Bridging Fashion Research Articles

Comparison of Bending Stiffness between String of Pearls Plate-Bone Substitute Constructs with and without Bending Tees in a Fracture Gap Model

Abstract Objective The aim of this study was to compare the bending properties of String of Pearls plate-bone substitute constructs with and without bending tees in the nodes over a simulated fracture gap. It is hypothesized that the constructs with tees will have higher bending stiffness. Study Design Acetal polymer tubes and 12-hole, 3.5-mm String of Pearls plates were used to create plate-bone substitute constructs simulating stabilization in a bridging fashion over a 45-mm gap. Twenty-four constructs were made with 12 containing tees in the nodes over the fracture gap. Single-cycle load-to-failure 4-point bending was performed in mediolateral and craniocaudal planes. Bending stiffness was compared with a t-test (p < 0.05). Results All plate-bone substitute constructs had a permanent loss of structural integrity via plastic deformation of the plate. The bending stiffness (mean ± standard deviation) of the craniocaudal group was 59.11 ± 1.98 N/mm with tees and 59.25 ± 1.69 N/mm without tees (p = 0.88). In the mediolateral group, the bending stiffness was 43.17 ± 0.75 N/mm with tees and 41.09 ± 0.91 N/mm without tees (p = 0.0042). Conclusion In 4-point bending, the plate-bone substitute constructs with tees had equivalent bending stiffness in the craniocaudal plane and increased bending stiffness in the mediolateral plane. However, with a small absolute difference in values, the clinical significance is unclear. Future studies for cyclic bending, torsional, and axial compression tests should be performed to further investigate the value of tees in the nodes over a comminuted or gap fracture repaired in a bridging fashion.

Catalytic Activity of Mono‐ and Bimetallic Rhodium(I) and Iridium(I) Complexes Bearing Carbon‐Ether‐Carbon (COC) Ligand for the Intramolecular Cyclization of 4‐Pentynoic Acid

AbstractThe catalytic performance of a series of mono‐ and bimetallic Ir(I) and Rh(I) complexes bearing the (COC) bis‐triazolylidene ligand, coordinated in a bridging or chelating fashion, was evaluated in the cyclization of 4‐pentynoic acid. The chelated mononuclear cationic complex [Ir(cod)(COC)]PF6 (cod=1,5‐cyclooctadiene; COC=biscarbene ether) displayed the highest reaction rate for 4‐pentynoic acid to form γ‐methyl‐ene‐γ‐butyrolactone (5‐methylenedihydrofuran‐2(3H)‐one). Density Functional Theory calculations were carried out to rationalize the reaction mechanism which proceeds in three steps, namely coordination of the alkyne to the active catalyst followed by intramolecular cyclization and final reductive elimination. Its catalytic performance was further assessed against different substituted 4‐pentynoic acid derivatives.

Spin Crossover Quenching by "Racemization" in a Family of trans-1,2-Di(tetrazol-1-yl)cyclopentane-Based Fe(II) 1D Coordination Polymers.

Optically pure (RR)- and racemic (RR/SS)-trans-1,2-di(tetrazol-1-yl)cyclopentane were synthesized and used to prepare homo- and heterochiral Fe(II) coordination compounds. [Fe((RR/SS)-C7H10N8)2(CH3CN)2](BF4)2 (1A), [Fe((RR/SS)-C7H10N8)2(C2H5CN)2](BF4)2 (2A), [Fe((RR)-C7H10N8)2(CH3CN)2](BF4)2·2CH3CN (1B·solv), and [Fe((RR)-C7H10N8)2(C2H5CN)2](BF4)2 (2B) form a family of one-dimensional coordination polymers. Fe(II) cations in these complexes are characterized by a heteroleptic coordination environment: the neighboring metal centers are bridged by two 1,2-di(tetrazol-1-yl)cyclopentane molecules, while the nitrile molecules (acetonitrile or propionitrile, respectively) occupy the axial positions. Independently of the kind of nitrile coligands, an ability to thermally induce spin crossover (SCO) is governed by chirality. 1B·solv and 2B exhibit abrupt and complete SCO occurring at T1/2 = 144 K and T1/2 = 228 K, respectively. Desolvated form, 1B (of the same stoichiometry as 2B), also exhibits SCO (T1/2 = 215 K). In contrast, an exchange within the polymeric chain of half of the RR molecules with the SS enantiomeric form results in formation of 1A and 2A, which remain in stable high-spin (HS) form down to 10 K. It has been shown that moving from a homochiral to a heterochiral system changes the structure of the polymeric unit (while maintaining the same polymer dimensionality and bridging fashion) that leads to the deep reorganization of the further coordination spheres, including the anion network.

Implementation of binarized neural networks immune to device variation and voltage drop employing resistive random access memory bridges and capacitive neurons

Resistive Random Access Memories (ReRAM) arrays provides a promising basement to deploy neural network accelerators based on near or in memory computing. However most popular accelerators rely on Ohm’s and Kirchhoff’s laws to achieve multiply and accumulate, and thus are prone to ReRAM variability and voltage drop in the memory array, and thus need sophisticated readout circuits. Here we propose a robust binary neural network, based on fully differential capacitive neurons and ReRAM synapses, used in a resistive bridge fashion. We fabricated a network layer with up to 23 inputs that we extrapolated to large numbers of inputs through simulation. Defining proper programming and reading conditions, we demonstrate the high resilience of this solution with a minimal accuracy drop, compared to a software baseline, on image classification tasks. Moreover, our solution can achieve a peak energy efficiency, comparable with the state of the art, when projected to a 22 nanometer technology.

Significant Control on Zero-field Quantum Tunneling of Magnetization in Dysprosium Based Single-Molecule Magnets via Orientation of the Anilato Ligand.

Tuning the bridging fashion of anilato ligand in dinuclear DyIII complexes, reveals a sizable effect on the slow relaxation of magnetization. Combined experimental and theoretical studies divulge that the geometry with high order axial symmetry (pseudo square antiprism) reduces the transverse crystal fields corresponding to QTM resulting in a significant increase in energy barrier (Ueff = 518 cm-1) through the Orbach relaxation process whereas the geometry with lower symmetry (triangular dodecahedron, pseudo D2d) enhances the transverse crystal fields that accelerate the ground state QTM process. Notably, the value 518 cm-1 represents the highest energy barrier among anilato ligand based SMMs.

Repair of a Comminuted Femur Fracture in a Komodo Dragon (Varanus komodoensis) Using a Double Plating Technique

This report describes double locking compression plate fixation of a moderately comminuted mid-diaphyseal right femur fracture in a Komodo dragon (Varanus komodoensis). The animal was restrained for a routine examination, during which the dragon struggled to escape restraint. When returned to the exhibit, the dragon did not use the right pelvic limb to walk. A right-sided, closed, mid-diaphyseal comminuted (type C3) femur fracture was diagnosed using palpation and radiographs, and the animal was transported to a specialty clinic within a few hours for fracture repair. Two locking compression plates (LCPs) were applied in bridging fashion for fracture repair. Radiographs performed at the four-month post-operative recheck revealed a healed fracture with significant callus formation and stable implants. The dragon was transitioned from cage rest in a restricted space to his normal large exhibit after healing was confirmed, no lameness was observed, and normal limb use was noted. After almost three years, he is still ambulating normally and without lameness. This is the first report of successful femur fracture stabilization using bone plate fixation in a Komodo dragon.

Oxidative addition of 8-bromo-9-ethyl-1,N6-ethenoadenine to d10 metals

The 8-bromoadenine derivative 8-bromo-9-ethyl-1,N6-ethenoadenine 3 was prepared from adenine in three steps. Treatment of 8-bromo-9-ethyl-1,N6-ethenoadenine 3 with the zero-valent metal precursors [M0(PPh3)4] (M = Pd, Pt) in the presence of NH4BF4 as proton source gave exclusively the compounds trans-[4]BF4 and trans-[5]BF4. The obtained complexes bear a modified C8-bound adenine derivative with a protonated endocyclic nitrogen atom N7. A stepwise reaction sequence consisting of an initial oxidative addition of the C8–Br bond of 3 to [Pt0(PPh3)4] followed by treatment with HBF4·Et2O as proton source led to the dinuclear complex [6]2+ after a reaction time of several days. This complex features two adenine-derived NHC ligands coordinating to two PtII ions in a µ-κC8:κN7 bridging fashion. Protonation of the NHC ligands occurred at the nitrogen atom N6 instead of N7 of the purine scaffold. The molecular structures of the three complexes were determined by X-ray diffraction studies.

Terminal N2 Dissociation in [(PNN)Fe(N2 )]2 (μ-N2 ) Leads to Local Spin-State Changes and Augmented Bridging N2 Activation.

Nitrogen fixation at iron centres is a fundamental catalytic step for N2 utilisation, relevant to biological (nitrogenase) and industrial (Haber-Bosch) processes. This step is coupled with important electronic structure changes which are currently poorly understood. We show here for the first time that terminal dinitrogen dissociation from iron complexes that coordinate N2 in a terminal and bridging fashion leaves the Fe-N2 -Fe unit intact but significantly enhances the degree of N2 activation (Δν≈180 cm-1 , Raman spectroscopy) through charge redistribution. The transformation proceeds with local spin state change at the iron centre (S= →S=3 /2 ). Further dissociation of the bridging N2 can be induced under thermolytic conditions, triggering a disproportionation reaction, from which the tetrahedral (PNN)2 Fe could be isolated. This work shows that dinitrogen activation can be induced in the absence of external chemical stimuli such as reducing agents or Lewis acids.

Variable hydrazine coordination modes from reactions with dichlorotris(triphenylphosphine)ruthenium(II)

The reactivity of the prominent ruthenium(II) catalyst and precursor, RuCl2(PPh3)3, was explored with hydrazine and its derivatives. The reactions produced 6-coordinate ruthenium(II) products that bond with the hydrazine moiety in bridging (NH2NH2 or NH2NHMe), end-on (NH2NHMe, NH2NHPh, or NH2NMe2), or side-on (NH2NMe2) fashions. The products have been characterized by single crystal X-ray diffraction and 31P NMR spectroscopy. With NH2NH2, the dimeric product, [RuCl2(PPh3)2]2(μ-N2H4)2, was formed under all conditions used. For other hydrazines, the reaction stoichiometry governed product formation to yield either bimetallic or monomeric products. When the RuCl2(PPh3)3 to hydrazine derivative ratio was 1:1 or lower, bimetallic complexes were formed while a 1:2 ratio produced monomeric compounds. The exception to the latter occurs with the production of the monomeric compound, RuCl2(PPh3)2(η2-NH2NMe2), that forms employing a 1:1 ratio. In addition to stoichiometry, steric factors and hydrogen bonding played a significant role in dictating the bonding mode of hydrazines. The bimetallic complexes were further reacted to yield the corresponding monomeric products, adopting the form RuCl2(PPh3)2(L)2 (L = NH2NHMe, NH2NHPh, or NH2NMe2). Reactions utilizing less than a 1:2 ratio of RuCl2(PPh3)3 to NH2NMe2 produced a mixture of products that appear to be in equilibrium. DFT calculations were performed to gain insight into the reaction energetics and molecular stability.

Dopamine Adsorption on Rutile TiO2(110): Geometry, Thermodynamics, and Core-Level Shifts from First Principles.

The modification of the rutile TiO2(110) surface with dopamine represents the best example of the functionalization of TiO2-based nanoparticles with catecholamines, which is of great interest for sunlight harvesting and drug delivery. However, there is little information on the dopamine–TiO2(110) adsorption complex in terms of thermodynamic properties and structural parameters such as bond coordination and orientation of the terminal ethyl–amino group. Here, we report a density functional theory (DFT) investigation of dopamine adsorption on the TiO2(110) surface using the optB86b-vdW functional with a Hubbard-type correction to the Ti 3d orbitals, where Ueff = 3 eV. Guided by available X-ray photoelectron spectroscopy (XPS) and near-edge X-ray absorption fine structure (NEXAFS) data, our simulations identify enolate species with bidentate coordination at a submonolayer coverage, which are bonded to two neighboring 5-fold-coordinated Ti atoms at the TiO2(110) surface through both deprotonated oxygen atoms of the dopamine, i.e., in a bridging fashion. The process is highly exothermic, involving an adsorption energy of −2.90 eV. Calculated structural parameters suggest that the molecule sits approximately upright on the surface with the amino group interacting with the π-like orbitals of the aromatic ring, leading to a gauche-like configuration. The resulting NH···π hydrogen bond in this configuration can be broken by overcoming an energy barrier of 0.22 eV; in this way, the amino group rotation leads to an anti-like conformation, making this terminal group able to bind to other biomolecules. This mechanism is endothermic by 0.07 eV. Comparison of existing spectroscopic data with DFT modeling shows that our computational setup can reproduce most experimentally determined parameters such as tilt angles from NEXAFS and chemical shifts in XPS, which allows us to identify the preferred mode of adsorption of dopamine on the TiO2(110) surface.

Dirhenium carbonyl compounds bearing cis-1,2-bis(diphenylphosphino)ethylene and cis-1,2-bis(diphenylphosphino)ethylene oxide ligands

Reaction of [Re2(CO)9(MeCN)] with cis-1,2-bis(diphenylphosphino)ethylene (cis-Ph2PCH=CHPPh2) in boiling benzene (80 °C) afforded two compounds, ax-[Re2(CO)9(κ1-cis-Ph2PCH=CHPPh2)] (1) and ax-[Re2(CO)9{κ1-cis-Ph2PCH=CHPh2P(O)}] (2) where the ligand is axially coordinated in a κ1 monodentate fashion through phosphorus. The close-bridged compound [Re2(CO)8(μ-κ2-cis-Ph2PCH=CHPPh2)] (3) was obtained from a similar reaction of the same ligand with [Re2(CO)8(NCMe)2] in refluxing benzene. In this case the diphosphine is equatorially coordinated to two Re atoms in a symmetrical bridging fashion. Compounds 1−3 have been characterized by IR, 1H NMR, 31P{1H} NMR spectroscopy and single crystal X-ray diffraction analyses.

Analysis of Solid-State Reaction Mechanisms with Two-Dimensional Fourier Transform Infrared Correlation Spectroscopy.

The utility of two-dimensional generalized correlation spectroscopy (2D-COS) for tracking complex solid-state reactions is demonstrated using infrared spectra acquired during a photochemically induced decomposition reaction. Eleven different thin films, consisting of six monometallic and five bimetallic 2-ethylhexanoate complexes, were tracked as a function of photolysis time. Overlapping peaks in the infrared fingerprint region are readily discriminated using 2D-COS, enabling individual vibrational components to be used to distinguish whether carboxylate ligands are free/ionic or bound in a chelating, bridging, or monodentate fashion. This classification enables the decomposition mechanism to be tracked for all 11 samples, revealing that ligands bound in monodentate and bridging fashions are first converted to chelates before being lost as volatile products for all samples. The magnitude of the measured first-order rate constants for loss of chelated ligands is found to correlate linearly to the asymmetric stretching frequency of monodentate ligands but exhibits a V shape when plotted against the electronegativity of the metal center. We propose that loss of chelated ligands proceeds via C-O scission for highly electronegative transition metals but M-O scission for transition metals with low electronegativity. These results establish 2D-COS as a powerful tool to deconvolute and correlate individual components, enabling mechanistic analysis of complex chemical reactions.

Internal Radioulnar Fixation for Treatment of Nonunion of Proximal Radius and Ulna Fractures in a Toy Breed Dog

AbstractIn this case report, we describe an alternative surgical procedure to treat proximal radius and ulnar nonunion in a toy breed dog. A 14-month-old, Maltese cross-breed dog was referred after previous treatment with external and internal fixation had failed, resulting in a nonunion of a fracture of the proximal radius and ulna with the proximal radius fragment too small and friable to be used for fixation. A craniomedial approach was made to debride the radius nonunion site and a second approach to the lateral aspect of the ulna was made. The fracture was realigned and a titanium locking plate was applied in bridging fashion, fixed to the proximal ulnar fragment with three locking screws in the most proximal plate holes, a fourth screw was inserted in the mid-shaft of the distal ulnar fragment and three locking screws were inserted in the distal most holes of the plate through the distal ulna to engage the distal radial fragment. A recombinant bone morphogenetic protein 2 graft was inserted into the radius and ulna fracture sites. The dog had a successful clinical and radiographic outcome with bridging of the defect 4 weeks postoperatively and complete callus formation 8 weeks postoperatively. Implants have undergone dynamization and then removal. Use of a locking plate as an internal fixator achieving fixation of the proximal ulna and distal radius can be considered an option for the treatment of proximal radioulnar nonunions with a small proximal radial fragment.

Catalytic conversion of alkynes to α-vinyl sulfides mediated by carbene-linker-carbene (CXC) rhodium and iridium complexes

The performance of a set of mono- and bimetallic Rh(i) and Ir(i) complexes bearing carbene-linker-carbene (CXC) bis-triazolylidene ligands (with X = O, N) coordinated in a bridging or chelating fashion was evaluated in the hydrothiolation of alkynes.

Evaluation of a Feline Bone Surrogate and In Vitro Mechanical Comparison of Small Interlocking Nail Systems in Mediolateral Bending.

The aim of this study was to (1) evaluate bending structural properties of a machined short fibre epoxy (SFE) feline bone surrogate (FBS), (2) compare the bending behaviour of small angle-stable interlocking nails (I-Loc; Targon) and locking compression plates (LCP) and (3) evaluate the effect of implant removal on FBS bending strength. Part 1: Feline cadaveric femurs (n = 10) and FBS (n = 4) underwent cyclic four-point bending and load to failure. Part 2: Fracture gap FBS constructs (n = 4/group) were stabilized in a bridging fashion with either I-Loc 3 and 4, Targon 2.5 and 3.0, LCP 2.0 and 2.4, then cyclically bent. Part 3: Intact FBS with pilot holes, simulating explantation, (n = 4/group) underwent destructive bending tests. Bending compliance, angular deformation and failure moment (FM) were statistically compared (p < 0.05). Native bone and FBS were similar for all outcome measures (p > 0.05). The smallest and largest bending compliance and angular deformation were seen in the I-Loc 4 and LCP 2.0 respectively (p < 0.05). While explanted Targon FBS had the lowest FM (p < 0.05), I-Loc and LCP constructs FM were not different (p > 0.05). The similar bending properties of short fibre epoxy made FBS and native feline femurs suggest that this model could be used for mechanical testing of implants designed for feline long bone osteosynthesis. The I-Loc constructs smaller angular deformation which also suggests that these implants represent a valid alternative to size-matched Targon and LCP for feline fracture osteosynthesis. The significantly lower FM of explanted Targon may increase the risk of secondary fracture following implant removal.

From solid state to in vitro anticancer activity of copper(II) compounds with electronically-modulated NNO Schiff base ligands.

The copper(ii) complexes of general formula [Cu(GL)(Cl)] (1-3, G = OMe, H and NO2, respectively), bearing tridentate Schiff base ligands (GL-) and a chloride as a fourth labile one, are here reported. The Schiff bases derive from the monocondensation of ethylenediamine and substituted salicylaldehyde, where the electronic properties are modulated by the releasing or withdrawing power of the G group. The compounds were structurally characterized through single crystal Synchrotron X-ray diffraction experiments in the solid state, revealing that 1 (OMe) and 2 (H) adopt a dimeric assembly [Cu(μ-Cl)(GL)]2 through apical interaction of the chloride ions of two monomeric units, while 3 embraces a 1D polymeric chain structure [Cu(μ-Cl)(NO2L)]n with a similar bridging fashion, all supported by extended intramolecular or intrachain hydrogen bonds. The redox properties of the complexes were also studied by cyclic voltammetry with no marked effect of the substituent on the potential of the CuII/CuI redox system. UV/Vis spectroscopic studies in mimicked physiological conditions highlighted the intactness and stability of the coordinated NNO tridentate ligand in 1-3 and the lability of the coordinated chloride ion with the formation of the aquo-complexes [Cu(GL)(H2O)]+ in aqueous solution, as confirmed by conductance measurements with a 1 : 1 electrolyte molar conductivity. In vitro tests on cell viability were conducted on malignant cell lines typical for their poor prognosis and curability, revealing time-dependent and differential cytotoxicity given by the substituent G. All compounds were capable of formation of intracellular reactive oxygen species and DNA intercalation, acting as nuclease and producing double-strand DNA breaks. This is especially effective for 3 (NO2), which revealed the highest anticancer activity against malignant triple-negative breast cancer MDA-MB-231 cells, with a two-to-four-fold cytotoxicity enhancement with respect to 1 (OMe) and 2 (H), and, most important, substantial differentiation of cytotoxicity with respect to healthy endothelial HUVEC cell line.

One pot synthesis of ZnO-CuO nanocomposites for catalytic peroxidase like activity and dye degradation

In this study, we report a low temperature chemical decomposition method for the synthesis of ZnO-CuO nanocomposites from ZnAl-layered double hydroxides (ZnAl-LDHs) supported copper terephthalate based metal organic frameworks [Cu-(BDC) MOFs]. The Cu-(BDC) MOFs arrays on the surface of ZnAl-LDHs nanosheets are obtained via in situ nucleation and directed growth from the terephthalate (BDC) anion intercalated ZnAl-LDHs. Cu(II) ion coordinates with BDC ligand in a bidentate bridging fashion to form Cu-(BDC) MOFs. The as prepared Cu-(BDC) MOFs are strongly and uniformly anchored onto the surfaces of ZnAl-LDHs. Decomposition of the resultant ZnAl-LDH supported Cu-(BDC) MOF precursor in alkaline solution for 24 h leads to the formation of ZnO-CuO nanocomposites. The structures and morphology of the nanocomposites are discussed with the results of scanning electron microscopy (SEM), transmission electron microscopy (TEM) combined with selected area electron diffraction (SAED) images, X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy and thermogravimetric analysis (TGA). The resulting ZnO-CuO nanocomposites show peroxidase like catalytic activity towards orthophenylene diamine oxidation (OPDox) and rhodamine 6 G (R6 G) dye degradation.

A new supramolecular isomer of p-aminobenzoate Zn(II) coordination polymer: Structure and photoluminescent property

A new supramolecular isomer of hydrated Zn(II) coordination polymer {[Zn(pABA)2(H2O)]·H2O}n (1) was prepared by a combination of multifunctional p-aminobenzoic acid (pABAH) with hydrated zinc tetrafluoroborate and then structurally compared with two previously known isomers IWORET and YIWDEO (refcodes in the Cambridge Structural Database). The new compound was characterized by FT-IR spectroscopy, thermogravimetric analysis, and single-crystal X-ray diffraction method. The crystallographic investigation shows that pABA anions bind the metal atoms in 1 and IWORET through the amine nitrogen and the carbonyl oxygen in a double-stranded bridge fashion giving rise a 1D coordination chain (1) and 2D layer (IWORET). In YIWDEO isomer, pABA− presents two different coordination modes (monodentate and bridging bidentate) extending the structure to 1D coordination polymer. The new solid reveals blue-violet and green photoluminescence, while IWORET crystals show violet emission upon excitation with ultraviolet light.

Safety and feasibility of radical surgery for giant desmoid in abdominal wall

To evaluate the safety and feasibility of radical surgery for giant desmoid in abdominal wall accompanied with the repair of giant myofascial defect using synthetic prosthesis. We analyzed the clinical and follow-up data of 31 patients with giant desmoid in abdominal wall undergoing radical resection and immediate abdominal wall reconstruction with synthetic prosthesis from January 2007 to January 2017 retrospectively. Patients were recruited at the Diagnostic and Therapeutic Center of Hernia and Abdominal Wall Diseases, the First Affiliated Hospital of Chinese PLA General Hospital and the Department of General Surgery, Chinese PLA General Hospital. Operative conditions, morbidity of complication, short- and long-term outcomes were summarized. All the patients underwent radical resection and infiltrated organs or tissues were simultaneously treated. Synthetic prosthesis was used to perform primary-intention reconstruction of giant myofascial defect in anterior or lateral abdominal wall. Bridging repair procedure for incisional hernia was used to perform double border fixation between prosthesis border and myofascial defect border. Placement and fixation of prosthesis followed the idea of "conformal repair", then prosthesis was finally repaired as arch in accordance with original abdominal wall. Of 31 patients, 28 cases were female with mean age of 35.2 (16-58) years and 3 were male with mean age of 42.6 (20-79) years. Six initial cases (19.4%) were diagnosed by preoperative biopsy, and 25 recurrent cases (60.6%) were diagnosed by medical history. The mean minimal diameter of tumors was 18.2 (14-25) cm, and the mean maximal diameter was 45.3 (32-53) cm. All 31 patients underwent radical resection and immediate abdominal wall reconstruction using synthetic prosthesis in bridging fashion successfully, and rapid pathological examination showed that all resection margins were negative. The average operative time was 335 (245-610) min, and the average intra-operative blood loss was 1260 (500-3500) ml. The size of abdominal wall defect after removal of desmoid ranged from 21 cm × 23 cm to 35 cm × 60 cm. The defects in 29 patients were repaired with compound synthetic prosthesis and the defects in 2 patients were repaired with compound prosthesis and polypropylene mesh. Four patients(12.9%) developed postoperative infection, in whom 3 patients had prosthesis infection during 1 month postoperatively, then 1 case recovered with conservative therapy, the other 2 cases were healed after the removal of infected prosthesis at 2 weeks and 3 months postoperatively, respectively; 1 patient had infection of artificial vessel prosthesis and received a second operation to remove the infected artificial vessel. The other 27 patients recovered smoothly and got primary intention wound healing. These 31 patients were followed up for a median of 60.5 (10-121) months with complete data. No marginal recurrence, incisional hernia, and abdominal wall bulge happened. One patient undergoing removal of all anterior and lateral abdominal wall had difficult defecation and urination during the first month after operation, and recovered through practising chest breathing. Ten patients developed fresh desmoids in other body positions postoperatively within 1-3 years, in whom 3 patients died of intestinal obstruction due to rapid neoplasm development and 7 patients survived with tumor receiving conservative therapy. All the 28 survival patients could restore normal life and workand have appropriate sports. Radical resection and immediate reconstruction of giant myofascial defect using synthetic prosthesis for patients with giant desmoid in abdominal wall is safe and effective.

Self‐Assembly of Discrete Copper(I)‐Halide Complexes with Diacylthioureas

Three diacylthioureas 1,4‐C6H4[C(O)NHC(S)NHAr]2 (Ar = 2,6‐iPr2C6H3) (L1, 1), 1,3‐C6H4[C(O)NHC(S)NHAr]2 (L2, 2), and 1,3‐C6H4[C(O)NHC(S)NHAr′]2 (Ar′ = 2,6‐Me2C6H3) (L3, 3) were synthesized and characterized. The CuI complexes from the reactions of bipodal ligands Ln with CuX (X = Cl, Br, I) were structurally investigated by single‐crystal X‐ray diffraction methods. Treatment of L1 with CuX gave the metallamacrocyclic complexes (L1CuX)2 [X = Cl (4), Br (5), I (6)] with the ligand to metal in a ratio of 2:2, where both sulfur and halide anions function as terminal substituents. In contrast, when L2 or L3 was reacted with CuBr, the two Ln ligands coordinate to four copper atoms each in a bridging and terminal fashion to yield [Ln(CuBr)2]2 [n = 2 (7), 3 (8)]. The obtained S4Cu4Br4 core contains all four bromide anions in bridging positions. The reaction of L3 with CuX (X = Cl, I) gave the 3:3 trinuclear complexes (L3CuX)3 [X = Cl (9) I (10)], interconnected by halide bridges. The obtained diacylthioureas (1–3) and their CuI complexes (4–10) were also characterized by elemental analysis, FT‐IR, 1H and 13C NMR spectroscopy.