Efficient Photoluminescence via Metal-Ligand Alteration in a New MOFs Family
|
|
- Ethelbert Baldwin
- 5 years ago
- Views:
Transcription
1 Supporting Information for: Efficient Photoluminescence via Metal-Ligand Alteration in a New MOFs Family Dorina F. Sava Gallis, Lauren E. S. Rohwer, Mark A. Rodriguez, and Tina M. Nenoff Nanoscale Sciences Department, Sandia National Laboratories, Albuquerque, NM 87185, USA. Microsystems Integration Department, Sandia National Laboratories, Albuquerque, NM 87185, USA. Materials Characterization Department, Sandia National Laboratories, Albuquerque, NM 87185, USA. S1
2 Table of Contents Section S1: Powder X-Ray Diffraction (PXRD) measurements Section S2: Thermogravimetric (TGA) analyses Section S3: SEM-EDS analysis Section S4: X-ray single-crystal data collection and determination Section S5: References S3 S9 S14 S15 S25 S2
3 Section S1: Powder X-Ray Diffraction (PXRD) measurements Powder X-Ray Diffraction (PXRD) measurements were performed on a Siemens Kristalloflex D500 diffractometer, CuKα radiation (λ = Å). Figure S1. Calculated (red) and experimental (blue) PXRD pattern for compound 1. S3
4 Figure S2. Calculated (red) and experimental (blue) PXRD pattern for (a) as synthesized and (b) thermally treated at 150 C for 10 hours compound 2. (a) As-synthesized (b) Experimental Calculated Intensity (a.u.) After thermal treatment at 150ºC, 10 hours theta/ 0 S4
5 Figure S3. Calculated (red) and experimental (blue) PXRD pattern for compound 3. S5
6 Figure S4. Calculated (red) and experimental as synthesized (magenta) and after thermal treatment at 150 C for 10 hours (blue) PXRD pattern for compound 4. S6
7 Figure S5. Experimental (blue) PXRD pattern for compound 5. Table S1. PXRD peak determination for compound 5. 2-Theta d(å) BG Height H% Area A% FWHM S7
8 In order to gather additional structural information about compound 5, additional analyses were performed. Microelemental analyses confirmed an equimolar metal to ligand ratio, as well as the anticipated guest exchange (DMA/MeOH with EtOH/H 2 O). Elemental analyses were conducted by the Galbraith Laboratories, Inc. on as synthesized and EtOH-exchanged compound 5. Suggested formula (as synthesized): Eu(TCBB)(DMA) 4.5 (MeOH); Found: C, 60.99; H, 5.64; N, 5.03; Eu, Calculated: C, 61.8; H, 5.79; N, 5.07; Eu, Suggested formula (EtOH exchanged): Eu(TCBB)(EtOH) 2 (H 2 O) 4 Found: C, 60.68; H 4.16; N <0.5; Eu, 15.4 Calculated: C, 59.8; H, 4.7; Eu, 15.4 FT-IR spectra of TCBB ligand (red) and compound 5 (blue). The data was recorded on a Thermo Scientific Nicolet is10 FT-IR Spectrometer. Compound 5 TCBB ligand S8
9 Section S2: Thermogravimetric analyses The structural thermal stability was investigated by TGA-DSC. Measurements used a SDTQ600 TA instrument. Samples were heated at 10 C/min to 800 C under nitrogen flow. Figure S6. TGA (red trace) and DSC (blue trace) for compound 1. S9
10 Figure S7. TGA (red trace) and DSC (blue trace) for compound 2. S10
11 Figure S8. TGA (red trace) and DSC (blue trace) for compound 3. Figure S. TGA (red trace) and DSC (blue trace) for compound 3. S11
12 Figure S9. TGA (red trace) and DSC (blue trace) for compound 4. S12
13 Figure S10. TGA (red trace) and DSC (blue trace) for compound 5. S13
14 Section S3: SEM-EDS analysis Scanning Electron Microscopy (SEM) images were captured on a FEI NovaNano SEM 230, and Energy Dispersive Spectroscopy (EDS) analyses were collected on a EDAX Genesis Apex 2 with an Apollo SDD detector. Iodine loading in compound 5 An activated sample of 5 (sample exchanged in EtOH for 24 hours and degassed at room temperature for 18 hours on a Micromeritics ASAP 2020 surface area and porosity analyzer) was sealed with excess I 2 in an adsorption chamber and placed in a convection oven at 75 C. The iodine loaded sample was recovered, allowed to cool in an inert environment and the mass change recorded. Figure S11. SEM-EDS analyses of I 5. S14
15 Section S4: X-ray single-crystal data collection and determination The X-ray intensities were measured using a Bruker-APEX/CCD diffractometer (Mo Kα,λ = Å). Indexing and frame integration was performed using the APEX-II software suite. S1 Absorption correction was performed using face-indexing (numerical method) also within the APEX-II software. The structures were solved and refined using SHELXS-97 contained in SHELXTL v6.10 packages. S2 The hydrogen atoms were placed in geometrically calculated positions and included in the refinement process using a riding model. Since many MOFs are inherently low-density materials, it is not uncommon to have significantly reduced X-ray scattering, especially at the higher theta angles. The main focus of the reported MOF structures in this manuscript is the establishment of the crystalline framework and connectivity of the metal nodes via the linker molecules. The main drawback in regard to the missing high-angle data for a structure typically has to do with reduced confidence in bond length values in particular for the shortest of these bonds (e.g. C-C ~1.4 Angstroms). This concern has been addressed in our datasets through the use of constraints/restraints. Since the linker molecules most susceptible to refinement error are well-known, S3 these molecules can be constrained in a reasonable fashion (i.e. equal C-C distance in 6 membered rings) so as to improve the overall refinement stability. While this is not ideal, it is not an uncommon tactic for other large molecules with low density (e.g. proteins). S4 The restraining of the linker bond lengths/angles facilitates the refinement of a reasonable structure in the absence of meaningful high angle data. Determinations of the theta max cutoff for each dataset were made based on usefulness of the observed scattered intensities above the background level. Further increase of the analysis to larger theta max values only served to decrease the quality of the refinement and subsequently move the R value higher. S15
16 Crystal data for compound 1, (SMOF-2) The BTB ligand illustrated some difficulty in refinement of a few carbon atoms. Since the BTB molecule is fairly well defined as containing 4 benzene rings, the carbon atoms within the problematic ring (C57 > C62) were constrained to exhibit the expected bond lengths (and angles). In addition, this troublesome ring was assumed to be planar, and was constrained to be flat (using the FLAT command). Also, the bond distances between the O and C atoms at the termination of the BTB ligand were constrained (i.e. O13 and O14 to C63). The FLAT command was extended from the C57 > C62 ring to include the C63, O13 and O14 atoms. Note that the most difficult ring to refine with stability was terminated by the monodentate bonding (where the terminal or non-bound oxygen was the O14). The O14 is an OH group but due to the low resolution of the data it was difficult to locate the hydrogen atom. Hence, the hydrogen atom was left off of the O14 oxygen in the refinement, but was accounted for in the formula of the final refinement. The problematic nature of the C57 > C62 ring and its subsequent terminal oxygen branches suggests that this particular ring was subject to some disorder due to the absence of a more rigid bidentate bonding configuration. Elsewhere in the structure some additional bond length and FLAT constraints were added to improve the bidentate bonding of the O9-C36-O10 bonding. The above listed constraints added considerable stability to the refinement. In addition to the OH group, there were two terminal water molecules in the structure that coordinate to the In metal center. These water molecules are associated with O15 and O16 oxygen atoms. The hydrogen atoms present on these water molecules were not included in the structure model, but were added to the total formula in the final refinement cycle, just as in the case of the O14 OH hydrogen. There was significant scatter observed within the large channels/voids in the structure; this suggested the presence of solvent in the void space. Solvent density was detected in at least three separate crystallographic locations. We list these three center-of-density locations but acknowledge that there are likely more sites necessary to completely elucidate the modeled solvent density. The fractional coordinates for the sites are as follows: Site 1 at ( ), Site 2 at ( ), and Site 3 S16
17 at ( ). Attempts to refine the highly disordered solvent were unproductive. Therefore, the program Platon/Squeeze S5 was employed to model the solvent presence. Thermogravimetric analysis (TGA) suggested that the solvent loss was from diethylformamide (DEF) which was employed in the crystallization process. The application of the Squeeze routine reported solvent accessible void space of Å 3 containing 6073 electrons/cell. Assuming all the density in the solvent voids was from DEF molecules, this roughly translated to approximately 108 DEF molecules per cell. Association of sites 1, 2 and 3 with DEF molecules would account for 54 of the 108 DEF molecules (or half of the solvent density predicted by the electron count determined by Squeeze). The remaining solvent sites proved more difficult to locate due a lack of clearly located electron density nodes. This suggests that the solvent is highly disordered at these alternative sites, resulting in smearing of the electron density. Even so, the Squeeze process was still able to model this density and account for the total DEF presence. The estimated weight of DEF present within the structure (based on the electron density of DEF detected via Squeeze) was 31 wt%. This is in good agreement with TGA analysis. Refinement of the structure after solvent modeling resulted in a significant drop in residual error. While the final structure factors do not reflect the now absent DEF solvent, the final refinement included the additional DEF chemical species within the chemical formula and the reported crystal data reflect the presence of 6 DEF molecules per formula unit for compound 1 reported in this manuscript. S17
18 Table S2. Crystal data and structure refinement for compound 1. Empirical formula C63 H40 Eu In O16, 6(C5 H11 O N) Formula weight Temperature Wavelength 193 K Å Crystal system, space group Trigonal, R-3 Unit cell dimensions a = (6) Å alpha = 90 b = (6) Å beta = 90 c = (5) Å gamma = 120 Volume 60330(14) Å 3 Z, Calculated density 18, Mg/m 3 F(000) Crystal size 0.46 x 0.36 x 0.25 mm Theta range for data collection 1.24 to Reflections collected / unique / 6776 R indices R1 = , wr2 = Largest diff. peak and hole and eå -3 S18
19 Crystal data for compound 3, (SMOF-5) The ligand illustrated some difficulty in refinement of carbon atoms. Since this molecule is fairly well defined as containing 3 benzene rings, connected via the central C3N3 ring, all the rings in both ligands were restrained to have the planar aromatic-type bonding. In addition, oxalate bridging ligands were also constrained to have the expected C-C, O-C bond lengths. This added considerable stability to the refinement without causing a significant increase in the overall residual error. There were two OH groups present in the lattice due to monodentate coordination of the linker molecule. These OH groups were associated with O14 and O18 oxygen atoms. The hydrogen atoms were left off of the O14 and O18 oxygen atoms in the refinement, but were accounted for in the formula of the final refinement. There was significant scatter observed within the large channels/voids in the structure; this suggested the presence of solvent in the void space. Solvent density was detected in at least 8 separate crystallographic locations. We list these eight center-of-density locations but acknowledge that there are likely more sites necessary to completely elucidate the modeled solvent density. The fractional coordinates for the sites are as follows: Site 1 at (0, 0.75, ), Site 2 at (0.542, 0.678, 0.259), Site 3 at (0.871, 0.786, 0.460), Site 4 at (0.737, 0.934, 0.187), Site 5 at (0.25, 0.873, 0.5), site 6 at (0, 0, 0), Site 7 at (0.145, 0.957, 0.429), Site 8 at (0.102, 0.977, 0.75). Attempts to refine the highly disordered solvent were unproductive. Therefore, the program Platon/Squeeze S3 was employed to model the solvent presence. Thermogravimetric analysis (TGA) suggested that the solvent loss was from dimethylformamide (DMF) which was employed in the crystallization process. The application of the Squeeze routine reported solvent accessible void space of Å 3 containing 4827 electrons/cell. Assuming all the density in the solvent voids was from DMF molecules, this roughly translated to approximately 120 DMF molecules per cell. Association of sites listed above with DMF molecules would account for 88 of the 120 DMF molecules (or about 70 percent of the solvent density predicted by the electron count determined by Squeeze). The remaining solvent sites proved more difficult to located due a lack of clearly located electron density nodes. This suggests that the S19
20 solvent is highly disordered, resulting in smearing of the electron density. Even so, the Squeeze process was still able to model this density and account for the total DMF presence. The estimated weight of DMF present within the structure (based on the electron density of DMF detected via Squeeze) was 27 wt%. This is in good agreement with TGA analysis. Refinement of the structure after solvent modeling resulted in a significant drop in residual error. While the final structure factors do not reflect the now absent DMF solvent, the final refinement included the additional DMF chemical species within the chemical formula and the reported crystal data reflect the presence of 15 DMF molecules per formula unit for compound s 3 structure. S20
21 Table S3. Crystal data and structure refinement for compound 3. Empirical formula C108 H64 In6 N12 O48, 15(C3 H7 N O) Formula weight Temperature Wavelength Crystal system, space group 193 K Å Orthorhombic, I b c a Unit cell dimensions a = (18) Å alpha = 90 b = Å beta = 90 c = (19) Å gamma = 90 Volume 37501(29) Å 3 Z, Calculated density 8, Mg/m 3 F(000) Crystal size 0.18 x 0.15 x 0.12 mm Theta range for data collection 1.19 to Reflections collected / unique 3611 / 2204 R indices R1 = , wr2 = Largest diff. peak and hole and eå -3 S21
22 Crystal data for compound 4, (SMOF-7) Special consideration was given to the O7 atom which appeared to be coordinated by a diethylformamide (DEF) molecule. This molecule showed significant disorder, but one orientation appeared to be the most consistent. Bond lengths and angles for a DEF molecule were employed to constrain this DEF molecule to coordinate to the metal site. Restraints regarding isotropic temperature parameters for this DEF molecule were also employed. It is important to bear in mind that this orientation is one of many possible orientations. There was a second oxygen atom, the O8 oxygen site, that might possibly be associated with a second coordinated DEF, but all attempts to model such a molecule to attach to the O8 atom were unsuccessful. It appeared that there was not sufficient clearly defined electron density to warrant placement of a DEF molecule off of the O8 atom. So in the case of O8 it was assumed that this terminal oxygen was a water molecule. The hydrogen atoms were left off of the O8 water as well as the DEF molecule coordinated via O7. However, these hydrogen atoms were included in the final refinement to generate proper crystallographic output. There was significant scatter observed within the large channels/voids in the structure; this suggested the presence of solvent in the void space. Solvent density was detected in at least 2 separate crystallographic locations: Site 1 at (0.598, 0.130, 0.516), Site 2 at (0.730, 0.126, 0.697). These were determined via significant Q peaks present in the Difference-Fourier maps. The program Platon/Squeeze S3 was employed to model the solvent presence. Thermogravimetric analysis (TGA) suggested that the mass loss was from the DEF solvent which was employed in the crystallization process. The application of the Squeeze routine reported solvent accessible void space of Å 3 containing 1115 electrons/cell. Assuming all the density in the solvent voids was from DEF molecules, this translated to approximately 20 DEF molecules per cell as uncoordinated solvent. Association of sites listed above with DEF molecules would account for 16 of the 20 DEF solvent molecules (or about 75 percent of the solvent density predicted by the electron count determined by Squeeze). The remaining solvent sites in the channels proved more difficult to locate due a lack of clearly located electron density nodes. This suggests that the solvent is highly S22
23 disordered, resulting in smearing of the electron density. Even so, the Squeeze process was still able to model this density and account for the total DEF presence via the electron count. The estimated weight of DEF present within the structure (based on the electron density of DEF detected via Squeeze) was 26.5 %. The inclusion of the coordinated solvent (O7) and the O8 water molecules resulted in an increase to 43.9 weight percent. This is in good agreement with the TGA analysis. Refinement of the structure after solvent modeling resulted in a significant drop in residual error. While the final structure factors do not reflect the now absent DEF solvent molecules, the final refinement included the additional DEF chemical species within the chemical formula and the reported crystal data reflect the presence of 7 DEF molecules per formula unit for the compound 4 structure. Of these DEF molecules, 2 of them are due to the O7 coordinated DEF and there are 5 additional DEF solvent molecules present as uncoordinated solvent. S23
24 Table S4. Crystal data and structure refinement for compound 4. Empirical formula C48 H30 N6 O12 Eu2, 7(C5 H11 N O), 2(H2O) Formula weight Temperature Wavelength 193 K Å Crystal system, space group Monoclinic, C 2/c Unit cell dimensions a = (8) Å alpha = 90 b = (3) Å beta = (3) c = (5) Å gamma = 90 Volume 8515(4) Å 3 Z, Calculated density 4, Mg/m 3 F(000) 3976 Crystal size 0.15 x 0.10 x 0.02 mm Theta range for data collection 1.29 to Reflections collected / unique 2548 / 1807 R indices R1 = , wr2 = Largest diff. peak and hole and eå -3 S24
25 Section S5: References S1. Bruker AXS, Inc. APEX2 ver Madison, Wisconsin, USA S2. (a) Sheldrick, G. M. Acta Cryst. 2008, A64, ; (b) Bruker AXS, Inc. XSHELL Version 4.01 and SHELXTL Version Madison, WI S3. Furukawa, H.; Ko, N.; Go, Y. B.; Aratani, N.; Choi, S. B.; Choi, E.; Yazaydin, A. O.; Snurr, R. Q.; O Keeffe, M.; Kim, J.; Yaghi, O. M. Science 2010, 329, 424. S4. (a) Chao, J. A.; Williamson, J. R. Structure 2004, 12, ; (b) Von Dreele, R. B. ; Stephens, P. W.; Smith, G. D.; Blessing, R. H. Acta Cryst. 2000, D56, ; (c) Prabhakaran, P.; Kale, S.S.; Puranik, V.G.; Rajamohanan, P. R.; Chetina, O.; Howard, J.A. K.; Hofmann, H.-J.; Sanjayan, G.J. J. Am. Chem. Soc. 2008, 130, S5. Spek, A. L. Platon, A Multipurpose Crystallographic Tool, Utrecht University, Utrecht, The Netherlands S25
Supporting Information
Electronic Supplementary Material (ESI) for CrystEngComm. This journal is The Royal Society of Chemistry 2015 Supporting Information Single-Crystal-to-Single-Crystal Transformation of an Anion Exchangeable
More informationSupplementary Information
Site-Selective Cyclometalation of a Metal-Organic Framework Phuong V. Dau, Min Kim, and Seth M. Cohen* Department of Chemistry and Biochemistry, University of California, San Diego, 9500 Gilman Drive,
More informationSupporting Information. Table of Contents
Supporting Information Selective Anion Exchange and Tunable Luminescent Behaviors of Metal-Organic Framework Based Supramolecular Isomers Biplab Manna, Shweta Singh, Avishek Karmakar, Aamod V.Desai and
More informationA supramoleculear self-assembled flexible open framework based on coordination honeycomb layers possessing octahedral and tetrahedral Co II geometries
Supporting Information A supramoleculear self-assembled flexible open framework based on coordination honeycomb layers possessing octahedral and tetrahedral Co II geometries Yang Zou,* a Yuanyuan Li, a
More informationElectronic Supplementary Information (ESI)
Electronic Supplementary Material (ESI) for ChemComm. This journal is The Royal Society of Chemistry 2018 Electronic Supplementary Information (ESI) A Large Spin, Magnetically Anisotropic, Octanuclear
More informationFluorous Metal Organic Frameworks with Superior Adsorption and Hydrophobic Properties toward Oil Spill Cleanup and Hydrocarbon Storage
SUPPORTING INFORMATION Fluorous Metal Organic Frameworks with Superior Adsorption and Hydrophobic Properties toward Oil Spill Cleanup and Hydrocarbon Storage Chi Yang, a Ushasree Kaipa, a Qian Zhang Mather,
More informationReversible uptake of HgCl 2 in a porous coordination polymer based on the dual functions of carboxylate and thioether
Supplementary Information Reversible uptake of HgCl 2 in a porous coordination polymer based on the dual functions of carboxylate and thioether Xiao-Ping Zhou, a Zhengtao Xu,*,a Matthias Zeller, b Allen
More informationSupporting Information
Submitted to Cryst. Growth Des. Version 1 of August 22, 2007 Supporting Information Engineering Hydrogen-Bonded Molecular Crystals Built from 1,3,5-Substituted Derivatives of Benzene: 6,6',6''-(1,3,5-Phenylene)tris-1,3,5-triazine-2,4-diamines
More informationCu(I)-MOF: naked-eye colorimetric sensor for humidity and. formaldehyde in single-crystal-to-single-crystal fashion
Supporting Information for Cu(I)-MOF: naked-eye colorimetric sensor for humidity and formaldehyde in single-crystal-to-single-crystal fashion Yang Yu, Xiao-Meng Zhang, Jian-Ping Ma, Qi-Kui Liu, Peng Wang,
More informationSupplementary Information. Single Crystal X-Ray Diffraction
Supplementary Information Single Crystal X-Ray Diffraction Single crystal diffraction data were collected on an Oxford Diffraction Gemini R Ultra diffractometer equipped with a Ruby CCD-detector with Mo-K
More informationSigma Bond Metathesis with Pentamethylcyclopentadienyl Ligands in Sterically. Thomas J. Mueller, Joseph W. Ziller, and William J.
Sigma Bond Metathesis with Pentamethylcyclopentadienyl Ligands in Sterically Crowded (C 5 Me 5 ) 3 M Complexes Thomas J. Mueller, Joseph W. Ziller, and William J. Evans * Department of Chemistry, University
More informationReaction Landscape of a Pentadentate N5-Ligated Mn II Complex with O 2
Electronic Supplementary Information for: Reaction Landscape of a Pentadentate N5-Ligated Mn II Complex with O - and H O Includes Conversion of a Peroxomanganese(III) Adduct to a Bis(µ- O)dimanganese(III,IV)
More information1. General Experiments... S2. 2. Synthesis and Experiments... S2 S3. 3. X-Ray Crystal Structures... S4 S8
Electronic Supplementary Material (ESI) for Dalton Transactions. This journal is The Royal Society of Chemistry 2017 Electronic Supplementary Information Gate-Opening upon CO 2 Adsorption on a Metal Organic
More informationSmall Molecule Crystallography Lab Department of Chemistry and Biochemistry University of Oklahoma 101 Stephenson Parkway Norman, OK
Small Molecule Crystallography Lab Department of Chemistry and Biochemistry University of Oklahoma 101 Stephenson Parkway Norman, OK 73019-5251 Sample: KP-XI-cinnamyl-chiral alcohol Lab ID: 12040 User:
More informationthe multiple helices
Supporting Information A 3D porous metal-organic framework containing nanotubes based on the multiple helices Lei Hou,* Li-Na Jia, Wen-Juan Shi, Li-Yun Du, Jiang Li, Yao-Yu Wang* and Qi-Zhen Shi Key Laboratory
More informationUnderstanding the relationship between crystal structure, plasticity and compaction behavior of theophylline, methyl gallate and their 1:1 cocrystal
Understanding the relationship between crystal structure, plasticity and compaction behavior of theophylline, methyl gallate and their 1:1 cocrystal Sayantan Chattoraj, Limin Shi and Changquan Calvin Sun
More informationSupporting Information
Supporting Information Three-dimensional frameworks of cubic (NH 4 ) 5 Ga 4 SbS 10, (NH 4 ) 4 Ga 4 SbS 9 (OH) H 2 O, and (NH 4 ) 3 Ga 4 SbS 9 (OH 2 ) 2H 2 O. Joshua L. Mertz, Nan Ding, and Mercouri G.
More informationA flexible MMOF exhibiting high selectivity for CO 2 over N 2, CH 4 and other small gases. Supporting Information
A flexible MMOF exhibiting high selectivity for CO 2 over N 2, CH 4 and other small gases Jingming Zhang, a Haohan Wu, a Thomas J. Emge, a and Jing Li* a a Department of Chemistry and Chemical Biology,
More informationSelective Binding and Removal of Organic Molecules in a Flexible Polymeric Material with Stretchable Metallosalen Chains
Selective Binding and Removal of Organic Molecules in a Flexible Polymeric Material with Stretchable Metallosalen Chains Gao Li, Chengfeng Zhu, Xiaobing Xi and Yong Cui* School of Chemistry and Chemical
More informationSmall Molecule Crystallography Lab Department of Chemistry and Biochemistry University of Oklahoma 101 Stephenson Parkway Norman, OK
Small Molecule Crystallography Lab Department of Chemistry and Biochemistry University of Oklahoma 101 Stephenson Parkway Norman, OK 73019-5251 Sample: KP-XI-furan-enzymatic alcohol Lab ID: 12042 User:
More informationSupporting Information. Directing the Breathing Behavior of Pillared-Layered. Metal Organic Frameworks via a Systematic Library of
Supporting Information Directing the Breathing Behavior of Pillared-Layered Metal Organic Frameworks via a Systematic Library of Functionalized Linkers Bearing Flexible Substituents Sebastian Henke, Andreas
More informationElectronic Supplementary Information. Pd(diimine)Cl 2 Embedded Heterometallic Compounds with Porous Structures as Efficient Heterogeneous Catalysts
Electronic Supplementary Information Pd(diimine)Cl 2 Embedded Heterometallic Compounds with Porous Structures as Efficient Heterogeneous Catalysts Sheng-Li Huang, Ai-Quan Jia and Guo-Xin Jin* Experimental
More informationElectronic Supporting Information
Electronic Supporting Information Solid-State Coexistence of {Zr 12 } and {Zr 6 } Zirconium Oxocarboxylate Clusters Iurie L. Malaestean, Meliha Kutluca Alıcı, Claire Besson, Arkady Ellern and Paul Kögerler*
More informationSupporting Information. A novel microporous metal-organic framework exhibiting high acetylene and methane storage capacities
Supporting Information A novel microporous metal-organic framework exhibiting high acetylene and methane storage capacities Xing Duan, a Chuande Wu, b Shengchang Xiang, c Wei Zhou, de Taner Yildirim, df
More informationElectronic Supplementary Information for: Gram-scale Synthesis of a Bench-Stable 5,5 -Unsubstituted Terpyrrole
Electronic Supplementary Information for: Gram-scale Synthesis of a Bench-Stable 5,5 -Unsubstituted Terpyrrole James T. Brewster II, a Hadiqa Zafar, a Matthew McVeigh, a Christopher D. Wight, a Gonzalo
More informationJuan Manuel Herrera, Enrique Colacio, Corine Mathonière, Duane Choquesillo-Lazarte, and Michael D. Ward. Supporting information
Cyanide-bridged tetradecanuclear Ru II 3M II 11 clusters (M II = Zn II and Cu II ) based on the high connectivity building block [Ru 3 (HAT)(CN) 12 ] 6+ : structural and photophysical properties Juan Manuel
More informationSupporting Information
Electronic Supplementary Material (ESI) for ChemComm. This journal is The Royal Society of Chemistry 2014 Supporting Information A cage-based cationic body-centered tetragonal metal-organic framework:
More informationion, as obtained from a search of the Cambridge Structural database (CSD), December 2013.
Electronic Supplementary Material (ESI) for Chemical Communications. This journal is The Royal Society of Chemistry 2014 SI Figure S1. The reported bridging modes of the CO 3 2- ion, as obtained from a
More informationRedetermination of Crystal Structure of Bis(2,4-pentanedionato)copper(II)
Asian Journal of Chemistry Vol. 20, No. 8 (2008), 5834-5838 Redetermination of Crystal Structure of Bis(2,4-pentanedionato)copper(II) HAMID GLCHUBIAN Department of Chemistry, Mazandaran University, P..
More informationReversible 1,2-Alkyl Migration to Carbene and Ammonia Activation in an NHC-Zirconium Complex.
Reversible 1,2-Alkyl Migration to Carbene and Ammonia Activation in an NHC-Zirconium Complex. Emmanuelle Despagnet-Ayoub, Michael K. Takase, Jay A. Labinger and John E. Bercaw Contents 1. Experimental
More informationAPPENDIX E. Crystallographic Data for TBA Eu(DO2A)(DPA) Temperature Dependence
APPENDIX E Crystallographic Data for TBA Eu(DO2A)(DPA) Temperature Dependence Temperature Designation CCDC Page 100 K MLC18 761599 E2 200 K MLC17 762705 E17 300 K MLC19 763335 E31 E2 CALIFORNIA INSTITUTE
More informationControllable Growth of Bulk Cubic-Phase CH 3 NH 3 PbI 3 Single Crystal with Exciting Room-Temperature Stability
Electronic Supplementary Material (ESI) for CrystEngComm. This journal is The Royal Society of Chemistry 2016 Electronic Supplementary Information Controllable Growth of Bulk Cubic-Phase CH 3 NH 3 PbI
More informationSupporting Information
Supporting Information A Sn IV -Porphyrin-Based Metal-Organic Framework for the Selective Photo-Oxygenation of Phenol and Sulfides Ming-Hua Xie, Xiu-Li Yang, Chao Zou and Chuan-De Wu* Department of Chemistry,
More informationOrthorhombic, Pbca a = (3) Å b = (15) Å c = (4) Å V = (9) Å 3. Data collection. Refinement
organic compounds Acta Crystallographica Section E Structure Reports Online ISSN 1600-5368 N 0 -(3,4-Dimethylbenzylidene)furan-2- carbohydrazide Yu-Feng Li a and Fang-Fang Jian b * a Microscale Science
More informationSupplementary Material (ESI) for CrystEngComm. An ideal metal-organic rhombic dodecahedron for highly efficient
Supplementary Material (ESI) for CrystEngComm An ideal metal-organic rhombic dodecahedron for highly efficient adsorption of dyes in an aqueous solution Yuan-Chun He, Jin Yang,* Wei-Qiu Kan, and Jian-Fang
More informationSupplementary Information. Supplementary Figure 1 Synthetic routes to the organic linker H 2 ATBDC.
Supplementary Information Supplementary Figure 1 Synthetic routes to the organic linker H 2 ATBDC. S1 Supplementary Figure 2 1 H NMR (D 2 O, 500MHz) spectrum of H 2 ATBDC. S2 Supplementary Figure 3 13
More informationCompetitive I 2 Sorption by Cu-BTC from Humid Gas Streams
Supporting Information for: Competitive I 2 Sorption by Cu-BTC from Humid Gas Streams Dorina F. Sava, Karena W. Chapman, Mark A. Rodriguez, Jeffery A. Greathouse, # Paul S. Crozier,^ Haiyan Zhao, Peter
More informationEur. J. Inorg. Chem WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim, 2013 ISSN SUPPORTING INFORMATION
Eur. J. Inorg. Chem. 2013 WILEY-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, 2013 ISSN 1099 0682 SUPPORTING INFORMATION DOI: 10.1002/ejic.201300309 Title: Hydrogen Evolution Catalyzed by Aluminum-Bridged
More informationCALIFORNIA INSTITUTE OF TECHNOLOGY BECKMAN INSTITUTE X-RAY CRYSTALLOGRAPHY LABORATORY
APPENDIX F Crystallographic Data for TBA Tb(DO2A)(F-DPA) CALIFORNIA INSTITUTE OF TECHNOLOGY BECKMAN INSTITUTE X-RAY CRYSTALLOGRAPHY LABORATORY Date 11 January 2010 Crystal Structure Analysis of: MLC23
More informationIron Complexes of a Bidentate Picolyl NHC Ligand: Synthesis, Structure and Reactivity
Electronic Supplementary Material (ESI) for Dalton Transactions. This journal is The Royal Society of Chemistry 2016 Supplementary Information for Iron Complexes of a Bidentate Picolyl HC Ligand: Synthesis,
More informationNickel-Mediated Stepwise Transformation of CO to Acetaldehyde and Ethanol
Nickel-Mediated Stepwise Transformation of CO to Acetaldehyde and Ethanol Ailing Zhang, Sakthi Raje, Jianguo Liu, Xiaoyan Li, Raja Angamuthu, Chen-Ho Tung, and Wenguang Wang* School of Chemistry and Chemical
More informationSupporting information for Eddaoudi et al. (2002) Proc. Natl. Acad. Sci. USA 99 (8), ( /pnas ) Supporting Information
Supporting information for Eddaoudi et al. (2002) Proc. Natl. Acad. Sci. USA 99 (8), 4900 4904. (10.1073/pnas.082051899) Supporting Information Table 1. Syntheses of MOF-102 112 MOFn MOF- 102 Link and
More informationElectronic Supporting Information for
Electronic Supporting Information for Microporous metal-organic open framework containing uncoordinated carbonyl groups as postsynthetic modification sites for cation exchange and Tb 3+ sensor Jianwei
More informationSynthetic, Structural, and Mechanistic Aspects of an Amine Activation Process Mediated at a Zwitterionic Pd(II) Center
Synthetic, Structural, and Mechanistic Aspects of an Amine Activation Process Mediated at a Zwitterionic Pd(II) Center Supporting Information Connie C. Lu and Jonas C. Peters* Division of Chemistry and
More informationSupporting Information for. Linker-Directed Vertex Desymmetrization for the Production of Coordination Polymers. with High Porosity
Supporting Information for Linker-Directed Vertex Desymmetrization for the Production of Coordination Polymers with High Porosity Jennifer K. Schnobrich, Olivier Lebel,, Katie A. Cychosz, Anne Dailly,
More informationSupplementary Figure S1 a, wireframe view of the crystal structure of compound 11. b, view of the pyridinium sites. c, crystal packing of compound
a b c Supplementary Figure S1 a, wireframe view of the crystal structure of compound 11. b, view of the pyridinium sites. c, crystal packing of compound 11. 1 a b c Supplementary Figure S2 a, wireframe
More informationBenzene Absorption in a Protuberant-Grid-Type Zinc(II) Organic Framework Triggered by the Migration of Guest Water Molecules
Electronic Supplementary Material (ESI) for Dalton Transactions. This journal is The Royal Society of Chemistry 2014 Electronic Supplementary Information Benzene Absorption in a Protuberant-Grid-Type Zinc(II)
More informationElectronic Supplementary Information (ESI)
Electronic Supplementary Information (ESI) Crystal Engineering of Multiple-Component Organic Solids: Pharmaceutical Cocrystals of Tadalafil with Persistent Hydrogen Bonding Motifs David R. Weyna, a Miranda
More informationA Third Generation Breathing MOF with Selective, Stepwise, Reversible and Hysteretic Adsorption properties
Supporting information for A Third Generation Breathing MOF with Selective, Stepwise, Reversible and Hysteretic Adsorption properties Suresh Sanda, Srinivasulu Parshamoni and SanjitKonar* Department of
More informationSupporting Information. Chiral phosphonite, phosphite and phosphoramidite η 6 -areneruthenium(ii)
Supporting Information Chiral phosphonite, phosphite and phosphoramidite η 6 -areneruthenium(ii) complexes: application to the kinetic resolution of allylic alcohols. Mariano A. Fernández-Zúmel, Beatriz
More informationElectronic Supplementary Information
Electronic Supplementary Information Thermally Reversible Single-Crystal to Single-Crystal Transformation of Mononuclear to Dinuclear Zn(II) Complexes By[2+2] Cycloaddition Reaction Raghavender Medishetty,
More information= (1) V = (12) Å 3 Z =4 Mo K radiation. Data collection. Refinement. R[F 2 >2(F 2 )] = wr(f 2 ) = S = reflections
organic compounds Acta Crystallographica Section E Structure Reports Online ISSN 1600-5368 S-Benzylisothiouronium nitrate P. Hemalatha a and V. Veeravazhuthi b * a Department of Physics, PSG College of
More informationSupporting Information
Supporting Information Dative Boron-Nitrogen Bonds in Structural Supramolecular Chemistry: Multicomponent Assembly of Prismatic Organic Cages Burcak Icli, Erin Sheepwash, Thomas Riis-Johannessen, Kurt
More informationWhite Phosphorus is Air-Stable Within a Self-Assembled Tetrahedral Capsule
www.sciencemag.org/cgi/content/full/324/5935/1697/dc1 Supporting Online Material for White Phosphorus is Air-Stable Within a Self-Assembled Tetrahedral Capsule Prasenjit Mal, Boris Breiner, Kari Rissanen,
More informationIridium Complexes Bearing a PNP Ligand, Favoring Facile C(sp 3 )- H Bond Cleavage
Iridium Complexes Bearing a PNP Ligand, Favoring Facile C(sp 3 )- H Bond Cleavage Kapil S. Lokare,* a Robert J. Nielsen, *b Muhammed Yousufuddin, c William A. Goddard III, b and Roy A. Periana*,a a Scripps
More informationSupporting Information
Electronic Supplementary Material (ESI) for Dalton Transactions. This journal is The Royal Society of Chemistry 2018 Supporting Information Rare metal-ion metathesis of tetrahedral Zn(II) core of a noncentrosymmetric
More informationmetal-organic compounds
metal-organic compounds Acta Crystallographica Section E Structure Reports Online ISSN 1600-5368 Poly[tetra-l-cyanido-dipyridinecadmium(II)zinc(II)] Sheng Li,* Kun Tang and Fu-Li Zhang College of Medicine,
More informationmetal-organic compounds
metal-organic compounds Acta Crystallographica Section E Structure Reports Online ISSN 1600-5368 = 86.130 (2) = 81.155 (2) = 76.289 (3) V = 699.69 (4) Å 3 Z =2 Mo K radiation = 1.58 mm 1 T = 293 (2) K
More informationCHAPTER 6 CRYSTAL STRUCTURE OF A DEHYDROACETIC ACID SUBSTITUTED SCHIFF BASE DERIVATIVE
139 CHAPTER 6 CRYSTAL STRUCTURE OF A DEHYDROACETIC ACID SUBSTITUTED SCHIFF BASE DERIVATIVE 6.1 INTRODUCTION This chapter describes the crystal and molecular structure of a dehydroacetic acid substituted
More information1. X-ray crystallography
From Selenidostannates to Silver-Selenidostannate: Structural Variation of Chalcogenidometallates Synthesized in Ionic Liquids Jian-Rong Li a, Wei-Wei Xiong a, Zai-Lai Xie a, Cheng-Feng Du a, Guo-Dong
More informationNerve Agent Surrogate
Supporting Information A Porous Metal-Organic Replica of α-pbo 2 for Capture of Nerve Agent Surrogate Ruqiang Zou, Ruiqin Zhong, Songbai Han, Hongwu Xu, Anthony K. Burrell, Neil Henson, Jonathan L. Cape,
More informationImpeller-like dodecameric water clusters in metal organic nanotubes
Electronic Supplementary Material (ESI) for CrystEngComm. This journal is The Royal Society of Chemistry 2014 Electronic Supplementary Information Impeller-like dodecameric water clusters in metal organic
More informationElectronic Supplementary Information (ESI)
Electronic Supplementary Information (ESI) S1 Experimental Section: Materials and methods: All commercially available chemicals were used as supplied without further purification. The Q[5] was synthesized
More informationElectronic Supplementary Information (ESI)
Electronic Supplementary Material (ESI) for Chemical Science. This journal is The Royal Society of Chemistry 2017 Electronic Supplementary Information (ESI) Enhancing stability and porosity of penetrated
More informationCentre for Advanced Scientific Research, Jakkur, Bangalore , India
Electronic Supplementary Material (ESI) for ChemComm. This journal is The Royal Society of Chemistry 2014 Supporting information A bimodal anionic MOF: Turn-off sensing for Cu II and specific sensitization
More informationSupporting Information
S1 Submitted to J. Am. Chem. Soc. Supporting Information A porous coordination copolymer with over 5000 m 2 /g BET surface area Kyoungmoo Koh, Antek G. Wong-Foy, and Adam J. Matzger* Department of Chemistry,
More informationSupporting Information. Table of Contents
Supporting Information Cyclo-P 3 Complexes of Vanadium. Redox Properties and Origin of the 31 P NMR Chemical Shift. Balazs Pinter,, Kyle T. Smith, Masahiro Kamitani, Eva M. Zolnhofer,ǁ Ba L. Tran, Skye
More information(Supporting Information: 47 pages including this page) Pradip Pachfule, Chandan Dey, Kumar Vanka and Rahul Banerjee*
Structural Diversity in Fluorinated Metal Organic Frameworks (F-MOFs) Composed of Divalent Transition Metals, 1,10-Phenanthroline and Fluorinated Carboxylic Acid (Supporting Information: 47 pages including
More informationSynthesis of Tetra-ortho-Substituted, Phosphorus- Containing and Carbonyl-Containing Biaryls Utilizing a Diels-Alder Approach
Synthesis of Tetra-ortho-Substituted, Phosphorus- Containing and Carbonyl-Containing Biaryls Utilizing a Diels-Alder Approach Bradley O. Ashburn and Rich G. Carter* and Lev N. Zakharov Department of Chemistry,
More informationSpain c Departament de Química Orgànica, Universitat de Barcelona, c/ Martí I Franqués 1-11, 08080, Barcelona, Spain.
a Institute of Chemical Research of Catalonia, Av. Països Catalans, 16, 43007 Tarragona, Spain. b Departament de Química, Universitat Autònoma de Barcelona, Cerdanyola del Vallès, E-08193 Barcelona, Spain
More informationSupporting Information. for. Advanced Functional Materials, adfm Wiley-VCH 2007
Supporting Information for Advanced Functional Materials, adfm.200601202 Wiley-VCH 2007 69451 Weinheim, Germany [Supporting Information] Optical Sensor Based on Nanomaterial for the Selective Detection
More informationConnection of zinc paddle-wheels in a pto-type metal-organic framework with 2-methylimidazolate and subsequent incorporation of charged organic guests
Electronic Supplementary Material (ESI) for ChemComm. This journal is The Royal Society of Chemistry 2014 Electronic Supplementary Information for Connection of zinc paddle-wheels in a pto-type metal-organic
More informationAn Anionic Metal Organic Framework For Adsorption and. Separation of Light Hydrocarbons
Supporting Information for An Anionic Metal Organic Framework For Adsorption and Separation of Light Hydrocarbons Jia Li, Hong-Ru Fu, Jian Zhang, Lan-Sun Zheng, and Jun Tao* State Key Laboratory of Physical
More informationInternational Journal of Innovative Research in Science, Engineering and Technology. (An ISO 3297: 2007 Certified Organization)
ISSN(Online) 2319-8753 ISSN (Print) 2347-6710 (An ISO 3297 2007 Certified Organization) Website www.ijirset.com X-Ray Crystallographic Investigation and Crystal Structure of 6-(2-Hydroxy-4,6- dimethyl-phenyl)-4-(2-methoxy-phenyl)5-
More informationAll materials and reagents were obtained commercially and used without further
Reversible shrinkage and expansion of a blue photofluorescene cadmium coordination polymer and in situ tetrazole ligand synthesis Hong Deng,* a Yong-Cai Qiu, a Ying-Hua Li, a Zhi-Hui liu, a Rong-Hua Zeng,
More informationElectronic supplementary information (ESI) Temperature dependent selective gas sorption of unprecedented
Electronic supplementary information (ESI) Temperature dependent selective gas sorption of unprecedented stable microporous metal-imidazolate framework Shui-Sheng Chen, a,c Min Chen, a Satoshi Takamizawa,
More informationStructure Report for J. Reibenspies
X-ray Diffraction Laboratory Center for Chemical Characterization and Analysis Department of Chemistry Texas A & M University Structure Report for J. Reibenspies Project Name: Sucrose Date: January 29,
More informationAn unprecedented 2D 3D metal-organic polyrotaxane. framework constructed from cadmium and flexible star-like
Electronic Supplementary Information An unprecedented 2D 3D metal-organic polyrotaxane framework constructed from cadmium and flexible star-like ligand Hua Wu, a,b Hai-Yan Liu, a Ying-Ying Liu, a Jin Yang,*
More informationSupporting Information
Supporting Information Self-Assembly of 4-(Diethylboryl)pyridine: Crystal Structures of Cyclic Pentamer and Hexamer and Their Solvent-Dependent Selective Crystallization Shigeharu Wakabayashi, * Yuka Hori,
More informationA mesoporous aluminium metal-organic framework with 3 nm open pores
Electronic Supplementary Information A mesoporous aluminium metal-organic framework with 3 nm open pores Sheng-Han Lo, a Ching-Hsuan Chien, a Yu-Lun Lai, b Chun-Chuen Yang, c Jey Jau Lee, d Duraisamy Senthil
More informationSupporting Information for the Article Entitled
Supporting Information for the Article Entitled Catalytic Production of Isothiocyanates via a Mo(II) / Mo(IV) Cycle for the Soft Sulfur Oxidation of Isonitriles authored by Wesley S. Farrell, Peter Y.
More information= (8) V = (8) Å 3 Z =4 Mo K radiation. Data collection. Refinement. R[F 2 >2(F 2 )] = wr(f 2 ) = S = reflections
organic compounds Acta Crystallographica Section E Structure Reports Online ISSN 1600-5368 1-(3-Amino-1H-inden-2-yl)ethanone Dong-Yue Hu and Zhi-Rong Qu* Ordered Matter Science Research Center, College
More informationmetal-organic compounds
metal-organic compounds Acta Crystallographica Section E Structure Reports Online ISSN 1600-5368 Tetraaquabis(nicotinamide-jN 1 )nickel(ii) bis(2-fluorobenzoate) Tuncer Hökelek, a * Hakan Dal, b Barış
More informationSynthesis, Structure and Reactivity of O-Donor Ir(III) Complexes: C-H Activation Studies with Benzene
Synthesis, Structure and Reactivity of O-Donor Ir(III) Complexes: C-H Activation Studies with Benzene Gaurav Bhalla, Xiang Yang Liu, Jonas Oxgaard, William A. Goddard, III, Roy A. Periana* Loker Hydrocarbon
More informationSupporting Information. Copyright Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim, 2008
Supporting Information pyright Wiley-VCH Verlag GmbH &. KGaA, 69451 Weinheim, 2008 Time-Evolving Self-rganization and Autonomous Structural Adaptation of balt(ii) rganic Framework Materials with Nets scu
More informationelectronic reprint 2-Hydroxy-3-methoxybenzaldehyde (o-vanillin) revisited David Shin and Peter Müller
Acta Crystallographica Section E Structure Reports Online ISSN 1600-5368 Editors: W.T. A. Harrison, H. Stoeckli-Evans, E. R.T. Tiekink and M. Weil 2-Hydroxy-3-methoxybenzaldehyde (o-vanillin) revisited
More informationSupporting Information
Electronic Supplementary Material (ESI) for CrystEngComm. This journal is The Royal Society of Chemistry 2015 Supporting Information Bridging different Co 4 -calix[4]arene building blocks into grids, cages
More informationSupporting Information
Supporting Information Selective Metal Cation Capture by Soft Anionic Metal-Organic Frameworks via Drastic Single-crystal-to-single-crystal Transformations Jian Tian, Laxmikant V. Saraf, Birgit Schwenzer,
More informationData collection. Refinement. R[F 2 >2(F 2 )] = wr(f 2 ) = S = reflections 92 parameters
organic compounds Acta Crystallographica Section E Structure Reports Online ISSN 1600-5368 1,1 0 -(Butane-1,4-diyl)dipyridinium dibromide dihydrate Ming-Qiang Wu, a Xin Xiao, a Yun-Qian Zhang, a * Sai-Feng
More informationA Mixed Crystal Lanthanide Zeolite-like Metal-Organic. Framework as a Fluorescent Indicator for Lysophosphatidic. Acid, a Cancer Biomarker
Supporting Information for A Mixed Crystal Lanthanide Zeolite-like Metal-Organic Framework as a Fluorescent Indicator for Lysophosphatidic Acid, a Cancer Biomarker Shi- Yuan Zhang,, Wei Shi, *, Peng Cheng,
More informationEfficient, scalable and solvent-free mechanochemical synthesis of the OLED material Alq 3 (q = 8-hydroxyquinolinate) Supporting Information
Efficient, scalable and solvent-free mechanochemical synthesis of the OLED material Alq 3 (q = 8-hydroxyquinolinate) Xiaohe Ma, Gin Keat Lim, Kenneth D.M. Harris, David C. Apperley, Peter N. Horton, Michael
More informationStephen F. Nelsen, Asgeir E. Konradsson, Rustem F. Ismagilov, Ilia A. Guzei N N
Supporting information for: Crystallographic characterization of the geometry changes upon electron loss from 2-tertbutyl-3-aryl-2,3-diazabicyclo[2.2.2]octanes Stephen F. Nelsen, Asgeir E. Konradsson,
More informationoligomerization to polymerization of 1-hexene catalyzed by an NHC-zirconium complex
Mechanistic insights on the controlled switch from oligomerization to polymerization of 1-hexene catalyzed by an NHC-zirconium complex Emmanuelle Despagnet-Ayoub, *,a,b Michael K. Takase, c Lawrence M.
More informationSupporting Information
Electronic Supplementary Material (ESI) for Dalton Transactions. This journal is The Royal Society of Chemistry 2016 Supporting Information Over or under: Hydride attack at the metal versus the coordinated
More informationaddenda and errata [N,N 0 -Bis(4-bromobenzylidene)-2,2-dimethylpropane-j Corrigendum Reza Kia, a Hoong-Kun Fun a * and Hadi Kargar b
addenda and errata Acta Crystallographica Section E Structure Reports Online ISSN 1600-5368 [N,N 0 -Bis(4-bromobenzylidene)-2,2-dimethylpropane-j 2 N,N 0 ]iodidocopper(i). Corrigendum Reza Kia, a Hoong-Kun
More informationPhotoactive and physical properties of an azobenzene-containing coordination framework
10.1071/CH17215_AC CSIRO 2017 Australian Journal of Chemistry 2017, 70(11), 1171-1179 SUPPLEMENTARY MATERIAL Photoactive and physical properties of an azobenzene-containing coordination framework James
More informationSupporting Information. for
Supporting Information for "Inverse-Electron-Demand" Ligand Substitution in Palladium(0) Olefin Complexes Shannon S. Stahl,* Joseph L. Thorman, Namal de Silva, Ilia A. Guzei, and Robert W. Clark Department
More informationDepartment of Chemistry, Tianjin University, Tianjin , P. R. China Tel:
Electronic Supplementary Information Analysis of factors governing the formation of single-stranded helical coordination polymers from a macrocyclic metalloligand and Ca 2+, Mn 2+, Fe 2+, Co 2+, Ni 2+,
More informationRemote Asymmetric Induction in an Intramolecular Ionic Diels-Alder Reaction: Application to the Total Synthesis of (+)-Dihydrocompactin
Page S16 Remote Asymmetric Induction in an Intramolecular Ionic Diels-Alder Reaction: Application to the Total Synthesis of (+)-Dihydrocompactin Tarek Sammakia,* Deidre M. Johns, Ganghyeok Kim, and Martin
More informationFunctional Group Effects on Metal- Organic Framework Topology
Functional Group Effects on Metal- Organic Framework Topology Phuong V. Dau, Kristine K. Tanabe, and Seth M. Cohen* Department of Chemistry and Biochemistry, University of California, San Diego, La Jolla,
More information