Donor Class Research Articles

Applications of Organosilanes in Visible Light‐induced Catalytic Asymmetric Reactions

Over the past decades, visible light‐mediated photocatalysis has found a mainstream of applications in synthetic chemistry. Organosilanes have been proven to be a useful class of electron donors to generate the highly active radical species via photoinduced single electron transfer oxidation/fragmentation sequence, which may undergo follow‐up radical coupling or addition process. This minireview highlights the comprehensive advances of organosilanes in photoredox catalyzed asymmetric organic synthesis, with particular emphasis placed on reaction mechanisms. We hope that this review will inspire further design and development of new reactions with such class of readily accessible reagents.

DFT and electrochemical determination of Hg2+ and Pb2+ in water using polyaniline–quinoxaline composite modified GCE electrode

In this study, we designed and synthesized a new class of donor–acceptor conjugated polymers containing the polyaniline-quinoxaline [Acenaptho [1, 2 -b] quinoxalin-9-amine] (PAni-QUA) composite, and we subsequently utilized it as an electrochemical sensor to detect Hg2+ and Pb2+ ions with good selectivity and sensitivity. Energy dispersive X-ray analysis spectroscopy (EDAX), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), and UV–Vis spectroscopy (UV–Vis) were employed to analyze the structural and morphological characteristics of the resulting composite. The electrochemical characteristics of the electrode modifiers were analyzed using cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). Several sensitivity-influencing factors, including chemical and electrochemical parameters like pH and the impact of the supporting electrolyte medium, were also identified to improve the efficiency of the developed sensor. In the presence of different hazardous metal ion species, the interference ability of the proposed sensor was also examined. They were also used to conduct individual and simultaneous sensing studies of various metal ions in different supportive electrolyte media utilizing the differential pulse voltammetry technique (DPV). The PAni-QUA composite modified GCE sensor shows remarkable selectivity and sensitivity towards Hg2+ and Pb2+ ions over the other heavy metal ions in 1 to 20 µM ranges, respectively. The detection limits (3σ/m) were 1.28 nM and 5.91 nM for Hg2+ and Pb2+ ions. Density Functional Theory (DFT) was used in the present study to accomplish the adsorption mechanism of the suggested sensors. The DFT calculation demonstrated that the PAni-QUA composite was formed with a lower band gap energy than QUA and DD PAni. These results showed that the suggested sensor (PAni-QUA) had the lowest detection limit in the acetate buffer medium compared to the specified electrolyte media. Based on these findings, it is possible to use this technology to identify harmful metal ions (Hg2+ and Pb2+) with high sensitivity in real water samples.

Synthesis of sialyl halides with various acyl protective groups

Glycosyl halides are historically one of the first glycosyl donors used in glycosylation reactions, and interest in glycosylation reactions involving this class of glycosyl donors is currently increasing. New methods for their activation have been proposed and effective syntheses of oligosaccharides with their participation have been developed. At the same time, the possibilities of using these approaches to the synthesis of sialosides are restricted by the limited diversity of known sialyl halides (previously, mainly sialyl chlorides, less often sialyl bromides and sialyl fluorides, with acetyl (Ac) groups at the oxygen atoms and AcNH, Ac2N and N3 groups at C-5 were used). This work describes the synthesis of six new N-acetyl- and N-trifluoroacetyl-sialyl chlorides and bromides with O-chloroacetyl and O-trifluoroacetyl protective groups. Preparation of N,O-trifluoroacetyl protected derivatives was made possible due to development of the synthesis of sialic acid methyl ester pentaol with N-trifluoroacetyl group.

Exploring the Glycosylation Reaction Inside the Resorcin[4]arene Capsule.

In the past decade, there has been an increased interest in applying supramolecular capsule and cage catalysis to the current challenges in synthetic organic chemistry. In this context, we recently reported the resorcin[4]arene capsule-catalyzed conversion of α-glycosyl halides into β-glycosides with high selectivity. Interestingly, this methodology enabled the formation of a wide range of β-pyranosides as well as β-furanosides, although these two donor classes exhibit different reactivities and usually require different reaction conditions and catalysts. Evidence was provided that a proton wire plays a key role in this reaction by enabling dual activation of the glycosyl donor and acceptor. Here, we describe a detailed investigation of several aspects of this reactivity. Besides a mechanistic study, we elucidated the size limitation, the origin of catalytic turnover, and the electrophile scope of nonglycosylic halides. Moreover, a screening of the sensitivity to changes in the reaction conditions provides guidelines to facilitate reproducibility. Furthermore, we demonstrate the compatibility with environmentally benign solvent alternatives, including the renewable solvent limonene.

A New Class of Donor‐π‐Acceptor Phosphonium Salt Exhibiting Intriguing Thermally Activated Delayed Fluorescence

AbstractThermally activated delayed fluorescence (TADF) behaviors in metal halide perovskite and perovskite derivatives are rarely reported due to the absence of suitable TADF molecules that can serve as the A‐site cations. Herein, a series of novel donor‐π‐acceptor type of molecules are developed by adopting substituted phosphine and phosphonium as the electron donor and acceptor linked by the polarized π‐spacer. The prepared ((diphenylphosphaneyl)phenyl)diphenylphosphonium‐X (BzDPP‐X, X = counterions: Cl−, Br−, I−, NO3−, CH3COO− etc.) salts show bright emission in the visible range with TADF characteristics due to the strong intramolecular charge transfer (ICT). Benefiting from the spatially separated highest occupied molecular orbital and lowest unoccupied molecular orbital, small singlet‐triplet energy splitting (ΔEST) is obtained, facilitating the reverse intersystem crossing process. It turns out that the emission of BzDPP‐X is dependent on the counter anions, and the counterions help to stabilize the ICT state. Intriguingly, the emission can be tuned by integrating metal‐halide units into the above phosphonium salt. Remarkably, the zinc‐based halide exhibits a higher photoluminescence quantum yield (36.2%) than the pure benzyl(2‐(diphenylphosphaneyl)phenyl)diphenylphosphonium bromide (26.9%). This work exemplifies an easy design concept and a facile synthetic method toward ionic luminescent materials.

Multivariate regression modelling for gender prediction using volatile organic compounds from hand odor profiles via HS-SPME-GC-MS.

The efficacy of using human volatile organic compounds (VOCs) as a form of forensic evidence has been well demonstrated with canines for crime scene response, suspect identification, and location checking. Although the use of human scent evidence in the field is well established, the laboratory evaluation of human VOC profiles has been limited. This study used Headspace-Solid Phase Microextraction-Gas Chromatography-Mass Spectrometry (HS-SPME-GC-MS) to analyze human hand odor samples collected from 60 individuals (30 Females and 30 Males). The human volatiles collected from the palm surfaces of each subject were interpreted for classification and prediction of gender. The volatile organic compound (VOC) signatures from subjects' hand odor profiles were evaluated with supervised dimensional reduction techniques: Partial Least Squares-Discriminant Analysis (PLS-DA), Orthogonal-Projections to Latent Structures Discriminant Analysis (OPLS-DA), and Linear Discriminant Analysis (LDA). The PLS-DA 2D model demonstrated clustering amongst male and female subjects. The addition of a third component to the PLS-DA model revealed clustering and minimal separation of male and female subjects in the 3D PLS-DA model. The OPLS-DA model displayed discrimination and clustering amongst gender groups with leave one out cross validation (LOOCV) and 95% confidence regions surrounding clustered groups without overlap. The LDA had a 96.67% accuracy rate for female and male subjects. The culminating knowledge establishes a working model for the prediction of donor class characteristics using human scent hand odor profiles.

Polythiophene-based terpolymers with modulated aggregation behaviors for high-performance organic solar cells with 16.6% efficiency

Polythiophenes (PTs) are an attractive class of polymer donors (PDs) for organic solar cells (OSCs) owing to their relatively simple structures and scalable synthesis. Herein, a series of chlorinated thiazole-incorporated PT terpolymers are designed and high-performance OSCs with a power conversion efficiency (PCE) of 16.6% are demonstrated. By incorporating two different units, 3,3′-difluoro-2,2′-bithiophene (T2F2) and thieno[3,2-b]thiophene (TT), the aggregation properties of the terpolymers (PTz-FX; X = 0, 30, 50, 70, and 100, where X represents the mole percentage of T2F2 to total T2F2 +TT) are modulated. Among the PTz-FX series, PTz-F70 is found to be the optimal PD because its suitably tuned aggregation property leads to an optimized blend morphology with well-developed crystalline structures and donor–acceptor intermixed domains. The balanced morphology not only promotes charge generation/transport but also suppresses charge recombination in OSC devices. Thus, the PTz-F70-based OSCs achieve the highest PCE (16.6%), outperforming the OSCs based on PTz-FX with extremely strong (PTz-F100, PCE = 14.7%) or weak (PTz-F0, PCE = 12.0%) aggregation properties. The PCE of the PTz-F70-based OSCs is one of the highest performances among PT-based binary OSCs. This study highlights the importance of controlling the aggregation property of PTs for achieving high-performance PT-based OSCs.

Philanthropic Foundations and Transnational Activist Networks: Ford and the Inter-American Institute of Human Rights

AbstractFoundations provide key funds for nongovernmental organizations. We know little about what they do for transnational activism or the mechanisms via which they seek/achieve influence. We carve a middle ground between those who see donors as supporting actors in transnational advocacy networks (TANs) and those who think they distort activism through impersonal market forces. Our negotiation-oriented approach looks at the micro-dynamics of donor–grantee relations. We argue that influence is a function of donors’ organizational characteristics. Only some, especially foundations, have the vision/means to shape grantees. However, internal complexity can cause coordination problems, complicating influence. Additionally, if many donors exist, recipients’ leverage increases. It does so too if their expertise is in short supply. Using archival evidence, we reconstruct how Ford tried to shape the Inter-American Human Rights Institute, a pillar of the region's human rights regime, and the factors conditioning success. For Ford, the Institute could play a role in a fledging TAN, but only if it downplayed its emphasis on research and directly engaged activists. Coupled with analyses of USAID’s relationship with the Institute and Ford's relationship with Americas Watch, we shed light on the activities of an important class of donor and illuminate foundations’ role in the development of TANs.

Nonlinear optical properties of superalkali@teetotum boron clusters with potential applications on the electro-optic modulator

The development of nonlinear optics has revolutionized the photonic and optoelectronic fields in recent years.In this paper, we have designed a new class of donor–acceptor frameworks with enhanced nonlinear optical (NLO)properties using a series of superalkalis including Li3O, Li2NaO, LiNa2O, Li2KO, LiK2O as donors and three sizes of teetotum boron clusters (B14, B18, and B22) as acceptors. A systematic first-principles study has been performed on the electronic, linear, and NLO properties of superalkali@Bnassemblies. Besides the static non-linearity, the frequency-dependent electro-optic Pockel's effect (EOPE), second harmonic generation (SHG), and nonlinear refractive index have also been evaluated. In the case of dynamic NLO, the SHG process has a stronger NLO response than EOPE. At the typical experimental frequency of the Nd:YAG laser (ω = 0.04282) a.u., the SHG coefficients are about 2–3 times larger than the corresponding EOPE at this wavelength. Also, the nonlinear refractive index shows a remarkable response atω = 0.04 a.u. for LiK2O@B14.

Exquisite use of Selenoesters as Recyclable Acyl Donors for Lipases‐catalyzed Kinetic Resolution

AbstractLipase‐catalyzed enantioselective synthetic reactions employing enol esters, activated esters, anhydrides, and oximes as acyl donors is a well‐consolidated strategy towards enantiopure compounds. However, lipases can also cleave the C−S bond of thioesters, proving that other classes of substances can be used as acyl donors in lipase‐catalyzed transformations. Herein we describe the application of selenoesters as a new class of acyl donors in enzymatic kinetic resolution of chiral alcohols. A series of selenoesters was successfully employed in the resolution of chiral primary and secondary alcohols, demonstrating that lipases can also cleave the C−Se bond. Assays using selenoesters as acyl donors in lipase‐catalyzed reactions furnished enantiopure compounds (e.e.>99 %) and enantiomeric ratio (E>200). We also observed that the enzymatic reaction is accelerated in an oxygen atmosphere and performing a preparative scale reaction could demonstrate how simple and easy the purification process is to recover the diselenide formed during the resolution.

Intramolecular Thiol- and Selenol-Assisted Delivery of Hydrogen Sulfide.

Arylthioamides have been frequently employed to assess the chemical biology and pharmacology of hydrogen sulfide (H2 S). From this class of donors, however, extremely low H2 S releasing efficiencies have been reported and proper mechanistic studies have been omitted. Consequently, millimolar concentrations of arylthioamides are required to liberate just trace amounts of H2 S, and via an unidentified mechanistic pathway, which obfuscates the interpretation of any biological activity that stems from their use. Herein, we report that H2 S release from this valuable class of donors can be markedly enhanced through intramolecular nucleophilic assistance. Specifically, we demonstrate that both disulfide- and diselenide-linked thioamides are responsive to biologically relevant concentrations of glutathione and release two molar equivalents of H2 S via an intramolecular cyclization that significantly augments their rate and efficiency of sulfide delivery in both buffer and live human cells.

Intramolecular Thiol‐ and Selenol‐Assisted Delivery of Hydrogen Sulfide

AbstractArylthioamides have been frequently employed to assess the chemical biology and pharmacology of hydrogen sulfide (H2S). From this class of donors, however, extremely low H2S releasing efficiencies have been reported and proper mechanistic studies have been omitted. Consequently, millimolar concentrations of arylthioamides are required to liberate just trace amounts of H2S, and via an unidentified mechanistic pathway, which obfuscates the interpretation of any biological activity that stems from their use. Herein, we report that H2S release from this valuable class of donors can be markedly enhanced through intramolecular nucleophilic assistance. Specifically, we demonstrate that both disulfide‐ and diselenide‐linked thioamides are responsive to biologically relevant concentrations of glutathione and release two molar equivalents of H2S via an intramolecular cyclization that significantly augments their rate and efficiency of sulfide delivery in both buffer and live human cells.

Donor with HLA-C2 is associated with acute rejection following liver transplantation in Southern Chinese.

Apart from presenting peptides to T cells, class I HLA molecules serve as ligands for killer cell immunoglobulin-like receptor (KIRs) and regulate the response of natural killer (NK) cells. The role played by HLA and KIR in the acute rejection (AR) following liver transplantation has been controversial. In this retrospective study, we assessed the influence of class I HLA alleles, HLA matching between donor-recipient pairs, recipient KIR and donor HLA ligands on AR following liver transplantation in southern Chinese. In total, 143 recipients and 78 donors obtained from a single transplant center were included in the study cohort. Thirty-three recipients with histologically confirmed AR were observed. We found that the incidence of AR did not correlate with donor or recipient class I HLA alleles and HLA matching. Neither recipient KIR gene nor the KIR genotype was associated with AR, moreover, high-resolution genotyping of 14 functional KIR genes of recipients showed that no KIR allele was independently associated with AR. However, the frequency of HLA-C2+ donor significantly increased in AR group compared with NAR group (52.9% vs. 24.6%, p=0.03). In the presence of HLA-C2 by the donor allograft, AR was more frequently observed in recipients with normal expressed KIR2DS4 (43.8% vs. 15.0%, p=0.03). Donor with HLA-C2 is therefore a major determinant of AR, which can confer risk effect in liver transplantation. Our findings can provide valuable clues for better understanding pathogenesis of AR and have important clinical implications in liver transplantation for Chinese.

America’s dark harbingers: a genealogical analysis of self-disposing right-wing subjects during the pandemic

ABSTRACT This essay will review the emergence of the anti-public health practices of politically motivated individuals during the SARS-CoV-2 pandemic. Thousands of Americans, largely part of the far-right and libertarian front, have died due to their insistence on ‘freedom’ from the imposition of public health and vaccine mandates. In the abstract, I define these as self-disposing political subjects. The historical factors which compose such political characteristics are discursively rooted in the shifting economic interests of elite donor classes under neoliberal arrangements of society. This analysis will examine the emergence, pre-existing factors, and the contingencies out of which these practices have come about as an outcome of dominant power and neoliberal relations perfected through biopolitical and psychopolitical technologies. The target of this analysis will be to understand the multiple contingencies from which these self-destructive acts of political resistance come from, how they express neoliberalism in times of crisis and what we might expect as we face a future defined by climate crisis, and the receding waters of liberal democracy.

Recent Advances in Catalysis Involving Bidentate N-Heterocyclic Carbene Ligands.

Since the discovery of persistent carbenes by the isolation of 1,3-di-l-adamantylimidazol-2-ylidene by Arduengo and coworkers, we witnessed a fast growth in the design and applications of this class of ligands and their metal complexes. Modular synthesis and ease of electronic and steric adjustability made this class of sigma donors highly popular among chemists. While the nature of the metal-carbon bond in transition metal complexes bearing N-heterocyclic carbenes (NHCs) is predominantly considered to be neutral sigma or dative bonds, the strength of the bond is highly dependent on the energy match between the highest occupied molecular orbital (HOMO) of the NHC ligand and that of the metal ion. Because of their versatility, the coordination chemistry of NHC ligands with was explored with almost all transition metal ions. Other than the transition metals, NHCs are also capable of establishing a chemical bond with the main group elements. The advances in the catalytic applications of the NHC ligands linked with a second tether are discussed. For clarity, more frequently targeted catalytic reactions are considered first. Carbon–carbon coupling reactions, transfer hydrogenation of alkenes and carbonyl compounds, ketone hydrosilylation, and chiral catalysis are among highly popular reactions. Areas where the efficacy of the NHC based catalytic systems were explored to a lesser extent include CO2 reduction, C-H borylation, alkyl amination, and hydroamination reactions. Furthermore, the synthesis and applications of transition metal complexes are covered.

Closed-Loop Electrolyte Design for Lithium-Mediated Ammonia Synthesis.

Novel methods for producing ammonia, a large-scale industrial chemical, are necessary for reducing the environmental impact of its production. Lithium-mediated electrochemical nitrogen reduction is one attractive alternative method for producing ammonia. In this work, we experimentally tested several classes of proton donors for activity in the lithium-mediated approach. From these data, an interpretable data-driven classification model is constructed to distinguish between active and inactive proton donors; solvatochromic Kamlet–Taft parameters emerged to be the key descriptors for predicting nitrogen reduction activity. A deep learning model is trained to predict these parameters using experimental data from the literature. The combination of the classification and deep learning models provides a predictive mapping from proton donor structure to activity for nitrogen reduction. We demonstrate that the two-model approach is superior to a purely mechanistic or a data-driven approach in accuracy and experimental data efficiency.

Donor HLA Class 1 Evolutionary Divergence Is a Major Predictor of Liver Allograft Rejection : A Retrospective Cohort Study.

The HLA evolutionary divergence (HED), a continuous metric quantifying the peptidic differences between 2 homologous HLA alleles, reflects the breadth of the immunopeptidome presented to T lymphocytes. To assess the potential effect of donor or recipient HED on liver transplant rejection. Retrospective cohort study. Liver transplant units. 1154 adults and 113 children who had a liver transplant between 2004 and 2018. Liver biopsies were done 1, 2, 5, and 10 years after the transplant and in case of liver dysfunction. Donor-specific anti-HLA antibodies (DSAs) were measured in children at the time of biopsy. The HED was calculated using the physicochemical Grantham distance for class I (HLA-A or HLA-B) and class II (HLA-DRB1 or HLA-DQB1) alleles. The influence of HED on the incidence of liver lesions was analyzed through the inverse probability weighting approach based on covariate balancing, generalized propensity scores. In adults, class I HED of the donor was associated with acute rejection (hazard ratio [HR], 1.09 [95% CI, 1.03 to 1.16]), chronic rejection (HR, 1.20 [CI, 1.10 to 1.31]), and ductopenia of 50% or more (HR, 1.33 [CI, 1.09 to 1.62]) but not with other histologic lesions. In children, class I HED of the donor was also associated with acute rejection (HR, 1.16 [CI, 1.03 to 1.30]) independent of the presence of DSAs. There was no effect of either donor class II HED or recipient class I or class II HED on the incidence of liver lesions in adults and children. The DSAs were measured only in children. Class I HED of the donor predicts acute or chronic rejection of liver transplant. This novel and accessible prognostic marker could orientate donor selection and guide immunosuppression. Institut National de la Santé et de la Recherche Médicale.

The Chloroazaphosphatrane Motif for Halogen Bonding in Solution

Chloroazaphosphatranes, the corresponding halogenophosphonium cations of the Verkade superbases, were evaluated as a new motif for halogen bonding (XB). Their modulable synthesis allowed for synthetizing chloroazaphosphatranes with various substituents on the nitrogen atoms. The binding constants determined from NMR titration experiments for Cl-, Br-, I-, AcO-, and CN- anions are comparable to those obtained with conventional iodine-based monodentate XB receptors. Remarkably, the protonated azaphosphatrane counterparts display no affinity for anions under the same conditions. The strength of the XB interaction is, to some extent, related to the basicity of the corresponding Verkade superbase. The halogen bonding abilities of this new class of halogen donor motif were also revealed by the Δδ(31P) NMR shift observed in CD2Cl2 solution in the presence of triethylphosphine oxide (TEPO). Thus, chloroazaphosphatranes constitute a new class of halogen bond donors, expanding the repertory of XB motifs mainly based on CAr-I bonds.

Selective acetate recognition and sensing using SWCNTs functionalized with croconamides

Croconamides are a new class of dual-hydrogen bond donors that have attracted interest in anion recognition and sensing applications due to their strong H-bond donation capability. In this work, we report chemiresistive sensors for the detection of anions based on poly(4-vinylpyridine) (P4VP)-wrapped single-walled carbon nanotubes (SWCNTs) functionalized with croconamide-based selectors. Model structures of asymmetric N,N-substituted croconamide selectors with N,N-substitutional groups of alkyl cationic pyridinium and electron-withdrawing moieties such as aniline (6) and 3,5-bis(trifluoromethyl)phenyl (7) groups were synthesized and their binding affinities for various anions were characterized using UV–vis and 1H NMR titrations. Switchable binding of oxoanions was observed with selector 7, wherein HSO4– formed hydrogen bonding interactions and acetate (AcO–) induced deprotonation of the NH protons of the croconamide. Large sensitivity transitions were obtained toward AcO– for both P4VP-6-SWCNT (S = 95.68 ± 2.11 %) and P4VP-7-SWCNT (S = 140.91 ± 3.68 %) at 83.33 mM, which was attributed to deprotonation of the croconamide selectors upon addition of AcO–. Three serial sensors were assembled in a sensor array that rapid and selective screening of AcO– was demonstrated against other oxoanions such as HSO4– and H2PO4– in real-time.

Donor and Recipient HLA Class I Molecule Are Required for Maximum NK Cells Cytotoxicity Reconstitution Post Haploidentical Hematopoietic Stem Cells Transplantation

Background: Our previous report had demonstrated that haploidentical stem cells transplantation (Haplo-SCT) recipients presenting class I for donor inhibitory KIRs promote NK-cell licensing, leading to decreased relapse rates. Hsu and colleagues had showed that both cell intrinsic and -extrinsic HLA cooperate to maintain and adjust NK cell education.Aim: We hypothesis that donor and recipient HLA class I molecule are required for maximum human NK cells education post haplo-SCT.Methods: In this study, we compared the cytotoxicity of reconstituting NK cells against K562 cells derived in patients 30-90 days in the first cohort of 76 patients after haplo-SCT. We also addressed whether both of donor and recipient expression of class I ligands for donor inhibitory KIRs could predict lowest relapse rate occurrence in the second cohort of 291 myeloid hematological malignant disease patient.Results: A longitudinal analysis in the first cohort indicated that donor and recipient HLA class I molecules contribute to NK cell education in patients following haplo-SCT. We compared NK cells exhibiting KIR2DL1, KIR2DL2/KIR2DL3, or KIR3DL1 as their sole receptor, stratifying based on the presence or absence of their ligands in the haplo-SCT donor and/or recipient. HLA-Bw4 contributed by both the donor and the recipient promoted KIR3DL1+ NK cell responsiveness to K562 cells: the highest responsiveness occurred when HLA-Bw4 was available in both, and however lowest NK cells responsiveness occurred when the KIR ligand was absent in both. The educating ligands for KIR2DL1 (HLA-C2) and KIR2DL2 or KIR2DL3 (HLA-C1) contributed similarly to NK cell education: ligand present in both the donor and recipient was associated with the highest reactivity, and similar NK cell responsiveness occurred when the KIR ligand was present in either the donor or the recipient. Multivariate analysis demonstrated in the second haplo-SCT cohort setting, the higher relapse rate was observed when donor KIRs were not ligated by donor class I compared to those donor KIRs ligated by donor class I(HR, 95%CI, 2.406(0.996-5.811), P=0.051). If we considering the donor-host partnerships, the lowest relapse rate was observed when donor KIRs were ligated by both of donor and recipient class I (n =36, 5.74%±4.0% vs. 8.76%±4.5% vs. 18.98%±4.4%, P=0.069 for relapse) compared with where donor KIRs were ligated by donor or recipient class I (n = 158) or where donor KIRs were not ligated by donor and recipient class I (n = 97). Meanwhile, highest leukemia free survival was observed when donor KIRs were ligated by both of donor and recipient class I (n =36) compared with where donor KIRs were ligated by donor or recipient class I (n = 158, 85.8%±5.9% vs. 66.9%±3.9%, P=0.047) or where donor KIRs were not ligated by donor and recipient class I (n = 97, 85.8%±5.9% vs. 68.8%±5.0%, P=0.076).Conclusion: This study suggests that both of donor and recipient HLA class I molecule are required for maximum NK cells functional reconstitution post haplo-SCT. DisclosuresNo relevant conflicts of interest to declare.