2-[2-(2-Pyrid­yl)eth­yl]isoindolinium perchlorate

In the title salt, C15H17N2 +·ClO4 −, the isoindoline N atom is protonated and an intra­molecular N—H⋯N hydrogen bond occurs. In the crystal, N—H⋯O and numerous weak C—H⋯O inter­actions occur between the cation and anion. The O atoms of the perchlorate anion are disordered over four sets of sites with occupancies of 0.438 (4), 0.270 (9), 0.155 (8) and 0.138 (5)

Bis[μ-2-(2-pyridylmethyl­amino­meth­yl)phenolato]-κ4 N,N′,O:O;κ4 O:N,N′,O-bis­[(thio­cyanato-κN)copper(II)]

The centrosymmetric binuclear complex, [Cu2(C13H13N2O)2(NCS)2], formed via phenolate oxygen bridges, involves the CuII atoms in a distorted square-pyramidal coordination [τ = 0.197 (1)]. A Cu⋯Cu separation of 3.2281 (3) Å is observed. The in-plane Cu—Ophenolate distance [1.9342 (8) Å] is shorter than the axial distance [2.252 (8) Å]. The Cu—Namine and Cu—Npy distances are similar [2.0095 (10) and 2.0192 (10) Å, respectively]. The Cu—Nthio­cyanate distance [1.9678 (11) Å] is in the range found for Cu—N distances in previously determined structures containing coordinated thio­cyanate anions. There is an inter­molecular hydrogen bond between the amine H atom and the S atom of a coordinated thio­cyanate anion

[2,2′-(2,6,9,13-Tetra­azatetra­decane-1,14-di­yl)diphenolato]iron(III) iodide

The title FeIII complex, [Fe(C22H32N4O2)]I, contains a six-coordinate FeN4O2 cation in which the ligand is a reduced Schiff base resulting from the NaBH4 reduction of the condensation product between salicylaldehyde and 1,5,8,12-tetra­azadodecane. In spite of the increased flexibility of the saturated backbone of the ligand compared to the Schiff base from which it was synthesized, the complex adopts a cis-FeN4O2 conformation for the phenolic O-atom donors, which contrasts with the trans conformation adopted by the analogous ClO4 − salt [Yisgedu et al. (2009 ▶). J. Chem. Crystallogr. 39, 315–319]. In addition to extensive N—H⋯I hydrogen bonding between the amine H atoms and the anion there is a weak C—H⋯I inter­action

(m-Phenyl­enedimethyl­ene)diammonium p-nitro­phenyl­phosphate perchlorate

The title compound, C8H14N2 2+·C12H8N2O8P−·ClO4 −, was formed by the reaction of α,α-bis-m-xylenediamine and sodium bis-p-nitro­phenyl­phosphate in the presence of Zn(ClO4)·6H2O in methanol solution. The two amine groups of the m-xylenediammonium ion are each protonated and each hydrogen-bonded to two O atoms of the phosphate anion, which acts as a 1,3-bridge. The ammonium groups are arranged matched face to face and each pair is doubly bridged by two perchlorate ions through hydrogen bonding. In addition, there are also weak C—H⋯O inter­actions. Both the N—H⋯O and C—H⋯O inter­actions are contained in a channel down the a axis. The perchlorate oxygen atoms are disordered over two positions with site occupancy factors of ca 0.7 and 0.3

(Acetonitrile)[bis­(2-pyridylmeth­yl)amine]bis­(perchlorato)copper(II)

In the title compound, [Cu(ClO4)2(C12H13N3)(C2H3N)], the CuII atom is six-coordinate in a Jahn–Teller distorted octahedral geometry, with coordination by the tridentate chelating ligand, an acetonitrile mol­ecule, and two axial perchlorate anions. The tridentate ligand bis­(2-pyridylmeth­yl)amine chelates meridionally and equatorially while an acetonitrile mol­ecule is coordinated at the fourth equatorial site. The two perchlorate anions are disordered with site occupancy factors of 0.72/0.28. The amine H is involved in intra­molecular hydrogen bonding to the perchlorate O atoms and there are extensive but weak inter­molecular C—H⋯O inter­actions

Di-μ-perchlorato-bis­{μ-2-[(2-pyrid­yl)methyl­amino­meth­yl]phenolato)dicopper(II) acetonitrile disolvate

In the crystal of the dinuclear title compound, [Cu2(C13H13N2O)2(ClO4)2]·2CH3CN, the two bridging perchlorate ions chelate to the two CuII atoms in a μ-O:O′ fashion on opposite sides of the equatorial plane. The CuII ions display a distorted octa­hedral coordination geometry (in the usual 4 + 2 Jahn–Teller arrangement), each being coordinated by two O atoms from the two perchlorate ligands, and two N and O atoms from the reduced Schiff base ligand. The asymmetric unit contains two acetonitrile solvent mol­ecules. In the crystal structure, in addition to N—H⋯O hydrogen bonds, there are weak C—H⋯O inter­actions between the perchlorate O atoms and the reduced Schiff base ligand. C—H⋯N inter­actions are also present

[(6-Methyl-2-pyridylmeth­yl)(2-pyridylmeth­yl)amine][(2-pyridylmeth­yl)amine]copper(II) bis­(perchlorate)

The title compound, [Cu(C6H8N2)(C13H15N3)](ClO4)2, is a mixed ligand complex with the CuII atom coordinated by (6-methyl-2-pyridylmeth­yl)(2-pyridylmeth­yl)amine, acting as a tridentate ligand, and 2-(2-amino­meth­yl)pyridine, as a bidentate ligand, leading to an N5 square-pyramidal geometry. The amine H atoms are involved in hydrogen bonding to the perchlorate O atoms and there are extensive but weak inter­molecular C—H⋯O inter­actions in the crystal structure. The perchlorate ions are each disordered over two positions, with site occupancies of 0.601 (8):0.399 (8) and 0.659 (11):0.341 (11)

Redetermination of di-μ-hydrido-hexa­hydridotetra­kis(tetra­hydro­furan)dialuminium(III)magnesium(II)

The structure of the title compound, [Mg(AlH4)2(C4H8O)4], has been redetermined at 150 K. The MgII ion is hexa­coordinated to four tetra­hydro­furan (THF) ligands, and two AlH4 − anions through bridging H atoms. The Al—H distances are more precise compared to those previously determined [Nöth et al. (1995 ▶). Chem. Ber. 128, 999–1006; Fichtner & Fuhr (2002 ▶). J. Alloys Compd, 345, 386–396]. The mol­ecule has twofold rotation symmetry

High-capacity hydrogen release through hydrolysis of NaB3H8

NaB3H8 has advantages over NaBH4 and NH3BH3, two most widely studied chemical hydrides for hydrogen storage via hydrolysis. NaB3H8 has an extraordinary high solubility in water and thus possesses a high theoretical capacity of 10.5 wt% H via hydrolysis, in contrast to 7.5 wt% for NaBH4 and 5.1 wt% for NH3BH3. NaB3H8 is reasonably stable in water which makes it unnecessary to add corrosive NaOH as a stabilizer as the case for NaBH4. Furthermore, hydrolysis of NaB3H8 can be catalyzed by a Co-based catalyst with fast kinetics that is comparable to Ru-based catalysts. Therefore, cost-effective hydrolysis of NaB3H8 is possible for practical applications. A high capacity of 7.4 wt% H was achieved when water was included in the materials weight

Ammonium octahydrotriborate (NH4B3H8): new synthesis, structure, and hydrolytic hydrogen release

A metathesis reaction between unsolvated NaB3H8 and NH4Cl provides a simple and high-yield synthesis of NH4B3H8. Structure determination through X-ray single crystal diffraction analysis reveals weak N—Hδ+- - -Hδ-—B interaction in NH4B3H8 and strong N—Hδ+—Hδ-—B interaction in NH4B3H8·18-crown-6·THF adduct. Pyrolysis of NH4B3H8 leads to the formation of hydrogen gas with appreciable amounts of other volatile boranes below 160°C. Hydrolysis experiments show that upon addition of catalysts, NH4B3H8 releases up to 7.5 materials wt % hydrogen