Crystallography Open Database

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Searching journal of publication like 'Chem.Commun.' volume of publication is 51

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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

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