex
Chem.Commun., 2015, 51, 7907
7117074 CIFC21 H45 Cu3 I6 N3P 2 21 218.52016; 31.2866; 13.2813
90; 90; 90		3540.35Shi-Li Li; Fu-Qiang Zhang; Xian-Ming Zhang
An organic-ligand-free thermochromic luminescent cuprous iodide trinuclear cluster: evidence for cluster centered emission and configuration distortion with temperature
Chem.Commun., 2015, 51, 8062
7117075 CIFC18 H42 Cu3 I6 N3P 2 21 218.5342; 31.3102; 13.3245
90; 90; 90		3560.4Shi-Li Li; Fu-Qiang Zhang; Xian-Ming Zhang
An organic-ligand-free thermochromic luminescent cuprous iodide trinuclear cluster: evidence for cluster centered emission and configuration distortion with temperature
Chem.Commun., 2015, 51, 8062
7117076 CIFC21 H45 Cu3.01 I6 N3P 2 21 218.5719; 13.4018; 31.305
90; 90; 90		3596.3Shi-Li Li; Fu-Qiang Zhang; Xian-Ming Zhang
An organic-ligand-free thermochromic luminescent cuprous iodide trinuclear cluster: evidence for cluster centered emission and configuration distortion with temperature
Chem.Commun., 2015, 51, 8062
7117077 CIFC21 H45 Cu3 I6 N3P 2 21 218.6; 31.212; 13.5728
90; 90; 90		3643.3Shi-Li Li; Fu-Qiang Zhang; Xian-Ming Zhang
An organic-ligand-free thermochromic luminescent cuprous iodide trinuclear cluster: evidence for cluster centered emission and configuration distortion with temperature
Chem.Commun., 2015, 51, 8062
7117078 CIFC21 H45 Cu2.99 I6 N3P 2 21 218.6034; 13.5945; 31.256
90; 90; 90		3655.7Shi-Li Li; Fu-Qiang Zhang; Xian-Ming Zhang
An organic-ligand-free thermochromic luminescent cuprous iodide trinuclear cluster: evidence for cluster centered emission and configuration distortion with temperature
Chem.Commun., 2015, 51, 8062
7117079 CIFC21 H45 Cu3.01 I6 N3P 2 21 218.6312; 13.6767; 31.2048
90; 90; 90		3683.6Shi-Li Li; Fu-Qiang Zhang; Xian-Ming Zhang
An organic-ligand-free thermochromic luminescent cuprous iodide trinuclear cluster: evidence for cluster centered emission and configuration distortion with temperature
Chem.Commun., 2015, 51, 8062
7117080 CIFC44 H32 Cd2 Cl2 N4 O8P -18.9041; 17.9362; 18.9879
100.842; 102.263; 103.409		2791.2Cheng Chen; Li-Xuan Cai; Bin Tan; Ya-Jun Zhang; Xiao-Dong Yang; Jie Zhang
Ammonia detection by using flexible Lewis acidic sites in luminescent porous frameworks constructed from a bipyridinium derivative
Chem.Commun., 2015, 51, 8189
7117081 CIFC44 H32 Br2 Cd2 N4 O8P -19.0867; 18.0356; 18.8207
102.462; 103.387; 100.625		2839.4Cheng Chen; Li-Xuan Cai; Bin Tan; Ya-Jun Zhang; Xiao-Dong Yang; Jie Zhang
Ammonia detection by using flexible Lewis acidic sites in luminescent porous frameworks constructed from a bipyridinium derivative
Chem.Commun., 2015, 51, 8189
7117082 CIFC20 H17 N O2 SP 1 21 15.7758; 20.087; 7.3139
90; 92.951; 90		847.42Li Lin; Yuhong Yang; Mei Wang; Luhao Lai; Yarong Guo; Rui Wang
Oxidative N-heterocyclic carbene catalyzed stereoselective annulation of simple aldehydes and 5-alkenyl thiazolones
Chem.Commun., 2015, 51, 8134
7117083 CIFC20 H17 N O2 SP 1 21 15.7825; 20.098; 7.311
90; 92.824; 90		848.6Li Lin; Yuhong Yang; Mei Wang; Luhao Lai; Yarong Guo; Rui Wang
Oxidative N-heterocyclic carbene catalyzed stereoselective annulation of simple aldehydes and 5-alkenyl thiazolones
Chem.Commun., 2015, 51, 8134
7117084 CIFC25 H21 Cl3 N2 SiP 1 21/c 110.681; 19.442; 11.152
90; 101.368; 90		2270.4Takayuki Tanaka; Atsuhiro Osuka
Tetracoordinate silicon complexes of 1,2-bis(indol-2-yl)benzene as blue-emitting dyes in the solid state
Chem.Commun., 2015, 51, 8123
7117085 CIFC26 H24 N2 SiP 1 21/a 114.1331; 7.8144; 18.4958
90; 102.186; 90		1996.68Takayuki Tanaka; Atsuhiro Osuka
Tetracoordinate silicon complexes of 1,2-bis(indol-2-yl)benzene as blue-emitting dyes in the solid state
Chem.Commun., 2015, 51, 8123
7117086 CIFC36 H28 N2 O0.5 SiC 1 2/c 121.767; 12.983; 19.854
90; 108.48; 90		5321.4Takayuki Tanaka; Atsuhiro Osuka
Tetracoordinate silicon complexes of 1,2-bis(indol-2-yl)benzene as blue-emitting dyes in the solid state
Chem.Commun., 2015, 51, 8123
7117087 CIFC73 H58 Cl2 N4 Si2P 32 2 113.156; 13.156; 28.415
90; 90; 120		4259.2Takayuki Tanaka; Atsuhiro Osuka
Tetracoordinate silicon complexes of 1,2-bis(indol-2-yl)benzene as blue-emitting dyes in the solid state
Chem.Commun., 2015, 51, 8123
7117088 CIFC22 H22 Cu4 N2 O18 S2F d d 224.748; 32.354; 21.712
90; 90; 90		17385Xing; Meng,ab; Shu-Yan Song; Xue-Zhi Song; Min Zhu; Shu-Na Zhao; Lan-Lan Wu; Hong-Jie Zhang
A tetranuclear copper cluster-based MOF with sulfonate-carboxylate ligands exhibiting high proton conduction properties
Chem.Commun., 2015, 51, 8150
7117089 CIFC40 H38 Cl2 Fe2 N2 O2P 1 21/n 110.271; 20.397; 17.702
90; 105.15; 90		3579.6Fabio Marchetti; Stefano Zacchini; Valerio Zanotti
Carbon monoxide-isocyanide coupling promoted by acetylide addition to a diiron complex
Chem.Commun., 2015, 51, 8101
7117090 CIFC42 H43 Fe2 N2 O2.5P 1 21/c 116.505; 14.661; 17.918
90; 111.59; 90		4031.6Fabio Marchetti; Stefano Zacchini; Valerio Zanotti
Carbon monoxide-isocyanide coupling promoted by acetylide addition to a diiron complex
Chem.Commun., 2015, 51, 8101
7117097 CIFC20 H19 BrP 1 n 16.0119; 15.806; 8.3765
90; 98.292; 90		787.65Xin-Xing Wu; Yi Shen; Wen-Long Chen; Si Chen; Xin-Hua Hao; Yu Xia; Peng-Fei Xu; Yong-Min Liang
Palladium-catalyzed ring opening of norbornene: efficient synthesis of methylenecyclopentane derivatives
Chem.Commun., 2015, 51, 8031
7117098 CIFC21 H22 OP 1 21/c 117.781; 15.3478; 6.0728
90; 99.114; 90		1636.34Xin-Xing Wu; Yi Shen; Wen-Long Chen; Si Chen; Xin-Hua Hao; Yu Xia; Peng-Fei Xu; Yong-Min Liang
Palladium-catalyzed ring opening of norbornene: efficient synthesis of methylenecyclopentane derivatives
Chem.Commun., 2015, 51, 8031
7117099 CIFC2 H11 Cl2 N3 O2 PtP -17.103; 9.028; 13.105
90.17; 94.67; 90.44		837.5Giorgio Pelosi; Mauro Ravera; Elisabetta Gabano; Federico Fregonese; Domenico Osella
Unprecedented one-pot synthesis of an unsymmetrical cisplatin-based Pt(IV)-acetamidato complex
Chem.Commun., 2015, 51, 8051
7117100 CIFC15 H21 N O4P 21 21 2110.9624; 11.2771; 12.2022
90; 90; 90		1508.49Alejandra Millan-Ortiz; German Lopez-Valdez; Fernando Cortez-Guzman; Luis D. Miranda
A novel carbamoyl radical based dearomatizing spiroacylation process
Chem.Commun., 2015, 51, 8345
7117101 CIFC15 H14 Br NP b c a19.318; 7.18486; 19.6634
90; 90; 90		2729.22Johannes F. Franz; Wolfgang B. Kraus; Kirsten Zeitler
No photocatalyst required ‒ versatile, visible light mediated transformations with polyhalomethanes
Chem.Commun., 2015, 51, 8280
7117102 CIFC76 H28 F10 O2I 41/a28.7283; 28.7283; 12.1809
90; 90; 90		10053.1Baddigam Kiran Reddy; Santosh C. Gadekar; Venkataramanarao G. Anand
Non-covalent composites of antiaromatic isophlorin-fullerene
Chem.Commun., 2015, 51, 8276
7117103 CIFC46 H20 Cl6 F10 O4P 1 21/c 110.3234; 15.5838; 13.5017
90; 102.531; 90		2120.4Baddigam Kiran Reddy; Santosh C. Gadekar; Venkataramanarao G. Anand
Non-covalent composites of antiaromatic isophlorin-fullerene
Chem.Commun., 2015, 51, 8276
7117104 CIFC82 H9 F5 O2C 1 2/c 126.962; 13.616; 24.071
90; 97.746; 90		8756Baddigam Kiran Reddy; Santosh C. Gadekar; Venkataramanarao G. Anand
Non-covalent composites of antiaromatic isophlorin-fullerene
Chem.Commun., 2015, 51, 8276
7117105 CIFC78.25 H24 F10 O4.75P -115.928; 19.014; 20.624
101.456; 110.099; 108.543		5218.1Baddigam Kiran Reddy; Santosh C. Gadekar; Venkataramanarao G. Anand
Non-covalent composites of antiaromatic isophlorin-fullerene
Chem.Commun., 2015, 51, 8276
7117106 CIFC32 H10 F10 O4P 1 21/c 114.649; 10.269; 8.425
90; 99.012; 90		1251.7Baddigam Kiran Reddy; Santosh C. Gadekar; Venkataramanarao G. Anand
Non-covalent composites of antiaromatic isophlorin-fullerene
Chem.Commun., 2015, 51, 8276
7117107 CIFC106 H26 F10 O4P 1 21/c 127.439; 9.7293; 23.787
90; 97.272; 90		6299.2Baddigam Kiran Reddy; Santosh C. Gadekar; Venkataramanarao G. Anand
Non-covalent composites of antiaromatic isophlorin-fullerene
Chem.Commun., 2015, 51, 8276
7117108 CIFC8 H14 Cr Mn N O12P -3 1 c8.2865; 8.2865; 13.88
90; 90; 120		825.4Jiong-Peng Zhao; Song-De Han; Xue Jiang; Sui-Jun Liu; Ran Zhao; Ze Chang; Xian-He Bu
A heterometallic strategy to achieve a large magnetocaloric effect in polymeric 3d complexes
Chem.Commun., 2015, 51, 8288
7117109 CIFC7 H12 Cr Mn N O12P -3 1 c8.2708; 8.2708; 14.088
90; 90; 120		834.6Jiong-Peng Zhao; Song-De Han; Xue Jiang; Sui-Jun Liu; Ran Zhao; Ze Chang; Xian-He Bu
A heterometallic strategy to achieve a large magnetocaloric effect in polymeric 3d complexes
Chem.Commun., 2015, 51, 8288
7117110 CIFC8 H14 Al Mn N O12P -3 1 c8.2179; 8.2179; 13.646
90; 90; 120		798.1Jiong-Peng Zhao; Song-De Han; Xue Jiang; Sui-Jun Liu; Ran Zhao; Ze Chang; Xian-He Bu
A heterometallic strategy to achieve a large magnetocaloric effect in polymeric 3d complexes
Chem.Commun., 2015, 51, 8288
7117111 CIFC8 H14 Cr Mg N O12P -3 1 c8.1565; 8.1565; 13.705
90; 90; 120		789.6Jiong-Peng Zhao; Song-De Han; Xue Jiang; Sui-Jun Liu; Ran Zhao; Ze Chang; Xian-He Bu
A heterometallic strategy to achieve a large magnetocaloric effect in polymeric 3d complexes
Chem.Commun., 2015, 51, 8288
7117112 CIFC34 H53 Cu N2 O S SiC 1 2/c 128.986; 12.887; 19.067
90; 92.619; 90		7115Mahmood Azizpoor Fard; Florian Weigend; John F. Corrigan
Simple but effective: thermally stable Cu-ESiMe3via NHC ligation
Chem.Commun., 2015, 51, 8361
7117113 CIFC34 H53 Cu N2 O Se SiC 1 2/c 129.597; 12.842; 19.184
90; 93.196; 90		7280Mahmood Azizpoor Fard; Florian Weigend; John F. Corrigan
Simple but effective: thermally stable Cu-ESiMe3via NHC ligation
Chem.Commun., 2015, 51, 8361
7117114 CIFC30 H45 Cu N2 Si TeP 1 21/n 19.789; 21.443; 15.58
90; 100.673; 90		3214Mahmood Azizpoor Fard; Florian Weigend; John F. Corrigan
Simple but effective: thermally stable Cu-ESiMe3via NHC ligation
Chem.Commun., 2015, 51, 8361
7117115 CIFC58 H80 Cl8 Cu2 Hg N4 S2P 1 21/n 113.026; 16.803; 16.264
90; 106.93; 90		3405.5Mahmood Azizpoor Fard; Florian Weigend; John F. Corrigan
Simple but effective: thermally stable Cu-ESiMe3via NHC ligation
Chem.Commun., 2015, 51, 8361
7117116 CIFC26 H15 N O4 S ZnP -17.9902; 11.043; 13.43
105.463; 102.922; 107.508		1028Zhi-Qiang Shi; Zi-Jian Guo; He-Gen Zheng
Two luminescent Zn(II) metal-organic frameworks for exceptionally selective detection of picric acid explosives
Chem.Commun., 2015, 51, 8300
7117117 CIFC36 H24 N4 O4 S ZnP b c a18.379; 10.6606; 31.736
90; 90; 90		6218.1Zhi-Qiang Shi; Zi-Jian Guo; He-Gen Zheng
Two luminescent Zn(II) metal-organic frameworks for exceptionally selective detection of picric acid explosives
Chem.Commun., 2015, 51, 8300
7117118 CIFC48 H47 Co N3 O8P -112.848; 14.185; 15.785
114.87; 97.126; 109.338		2343.4Chuan-Lei Zhang; Yan-Le Li; Ting Wang; Ze-Min Ju; He-Gen Zheng; Jing Ma
Three different metal-organic frameworks derived from a one-pot crystallization and their controllable synthesis
Chem.Commun., 2015, 51, 8338
7117119 CIFC60 H65 Co N4 O11P -110.6129; 14.9365; 18.7658
108.987; 92.348; 106.134		2673.7Chuan-Lei Zhang; Yan-Le Li; Ting Wang; Ze-Min Ju; He-Gen Zheng; Jing Ma
Three different metal-organic frameworks derived from a one-pot crystallization and their controllable synthesis
Chem.Commun., 2015, 51, 8338
7117120 CIFC72 H64 Co3 N4 O14C 1 2/c 126.758; 10.635; 29.565
90; 116.906; 90		7503Chuan-Lei Zhang; Yan-Le Li; Ting Wang; Ze-Min Ju; He-Gen Zheng; Jing Ma
Three different metal-organic frameworks derived from a one-pot crystallization and their controllable synthesis
Chem.Commun., 2015, 51, 8338
7117121 CIFC46 H25 Cl3 F10 N6 O2P 4113.62; 13.62; 22.0245
90; 90; 90		4085.64Rafal Orlowski; Olena Vakuliuk; Maria Pia Gullo; Oksana Danylyuk; Barbara Ventura; Beata Koszarna; Anna Tarnowska; Nina Jaworska; Andrea Barbieri; Daniel T. Gryko
Self-assembling corroles
Chem.Commun., 2015, 51, 8284
7117122 CIFC44 H28 Cl3 F10 N5 O2P -111.084; 13.9124; 15.6917
95.169; 107.245; 111.916		2088.2Rafal Orlowski; Olena Vakuliuk; Maria Pia Gullo; Oksana Danylyuk; Barbara Ventura; Beata Koszarna; Anna Tarnowska; Nina Jaworska; Andrea Barbieri; Daniel T. Gryko
Self-assembling corroles
Chem.Commun., 2015, 51, 8284
7117123 CIFC30 H8 F10 N4P -15.996; 7.348; 13.198
87.325; 86.01; 71.49		549.9Santosh C. Gadekar; Baddigam Kiran Reddy; Venkataramanarao G. Anand
Metal assisted cyclodimerization of doubly N-confused dipyrrins into planar aza-heptalenes
Chem.Commun., 2015, 51, 8342
7117124 CIFC30 H8 F10 N4 OP 1 21/c 128.021; 11.565; 7.319
90; 95.576; 90		2360.6Santosh C. Gadekar; Baddigam Kiran Reddy; Venkataramanarao G. Anand
Metal assisted cyclodimerization of doubly N-confused dipyrrins into planar aza-heptalenes
Chem.Commun., 2015, 51, 8342
7117125 CIFC31 H10 F10 N4P 16.1461; 7.3648; 14.031
76.834; 82.082; 72.763		588.95Santosh C. Gadekar; Baddigam Kiran Reddy; Venkataramanarao G. Anand
Metal assisted cyclodimerization of doubly N-confused dipyrrins into planar aza-heptalenes
Chem.Commun., 2015, 51, 8342
7117126 CIFC40 H72 Mo2 N32 O11 Zn4P c a 2114.7778; 14.8566; 31.0576
90; 90; 90		6818.6N. Bridonneau; J. Long; J.-L. Cantin; J. von Bardeleben; S. Pillet; E.-E. Bendeif; D. Aravena; E. Ruiz; V. Marvaud
First evidence of light-induced spin transition in molybdenum(IV)
Chem.Commun., 2015, 51, 8229
7117127 CIFC34 H42 N4 O11 SP 1 21/n 18.6053; 18.642; 12.19
90; 98.319; 90		1934.9M. Pandeeswar; Harshavardhan Khare; Suryanarayanarao Ramakumar; T. Govindaraju
Crystallographic insight-guided nanoarchitectonics and conductivity modulation of an n-type organic semiconductor through peptide conjugation
Chem.Commun., 2015, 51, 8315
7117128 CIFC28 H28 N4 O10P 21 21 219.942; 14.412; 18.805
90; 90; 90		2694.5M. Pandeeswar; Harshavardhan Khare; Suryanarayanarao Ramakumar; T. Govindaraju
Crystallographic insight-guided nanoarchitectonics and conductivity modulation of an n-type organic semiconductor through peptide conjugation
Chem.Commun., 2015, 51, 8315
7117129 CIFC28 H28 N4 O10P 21 21 219.9943; 14.47; 18.796
90; 90; 90		2718.2M. Pandeeswar; Harshavardhan Khare; Suryanarayanarao Ramakumar; T. Govindaraju
Crystallographic insight-guided nanoarchitectonics and conductivity modulation of an n-type organic semiconductor through peptide conjugation
Chem.Commun., 2015, 51, 8315
7117130 CIFC27 H21 Br O5P 1 21/n 18.0879; 27.2026; 10.7134
90; 93.374; 90		2352.99Jieru Yang; Ao Mao; Zhenting Yue; Wenxuan Zhu; Xuewei Luo; Chuwei Zhu; Yuanjing Xiao; Junliang Zhang
A simple base-mediated synthesis of diverse functionalized ring-fluorinated 4H-pyrans via double direct C-F substitutions
Chem.Commun., 2015, 51, 8326
7117131 CIFC16 H13 F O2C 1 2/c 125.8977; 8.7711; 11.9279
90; 111.181; 90		2526.4Jieru Yang; Ao Mao; Zhenting Yue; Wenxuan Zhu; Xuewei Luo; Chuwei Zhu; Yuanjing Xiao; Junliang Zhang
A simple base-mediated synthesis of diverse functionalized ring-fluorinated 4H-pyrans via double direct C-F substitutions
Chem.Commun., 2015, 51, 8326
7117133 CIFC20 H16 Cl3 F2 N O Pt SP 1 21 15.897; 13.924; 12.852
90; 96.001; 90		1049.5Paul A. Shaw; Jessica M. Phillips; Christopher P. Newman; Guy J. Clarkson; Jonathan P. Rourke
Intramolecular transcyclometallation: the exchange of an aryl-Pt bond for an alkyl-Pt bond via an agostic intermediate
Chem.Commun., 2015, 51, 8365
7117134 CIFC20 H18 F2 N P PtC 1 2/c 123.9938; 12.5106; 12.1687
90; 107.325; 90		3487.04Paul A. Shaw; Jessica M. Phillips; Christopher P. Newman; Guy J. Clarkson; Jonathan P. Rourke
Intramolecular transcyclometallation: the exchange of an aryl-Pt bond for an alkyl-Pt bond via an agostic intermediate
Chem.Commun., 2015, 51, 8365
7117135 CIFC29 H36 Cl2 F2 N P PtP b c a14.9738; 15.8809; 24.6498
90; 90; 90		5861.7Paul A. Shaw; Jessica M. Phillips; Christopher P. Newman; Guy J. Clarkson; Jonathan P. Rourke
Intramolecular transcyclometallation: the exchange of an aryl-Pt bond for an alkyl-Pt bond via an agostic intermediate
Chem.Commun., 2015, 51, 8365
7117136 CIFC29.5 H36.5 Cl3.5 F2 N P PtP 1 21/c 142.5003; 8.95573; 15.7762
90; 92.949; 90		5996.8Paul A. Shaw; Jessica M. Phillips; Christopher P. Newman; Guy J. Clarkson; Jonathan P. Rourke
Intramolecular transcyclometallation: the exchange of an aryl-Pt bond for an alkyl-Pt bond via an agostic intermediate
Chem.Commun., 2015, 51, 8365
7117137 CIFC29 H36 Cl2 F2 N P PtP n a 2117.9634; 13.9987; 11.0698
90; 90; 90		2783.66Paul A. Shaw; Jessica M. Phillips; Christopher P. Newman; Guy J. Clarkson; Jonathan P. Rourke
Intramolecular transcyclometallation: the exchange of an aryl-Pt bond for an alkyl-Pt bond via an agostic intermediate
Chem.Commun., 2015, 51, 8365
7117138 CIFC82 H20 Cl4P b c a17.0287; 18.1277; 29.437
90; 90; 90		9086.9Ran Tao; Tomokazu Umeyama; Tomohiro Higashino; Tomoyuki Koganezawa; Hiroshi Imahori
A single cis-2 regioisomer of ethylene-tethered indene dimer-fullerene adduct as an electron-acceptor in polymer solar cells
Chem.Commun., 2015, 51, 8233
7117139 CIFC44 H71 B2 F8 N4 Ni O6.5P 1 21 116.4359; 15.6364; 19.2398
90; 92.863; 90		4938.4Yulong Zhang; Na Yang; Xiaohua Liu; Jing Guo; Xiying Zhang; Lili Lin; Changwei Hu; Xiaoming Feng
Reversal of enantioselective Friedel-Crafts C3-alkylation of pyrrole by slightly tuning the amide units of N,N'-dioxide ligands
Chem.Commun., 2015, 51, 8432
7117140 CIFC55 H92 B2 F8 N4 Ni O8I 1 2 116.452; 8.8684; 22.2394
90; 110.682; 90		3035.68Yulong Zhang; Na Yang; Xiaohua Liu; Jing Guo; Xiying Zhang; Lili Lin; Changwei Hu; Xiaoming Feng
Reversal of enantioselective Friedel-Crafts C3-alkylation of pyrrole by slightly tuning the amide units of N,N'-dioxide ligands
Chem.Commun., 2015, 51, 8432
7117141 CIFC32 H24 B F15 Si2P -113.8787; 14.2041; 19.8693
101.859; 98.658; 117.694		3254.49Christina Eller; Gerald Kehr; Constantin G. Daniliuc; Gerhard Erker
Unusual product formation in a 1,1-carboboration reaction
Chem.Commun., 2015, 51, 8436
7117142 CIFC23 H20 Fe O4P 1 21/n 18.6879; 6.4163; 34.7054
90; 94.776; 90		1927.91Tatsuo Okauchi; Naoki Sata; Akihiro Urakawa; Mitsuru Kitamura
Unprecedented formation of eta^46-(vinylketene)iron complexes from eta^4^-(diene)iron complexes and aromatic compounds in the presence of a Lewis acid
Chem.Commun., 2015, 51, 8454
7117143 CIFC21 H33 Cu N3 O11.5R -3 m :H18.483; 18.483; 46.758
90; 90; 120		13833Chengling Song; Yajing Ling; Yunlong Feng; Wei Zhou; Taner Yildirim; Yabing He
A NbO-type metal-organic framework exhibiting high deliverable capacity for methane storage
Chem.Commun., 2015, 51, 8508
7117144 CIFC147 H182 N14 O56 Zn6P m n a19.7928; 17.7591; 28.543
90; 90; 90		10032.9Fei-Yan Yi; Hai-Long Jiang; Zhong-Ming Sun
Linearly bridging CO2 in a metal-organic framework
Chem.Commun., 2015, 51, 8446
7117145 CIFC24 H17 NP 1 21/c 113.0849; 9.1297; 13.5767
90; 93.893; 90		1618.15Sisir Lohar; Damir A. Safin; Archya Sengupta; Ansuman Chattopadhyay; Jesus Sanmartin Matalobos; Maria G. Babashkina; Koen Robeyns; Mariusz P. Mitoraj; Piotr Kubisiak; Yann Garcia; Debasis Das
Ratiometric sensing of lysine through the formation of the pyrene excimer: experimental and computational studies
Chem.Commun., 2015, 51, 8536
7117146 CIFC22 H17 NP 1 21/n 14.2713; 14.11; 25.725
90; 91.832; 90		1549.6Sisir Lohar; Damir A. Safin; Archya Sengupta; Ansuman Chattopadhyay; Jesus Sanmartin Matalobos; Maria G. Babashkina; Koen Robeyns; Mariusz P. Mitoraj; Piotr Kubisiak; Yann Garcia; Debasis Das
Ratiometric sensing of lysine through the formation of the pyrene excimer: experimental and computational studies
Chem.Commun., 2015, 51, 8536
7117147 CIFC31 H30 Al Cr F24 O7P 1 21/n 125.012; 13.9336; 25.099
90; 111.913; 90		8115.2Wenqing Wang; Xingyong Wang; Zaichao Zhang; Ningning Yuan; Xinping Wang
The long-sought seventeen-electron radical [(C6Me6)Cr(CO)3]+: isolation, crystal structure and substitution reaction
Chem.Commun., 2015, 51, 8410
7117148 CIFC48 H33 Al Cr F36 O6 PP 1 21/n 119.1442; 34.536; 19.5979
90; 119.074; 90		11324.7Wenqing Wang; Xingyong Wang; Zaichao Zhang; Ningning Yuan; Xinping Wang
The long-sought seventeen-electron radical [(C6Me6)Cr(CO)3]+: isolation, crystal structure and substitution reaction
Chem.Commun., 2015, 51, 8410
7117149 CIFC32 H33 Cr O2 PP -18.649; 9.593; 17.771
90.671; 99.551; 116.355		1296.8Wenqing Wang; Xingyong Wang; Zaichao Zhang; Ningning Yuan; Xinping Wang
The long-sought seventeen-electron radical [(C6Me6)Cr(CO)3]+: isolation, crystal structure and substitution reaction
Chem.Commun., 2015, 51, 8410
7117150 CIFC18 H20 O2 SP 1 21 17.323; 12.346; 9.152
90; 108.447; 90		784.9Ryosuke Takechi; Takahiro Nishimura
Enantioselective 1,4-addition of cyclopropylboronic acid catalyzed by rhodium/chiral diene complexes
Chem.Commun., 2015, 51, 8528
7117151 CIFC51 H50 N2 O2 S6C 1 2/c 137.215; 14.101; 9.619
90; 96.595; 90		5014.3Minh T. Nguyen; Bradley J. Holliday
Direct insights into metal-induced conductivity enhancement in conducting metallopolymers
Chem.Commun., 2015, 51, 8610
7117152 CIFC18.86 H19 Ag I0.14 N3.86P 1 21/n 19.6546; 10.6457; 17.115
90; 90.385; 90		1759.04Rachael Heath; Helge Muller-Bunz; Martin Albrecht
Silver(I) NHC mediated C-C bond activation of alkyl nitriles and catalytic efficiency in oxazoline synthesis
Chem.Commun., 2015, 51, 8699
7117153 CIFC19 H19 Ag N4P 1 21/n 19.59019; 10.57651; 17.1999
90; 90.1567; 90		1744.59Rachael Heath; Helge Muller-Bunz; Martin Albrecht
Silver(I) NHC mediated C-C bond activation of alkyl nitriles and catalytic efficiency in oxazoline synthesis
Chem.Commun., 2015, 51, 8699
7117154 CIFC20 H16 Cl F3 N2 O2P 1 21 110.4449; 7.9864; 11.2224
90; 93.069; 90		934.8Mingxia Ma; Yuanyuan Zhu; Quantao Sun; Xiaoyuan Li; Jinhuan Su; Long Zhao; Yanyan Zhao; Shuai Qiu; Wenjin Yan; Kairong Wang; Rui Wang
The asymmetric synthesis of CF3-containing spiro[pyrrolidin-3,2'-oxindole] through the organocatalytic 1,3-dipolar cycloaddition reaction
Chem.Commun., 2015, 51, 8789
7117155 CIFC11 H8 Br F3 N2 OP 1 21/n 16.8291; 12.139; 14.882
90; 101.467; 90		1209.1Mingxia Ma; Yuanyuan Zhu; Quantao Sun; Xiaoyuan Li; Jinhuan Su; Long Zhao; Yanyan Zhao; Shuai Qiu; Wenjin Yan; Kairong Wang; Rui Wang
The asymmetric synthesis of CF3-containing spiro[pyrrolidin-3,2'-oxindole] through the organocatalytic 1,3-dipolar cycloaddition reaction
Chem.Commun., 2015, 51, 8789
7117156 CIFC15 H11 N O SP 1 21/c 116.112; 7.8274; 9.593
90; 101.081; 90		1187.27Bhaskar Garg; Yong-Chien Ling
A highly selective phenothiazine-based fluorescence 'turn-on' indicator based on cyanide-promoted novel protection/deprotection mechanism
Chem.Commun., 2015, 51, 8809
7117157 CIFC29 H23 Br O2P -19.845; 10.37; 12.763
89.509; 70.585; 71.497		1158.5Ya-Jing Chen; Tian-Jiao Hu; Chen-Guo Feng; Guo-Qiang Lin
Synthesis of chiral cyclobutanes via rhodium/diene-catalyzed asymmetric 1,4-addition: a dramatic ligand effect on the diastereoselectivity
Chem.Commun., 2015, 51, 8773
7117158 CIFC15 H4 F4 I NP -17.4665; 9.3784; 10.5061
85.468; 75.25; 67.203		655.7Fanny Frausto; Zachary C. Smith; Terry E. Haas; Samuel W. Thomas III
Two-dimensional bricklayer arrangements of tolans using halogen bonding interactions
Chem.Commun., 2015, 51, 8825
7117159 CIFC15 H8 I NF d d 218.421; 7.6185; 17.387
90; 90; 90		2440.1Fanny Frausto; Zachary C. Smith; Terry E. Haas; Samuel W. Thomas III
Two-dimensional bricklayer arrangements of tolans using halogen bonding interactions
Chem.Commun., 2015, 51, 8825
7117160 CIFC15 H4 Br F4 NP 1 21/c 113.2997; 9.7019; 19.917
90; 102.415; 90		2509.8Fanny Frausto; Zachary C. Smith; Terry E. Haas; Samuel W. Thomas III
Two-dimensional bricklayer arrangements of tolans using halogen bonding interactions
Chem.Commun., 2015, 51, 8825
7117161 CIFC15 H6 Br F2 NP -15.7972; 8.6736; 12.715
73.612; 85.418; 86.061		610.7Fanny Frausto; Zachary C. Smith; Terry E. Haas; Samuel W. Thomas III
Two-dimensional bricklayer arrangements of tolans using halogen bonding interactions
Chem.Commun., 2015, 51, 8825
7117162 CIFC15 H8 Br NF d d 217.893; 7.5409; 17.168
90; 90; 90		2316.5Fanny Frausto; Zachary C. Smith; Terry E. Haas; Samuel W. Thomas III
Two-dimensional bricklayer arrangements of tolans using halogen bonding interactions
Chem.Commun., 2015, 51, 8825
7117163 CIFC15 H9 NP -19.404; 9.48; 13.047
94.412; 102.356; 103.038		1097.3Fanny Frausto; Zachary C. Smith; Terry E. Haas; Samuel W. Thomas III
Two-dimensional bricklayer arrangements of tolans using halogen bonding interactions
Chem.Commun., 2015, 51, 8825
7117164 CIFC16 H12 F2 N O4P 1 21/c 122.639; 5.0207; 11.438
90; 93.54; 90		1297.6Rui Guo; Haodong Yang; Pingping Tang
Silver-catalyzed Meerwein arylation: intermolecular and intramolecular fluoroarylation of styrenes
Chem.Commun., 2015, 51, 8829
7117166 CIFC10 H16 N4 O4 SC 1 2/c 19.642; 15.986; 9.334
90; 92.708; 90		1437Cristina Mottillo; Tomislav Friscic
Supramolecular imidazolium frameworks: direct analogues of metal azolate frameworks with charge-inverted node-and-linker structure
Chem.Commun., 2015, 51, 8924
7117167 CIFC14 H14 N4 O4 SF d d 214.6766; 18.8388; 11.8862
90; 90; 90		3286.4Cristina Mottillo; Tomislav Friscic
Supramolecular imidazolium frameworks: direct analogues of metal azolate frameworks with charge-inverted node-and-linker structure
Chem.Commun., 2015, 51, 8924
7117168 CIFC16 H18 N4 O4 SC 1 2/c 117.398; 7.4436; 14.051
90; 105.38; 90		1754.5Cristina Mottillo; Tomislav Friscic
Supramolecular imidazolium frameworks: direct analogues of metal azolate frameworks with charge-inverted node-and-linker structure
Chem.Commun., 2015, 51, 8924
7117169 CIFC28 H28 N4 O5 SP b c n16.62; 8.218; 19.159
90; 90; 90		2616.8Cristina Mottillo; Tomislav Friscic
Supramolecular imidazolium frameworks: direct analogues of metal azolate frameworks with charge-inverted node-and-linker structure
Chem.Commun., 2015, 51, 8924
7117170 CIFC28 H30 N4 O6 SP b c n16.933; 8.0337; 19.688
90; 90; 90		2678.3Cristina Mottillo; Tomislav Friscic
Supramolecular imidazolium frameworks: direct analogues of metal azolate frameworks with charge-inverted node-and-linker structure
Chem.Commun., 2015, 51, 8924
7117171 CIFC14 H14 N4 O4 SeP 43 21 218.5107; 18.5107; 18.953
90; 90; 90		6494.2Cristina Mottillo; Tomislav Friscic
Supramolecular imidazolium frameworks: direct analogues of metal azolate frameworks with charge-inverted node-and-linker structure
Chem.Commun., 2015, 51, 8924
7117172 CIFC17 H23 N4 O5.5 SeC 1 2/c 125.917; 8.7717; 17.5915
90; 100.377; 90		3933.8Cristina Mottillo; Tomislav Friscic
Supramolecular imidazolium frameworks: direct analogues of metal azolate frameworks with charge-inverted node-and-linker structure
Chem.Commun., 2015, 51, 8924
7117173 CIFC26 H22 N4 O4 SeP -19.611; 10.852; 11.918
83.339; 72.175; 88.808		1175.2Cristina Mottillo; Tomislav Friscic
Supramolecular imidazolium frameworks: direct analogues of metal azolate frameworks with charge-inverted node-and-linker structure
Chem.Commun., 2015, 51, 8924
7117174 CIFC28 H30 N4 O6 SeP b c n17.3442; 8.0712; 19.5768
90; 90; 90		2740.5Cristina Mottillo; Tomislav Friscic
Supramolecular imidazolium frameworks: direct analogues of metal azolate frameworks with charge-inverted node-and-linker structure
Chem.Commun., 2015, 51, 8924
7117175 CIFC30 H24 O2C 1 2/c 131.067; 13.835; 15.67
90; 93.254; 90		6724Suman Kalyan Samanta; Eduard Preis; Christian W. Lehmann; Richard Goddard; Saientan Bag; Prabal K. Maiti; Gunther Brunklaus; Ullrich Scherf
One-step synthesis of a cyclic 2,17-dioxo[3,3](4,4') biphenylophane and first preparation of a microporous polymer network from a macrocyclic precursor by cyclotrimerization
Chem.Commun., 2015, 51, 9046
7117176 CIFC18 H11 F3 O SP 1 21 15.593; 8.107; 17.57
90; 95.029; 90		793.6Amparo Sanz-Marco; Gonzalo Blay; M. Carmen Munoz; Jose R. Pedro
Highly enantioselective copper(I)-catalyzed conjugate addition of 1,3-diynes to alpha,beta-unsaturated trifluoromethyl ketones
Chem.Commun., 2015, 51, 8958
7117177 CIFC29 H31 N3 O6P 1 21/c 119.2486; 10.9164; 12.4114
90; 93.117; 90		2604.09Dan Preston; Alyssa Fox-Charles; Warrick K. C. Lo; James D. Crowley
Chloride triggered reversible switching from a metallosupramolecular [Pd2L4]^4+^ cage to a [Pd2L2Cl4] metallo-macrocycle with release of endo- and exo-hedrally bound guests
Chem.Commun., 2015, 51, 9042
7117178 CIFC116 H132 B4 F16 N12 O28 Pd2P -114.8562; 16.5839; 16.9982
117.401; 93.11; 114.691		3216.5Dan Preston; Alyssa Fox-Charles; Warrick K. C. Lo; James D. Crowley
Chloride triggered reversible switching from a metallosupramolecular [Pd2L4]^4+^ cage to a [Pd2L2Cl4] metallo-macrocycle with release of endo- and exo-hedrally bound guests
Chem.Commun., 2015, 51, 9042
7117179 CIFC58 H62 Cl4 N6 O12 Pd2C 1 2/m 113.8958; 21.0537; 11.1192
90; 101.982; 90		3182.1Dan Preston; Alyssa Fox-Charles; Warrick K. C. Lo; James D. Crowley
Chloride triggered reversible switching from a metallosupramolecular [Pd2L4]^4+^ cage to a [Pd2L2Cl4] metallo-macrocycle with release of endo- and exo-hedrally bound guests
Chem.Commun., 2015, 51, 9042
7117180 CIFC126 H150 N16 O38 Pd2 S4P 1 21/n 113.099; 17.179; 32.25
90; 91.566; 90		7254.4Dan Preston; Alyssa Fox-Charles; Warrick K. C. Lo; James D. Crowley
Chloride triggered reversible switching from a metallosupramolecular [Pd2L4]^4+^ cage to a [Pd2L2Cl4] metallo-macrocycle with release of endo- and exo-hedrally bound guests
Chem.Commun., 2015, 51, 9042
7117181 CIFC24 H44 Cu7 I8 N8R -3 :H25.9051; 25.9051; 20.4603
90; 90; 120		11890.9Yao Kang; Wei-Hui Fang; Lei Zhang; Jian Zhang
A structure-directing method to prepare semiconductive zeolitic cluster-organic frameworks with Cu3I4 building units
Chem.Commun., 2015, 51, 8994
7117182 CIFC15 H29 Cu4 I4 N4I 4 2 218.5097; 18.5097; 36.1113
90; 90; 90		12372.1Yao Kang; Wei-Hui Fang; Lei Zhang; Jian Zhang
A structure-directing method to prepare semiconductive zeolitic cluster-organic frameworks with Cu3I4 building units
Chem.Commun., 2015, 51, 8994
7117183 CIFC26 H16 N2 O8 S UP 21 21 218.435; 12.595; 22.468
90; 90; 90		2387Shu-wen An; Lei Mei; Cong-zhi Wang; Chuan-qin Xia; Zhi-fang Chai; Wei-qun Shi
The first case of actinide triple helices: pH-dependent structural evolution and kinetically-controlled transformation of two supramolecular conformational isomers
Chem.Commun., 2015, 51, 8978
7117184 CIFC26 H18 N2 O9 S UP 1 21/c 114.395; 8.675; 20.368
90; 95.16; 90		2533.2Shu-wen An; Lei Mei; Cong-zhi Wang; Chuan-qin Xia; Zhi-fang Chai; Wei-qun Shi
The first case of actinide triple helices: pH-dependent structural evolution and kinetically-controlled transformation of two supramolecular conformational isomers
Chem.Commun., 2015, 51, 8978
7117185 CIFC11 H9 F3 N2 O3P -15.736; 7.686; 15.026
102.598; 92.769; 110.155		601.4Ai-Jie Cai; Yan Zheng; Jun-An Ma
Copper-triggered three-component reaction of CF3CHN2, nitriles, and aldehydes: highly diastereoselective synthesis of CF3-substituted oxazolines and vicinal amino alcohols
Chem.Commun., 2015, 51, 8946
7117186 CIFC11 H9 Cl F3 N O2P 1 21/c 17.764; 22.824; 7.398
90; 112.915; 90		1207.5Ai-Jie Cai; Yan Zheng; Jun-An Ma
Copper-triggered three-component reaction of CF3CHN2, nitriles, and aldehydes: highly diastereoselective synthesis of CF3-substituted oxazolines and vicinal amino alcohols
Chem.Commun., 2015, 51, 8946
7117188 CIFC46 H43 Cl3 S6P b c a9.4165; 19.7949; 45.588
90; 90; 90		8497.5Shu-Wei Chang; Masaki Horie
A donor-acceptor conjugated block copolymer of poly(arylenevinylene)s by ring-opening metathesis polymerization
Chem.Commun., 2015, 51, 9113
7117189 CIFC16 H17.13 Cu2 O19.5 S2P -17.6226; 8.0332; 19.2709
89.772; 88.902; 76.322		1146.36Xiao-Qin Wu; Jian-Gong Ma; Han Li; Di-Ming Chen; Wen Gu; Guang-Ming Yang; Peng Cheng
Metal-organic framework biosensor with high stability and selectivity in a bio-mimic environment
Chem.Commun., 2015, 51, 9161
7117190 CIFC17 H21 F4 N O4 SP 21 21 217.7459; 9.8069; 25.602
90; 90; 90		1944.8Chen Xie; Yanling Dai; Haibo Mei; Jianlin Han; Vadim A. Soloshonok; Yi Pan
Asymmetric synthesis of quaternary alpha-fluoro-beta-keto-amines via detrifluoroacetylative Mannich reactions
Chem.Commun., 2015, 51, 9149
7117191 CIFC22 H19 Br Cl3 N2 O4P 21 21 2110.2175; 12.1386; 19.641
90; 90; 90		2436Wu-Lin Yang; Yang-Zi Liu; Shuai Luo; Xingxin Yu; John S. Fossey; Wei-Ping Deng
The copper-catalyzed asymmetric construction of a dispiropyrrolidine skeleton via 1,3-dipolar cycloaddition of azomethine ylides to alpha-alkylidene succinimides
Chem.Commun., 2015, 51, 9212
7117192 CIFC24 H18 F6 O6P -18.917; 11.888; 12.165
62.137; 81.719; 78.834		1116.3Jingbo Wu; Scott T. Iacono; Gregory T. McCandless; Dennis W. Smith; Bruce M. Novak
Utilization of a Meldrum's acid towards functionalized fluoropolymers possessing dual reactivity for thermal crosslinking and post-polymerization modification
Chem.Commun., 2015, 51, 9220
7117193 CIFC19 H14 B F2 N3 SP 1 21/c 113.4997; 13.9995; 10.1052
90; 111.458; 90		1777.4Roop Shikha Singh; Rakesh Kumar Gupta; Rajendra Prasad Paitandi; Mrigendra Dubey; Gunjan Sharma; Biplob Koch; Daya Shankar Pandey
Morphological tuning via structural modulations in AIE luminogens with the minimum number of possible variables and their use in live cell imaging
Chem.Commun., 2015, 51, 9125
7117194 CIFC23 H23 B F2 N3 SP 1 21/n 116.3271; 8.327; 16.9926
90; 109.759; 90		2174.2Roop Shikha Singh; Rakesh Kumar Gupta; Rajendra Prasad Paitandi; Mrigendra Dubey; Gunjan Sharma; Biplob Koch; Daya Shankar Pandey
Morphological tuning via structural modulations in AIE luminogens with the minimum number of possible variables and their use in live cell imaging
Chem.Commun., 2015, 51, 9125
7117195 CIFC20 H16 B F2 N3 O SP 1 21/c 110.5497; 19.995; 9.2865
90; 104.898; 90		1893.1Roop Shikha Singh; Rakesh Kumar Gupta; Rajendra Prasad Paitandi; Mrigendra Dubey; Gunjan Sharma; Biplob Koch; Daya Shankar Pandey
Morphological tuning via structural modulations in AIE luminogens with the minimum number of possible variables and their use in live cell imaging
Chem.Commun., 2015, 51, 9125
7117196 CIFC18 H11 B Cl F2 N3P 1 21/c 19.7361; 14.5464; 12.214
90; 111.146; 90		1613.33Roop Shikha Singh; Rakesh Kumar Gupta; Rajendra Prasad Paitandi; Mrigendra Dubey; Gunjan Sharma; Biplob Koch; Daya Shankar Pandey
Morphological tuning via structural modulations in AIE luminogens with the minimum number of possible variables and their use in live cell imaging
Chem.Commun., 2015, 51, 9125
7117197 CIFC90 H106 Cl4 N10 O92.75 V16P 1 21/a 121.2958; 21.33; 21.9581
90; 105.868; 90		9594.2Zhuxiu Zhang; Wen-Yang Gao; Lukasz Wojtas; Zhenjie Zhang; Michael J. Zaworotko
A new family of anionic organic-inorganic hybrid doughnut-like nanostructures
Chem.Commun., 2015, 51, 9223
7117198 CIFC80 H80 Cl4 N4 O81.5 V16I 4/m m m14.9098; 14.9098; 38.069
90; 90; 90		8462.8Zhuxiu Zhang; Wen-Yang Gao; Lukasz Wojtas; Zhenjie Zhang; Michael J. Zaworotko
A new family of anionic organic-inorganic hybrid doughnut-like nanostructures
Chem.Commun., 2015, 51, 9223
7117199 CIFC51.75 H64.75 Br4 Cl2 N7.25 O42.75 V8P -115.1975; 19.1532; 19.3115
103.817; 95.3294; 98.3478		5352.9Zhuxiu Zhang; Wen-Yang Gao; Lukasz Wojtas; Zhenjie Zhang; Michael J. Zaworotko
A new family of anionic organic-inorganic hybrid doughnut-like nanostructures
Chem.Commun., 2015, 51, 9223
7117200 CIFC91 H119 Cl7 N9 O83.25 V16P -114.9214; 16.0334; 16.7794
79.476; 82.828; 81.284		3881.7Zhuxiu Zhang; Wen-Yang Gao; Lukasz Wojtas; Zhenjie Zhang; Michael J. Zaworotko
A new family of anionic organic-inorganic hybrid doughnut-like nanostructures
Chem.Commun., 2015, 51, 9223
7117201 CIFC45 H109 Cr Mo6 N6 O29P -113.554; 13.7899; 21.0955
86.768; 88.944; 63.016		3508Jiangwei Zhang; Zhenhua Liu; Yichao Huang; Jin zhang; Jian Hao; Yongge Wei
Unprecedented chi isomers of single-side triol-functionalized Anderson polyoxometalates and their proton-controlled isomer transformation
Chem.Commun., 2015, 51, 9097
7117202 CIFC62 H143 Br Cr Mo6 N5 O27P 1 21/c 124.0245; 13.9963; 26.7955
90; 94.54; 90		8981.8Jiangwei Zhang; Zhenhua Liu; Yichao Huang; Jin zhang; Jian Hao; Yongge Wei
Unprecedented chi isomers of single-side triol-functionalized Anderson polyoxometalates and their proton-controlled isomer transformation
Chem.Commun., 2015, 51, 9097
7117203 CIFC69 H158 Br Cr Mo6 N8 O29P 113.2494; 14.7378; 14.8892
119.221; 103.752; 96.589		2371.5Jiangwei Zhang; Zhenhua Liu; Yichao Huang; Jin zhang; Jian Hao; Yongge Wei
Unprecedented chi isomers of single-side triol-functionalized Anderson polyoxometalates and their proton-controlled isomer transformation
Chem.Commun., 2015, 51, 9097
7117204 CIFC46 H108 Cr Mo6 N5 O28P -113.6865; 13.7366; 21.5248
86.727; 83.692; 62.304		3561.4Jiangwei Zhang; Zhenhua Liu; Yichao Huang; Jin zhang; Jian Hao; Yongge Wei
Unprecedented chi isomers of single-side triol-functionalized Anderson polyoxometalates and their proton-controlled isomer transformation
Chem.Commun., 2015, 51, 9097
7117205 CIFC67 H155 Br Mn Mo6 N9 O29P 113.2671; 14.756; 14.887
119.33; 103.729; 96.883		2370.4Jiangwei Zhang; Zhenhua Liu; Yichao Huang; Jin zhang; Jian Hao; Yongge Wei
Unprecedented chi isomers of single-side triol-functionalized Anderson polyoxometalates and their proton-controlled isomer transformation
Chem.Commun., 2015, 51, 9097
7117206 CIFC8 H43 Cr Mo6 N2 O30P 1 21/n 115.0834; 11.5341; 23.0245
90; 98.122; 90		3965.47Jiangwei Zhang; Zhenhua Liu; Yichao Huang; Jin zhang; Jian Hao; Yongge Wei
Unprecedented chi isomers of single-side triol-functionalized Anderson polyoxometalates and their proton-controlled isomer transformation
Chem.Commun., 2015, 51, 9097
7117207 CIFC62 H54 Cl6 P4 RuP -112.3129; 14.9215; 18.0053
67.588; 85.054; 78.028		2991.6Samantha G. Eaves; Sam J. Hart; Adrian C. Whitwood; Dmitry S. Yufit; Paul J. Low; Jason M. Lynam
Rapid Markovnikov addition of HCl to a pendant alkyne: evidence for a quinoidal cumulene
Chem.Commun., 2015, 51, 9362
7117208 CIFC63.5 H57 Cl5 P4 RuP -111.3506; 12.3819; 21.4222
80.7264; 74.684; 83.7147		2858.75Samantha G. Eaves; Sam J. Hart; Adrian C. Whitwood; Dmitry S. Yufit; Paul J. Low; Jason M. Lynam
Rapid Markovnikov addition of HCl to a pendant alkyne: evidence for a quinoidal cumulene
Chem.Commun., 2015, 51, 9362
7117210 CIFC67.99 H56.99 F11.99 N14 O P2 RuR -317.6408; 17.6408; 44.355
90; 90; 120		11953.9E. Rousset; D. Chartrand; I. Ciofini; V. Marvaud; G. S. Hanan
Red-light-driven photocatalytic hydrogen evolution using a ruthenium quaterpyridine complex
Chem.Commun., 2015, 51, 9261
7117211 CIFC60 H42 Cl2 N12 O5 RuP 41 3 221.1118; 21.1118; 21.1118
90; 90; 90		9409.7E. Rousset; D. Chartrand; I. Ciofini; V. Marvaud; G. S. Hanan
Red-light-driven photocatalytic hydrogen evolution using a ruthenium quaterpyridine complex
Chem.Commun., 2015, 51, 9261
7117212 CIFC17 H13 N3 OP 1 21/n 15.212; 17.471; 15.196
90; 92.267; 90		1382.6Liang Zhang; Mingzhu Zhao; Xiaoming Zhao
The synthesis of carbonyl 2-amino-pyrimidines via tandem regioselective heterocyclization of 1,3-diynes with guanidine and selective oxidation
Chem.Commun., 2015, 51, 9370
7117213 CIFAl4 H3 Na3 O19 P4P 1 21/m 17.537; 12.525; 9.7
90; 98.51; 90		905.6Yanjun Sun; Yan Yan; Yanyan Wang; Yi Li; Jiyang Li; Jihong Yu
High proton conduction in a new alkali metal-templated open-framework aluminophosphate
Chem.Commun., 2015, 51, 9317
7117214 CIFC96 H40 Cd5 O34R -3 c :H29.1653; 29.1653; 83.513
90; 90; 120		61520Hongming He; Yang Song; Chuanqi Zhang; Fuxing Sun; Rongrong Yuan; Zheng Bian; Lianxun Gao; Guangshan Zhu
A highly robust metal-organic framework based on an aromatic 12-carboxyl ligand with highly selective adsorption of CO2 over CH4
Chem.Commun., 2015, 51, 9463
7117215 CIFCl7 Cu10 O16 Pb2 Se4C 1 2/m 118.605; 6.204; 12.673
90; 109.869; 90		1376Vadim M. Kovrugin; Marie Colmont; Oleg I. Siidra; Olivier Mentre; Alexander Al-Shuray; Vladislav V. Gurzhiy; Sergey V. Krivovichev
Oxocentered Cu(II) lead selenite honeycomb lattices hosting Cu(I)Cl2 groups obtained by chemical vapor transport reactions
Chem.Commun., 2015, 51, 9563
7117216 CIFCl10 Cu12 O16 Pb2 Se4C 1 2/m 118.4956; 6.1454; 15.2985
90; 119.311; 90		1516.25Vadim M. Kovrugin; Marie Colmont; Oleg I. Siidra; Olivier Mentre; Alexander Al-Shuray; Vladislav V. Gurzhiy; Sergey V. Krivovichev
Oxocentered Cu(II) lead selenite honeycomb lattices hosting Cu(I)Cl2 groups obtained by chemical vapor transport reactions
Chem.Commun., 2015, 51, 9563
7117217 CIFCl11.6 Cu13.6 K1.6 O16 Pb0.4 Se4C 1 2/m 115.1158; 6.1853; 9.2672
90; 95.965; 90		861.75Vadim M. Kovrugin; Marie Colmont; Oleg I. Siidra; Olivier Mentre; Alexander Al-Shuray; Vladislav V. Gurzhiy; Sergey V. Krivovichev
Oxocentered Cu(II) lead selenite honeycomb lattices hosting Cu(I)Cl2 groups obtained by chemical vapor transport reactions
Chem.Commun., 2015, 51, 9563
7117218 CIFC15 H9 Ag Cl N9 O4I -4 3 d20.2313; 20.2313; 20.2313
90; 90; 90		8280.8Damir A. Safin; Amelie Pialat; Alicea A. Leitch; Nikolay A. Tumanov; Ilia Korobkov; Yaroslav Filinchuk; Jaclyn L. Brusso; Muralee Murugesu
Anion-induced Ag^I^ self-assemblies with electron deficient aromatic ligands: anion-pi-system interactions as a driving force for templated coordination networks
Chem.Commun., 2015, 51, 9547
7117219 CIFC40 H27 Ag4 F12 N27 O12 S4P 1 21/n 110.6023; 18.0069; 33.316
90; 90.1374; 90		6360.5Damir A. Safin; Amelie Pialat; Alicea A. Leitch; Nikolay A. Tumanov; Ilia Korobkov; Yaroslav Filinchuk; Jaclyn L. Brusso; Muralee Murugesu
Anion-induced Ag^I^ self-assemblies with electron deficient aromatic ligands: anion-pi-system interactions as a driving force for templated coordination networks
Chem.Commun., 2015, 51, 9547
7117220 CIFC24 H18 Ag2 F12 N18 P2P n m a10.6565; 16.8754; 19.1418
90; 90; 90		3442.3Damir A. Safin; Amelie Pialat; Alicea A. Leitch; Nikolay A. Tumanov; Ilia Korobkov; Yaroslav Filinchuk; Jaclyn L. Brusso; Muralee Murugesu
Anion-induced Ag^I^ self-assemblies with electron deficient aromatic ligands: anion-pi-system interactions as a driving force for templated coordination networks
Chem.Commun., 2015, 51, 9547
7117221 CIFC30 H24 Cl2 N Ni O3 PP -110.2518; 11.9007; 13.0245
111.438; 97.586; 98.593		1432.11Wenfeng Lo; Chunhua Hu; Tyler Berenson; Nathaniel Tracer; Daniel Shlian; Michael Khaloo; Avraham Benhaim; Jianfeng Jiang
Oxidation of carbon monoxide in basic solution catalyzed by nickel cyano carbonyls under ambient conditions and the prototype of a CO-powered alkaline fuel cell
Chem.Commun., 2015, 51, 9432
7117222 CIFC20 H40 N4 Ni O2C 1 2/c 114.857; 10.303; 15.562
90; 99.009; 90		2352.7Wenfeng Lo; Chunhua Hu; Tyler Berenson; Nathaniel Tracer; Daniel Shlian; Michael Khaloo; Avraham Benhaim; Jianfeng Jiang
Oxidation of carbon monoxide in basic solution catalyzed by nickel cyano carbonyls under ambient conditions and the prototype of a CO-powered alkaline fuel cell
Chem.Commun., 2015, 51, 9432
7117223 CIFC62 H42 N6 Ni2 O18P 1 21/n 113.142; 12.337; 17.656
90; 108.519; 90		2714Jun Zhao; Yenan Wang; Wenwen Dong; Yapan Wu; Dongsheng Li; Bin Liu; Qichun Zhang
A new surfactant-introduction strategy for separating the pure single-phase of metal-organic frameworks
Chem.Commun., 2015, 51, 9479
7117224 CIFC36 H21 N4 Ni2 O8C m c a31.395; 13.702; 15.808
90; 90; 90		6800Jun Zhao; Yenan Wang; Wenwen Dong; Yapan Wu; Dongsheng Li; Bin Liu; Qichun Zhang
A new surfactant-introduction strategy for separating the pure single-phase of metal-organic frameworks
Chem.Commun., 2015, 51, 9479
7117225 CIFC18 H12 N2 O2P 1 21/n 17.72; 21.073; 8.161
90; 92.202; 90		1326.7David E. Stephens; Johant Lakey-Beitia; Gabriel Chavez; Carla Ilie; Hadi D. Arman; Oleg V. Larionov
Experimental and mechanistic analysis of the palladium-catalyzed oxidative C8-selective C-H homocoupling of quinoline N-oxides
Chem.Commun., 2015, 51, 9507
7117227 CIFC28 H31 N3C 1 2/c 131.282; 8.8017; 19.4725
90; 121.27; 90		4582.6Qian Gao; Peng Zhou; Feng Liu; Wen-Juan Hao; Changsheng Yao; Bo Jiang; Shu-Jiang Tu
Cobalt(II)/silver relay catalytic isocyanide insertion/cycloaddition cascades: a new access to pyrrolo[2,3-b]indoles
Chem.Commun., 2015, 51, 9519
7117228 CIFC23 H18 N2 O4P 1 21/c 110.8247; 12.1491; 14.009
90; 96.356; 90		1831Subrata Mukherjee; Santigopal Mondal; Atanu Patra; Rajesh G. Gonnade; Akkattu T. Biju
N-Heterocyclic carbene-catalyzed diastereoselective synthesis of beta-lactone-fused cyclopentanes using homoenolate annulation reaction
Chem.Commun., 2015, 51, 9559
7117229 CIFC24 H20 Cl3 N O3P 1 21/c 115.3285; 11.4221; 12.7961
90; 95.471; 90		2230.2Subrata Mukherjee; Santigopal Mondal; Atanu Patra; Rajesh G. Gonnade; Akkattu T. Biju
N-Heterocyclic carbene-catalyzed diastereoselective synthesis of beta-lactone-fused cyclopentanes using homoenolate annulation reaction
Chem.Commun., 2015, 51, 9559
7117230 CIFC50 H60 B F24 Na P6P 1 21/c 118.4514; 13.2631; 26.133
90; 90.826; 90		6394.7Marina Carravetta; Maria Concistre; William Levason; Gillian Reid; Wenjian Zhang
Unique Group 1 cations stabilised by homoleptic neutral phosphine coordination
Chem.Commun., 2015, 51, 9555
7117231 CIFC62 H60 B F24 Na P6P -112.5084; 16.4798; 17.5637
79.047; 78.403; 81.625		3460.2Marina Carravetta; Maria Concistre; William Levason; Gillian Reid; Wenjian Zhang
Unique Group 1 cations stabilised by homoleptic neutral phosphine coordination
Chem.Commun., 2015, 51, 9555
7117232 CIFC46 H48 Al F36 Li O4 P6P n a 2115.092; 27.737; 15.405
90; 90; 90		6448.6Marina Carravetta; Maria Concistre; William Levason; Gillian Reid; Wenjian Zhang
Unique Group 1 cations stabilised by homoleptic neutral phosphine coordination
Chem.Commun., 2015, 51, 9555
7117233 CIFC48 H68 Cl Fe In N2 O4P 21 21 2110.3658; 18.6942; 23.794
90; 90; 90		4610.8Stephanie M. Quan; Paula L. Diaconescu
High activity of an indium alkoxide complex toward ring opening polymerization of cyclic esters
Chem.Commun., 2015, 51, 9643
7117234 CIFC27 H18 Br N3 OP 1 21 18.1413; 13.747; 10.606
90; 108.05; 90		1128.6Tianyou Qin; Lu Cheng; Sean Xiao-An Zhang; Weiwei Liao
Stereoselective synthesis of organosulfur compounds incorporating N-aromatic heterocyclic motifs and quaternary carbon centers via a sulfa-Michael triggered tandem reaction
Chem.Commun., 2015, 51, 9714
7117235 CIFC32 H24 N2 O SP -19.4724; 12.292; 12.563
104; 109.97; 102.72		1258.3Tianyou Qin; Lu Cheng; Sean Xiao-An Zhang; Weiwei Liao
Stereoselective synthesis of organosulfur compounds incorporating N-aromatic heterocyclic motifs and quaternary carbon centers via a sulfa-Michael triggered tandem reaction
Chem.Commun., 2015, 51, 9714
7117236 CIFC33 H15 Cu6 N6 O19F m -3 m44.588; 44.588; 44.588
90; 90; 90		88645Wen-Yang Gao; Tony Pham; Katherine A. Forrest; Brian Space; Lukasz Wojtas; Yu-Sheng Chen; Shengqian Ma
The local electric field favours more than exposed nitrogen atoms on CO2 capture: a case study on the rht-type MOF platform
Chem.Commun., 2015, 51, 9636
7117237 CIFC69 H65 Au2 F6 N P SbP 1 21/c 116.83401; 18.4515; 19.639
90; 100.054; 90		6006.44Luisa Ciano; Natalie Fey; Connor J. V. Halliday; Jason M. Lynam; Lucy M. Milner; Nimesh Mistry; Natalie E. Pridmore; Nell S. Townsend; Adrian C. Whitwood
Dispersion, solvent and metal effects in the binding of gold cations to alkynyl ligands: implications for Au(I) catalysis
Chem.Commun., 2015, 51, 9702
7117238 CIFC58.01 H55.02 Au2 F6 N P SbP b c n24.291; 17.933; 24.334
90; 90; 90		10600Luisa Ciano; Natalie Fey; Connor J. V. Halliday; Jason M. Lynam; Lucy M. Milner; Nimesh Mistry; Natalie E. Pridmore; Nell S. Townsend; Adrian C. Whitwood
Dispersion, solvent and metal effects in the binding of gold cations to alkynyl ligands: implications for Au(I) catalysis
Chem.Commun., 2015, 51, 9702
7117239 CIFC66 H64 Au3 F6 N2 SbP 1 21/c 116.33309; 18.64797; 18.79354
90; 91.0581; 90		5723.14Luisa Ciano; Natalie Fey; Connor J. V. Halliday; Jason M. Lynam; Lucy M. Milner; Nimesh Mistry; Natalie E. Pridmore; Nell S. Townsend; Adrian C. Whitwood
Dispersion, solvent and metal effects in the binding of gold cations to alkynyl ligands: implications for Au(I) catalysis
Chem.Commun., 2015, 51, 9702
7117240 CIFC32 H42 Cl3 N3 PdP 1 21/c 19.2943; 21.212; 18.121
90; 114.171; 90		3259.4Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117241 CIFC26 H30 Cl3 N3 PtP 21 21 235.0384; 9.1217; 16.6331
90; 90; 90		5316.1Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117242 CIFC32 H42 Cl3 N3 PtP 1 21/c 19.3227; 21.1418; 18.1068
90; 115.162; 90		3230.18Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117243 CIFC32 H41 Cl2 N3 PdP 1 21/c 19.7411; 22.3057; 14.8046
90; 98.163; 90		3184.2Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117244 CIFC33 H43 Cl4 N3 PdI 41/a :233.4882; 33.4882; 12.9635
90; 90; 90		14538Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117245 CIFC39 H49 Cl2 N3 PdP 1 21/c 114.8545; 17.1043; 14.8749
90; 102.243; 90		3693.4Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117246 CIFC22 H21 Cl2 N3 PdP 1 21/c 19.0414; 25.274; 10.5618
90; 120.856; 90		2071.9Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117247 CIFC44 H42 Br1.81 Cl2.18 N6 Pd2C 1 c 114.907; 15.9956; 18.4249
90; 99.438; 90		4333.9Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117248 CIFC26 H29 Cl2 N3 PdP 1 21/c 111.5869; 14.0962; 15.7142
90; 100.524; 90		2523.45Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117249 CIFC27 H31 Cl4 N3 PtP 1 21/c 116.5349; 11.8855; 14.5488
90; 91.162; 90		2858.62Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117250 CIFC22 H21 Cl2 N3 PtP 1 21/c 19.0255; 25.338; 10.5412
90; 120.716; 90		2072.5Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117251 CIFC79 H21 Cl2 NP 1 21/c 110.4764; 25.5317; 16.5265
90; 102.296; 90		4319.1Bolong Zhang; Jegadesan Subbiah; Yu-Ying Lai; Jonathan M. White; David J. Jones; Wallace W. H. Wong
One-pot selective synthesis of a fullerene bisadduct for organic solar cell applications
Chem.Commun., 2015, 51, 9837
7117252 CIFC21 H19 Cl N2 O3P 21 21 216.1999; 13.2765; 23.277
90; 90; 90		1916Santosh Agrawal; Nagaraju Molleti; Vinod K. Singh
Organocatalytic enantio- and diastereoselective synthesis of highly substituted ?-lactones via a Michael-cyclization cascade
Chem.Commun., 2015, 51, 9793
7117253 CIFC116 H150 Ag24 F12 N2 O16P 1 21/n 123.5527; 20.9694; 29.346
90; 95.231; 90		14433.2Kuan-Guan Liu; Su-Kun Chen; Yu-Mei Lin; Quan-Ming Wang
An organic anion template: a 24-nucleus silver cluster encapsulating a squarate dimer
Chem.Commun., 2015, 51, 9896
7117254 CIFC12 H18P -15.246; 6.1956; 7.9824
103.859; 98.602; 100.131		242.93Viswanadha G. Saraswatula; Binoy K. Saha
A thermal expansion investigation of the melting point anomaly in trihalomesitylenes
Chem.Commun., 2015, 51, 9829

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